214 results on '"Fyfe, Janet"'
Search Results
2. Seasonal Pattern of Mycobacterium ulcerans , the Causative Agent of Buruli Ulcer, in the Environment in Ghana
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Aboagye, Samuel Yaw, Ampah, Kobina Assan, Ross, Amanda, Asare, Prince, Otchere, Isaac Darko, Fyfe, Janet, and Yeboah-Manu, Dorothy
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- 2017
3. MYCOBACTERIUM PINNIPEDII TUBERCULOSIS IN A FREE-RANGING AUSTRALIAN FUR SEAL (ARCTOCEPHALUS PUSILLUS DORIFERUS) IN SOUTH AUSTRALIA
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Boardman, Wayne S. J., Shephard, Lisa, Bastian, Ivan, Globan, Maria, Fyfe, Janet A. M., Cousins, Debby V., Machado, Aaron, and Woolford, Lucy
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- 2014
4. Genetic diversity of Mycobacterium tuberculosis isolates obtained from patients with pulmonary tuberculosis in Beira city, Mozambique
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Saifodine, Abuchahama, Fyfe, Janet, Sievers, Aina, Coelho, Elizabeth, Azam, Khalide, and Black, James
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- 2014
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5. Statistical modeling based on structured surveys of Australian native possum excreta harboring Mycobacterium ulcerans predicts Buruli ulcer occurrence in humans.
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Vandelannoote, Koen, Buultjens, Andrew H., Porter, Jessica L., Velink, Anita, Wallace, John R., Blasdell, Kim R., Dunn, Michael, Boyd, Victoria, Fyfe, Janet A. M., Tay, Ee Laine, Johnson, Paul D. R., Windecker, Saras M., Golding, Nick, and Stinear, Timothy P.
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- 2023
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6. The performance of the Xpert MTB/RIF Version G4 in a low tuberculosis incidence setting
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Foley, David A., Phuong, Linny K., Globan, Maria, Fyfe, Janet M., Lavender, Caroline, and Williamson, Deborah A.
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- 2022
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7. Case clusters of leproid granulomas in foxhounds in New Zealand and Australia
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Smits, Bronwyn, Willis, Richard, Malik, Richard, Studdert, Virginia, Collins, Desmond M., Kawakami, Pamela, Graham, Duncan, and Fyfe, Janet A.
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- 2012
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8. Local adaptation in populations of Mycobacterium tuberculosis endemic to the Indian Ocean Rim [version 2; peer review: 3 approved]
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Menardo, Fabrizio, Rutaihwa, Liliana K, Zwyer, Michaela, Borrell, Sonia, Comas, Iñaki, Conceição, Emilyn Costa, Coscolla, Mireia, Cox, Helen, Joloba, Moses, Dou, Horng-Yunn, Feldmann, Julia, Fenner, Lukas, Fyfe, Janet, Gao, Qian, García de Viedma, Darío, Garcia-Basteiro, Alberto L, Gygli, Sebastian M, Hella, Jerry, Hiza, Hellen, Jugheli, Levan, Kamwela, Lujeko, Kato-Maeda, Midori, Liu, Qingyun, Ley, Serej D, Loiseau, Chloe, Mahasirimongkol, Surakameth, Malla, Bijaya, Palittapongarnpim, Prasit, Rakotosamimanana, Niaina, Rasolofo, Voahangy, Reinhard, Miriam, Reither, Klaus, Sasamalo, Mohamed, Silva Duarte, Rafael, Sola, Christophe, Suffys, Philip, Batista Lima, Karla Valeria, Yeboah-Manu, Dorothy, Beisel, Christian, Brites, Daniela, and Gagneux, Sebastien
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360 Social problems & social services ,lcsh:R ,lcsh:Medicine ,610 Medicine & health ,lcsh:Q ,lcsh:Science - Abstract
Background: Lineage 1 (L1) and 3 (L3) are two lineages of the Mycobacterium tuberculosis complex (MTBC) causing tuberculosis (TB) in humans. L1 and L3 are prevalent around the rim of the Indian Ocean, the region that accounts for most of the world's new TB cases. Despite their relevance for this region, L1 and L3 remain understudied. Methods: We analyzed 2,938 L1 and 2,030 L3 whole genome sequences originating from 69 countries. We reconstructed the evolutionary history of these two lineages and identified genes under positive selection. Results: We found a strongly asymmetric pattern of migration from South Asia toward neighboring regions, highlighting the historical role of South Asia in the dispersion of L1 and L3. Moreover, we found that several genes were under positive selection, including genes involved in virulence and resistance to antibiotics . For L1 we identified signatures of local adaptation at the esxH locus, a gene coding for a secreted effector that targets the human endosomal sorting complex, and is included in several vaccine candidates. Conclusions: Our study highlights the importance of genetic diversity in the MTBC, and sheds new light on two of the most important MTBC lineages affecting humans.
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- 2021
9. Feline cutaneous mycobacteriosis: a review of clinical, pathological and molecular characterization of one case of Mycobacterium microti skin infection and nine cases of feline leprosy syndrome from France and New Caledonia
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Laprie, Caroline, Duboy, Julie, Malik, Richard, and Fyfe, Janet
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- 2013
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10. Mycobacterium ulcerans in mosquitoes captured during outbreak of Buruli ulcer, Southeastern Australia
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Johnson, Paul D.R., Azoulas, Joseph, Lavender, Caroline J., Wishart, Elwyn, Stinear, Timothy P., Hayman, John A., Brown, Lynne, Jenkin, Grant A., and Fyfe, Janet A.M.
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Company legal issue ,Mosquitoes -- Physiological aspects ,Mosquitoes -- Genetic aspects ,Mosquitoes -- Testing ,Mycobacteria -- Health aspects ,Mycobacteria -- Physiological aspects ,Mycobacteria -- Genetic aspects ,Mycobacterium -- Health aspects ,Mycobacterium -- Physiological aspects ,Mycobacterium -- Genetic aspects ,Vector-borne diseases -- Physiological aspects ,Vector-borne diseases -- Genetic aspects ,Mycobacterial infections -- Development and progression ,Mycobacterial infections -- Causes of ,Epidemics -- Australia ,Epidemics -- Investigations ,Disease transmission -- Evaluation ,Skin -- Ulcers ,Skin -- Diagnosis ,Skin -- Causes of ,Skin -- Development and progression - Abstract
Buruli ulcer (BU) occurs in >30 countries. The causative organism, Mycobacterium ulcerans, is acquired from the environment, but the exact mode of transmission is unknown. We investigated an outbreak of [...]
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- 2007
11. Evolution of Mycobacterium ulcerans and other mycolactone-producing mycobacteria from a common Mycobacterium magnum progenitor
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Yip, Marcus J., Porter, Jessica L., Fyfe, Janet A.M., Lavender, Caroline J., Portaels, Francoise, Rhodes, Martha, Kator, Howard, Colorni, Angelo, Jenkin, Grant A., and Stinear, Tim
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Mycobacteria -- Genetic aspects ,Mycobacteria -- Research ,Mycobacterium -- Genetic aspects ,Mycobacterium -- Research ,Polyketides -- Production processes ,Polyketides -- Research ,Molecular evolution -- Research ,Biological sciences - Abstract
It had been assumed that production of the cytotoxie polyketide mycolactone was strictly associated with Mycobacterium ulcerans, the causative agent of Buruli ulcer. However, a recent study has uncovered a broader distribution of mycolactone-producing mycobacteria (MPM) that includes mycobacteria cultured from diseased fish and frogs in the United States and from diseased fish in the Red and Mediterranean Seas. All of these mycobacteria contain versions of the M. ulcerans pMUM plasmid, produce mycolactones, and show a high degree of genetic relatedness to both M. ulcerans and Mycobacterium marinum. Here, we show by multiple genetic methods, including multilocus sequence analysis and DNA-DNA hybridization, that all MPM have evolved from a common M. marinum progenitor to form a genetically cohesive group among a more diverse assemblage of M. marinum strains. Like M. ulcerans, the fish and frog MPM show multiple copies of the insertion sequence IS2404. Comparisons of pMUM and chromosomal gene sequences demonstrate that plasmid acquisition and the subsequent ability to produce mycolactone were probably the key drivers of speciation. Ongoing evolution among MPM has since produced at least two genetically distinct ecotypes that can be broadly divided into those typically causing disease in ectotherms (but also having a high zoonotic potential) and those causing disease in endotherms, such as humans.
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- 2007
12. Global phylogeny of Mycobacterium tuberculosis based on single nucleotide polymorphism (SNP) analysis: insights into tuberculosis evolution, phylogenetic accuracy of other DNA fingerprinting systems, and recommendations for a minimal standard SNP set
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Filliol, Ingrid, Motiwala, Alifiya S., Cavatore, Magali, Qi, Weihong, Hazbon, Manzour Hernando, del Valle, Miriam Bobadilla, Fyfe, Janet, Garcia-Garcia, Lourdes, Rastogi, Nalin, Sola, Christophe, Zozio, Thierry, Inirida Guerrero, Marta, Leon, Clara Ines, Crabtree, Jonathan, Angiuoli, Sam, Eisenach, Kathleen D., Durmaz, Riza, Joloba, Moses L., Rendon, Adrian, Sifuentes-Osornio, Jose, de Leon, Alfredo Ponce, Cave, M. Donald, Fleischmann, Robert, Whittam, Thomas S., and Alland, David
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Single nucleotide polymorphisms -- Research ,Mycobacterium tuberculosis -- Research ,Biological sciences - Abstract
We analyzed a global collection of Mycobacterium tuberculosis strains using 212 single nucleotide polymorphism (SNP) markers. SNP nucleotide diversity was high (average across all SNPs, 0.19), and 96% of the SNP locus pairs were in complete linkage disequilibrium. Cluster analyses identified six deeply branching, phylogenetically distinct SNP cluster groups (SCGs) and five subgroups. The SCGs were strongly associated with the geographical origin of the M. tuberculosis samples and the birthplace of the human hosts. The most ancestral cluster (SCG-1) predominated in patients from the Indian subcontinent, while SCG-1 and another ancestral cluster (SCG-2) predominated in patients from East Asia, suggesting that M. tuberculosis first arose in the Indian subcontinent and spread worldwide through East Asia. Restricted SCG diversity and the prevalence of less ancestral SCGs in indigenous populations in Uganda and Mexico suggested a more recent introduction of M. tuberculosis into these regions. The East African Indian and Beijing spoligotypes were concordant with SCG-1 and SCG-2, respectively; X and Central Asian spoligotypes were also associated with one SCG or subgroup combination. Other clades had less consistent associations with SCGs. Mycobacterial interspersed repetitive unit (MIRU) analysis provided less robust phylogenetic information, and only 6 of the 12 MIRU microsatellite loci were highly differentiated between SCGs as measured by [G.sub.ST]. Finally, an algorithm was devised to identify two minimal sets of either 45 or 6 SNPs that could be used in future investigations to enable global collaborations for studies on evolution, strain differentiation, and biological differences of M. tuberculosis.
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- 2006
13. The RpoH-mediated stress response in Neisseria gonorrhoeae is regulated at the level of activity
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Laskos, Lina, Ryan, Catherine S., Fyfe, Janet A.M., and Davies, John K.
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Neisseria gonorrhoeae -- Research ,Neisseria gonorrhoeae -- Genetic aspects ,Bacteriology -- Research ,Biological sciences - Abstract
The general stress response in Neisseria gonorrhoeae was investigated. Transcriptional analyses of the genes encoding the molecular chaperones DnaK, DnaJ, and GrpE suggested that they are transcribed from [[sigma].sup.32] (RpoH)-dependent promoters upon exposure to stress. This was confirmed by mutational analysis of the [[sigma].sup.32] promoter of dnaK. The gene encoding the gonococcal RpoH sigma factor appears to be essential, as we could not isolate viable mutants. Deletion of an unusually long rpoH leader sequence resulted in elevated levels of transcription, suggesting that this region is involved in negative regulation of RpoH expression during normal growth. Transcriptional analyses and protein studies determined that regulation of the RpoH-mediated stress response is different from that observed in most other species, in which regulation occurs predominantly at the transcriptional and translational levels. We suggest that an increase in the activity of preformed RpoH is primarily responsible for induction of the stress response in N. gonorrhoeae.
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- 2004
14. Ulcerated and nonulcerated nontuberculous cutaneous mycobacterial granulomas in cats and dogs
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Malik, Richard, Smits, Bronwyn, Reppas, George, Laprie, Caroline, O’Brien, Carolyn, and Fyfe, Janet
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- 2013
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15. On the origin of Mycobacterium ulcerans, the causative agent of Buruli ulcer
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Doig Kenneth D, Holt Kathryn E, Fyfe Janet AM, Lavender Caroline J, Eddyani Miriam, Portaels Françoise, Yeboah-Manu Dorothy, Pluschke Gerd, Seemann Torsten, and Stinear Timothy P
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Biotechnology ,TP248.13-248.65 ,Genetics ,QH426-470 - Abstract
Abstract Background Mycobacterium ulcerans is an unusual bacterial pathogen with elusive origins. While closely related to the aquatic dwelling M. marinum, M. ulcerans has evolved the ability to produce the immunosuppressive polyketide toxin mycolactone and cause the neglected tropical disease Buruli ulcer. Other mycolactone-producing mycobacteria (MPM) have been identified in fish and frogs and given distinct species designations (M. pseudoshottsii, M. shinshuense, M. liflandii and M. marinum), however the evolution of M. ulcerans and its relationship to other MPM has not been defined. Here we report the comparative analysis of whole genome sequences from 30 MPM and five M. marinum. Results A high-resolution phylogeny based on genome-wide single nucleotide polymorphisms (SNPs) showed that M. ulcerans and all other MPM represent a single clonal group that evolved from a common M. marinum progenitor. The emergence of the MPM was driven by the acquisition of the pMUM plasmid encoding genes for the biosynthesis of mycolactones. This change was accompanied by the loss of at least 185 genes, with a significant overrepresentation of genes associated with cell wall functions. Cell wall associated genes also showed evidence of substantial adaptive selection, suggesting cell wall remodeling has been critical for the survival of MPM. Fine-grain analysis of the MPM complex revealed at least three distinct lineages, one of which comprised a highly clonal group, responsible for Buruli ulcer in Africa and Australia. This indicates relatively recent transfer of M. ulcerans between these continents, which represent the vast majority of the global Buruli ulcer burden. Our data provide SNPs and gene sequences that can differentiate M. ulcerans lineages, suitable for use in the diagnosis and surveillance of Buruli ulcer. Conclusions M. ulcerans and all mycolactone-producing mycobacteria are specialized variants of a common Mycobacterium marinum progenitor that have adapted to live in restricted environments. Examination of genes lost or retained and now under selective pressure suggests these environments might be aerobic, and extracellular, where slow growth, production of an immune suppressor, cell wall remodeling, loss or modification of cell wall antigens, and biofilm-forming ability provide a survival advantage. These insights will guide our efforts to find the elusive reservoir(s) of M. ulcerans and to understand transmission of Buruli ulcer.
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- 2012
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16. Reduced Antigenicity of the Hepatitis B Virus HBsAg Protein Arising as a Consequence of Sequence Changes in the Overlapping Polymerase Gene That Are Selected by Lamivudine Therapy
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Torresi, Joseph, Earnest-Silveira, Linda, Deliyannis, Georgia, Edgtton, Kristy, Zhuang, Hui, Locarnini, Stephen A, Fyfe, Janet, Sozzi, Tina, and Jackson, David C
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- 2002
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17. Restoration of Replication Phenotype of Lamivudine-Resistant Hepatitis B Virus Mutants by Compensatory Changes in the “Fingers” Subdomain of the Viral Polymerase Selected as a Consequence of Mutations in the Overlapping S Gene
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Torresi, Joseph, Earnest-Silveira, Linda, Civitico, Gilda, Walters, Tomos E., Lewin, Sharon R., Fyfe, Janet, Locarnini, Stephen A., Manns, Michael, Trautwein, Christian, and Bock, Thomas C.
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- 2002
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18. Scottish Volunteers with Garibaldi
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Fyfe, Janet
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- 1978
19. Development and application of two multiplex real-time PCR assays for the detection of Mycobacterium ulcerans in clinical and environmental samples
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Fyfe, Janet A.M., Lavender, Caroline J., Globan, Maria, Sievers, Aina, Azuolas, Joseph, and Stinear, Tomothy P.
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Mycobacteria -- Genetic aspects ,Mycobacteria -- Environmental aspects ,Mycobacterium -- Genetic aspects ,Mycobacterium -- Environmental aspects ,Nucleotide sequence -- Analysis ,Biological sciences - Abstract
The development and application of two multiplex real-time PCR assays targeting three distinct repeated sequences in Mycobacterium ulcerans genome is presented. The assay improves the turnaround time for diagnosis and replaces conventional gel-based PCR as the routine method for laboratory confirmation of Mycobacterium ulcerans infection.
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- 2007
20. A New Phylogenetic Framework for the Animal-Adapted Mycobacterium tuberculosis Complex.
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Brites, Daniela, Loiseau, Chloé, Menardo, Fabrizio, Borrell, Sonia, Boniotti, Maria Beatrice, Warren, Robin, Dippenaar, Anzaan, Parsons, Sven David Charles, Beisel, Christian, Behr, Marcel A., Fyfe, Janet A., Coscolla, Mireia, and Gagneux, Sebastien
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Tuberculosis (TB) affects humans and other animals and is caused by bacteria from the Mycobacterium tuberculosis complex (MTBC). Previous studies have shown that there are at least nine members of the MTBC infecting animals other than humans; these have also been referred to as ecotypes. However, the ecology and the evolution of these animal-adapted MTBC ecotypes are poorly understood. Here we screened 12,886 publicly available MTBC genomes and newly sequenced 17 animal-adapted MTBC strains, gathering a total of 529 genomes of animal-adapted MTBC strains. Phylogenomic and comparative analyses confirm that the animal-adapted MTBC members are paraphyletic with some members more closely related to the human-adapted Mycobacterium africanum Lineage 6 than to other animal-adapted strains. Furthermore, we identified four main animal-adapted MTBC clades that might correspond to four main host shifts; two of these clades are hypothesized to reflect independent cattle domestication events. Contrary to what would be expected from an obligate pathogen, MTBC nucleotide diversity was not positively correlated with host phylogenetic distances, suggesting that host tropism in the animal-adapted MTBC seems to be driven by contact rates and demographic aspects of the host population rather by than host relatedness. By combining phylogenomics with ecological data, we propose an evolutionary scenario in which the ancestor of Lineage 6 and all animal-adapted MTBC ecotypes was a generalist pathogen that subsequently adapted to different host species. This study provides a new phylogenetic framework to better understand the evolution of the different ecotypes of the MTBC and guide future work aimed at elucidating the molecular mechanisms underlying host range. [ABSTRACT FROM AUTHOR]
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- 2018
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21. Epidemiology of Buruli Ulcer Infections, Victoria, Australia, 2011-2016.
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Loftus, Michael J., Ee Laine Tay, Globan, Maria, Lavender, Caroline J., Crouch, Simon R., Johnson, Paul D. R., Fyfe, Janet A. M., and Tay, Ee Laine
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MYCOBACTERIUM ,ULCERS ,ENDEMIC diseases ,BURULI ulcer - Abstract
Buruli ulcer (BU) is a destructive soft-tissue infection caused by the environmental pathogen Mycobacterium ulcerans. In response to rising BU notifications in the state of Victoria, Australia, we reviewed all cases that occurred during 2011-2016 to precisely map the time and likely place of M. ulcerans acquisition. We found that 600 cases of BU had been notified; just over half were in residents and the remainder in visitors to defined BU-endemic areas. During the study period, notifications increased almost 3-fold, from 66 in 2013 to 182 in 2016. We identified 4 BU-endemic areas: Bellarine Peninsula, Mornington Peninsula, Frankston region, and the southeastern Bayside suburbs of Melbourne. We observed a decline in cases on the Bellarine Peninsula but a progressive increase elsewhere. Acquisitions peaked in late summer. The appearance of new BU-endemic areas and the decline in established areas probably correlate with changes in the level of local environmental contamination with M. ulcerans. [ABSTRACT FROM AUTHOR]
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- 2018
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22. First case of Mycobacterium ulcerans disease (Bairnsdale or Buruli ulcer) acquired in New South Wales
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Lavender, Caroline J., Senanayake, Sanjaya N., Fyfe, Janet A.M., Buntine, John A., Globan, Maria, Stinear, Timothy P., Hayman, John A., and Johnson, Paul D.R.
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Mycobacteria -- Case studies ,Mycobacterium -- Case studies ,Health - Abstract
A molecular epidemiological investigation is conducted to study the case-histories of two patients with laboratory-confirmed Buruli or Bairnsdale ulcer (BU), caused by Mycobacterium ulcerans, who were infected in New South Wales (NSW) or overseas. The case studied is supposedly the first case of the disease acquired in NSW and hence makes the clinicians aware of the occurrence of the disease to ensure early diagnosis and treatment to minimize disability.
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- 2007
23. Consensus recommendations for the diagnosis, treatment and control of Mycobacterium ulcerans infection (Bairnsdale or Buruli ulcer) in Victoria, Australia
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Johnson, Paul D.R., Hayman, John A., Quek, Tricia Y., Fyfe, Janet A.M., Jenkin, Grant A., Buntine, John A., Athan, Eugene, Birrell, Mike, Graham, Justin, and Lavender, Caroline J.
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Mycobacteria -- Diagnosis ,Mycobacteria -- Risk factors ,Mycobacteria -- Care and treatment ,Mycobacterium -- Diagnosis ,Mycobacterium -- Risk factors ,Mycobacterium -- Care and treatment ,Health - Abstract
Various discussions are conducted in Victoria, Australia to develop and identify a consensus approach for the diagnosis, treatment and control of the skin and soft tissue infections, Bairnsdale or Buruli ulcer (BU), caused by Mycobacterium ulcerans. The results show that the local populations should be kept aware of the outbreaks to obtain an early diagnosis of the infection, as the use of the antibiotics might allow more conservative surgery.
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- 2007
24. The association of rainfall and Buruli ulcer in southeastern Australia.
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Yerramilli, Arvind, Tay, Ee Laine, Stewardson, Andrew J., Fyfe, Janet, O’Brien, Daniel P., and Johnson, Paul D. R.
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BURULI ulcer ,RAINFALL ,ENDEMIC diseases ,INFECTIOUS disease transmission ,GENETICS - Abstract
Background: Buruli ulcer has been increasing in incidence in southeastern Australia with unclear transmission mechanisms. We aimed to investigate the link between rainfall and case numbers in two endemic areas of the state of Victoria; the Bellarine and Mornington Peninsulas. Methodology: We created yearly and monthly graphs comparing rainfall with local Buruli ulcer incidence for the period 2004–2016 by endemic region and then considered a range of time lag intervals of 0–24 months to investigate patterns of correlation. Conclusions: Optimal positive correlation for the Bellarine Peninsula occurred with a 12-month prior rainfall lag, however, no significant correlation was observed on the Mornington Peninsula for any time lag. These results provide an update in evidence to further explore transmission mechanisms which may differ between these geographically proximate endemic regions. [ABSTRACT FROM AUTHOR]
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- 2018
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25. Analysis of a Novel pncA Mutation for Susceptibility to Pyrazinamide Therapy.
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Karmakar, Malancha, Globan, Maria, Fyfe, Janet A M, Stinear, Timothy P, Johnson, Paul D R, Holmes, Natasha E, Denholm, Justin T, and Ascher, David B
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- 2018
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26. The incubation period of Buruli ulcer (Mycobacterium ulcerans infection) in Victoria, Australia – Remains similar despite changing geographic distribution of disease.
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Loftus, Michael J., Trubiano, Jason A., Tay, Ee Laine, Lavender, Caroline J., Globan, Maria, Fyfe, Janet A. M., and Johnson, Paul D. R.
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BURULI ulcer ,MYCOBACTERIAL diseases ,BIOGEOGRAPHY ,DISEASE risk factors ,INFECTIOUS disease transmission - Abstract
Background: Buruli ulcer (BU) is a geographically-restricted infection caused by Mycobacterium ulcerans; contact with an endemic region is the primary risk factor for disease acquisition. Globally, efforts to estimate the incubation period of BU are often hindered as most patients reside permanently in endemic areas. However, in the south-eastern Australian state of Victoria, a significant proportion of people who acquire BU are visitors to endemic regions. During a sustained outbreak of BU on the Bellarine peninsula we estimated a mean incubation period of 4.5 months. Since then cases on the Bellarine peninsula have declined but a new endemic area has developed centred on the Mornington peninsula. Method: Retrospective review of 443 cases of BU notified in Victoria between 2013 and 2016. Telephone interviews were performed to identify all cases with a single visit to an endemic region, or multiple visits within a one month period. The incubation period was defined as the time between exposure to an endemic region and symptom onset. Data were subsequently combined with those from our earlier study incorporating cases from 2002 to 2012. Results: Among the 20 new cases identified in short-term visitors, the mean incubation period was 143 days (4.8 months), very similar to the previous estimate of 135 days (4.5 months). This was despite the predominant exposure location shifting from the Bellarine peninsula to the Mornington peninsula. We found no association between incubation period and age, sex, location of exposure, duration of exposure to an endemic region or location of BU lesion. Conclusions: Our study confirms the mean incubation period of BU in Victoria to be between 4 and 5 months. This knowledge can guide clinicians and suggests that the mode of transmission of BU is similar in different geographic regions in Victoria. [ABSTRACT FROM AUTHOR]
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- 2018
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27. Molecular epidemiology of tuberculosis in Tasmania and genomic characterisation of its first known multi-drug resistant case.
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Gautam, Sanjay S., Mac Aogáin, Micheál, Cooley, Louise A., Haug, Greg, Fyfe, Janet A., Globan, Maria, and O’Toole, Ronan F.
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TUBERCULOSIS treatment ,MOLECULAR epidemiology ,GENETICS of tuberculosis ,MYCOBACTERIUM tuberculosis ,MULTIDRUG resistance in bacteria - Abstract
Background: The origin and spread of tuberculosis (TB) in Tasmania and the types of strains of Mycobacterium tuberculosis complex (MTBC) present in the population are largely unknown. Objective: The aim of this study was to perform the first genomic analysis of MTBC isolates from Tasmania to better understand the epidemiology of TB in the state. Methods: Whole-genome sequencing was performed on cultured isolates of MTBC collected from 2014–2016. Single-locus variant analysis was applied to determine the phylogeny of the isolates and the presence of drug-resistance mutations. The genomic data were then cross-referenced against public health surveillance records on each of the cases. Results: We determined that 83.3% of TB cases in Tasmania from 2014–2016 occurred in non-Australian born individuals. Two possible TB clusters were identified based on single locus variant analysis, one from November-December 2014 (n = 2), with the second from May-August 2015 (n = 4). We report here the first known isolate of multi-drug resistant (MDR) M. tuberculosis in Tasmania from 2016 for which we established its drug resistance mutations and potential overseas origin. In addition, we characterised a case of M. bovis TB in a Tasmanian-born person who presented in 2014, approximately 40 years after the last confirmed case in the state’s bovids. Conclusions: TB in Tasmania is predominantly of overseas origin with genotypically-unique drug-susceptible isolates of M. tuberculosis. However, the state also exhibits features of TB that are observed in other jurisdictions, namely, the clustering of cases, and drug resistance. Early detection of TB and contact tracing, particularly of overseas-born cases, coordinated with rapid laboratory drug-susceptibility testing and molecular typing, will be essential for Tasmania to reach the World Health Organisation’s TB eradication goals for low-incidence settings. [ABSTRACT FROM AUTHOR]
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- 2018
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28. Mycobacterium ulcerans DNA in Bandicoot Excreta in Buruli Ulcer-Endemic Area, Northern Queensland, Australia.
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Röltgen, Katharina, Pluschke, Gerd, Johnson, Paul D. R., and Fyfe, Janet
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MYCOBACTERIUM ,BANDICOTA ,BURULI ulcer ,ENVIRONMENTAL sampling ,MARSUPIALS - Abstract
To identify potential reservoirs/vectors of Mycobacterium ulcerans in northern Queensland, Australia, we analyzed environmental samples collected from the Daintree River catchment area, to which Buruli ulcer is endemic, and adjacent coastal lowlands by species-specific PCR. We detected M. ulcerans DNA in soil, mosquitoes, and excreta of bandicoots, which are small terrestrial marsupials. [ABSTRACT FROM AUTHOR]
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- 2017
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29. SCOTTISH COLLECTIONS IN CANADIAN LIBRARIES
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Fyfe, Janet
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- 1965
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30. Feline leprosy due to Candidatus ‘Mycobacterium lepraefelis’: Further clinical and molecular characterisation of eight previously reported cases and an additional 30 cases.
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O’Brien, Carolyn R., Malik, Richard, Globan, Maria, Reppas, George, McCowan, Christina, and Fyfe, Janet A.
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Objectives: This paper, the last in a series of three on ‘feline leprosy’, provides a detailed description of disease referable to the previously unnamed species, Candidatus ‘Mycobacterium lepraefelis’, a close relative of the human pathogens Mycobacterium leprae and Mycobacterium lepromatosis. Methods: Cases were sourced retrospectively and prospectively for this observational study, describing clinical, geographical and molecular microbiological data for cats definitively diagnosed with Candidatus ‘M lepraefelis’ infection. Results: A total of 145 cases of feline leprosy were scrutinised; 114 ‘new’ cases were sourced from the Victorian Infectious Diseases Reference Laboratory (VIDRL) records, veterinary pathology laboratories or veterinarians, and 31 cases were derived from six published studies. Thirty-eight cats were definitively diagnosed with Candidatus ‘M lepraefelis’ infection. Typically, cats tended to be middle-aged or older when first infected, with a male predilection. Affected cats typically had widespread cutaneous lesions, in some cases after initially localised disease. Advanced cases were often systemically unwell. All cats had outdoor access. The histological picture was lepromatous in the majority of patients, although two cases had tuberculoid disease. In one case that underwent necropsy, lesions were evident in the liver, spleen and lungs. Treatment was varied, although most cats received a combination of oral clarithromycin and rifampicin. Prognosis for recovery was variable, but typically poor. Conclusions and relevance: Candidatus ‘M lepraefelis’ typically causes high bacterial index (lepromatous) feline leprosy that in some cases progresses to systemic mycobacteriosis. The disease has a variable clinical course and prognosis. Many cases either died or were euthanased due to the infection. Multilocus sequence analysis reveals a heterogeneous picture and further analysis of draft genome sequencing may give clues to the taxonomy and epidemiology of this organism. Prospective treatment trials and/or additional drug susceptibility testing in specialised systems would further inform treatment recommendations. Comparative aspects: This paper finishes with a discussion of comparative aspects of infection caused by the three feline leproid disease agents that have been the subject of this series: Candidatus ’Mycobacterium tarwinense’, Mycobacterium lepraemurium and Candidatus ‘M lepraefelis’. [ABSTRACT FROM AUTHOR]
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- 2017
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31. Feline leprosy due to Mycobacterium lepraemurium.
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O’Brien, Carolyn R., Malik, Richard, Globan, Maria, Reppas, George, McCowan, Christina, and Fyfe, Janet A.
- Abstract
Objectives: This paper, the second in a series of three on ‘feline leprosy’, provides a detailed description of disease referable to Mycobacterium lepraemurium, the most common cause of feline leprosy worldwide. Methods: Cases were sourced retrospectively and prospectively for this observational study, describing clinical, geographical and molecular microbiological data for cats definitively diagnosed with M lepraemurium infection. Results: A total of 145 cases of feline leprosy were scrutinised; 114 ‘new’ cases were sourced from the Victorian Infectious Diseases Reference Laboratory records, veterinary pathology laboratories or veterinarians, and 31 cases were derived from six published studies. Sixty-five cats were definitively diagnosed with M lepraemurium infection. Typically, cats were 1–3 years of age when first infected, with a male gender predilection. Affected cats were generally systemically well. All had outdoor access. Lesions tended to consist of one or more cutaneous/subcutaneous nodules, typically located on the head and/or forelimbs, possibly reflecting the most likely locations for a rodent bite as the site of inoculation for organisms. Nodules had the propensity to ulcerate at some stage in the clinical course. The cytological and histological picture varied from tuberculoid, with relatively low bacterial numbers, to lepromatous with moderate to high bacterial numbers. Treatment was varied, although most cats underwent surgical resection of lesions with adjunctive medical therapy, most often using a combination of oral clarithromycin and rifampicin. Prognosis for recovery was generally good, and in two cases there was spontaneous remission without the requirement for medical intervention. Untreated cats continued to enjoy an acceptable quality of life despite persistence of the disease, which extended locally but had no apparent tendency to disseminate to internal organs. Conclusions and relevance: M lepraemurium causes high bacterial index (lepromatous) or low bacterial index (tuberculoid) feline leprosy. The infection typically causes nodules of the skin and/or subcutis (which tend towards ulceration) on the head and/or forelimbs. The disease usually has an indolent clinical course and infected cats have a generally favourable response to therapeutic interventions, with rare cases undergoing spontaneous resolution. Genomic analysis may yield clues as to the environmental niche and culture requirements of this elusive organism. Prospective treatment trials and/or additional drug susceptibility testing in specialised systems would further inform treatment recommendations. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
32. Role of embB Codon 306 Mutations in Mycobacterium tuberculosis Revisited: a Novel Association with Broad Drug Resistance and IS6110 Clustering Rather than Ethambutol Resistance
- Author
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Hazbón, Manzour Hernando, Bobadilla del Valle, Miriam, Guerrero, Marta Inírida, Varma-Basil, Mandira, Filliol, Ingrid, Cavatore, Magali, Colangeli, Roberto, Safi, Hassan, Billman-Jacobe, Helen, Lavender, Caroline, Fyfe, Janet, García-García, Lourdes, Davidow, Amy, Brimacombe, Michael, León, Clara Inés, Porras, Tania, Bose, Mridula, Chaves, Fernando, Eisenach, Kathleen D., Sifuentes-Osornio, José, Ponce de León, Alfredo, Cave, M. Donald, and Alland, David
- Subjects
DNA, Bacterial ,Base Sequence ,Molecular Sequence Data ,Antitubercular Agents ,Microbial Sensitivity Tests ,Mycobacterium tuberculosis ,Mechanisms of Resistance ,Genes, Bacterial ,Multigene Family ,Drug Resistance, Bacterial ,Multivariate Analysis ,Mutation ,Cluster Analysis ,Ethambutol ,Phylogeny - Abstract
Mutations at position 306 of embB (embB306) have been proposed as a marker for ethambutol resistance in Mycobacterium tuberculosis; however, recent reports of embB306 mutations in ethambutol-susceptible isolates caused us to question the biological role of this mutation. We tested 1,020 clinical M. tuberculosis isolates with different drug susceptibility patterns and of different geographical origins for associations between embB306 mutations, drug resistance patterns, and major genetic group. One hundred isolates (10%) contained a mutation in embB306; however, only 55 of these mutants were ethambutol resistant. Mutations in embB306 could not be uniquely associated with any particular type of drug resistance and were found in all three major genetic groups. A striking association was observed between these mutations and resistance to any drug (P < 0.001), and the association between embB306 mutations and resistance to increasing numbers of drugs was highly significant (P < 0.001 for trend). We examined the association between embB306 mutations and IS6110 clustering (as a proxy for transmission) among all drug-resistant isolates. Mutations in embB306 were significantly associated with clustering by univariate analysis (odds ratio, 2.44; P = 0.004). In a multivariate model that also included mutations in katG315, katG463, gyrA95, and kasA269, only mutations in embB306 (odds ratio, 2.14; P = 0.008) and katG315 (odds ratio, 1.99; P = 0.015) were found to be independently associated with clustering. In conclusion, embB306 mutations do not cause classical ethambutol resistance but may predispose M. tuberculosis isolates to the development of resistance to increasing numbers of antibiotics and may increase the ability of drug-resistant isolates to be transmitted between subjects.
- Published
- 2005
33. Feline leprosy due to Candidatus ‘Mycobacterium tarwinense’.
- Author
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O’Brien, Carolyn R., Malik, Richard, Globan, Maria, Reppas, George, McCowan, Christina, and Fyfe, Janet A.
- Abstract
Objectives: This paper, the first in a series of three on ‘feline leprosy’, provides a detailed description of disease referable to Candidatus ‘Mycobacterium tarwinense’, the most common cause of feline leprosy in Victoria, Australia. Methods: Cases were sourced retrospectively and prospectively for this observational study, describing clinical, geographical and molecular microbiological data for cats definitively diagnosed with Candidatus ‘M tarwinense’ infection. Results: A total of 145 cases of feline leprosy were scrutinised; 114 ‘new’ cases were sourced from the Victorian Infectious Diseases Reference Laboratory records, veterinary pathology laboratories or veterinarians, and 31 cases were derived from six published studies. Forty-two cats were definitively diagnosed with Candidatus ‘M tarwinense’ infection. Typically, cats were between 3 and 11 years of age, with no gender predilection, and were generally systemically well. All had outdoor access. Most cats underwent surgical resection of lesions with adjunctive medical therapy, often utilising a combination of oral clarithromycin and rifampicin for at least 3 months. Prognosis for recovery was generally good. Resolution of lesions was not observed in the absence of treatment, but a number of untreated cats continued to enjoy an acceptable quality of life despite persistence of the disease, which extended locally but did not appear to disseminate to internal organs. Preliminary results of draft genome sequencing confirmed that the species is a member of the Mycobacterium simiae complex. Conclusions and relevance: Candidatus ‘M tarwinense’, a fastidious member of the M simiae complex, is capable of causing feline leprosy with a tendency to produce lesions on the head, particularly involving the eyes and periocular skin. The disease has an indolent clinical course and generally responds favourably to therapy despite lesions often containing large numbers of organisms. Detailed genomic analysis may yield clues as to the environmental niche and culture requirement of this elusive organism. Prospective treatment trials and/or drug susceptibility testing in specialised systems would further inform treatment recommendations. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
34. Localised Mycobacterium ulcerans infection in a cat in Australia
- Author
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Elsner, Lisa, Wayne, Julie, O'Brien, Carolyn R., McCowan, Christina, Malik, Richard, Hayman, John A., Globan, Maria, Lavender, Caroline J., and Fyfe, Janet A.
- Published
- 2008
- Full Text
- View/download PDF
35. A case of feline leprosy caused by Mycobacterium lepraemurium originating from the island of Kythira (Greece): diagnosis and treatment
- Author
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Courtin, Francois, Huerre, Michel, Fyfe, Janet, Dumas, Paul, and Boschiroli, Maria L.
- Published
- 2007
- Full Text
- View/download PDF
36. Mycobacterium Ulcerans Treatment – Can Antibiotic Duration Be Reduced in Selected Patients?
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Cowan, Raquel, Athan, Eugene, Friedman, N. Deborah, Hughes, Andrew J., McDonald, Anthony, Callan, Peter, Fyfe, Janet, and O'Brien, Daniel P.
- Subjects
BURULI ulcer ,ANTIBIOTICS ,MYCOBACTERIUM ,MYCOBACTERIAL diseases ,ENDEMIC diseases ,SURGICAL excision ,TREATMENT duration - Abstract
Introduction: Mycobacterium ulcerans (M. ulcerans) is a necrotizing skin infection endemic to the Bellarine Peninsula, Australia. Current treatment recommendations include 8 weeks of combination antibiotics, with adjuvant surgery if necessary. However, antibiotic toxicity often results in early treatment cessation and local experience suggests that shorter antibiotic courses may be effective with concurrent surgery. We report the outcomes of patients in the Barwon Health M. ulcerans cohort who received shorter courses of antibiotic therapy than 8 weeks. Methodology / Principal findings: A retrospective analysis was performed of all M. ulcerans infections treated at Barwon Health from March 1, 1998 to July 31, 2013. Sixty-two patients, with a median age of 65 years, received < 56 days of antibiotics and 51 (82%) of these patients underwent concurrent surgical excision. Most received a two-drug regimen of rifampicin combined with either ciprofloxacin or clarithromycin for a median 29 days (IQR 21–41days). Cessation rates were 55% for adverse events and 36% based on clinician decision. The overall success rate was 95% (98% with concurrent surgery; 82% with antibiotics alone) with a 50% success rate for those who received < 14 days of antibiotics increasing to 94% if they received 14–27 days and 100% for 28–55 days (p<0.01). A 100% success rate was seen for concurrent surgery and 14–27 days of antibiotics versus 67% for concurrent surgery and < 14 days of antibiotics (p = 0.12). No previously identified risk factors for treatment failure with surgery alone were associated with reduced treatment success rates with < 56 days of antibiotics. Conclusion: In selected patients, antibiotic treatment durations for M. ulcerans shorter than the current WHO recommended 8 weeks duration may be associated with successful outcomes. Author Summary: Buruli ulcer is a necrotizing skin and subcutaneous tissue infection caused by Mycobacterium ulcerans and is the third most common mycobacterial infection, behind tuberculosis and leprosy, world-wide. In recent years, the World Health Organisation has modified its guidelines for M. ulcerans treatment, moving from predominantly surgical to predominantly medical based management. It now recommends the combination of oral rifampicin and intramuscular streptomycin for a period of eight weeks as first-line therapy, with surgery as adjunctive therapy if necessary. The Barwon Health experience from south-eastern Australia has demonstrated that the entirely oral combination of rifampicin with either ciprofloxacin or clarithromycin for eight weeks can be an effective treatment option. However, these antibiotics are often toxic leading to early cessation, especially in the elderly. In addition, clinicians have been using a shorter duration of therapy for smaller lesions that have also been surgically managed. This study reviews our experience treating M. ulcerans with antibiotic durations of less than 8 weeks and demonstrates that successful outcomes can be achieved in selected patients, with success rates influenced by the duration of treatment and the use of surgical excision. This finding needs confirmation in further studies, but could have significant benefits in terms of reducing toxicity and improving adherence associated with Buruli ulcer antibiotic treatment. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
37. Direct Detection of Mycobacterium ulcerans in Clinical Specimens and Environmental Samples.
- Author
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Lavender, Caroline J. and Fyfe, Janet A. M.
- Published
- 2013
- Full Text
- View/download PDF
38. Multicenter External Quality Assessment Program for PCR Detection of Mycobacterium ulcerans in Clinical and Environmental Specimens.
- Author
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Eddyani, Miriam, Lavender, Caroline, de Rijk, Willem Bram, Bomans, Pieter, Fyfe, Janet, de Jong, Bouke, and Portaels, Françoise
- Subjects
MYCOBACTERIUM ,DETECTION of microorganisms ,POLYMERASE chain reaction ,DIAGNOSTIC specimens ,BURULI ulcer ,PERFORMANCE evaluation ,MEDICAL microbiology - Abstract
Background: Mycobacterium ulcerans is the causative agent of Buruli ulcer (BU), a necrotizing disease of the skin, soft tissue and bone. PCR is increasingly used in the diagnosis of BU and in research on the mode of transmission and environmental reservoir of M. ulcerans. Methodology/Principal Findings: The aim of this study was to evaluate the performance of laboratories in detecting M. ulcerans using molecular tests in clinical and environmental samples by implementing sequential multicenter external quality assessment (EQA) programs. The second round of the clinical EQA program revealed somewhat improved performance. Conclusions/Significance: Ongoing EQA programs remain essential and continued participation in future EQA programs by laboratories involved in the molecular testing of clinical and environmental samples for M. ulcerans for diagnostic and research purposes is strongly encouraged. Broad participation in such EQA programs also benefits the harmonization of quality in the BU research community and enhances the credibility of advances made in solving the transmission enigma of M. ulcerans. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
- View/download PDF
39. Potential Wildlife Sentinels for Monitoring the Endemic Spread of Human Buruli Ulcer in South-East Australia.
- Author
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Carson, Connor, Lavender, Caroline J., Handasyde, Kathrine A., O'Brien, Carolyn R., Hewitt, Nick, Johnson, Paul D. R., and Fyfe, Janet A. M.
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BURULI ulcer ,WILDLIFE monitoring ,HEALTH planning ,ENVIRONMENTAL sampling - Abstract
The last 20 years has seen a significant series of outbreaks of Buruli/Bairnsdale Ulcer (BU), caused by Mycobacterium ulcerans, in temperate south-eastern Australia (state of Victoria). Here, the prevailing view of M. ulcerans as an aquatic pathogen has been questioned by recent research identifying native wildlife as potential terrestrial reservoirs of infection; specifically, tree-dwelling common ringtail and brushtail possums. In that previous work, sampling of environmental possum faeces detected a high prevalence of M. ulcerans DNA in established endemic areas for human BU on the Bellarine Peninsula, compared with non-endemic areas. Here, we report research from an emergent BU focus recently identified on the Mornington Peninsula, confirming associations between human BU and the presence of the aetiological agent in possum faeces, detected by real-time PCR targeting M. ulcerans IS2404, IS2606 and KR. Mycobacterium ulcerans DNA was detected in 20/216 (9.3%) ground collected ringtail possum faecal samples and 4/6 (66.6%) brushtail possum faecal samples. The distribution of the PCR positive possum faecal samples and human BU cases was highly focal: there was a significant non-random cluster of 16 M. ulcerans positive possum faecal sample points detected by spatial scan statistics (P<0.0001) within a circle of radius 0.42 km, within which were located the addresses of 6/12 human cases reported from the area to date; moreover, the highest sample PCR signal strength (equivalent to ≥10
6 organisms per gram of faeces) was found in a sample point located within this cluster radius. Corresponding faecal samples collected from closely adjacent BU-free areas were predominantly negative. Possums may be useful sentinels to predict endemic spread of human BU in Victoria, for public health planning. Further research is needed to establish whether spatial associations represent evidence of direct or indirect transmission between possums and humans, and the mechanism by which this may occur. Author Summary: Mycobacterium ulcerans causes the disfiguring human skin disease Buruli ulcer (BU). The mechanism of transmission and reservoir for human infection remain unknown. In previous research, we reported the detection of M. ulcerans DNA in the faeces of possums (small tree-dwelling marsupials) in an area of South-East Australia (the Bellarine peninsula) where the largest recorded outbreak of human BU has been in progress for the last decade. The current study was carried out in a new outbreak area (the Mornington peninsula), and describes the detection of M. ulcerans DNA in possum faeces collected from the ground, in locations which correspond closely with the addresses of human BU cases. The association of new human BU cases with areas where M. ulcerans positive possum faeces are found contributes further evidence to the possible role of possums as an environmental reservoir of infection. Possums may be useful sentinel animals to monitor the spread of BU in Australia. [ABSTRACT FROM AUTHOR]- Published
- 2014
- Full Text
- View/download PDF
40. Clinical, Microbiological and Pathological Findings of Mycobacterium ulcerans Infection in Three Australian Possum Species.
- Author
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O'Brien, Carolyn R., Handasyde, Kathrine A., Hibble, Jennifer, Lavender, Caroline J., Legione, Alistair R., McCowan, Christina, Globan, Maria, Mitchell, Anthony T., McCracken, Helen E., Johnson, Paul D. R., and Fyfe, Janet A. M.
- Subjects
BURULI ulcer ,MYCOBACTERIAL diseases ,AUTOPSY ,SKIN ulcers ,SKIN diseases ,ENVIRONMENTAL sampling - Abstract
Background: Buruli ulcer (BU) is a skin disease caused by Mycobacterium ulcerans, with endemicity predominantly in sub-Saharan Africa and south-eastern Australia. The mode of transmission and the environmental reservoir(s) of the bacterium and remain elusive. Real-time PCR investigations have detected M. ulcerans DNA in a variety of Australian environmental samples, including the faeces of native possums with and without clinical evidence of infection. This report seeks to expand on previously published findings by the authors' investigative group with regards to clinical and subclinical disease in selected wild possum species in BU-endemic areas of Victoria, Australia. Methodology/Principal Findings: Twenty-seven clinical cases of M. ulcerans infection in free-ranging possums from southeastern Australia were identified retrospectively and prospectively between 1998–2011. Common ringtail possums (Pseudocheirus peregrinus), a common brushtail possum (Trichosurus vulpecula) and a mountain brushtail possum (Trichosurus cunninghami) were included in the clinically affected cohort. Most clinically apparent cases were adults with solitary or multiple ulcerative cutaneous lesions, generally confined to the face, limbs and/or tail. The disease was minor and self-limiting in the case of both Trichosurus spp. possums. In contrast, many of the common ringtail possums had cutaneous disease involving disparate anatomical sites, and in four cases there was evidence of systemic disease at post mortem examination. Where tested using real-time PCR targeted at IS2404, animals typically had significant levels of M. ulcerans DNA throughout the gut and/or faeces. A further 12 possums without cutaneous lesions were found to have PCR-positive gut contents and/or faeces (subclinical cases), and in one of these the organism was cultured from liver tissue. Comparisons were made between clinically and subclinically affected possums, and 61 PCR-negative, non-affected individuals, with regards to disease category and the categorical variables of species (common ringtail possums v others) and sex. Animals with clinical lesions were significantly more likely to be male common ringtail possums. Conclusions/Significance: There is significant disease burden in common ringtail possums (especially males) in some areas of Victoria endemic for M. ulcerans disease. The natural history of the disease generally remains unknown, however it appears that some mildly affected common brushtail and mountain brushtail possums can spontaneously overcome the infection, whereas some severely affected animals, especially common ringtail possums, may become systemically, and potentially fatally affected. Subclinical gut carriage of M. ulcerans DNA in possums is quite common and in some common brushtail and mountain brushtail possums this is transient. Further work is required to determine whether M. ulcerans infection poses a potential threat to possum populations, and whether these animals are acting as environmental reservoirs in certain geographical areas. Author Summary: Mycobacterium ulcerans causes skin disease predominantly in sub-Saharan Africa and southeastern Australia. The mode of transmission and the environmental reservoir(s) of the bacterium are unknown. Investigations have detected M. ulcerans DNA in a variety of Australian environmental samples, including the faeces of native possums. This report expands on these studies by detailing the clinical, pathological and microbiological findings in affected wild possum species in endemic areas. Twenty-seven clinically and 12 subclinically affected individuals were identified. Most clinical cases were adults with skin ulcers of the face, limbs and/or tail. The disease was mild and self-limiting in both Trichosurus spp. possums. In contrast, many of the common ringtail possums had multiple skin ulcers and in some there was evidence of internal disease. There were also significant levels of M. ulcerans DNA throughout the gut. Comparisons were made with regards to disease category, species and sex; with clinical cases more likely to be male common ringtail possums. Asymptomatic gut carriage of M. ulcerans DNA is quite common and may be transient in some individuals. Further work is needed to determine whether M. ulcerans infection poses a potential threat to possum populations, and whether these animals are acting as reservoirs in some areas. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
- View/download PDF
41. Clinical, Microbiological and Pathological Findings of Mycobacterium ulcerans Infection in Three Australian Possum Species.
- Author
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O'Brien, Carolyn R., Handasyde, Kathrine A., Hibble, Jennifer, Lavender, Caroline J., Legione, Alistair R., McCowan, Christina, Globan, Maria, Mitchell, Anthony T., McCracken, Helen E., Johnson, Paul D. R., and Fyfe, Janet A. M.
- Subjects
CACOMISTLE ,BRUSH-tailed possums ,NUCLEIC acids ,DEOXYRIBOSE ,TRICHOSURUS vulpecula ,MYCOBACTERIUM ,PHALANGERIDAE ,GENES - Abstract
Background: Buruli ulcer (BU) is a skin disease caused by Mycobacterium ulcerans, with endemicity predominantly in sub-Saharan Africa and south-eastern Australia. The mode of transmission and the environmental reservoir(s) of the bacterium and remain elusive. Real-time PCR investigations have detected M. ulcerans DNA in a variety of Australian environmental samples, including the faeces of native possums with and without clinical evidence of infection. This report seeks to expand on previously published findings by the authors' investigative group with regards to clinical and subclinical disease in selected wild possum species in BU-endemic areas of Victoria, Australia. Methodology/Principal Findings: Twenty-seven clinical cases of M. ulcerans infection in free-ranging possums from southeastern Australia were identified retrospectively and prospectively between 1998–2011. Common ringtail possums (Pseudocheirus peregrinus), a common brushtail possum (Trichosurus vulpecula) and a mountain brushtail possum (Trichosurus cunninghami) were included in the clinically affected cohort. Most clinically apparent cases were adults with solitary or multiple ulcerative cutaneous lesions, generally confined to the face, limbs and/or tail. The disease was minor and self-limiting in the case of both Trichosurus spp. possums. In contrast, many of the common ringtail possums had cutaneous disease involving disparate anatomical sites, and in four cases there was evidence of systemic disease at post mortem examination. Where tested using real-time PCR targeted at IS2404, animals typically had significant levels of M. ulcerans DNA throughout the gut and/or faeces. A further 12 possums without cutaneous lesions were found to have PCR-positive gut contents and/or faeces (subclinical cases), and in one of these the organism was cultured from liver tissue. Comparisons were made between clinically and subclinically affected possums, and 61 PCR-negative, non-affected individuals, with regards to disease category and the categorical variables of species (common ringtail possums v others) and sex. Animals with clinical lesions were significantly more likely to be male common ringtail possums. Conclusions/Significance: There is significant disease burden in common ringtail possums (especially males) in some areas of Victoria endemic for M. ulcerans disease. The natural history of the disease generally remains unknown, however it appears that some mildly affected common brushtail and mountain brushtail possums can spontaneously overcome the infection, whereas some severely affected animals, especially common ringtail possums, may become systemically, and potentially fatally affected. Subclinical gut carriage of M. ulcerans DNA in possums is quite common and in some common brushtail and mountain brushtail possums this is transient. Further work is required to determine whether M. ulcerans infection poses a potential threat to possum populations, and whether these animals are acting as environmental reservoirs in certain geographical areas. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
- View/download PDF
42. The Incubation Period of Buruli Ulcer (Mycobacterium ulcerans Infection).
- Author
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Trubiano, Jason A., Lavender, Caroline J., Fyfe, Janet A. M., Bittmann, Simone, and Johnson, Paul D. R.
- Subjects
BURULI ulcer ,MYCOBACTERIAL diseases ,SKIN infections ,TELEPHONE interviewing ,MEDICAL history taking ,MYCOBACTERIUM - Abstract
Introduction: Buruli Ulcer (BU) is caused by the environmental microbe Mycobacterium ulcerans. Despite unclear transmission, contact with a BU endemic region is the key known risk factor. In Victoria, Australia, where endemic areas have been carefully mapped, we aimed to estimate the Incubation Period (IP) of BU by interviewing patients who reported defined periods of contact with an endemic area prior to BU diagnosis. Method: A retrospective review was undertaken of 408 notifications of BU in Victoria from 2002 to 2012. Telephone interviews using a structured questionnaire and review of notification records were performed. Patients with a single visit exposure to a defined endemic area were included and the period from exposure to disease onset determined (IP). Results: We identified 111 of 408 notified patients (27%) who had a residential address outside a known endemic area, of whom 23 (6%) reported a single visit exposure within the previous 24 months. The median age of included patients was 30 years (range: 6 to 73) and 65% were male. 61% had visited the Bellarine Peninsula, currently the most active endemic area. The median time from symptom onset to diagnosis was 71 days (range: 34–204 days). The midpoint of the reported IP range was utilized to calculate a point estimate of the IP for each case. Subsequently, the mean IP for the cohort was calculated at 135 days (IQR: 109–160; CI 95%: 113.9–156), corresponding to 4.5 months or 19.2 weeks. The shortest IP recorded was 32 days and longest 264 days (Figure 1 & 2). IP did not vary for variables investigated. Conclusions: The estimated mean IP of BU in Victoria is 135 days (IQR: 109–160 days), 4.5 months. The shortest recorded was IP 34 days and longest 264 days. A greater understanding of BU IP will aid clinical risk assessment and future research. Author Summary: Buruli Ulcer (BU) is a necrotizing skin infection caused by the environmental organism Mycobacterium ulcerans. Despite an unknown mode of transmission, contact with a BU endemic region is the known key risk factor. In Victoria, Australia, endemic areas have been carefully mapped and patients are known to report single visits or defined exposures to these areas. From a retrospective review, we identified 23 patients with a single visit exposure to BU endemic regions from a total of 408 notifications of BU in Victoria (2002–2012). We were able to estimate the time from exposure to disease onset, incubation period (IP), via notification record review and telephone questionnaire. The IP of the cohort was subsequently estimated at 4.5 months (Range 1–9 months). An understanding of the IP of BU will be of value to communities, clinicians and government health bodies via aiding clinical risk assessment, epidemiological studies and public health investigations in the future. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
43. The Incubation Period of Buruli Ulcer (Mycobacterium ulcerans Infection).
- Author
-
Trubiano, Jason A., Lavender, Caroline J., Fyfe, Janet A. M., Bittmann, Simone, and Johnson, Paul D. R.
- Subjects
BURULI ulcer ,PATIENTS ,TELEPHONE interviewing ,MYCOBACTERIUM ,HEALTH risk assessment ,HEALTH surveys - Abstract
Introduction: Buruli Ulcer (BU) is caused by the environmental microbe Mycobacterium ulcerans. Despite unclear transmission, contact with a BU endemic region is the key known risk factor. In Victoria, Australia, where endemic areas have been carefully mapped, we aimed to estimate the Incubation Period (IP) of BU by interviewing patients who reported defined periods of contact with an endemic area prior to BU diagnosis. Method: A retrospective review was undertaken of 408 notifications of BU in Victoria from 2002 to 2012. Telephone interviews using a structured questionnaire and review of notification records were performed. Patients with a single visit exposure to a defined endemic area were included and the period from exposure to disease onset determined (IP). Results: We identified 111 of 408 notified patients (27%) who had a residential address outside a known endemic area, of whom 23 (6%) reported a single visit exposure within the previous 24 months. The median age of included patients was 30 years (range: 6 to 73) and 65% were male. 61% had visited the Bellarine Peninsula, currently the most active endemic area. The median time from symptom onset to diagnosis was 71 days (range: 34–204 days). The midpoint of the reported IP range was utilized to calculate a point estimate of the IP for each case. Subsequently, the mean IP for the cohort was calculated at 135 days (IQR: 109–160; CI 95%: 113.9–156), corresponding to 4.5 months or 19.2 weeks. The shortest IP recorded was 32 days and longest 264 days (Figure 1 & 2). IP did not vary for variables investigated. Conclusions: The estimated mean IP of BU in Victoria is 135 days (IQR: 109–160 days), 4.5 months. The shortest recorded was IP 34 days and longest 264 days. A greater understanding of BU IP will aid clinical risk assessment and future research. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
44. Climate and Landscape Factors Associated with Buruli Ulcer Incidence in Victoria, Australia.
- Author
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Ravensway, Jenni van, Benbow, M. Eric, Tsonis, Anastasios A., Pierce, Steven J., Campbell, Lindsay P., Fyfe, Janet A. M., Hayman, John A., Johnson, Paul D. R., Wallace, John R., and Qi, Jiaguo
- Subjects
BURULI ulcer ,MYCOBACTERIUM ,SKIN diseases ,CLIMATOLOGY ,INFECTIOUS disease transmission - Abstract
Background: Buruli ulcer (BU), caused by Mycobacterium ulcerans (M. ulcerans), is a necrotizing skin disease found in more than 30 countries worldwide. BU incidence is highest in West Africa; however, cases have substantially increased in coastal regions of southern Australia over the past 30 years. Although the mode of transmission remains uncertain, the spatial pattern of BU emergence in recent years seems to suggest that there is an environmental niche for M. ulcerans and BU prevalence. Methodology/Principal Findings: Network analysis was applied to BU cases in Victoria, Australia, from 1981-2008. Results revealed a non-random spatio-temporal pattern at the regional scale as well as a stable and efficient BU disease network, indicating that deterministic factors influence the occurrence of this disease. Monthly BU incidence reported by locality was analyzed with landscape and climate data using a multilevel Poisson regression approach. The results suggest the highest BU risk areas occur at low elevations with forested land cover, similar to previous studies of BU risk in West Africa. Additionally, climate conditions as far as 1.5 years in advance appear to impact disease incidence. Warmer and wetter conditions 18-19 months prior to case emergence, followed by a dry period approximately 5 months prior to case emergence seem to favor the occurrence of BU. Conclusions/Significance: The BU network structure in Victoria, Australia, suggests external environmental factors favor M. ulcerans transmission and, therefore, BU incidence. A unique combination of environmental conditions, including land cover type, temperature and a wet-dry sequence, may produce habitat characteristics that support M. ulcerans transmission and BU prevalence. These findings imply that future BU research efforts on transmission mechanisms should focus on potential vectors/reservoirs found in those environmental niches. Further, this study is the first to quantitatively estimate environmental lag times associated with BU outbreaks, providing insights for future transmission investigations. [ABSTRACT FROM AUTHOR]
- Published
- 2012
- Full Text
- View/download PDF
45. Sero-Epidemiology as a Tool to Screen Populations for Exposure to Mycobacterium ulcerans.
- Author
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Yeboah-Manu, Dorothy, Röltgen, Katharina, Opare, William, Asan-Ampah, Kobina, Quenin-Fosu, Kwabena, Asante-Poku, Adwoa, Ampadu, Edwin, Fyfe, Janet, Koram, Kwadwo, Ahorlu, Collins, and Pluschke, Gerd
- Subjects
BURULI ulcer ,HEAT shock proteins ,MYCOBACTERIUM ,ANTIBODY formation ,ANTIBODY titer ,ENVIRONMENTAL sampling - Abstract
Background: Previous analyses of sera from a limited number of Ghanaian Buruli ulcer (BU) patients, their household contacts, individuals living in BU non-endemic regions as well as European controls have indicated that antibody responses to the M. ulcerans 18 kDa small heat shock protein (shsp) reflect exposure to this pathogen. Here, we have investigated to what extent inhabitants of regions in Ghana regarded as non-endemic for BU develop anti-18 kDa shsp antibody titers. Methodology/Principal Findings: For this purpose we determined anti-18 kDa shsp IgG titers in sera collected from healthy inhabitants of the BU endemic Densu River Valley and the Volta Region, which was so far regarded as BU non-endemic. Significantly more sera from the Densu River Valley contained anti-18 kDa shsp IgG (32% versus 12%, respectively). However, some sera from the Volta Region also showed high titers. When interviewing these sero-responders, it was revealed that the person with the highest titer had a chronic wound, which was clinically diagnosed and laboratory reconfirmed as active BU. After identification of this BU index case, further BU cases were clinically diagnosed by the Volta Region local health authorities and laboratory reconfirmed. Interestingly, there was neither a difference in sero-prevalence nor in IS2404 PCR positivity of environmental samples between BU endemic and non-endemic communities located in the Densu River Valley. Conclusions: These data indicate that the intensity of exposure to M. ulcerans in endemic and non-endemic communities along the Densu River is comparable and that currently unknown host and/or pathogen factors may determine how frequently exposure is leading to clinical disease. While even high serum titers of anti-18 kDa shsp IgG do not indicate active disease, sero-epidemiological studies can be used to identify new BU endemic areas. Author Summary: Sero-epidemiological analyses revealed that a higher proportion of sera from individuals living in the Buruli ulcer (BU) endemic Densu River Valley of Ghana contain Mycobacterium ulcerans 18 kDa small heat shock protein (shsp)-specific IgG than sera from inhabitants of the Volta Region, which was regarded so far as BU non-endemic. However, follow-up studies in the Volta Region showed that the individual with the highest anti-18 kDa shsp-specific serum IgG titer of all participants from the Volta Region had a BU lesion. Identification of more BU patients in the Volta Region by subsequent active case search demonstrated that sero-epidemiology can help identify low endemicity areas. Endemic and non-endemic communities along the Densu River Valley differed neither in sero-prevalence nor in positivity of environmental samples in PCR targeting M. ulcerans genomic and plasmid DNA sequences. A lower risk of developing M. ulcerans disease in the non-endemic communities may either be related to host factors or a lower virulence of local M. ulcerans strains. [ABSTRACT FROM AUTHOR]
- Published
- 2012
- Full Text
- View/download PDF
46. Risk of Buruli Ulcer and Detection of Mycobacterium ulcerans in Mosquitoes in Southeastern Australia.
- Author
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Lavender, Caroline J., Fyfe, Janet A. M., Azuolas, Joseph, Brown, Karen, Evans, Rachel N., Ray, Lyndon R., and Johnson, Paul D. R.
- Subjects
- *
BURULI ulcer , *MOSQUITOES , *MYCOBACTERIUM , *PEARSON correlation (Statistics) , *DISEASE incidence - Abstract
Background: Buruli ulcer (BU) is a destructive skin condition caused by infection with the environmental bacterium, Mycobacterium ulcerans. The mode of transmission of M. ulcerans is not completely understood, but several studies have explored the role of biting insects. In this study, we tested for an association between the detection of M. ulcerans in mosquitoes and the risk of BU disease in humans in an endemic area of southeastern Australia. Methodology/Principal Findings: Adult mosquitoes were trapped in seven towns on the Bellarine Peninsula in Victoria, Australia, from December 2004 to December 2009 and screened for M. ulcerans by real-time PCR. The number of laboratory-confirmed cases of BU in permanent residents of these towns diagnosed during the same period was tallied to determine the average cumulative incidence of BU in each location. Pearson's correlation coefficient (r) was calculated for the proportion of M. ulcerans-positive mosquitoes per town correlated with the incidence of BU per town. We found a strong dose-response relationship between the detection of M. ulcerans in mosquitoes and the risk of human disease (r, 0.99; 95% CI, 0.92–0.99; p<0.001). Conclusions/Significance: The results of this study strengthen the hypothesis that mosquitoes are involved in the transmission of M. ulcerans in southeastern Australia. This has implications for the development of intervention strategies to control and prevent BU. Author Summary: Buruli ulcer (BU) is a destructive skin condition caused by infection with the environmental bacterium, Mycobacterium ulcerans. BU has been reported in more than 30 countries in Africa, the Americas, Asia and the Western Pacific. How people become infected with M. ulcerans is not completely understood, but numerous studies have explored the role of biting insects. In 2007, it was discovered that M. ulcerans could be detected in association with mosquitoes trapped in one town in southeastern Australia during a large outbreak of BU. In the present study we investigated whether there was a relationship between the incidence of BU in humans in several towns and the likelihood of detecting M. ulcerans in mosquitoes trapped in those locations. We found a strong association between the proportion of M. ulcerans-positive mosquitoes and the incidence of human disease. The results of this study strengthen the hypothesis that mosquitoes are involved in the transmission of M. ulcerans in southeastern Australia. This has implications for the development of strategies to control and prevent BU. [ABSTRACT FROM AUTHOR]
- Published
- 2011
- Full Text
- View/download PDF
47. Mycobacterium ulcerans DNA Not Detected in Faecal Samples from Buruli Ulcer Patients: Results of a Pilot Study.
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Sarfo, Fred S., Lavender, Caroline J., Fyfe, Janet A. M., Johnson, Paul D. R., Stinear, Timothy P., and Phillips, Richard O.
- Subjects
MYCOBACTERIUM ,GASTROINTESTINAL system ,ALIMENTARY canal ,FUNGUS-bacterium relationships ,NUCLEIC acids - Abstract
It has recently been shown that in a Buruli ulcer (BU) endemic region of southeastern Australia, significant numbers of possums (native tree-dwelling marsupials) have clinical BU disease. Furthermore, based on quantitative PCR (qPCR) analysis, animals with BU lesions (and some without) shed M. ulcerans DNA in their faeces, indicative of bacterial loads of up to 10
8 organisms/gram. These findings led us to propose that humans might also harbour M. ulcerans in their gastrointestinal tract and shed the bacterium in their faeces. We conducted a pilot study and collected faecal swabs from 26 patients with confirmed BU and 31 healthy household controls. Faecal samples were also collected from 10 healthy controls from nonendemic regions in Ghana. All 67 specimens were negative when tested by IS2404 PCR. The detection sensitivity of this method was ≥104, bacteria per gram (wet-weight) of human faecal material. We conclude that the human gastrointestinal tract is unlikely to be a significant reservoir of M. ulcerans. [ABSTRACT FROM AUTHOR]- Published
- 2011
- Full Text
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48. All-Oral Antibiotic Treatment for Buruli Ulcer: A Report of Four Patients.
- Author
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Gordon, Claire L., Buntine, John A., Hayman, John A., Lavender, Caroline J., Fyfe, Janet A. M., Hosking, Patrick, Starr, Mike, and Johnson, Paul D. R.
- Subjects
BURULI ulcer ,SKIN infections ,ANTIBIOTICS ,MYCOBACTERIAL diseases ,THERAPEUTICS - Abstract
This article explores the treatment of Buruli ulcer (BU), a skin infection caused by Mycobacterium ulcerans. Traditionally, surgery has been the main treatment, but recent studies have shown the effectiveness of oral antibiotics. The article presents four cases where patients were treated with oral antibiotics, either followed by surgery or as the sole treatment. After several weeks of antibiotic therapy, three patients showed no signs of the bacteria. The article provides detailed information about the patients' characteristics, diagnosis, treatment, and histopathology. It suggests that using oral antibiotics before surgery may simplify management and prevent relapse. [Extracted from the article]
- Published
- 2010
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49. A Major Role for Mammals in the Ecology of Mycobacterium ulcerans.
- Author
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Fyfe, Janet A. M., Lavender, Caroline J., Handasyde, Kathrine A., Legione, Alistair R., O'Brien, Carolyn R., Stinear, Timothy P., Pidot, Sacha J., Seemann, Torsten, Benbow, M. Eric, Wallace, John R., McCowan, Christina, and Johnson, Paul D. R.
- Subjects
- *
MYCOBACTERIUM , *BURULI ulcer , *WHOLE genome sequencing , *AQUATIC insects , *MAMMALS - Abstract
Background: Mycobacterium ulcerans is the causative agent of Buruli ulcer (BU), a destructive skin disease found predominantly in sub-Saharan Africa and south-eastern Australia. The precise mode(s) of transmission and environmental reservoir(s) remain unknown, but several studies have explored the role of aquatic invertebrate species. The purpose of this study was to investigate the environmental distribution of M. ulcerans in south-eastern Australia. Methodology/Principal Findings: A range of environmental samples was collected from Point Lonsdale (a small coastal town southwest of Melbourne, Australia, endemic for BU) and from areas with fewer or no reported incident cases of BU. Mycobacterium ulcerans DNA was detected at low levels by real-time PCR in soil, sediment, water residue, aquatic plant biofilm and terrestrial vegetation collected in Point Lonsdale. Higher levels of M. ulcerans DNA were detected in the faeces of common ringtail (Pseudocheirus peregrinus) and common brushtail (Trichosurus vulpecula) possums. Systematic testing of possum faeces revealed that M. ulcerans DNA could be detected in 41% of faecal samples collected in Point Lonsdale compared with less than 1% of faecal samples collected from non-endemic areas (p<0.0001). Capture and clinical examination of live possums in Point Lonsdale validated the accuracy of the predictive value of the faecal surveys by revealing that 38% of ringtail possums and 24% of brushtail possums had laboratory-confirmed M. ulcerans skin lesions and/or M. ulcerans PCR positive faeces. Whole genome sequencing revealed an extremely close genetic relationship between human and possum M. ulcerans isolates. Conclusions/Significance: The prevailing wisdom is that M. ulcerans is an aquatic pathogen and that BU is acquired by contact with certain aquatic environments (swamps, slow-flowing water). Now, after 70 years of research, we propose a transmission model for BU in which terrestrial mammals are implicated as reservoirs for M. ulcerans. Author Summary: Mycobacterium ulcerans is the causative agent of Buruli ulcer (BU), a destructive skin disease found predominantly in sub-Saharan Africa and south-eastern Australia. The mode of transmission and environmental reservoir remain unknown, but several studies have explored the role of aquatic insects, such as water bugs, and biting insects, such as mosquitoes. In the present study we investigated possible environmental source(s) of M. ulcerans in Victoria, Australia. Our results revealed that although M. ulcerans DNA could be detected at low levels in a variety of environmental samples, the highest concentrations of M. ulcerans DNA were found in the faeces of two species of possums, common ringtails and common brushtails. Possums are small arboreal marsupial mammals, native to Australia, and these particular species occur in both urban and rural areas. Examination and sampling of live captured possums in an area endemic for BU revealed that 38% of ringtail possums and 24% of brushtail possums, respectively, had laboratory-confirmed M. ulcerans lesions and/or M. ulcerans PCR-positive faeces. The finding that large numbers of possums in a BU-endemic area are infected with M. ulcerans raises the possibility that mammals are an environmental reservoir for M. ulcerans. [ABSTRACT FROM AUTHOR]
- Published
- 2010
- Full Text
- View/download PDF
50. Evaluation of VNTR typing for the identification of Mycobacterium ulcerans in environmental samples from Victoria, Australia.
- Author
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Lavender, Caroline J., Stinear, Timothy P., Johnson, Paul D. R., Azuolas, Joseph, Benbow, Mark Eric, Wallace, John R., and Fyfe, Janet A.M.
- Subjects
MYCOBACTERIUM ,PATHOGENIC microorganisms ,MICROORGANISMS ,MICROBIOLOGY ,ENVIRONMENTAL sciences ,ECOLOGY ,POPULATION biology - Abstract
Reliable molecular detection of Mycobacterium ulcerans in environmental samples is essential to study the ecology and transmission of this important human pathogen. Variable number tandem repeat (VNTR) typing is a valuable method for distinguishing M. ulcerans isolates from different geographic regions and for distinguishing M. ulcerans from other members of the Mycobacterium marinum/ M. ulcerans complex, but its application to environmental samples has not yet been evaluated systematically. This study compares the sensitivity and specificity of PCR detection of 13 VNTR loci to determine the best loci for the analysis of environmental samples. This study demonstrates that VNTR typing using selected loci can be a useful addition to established molecular methods for detecting M. ulcerans in the environment and highlights some of the issues encountered when using molecular methods to detect microorganisms in environmental samples. When applied to environmental samples collected from an endemic region in Victoria, Australia, VNTR typing confirmed that the strain of M. ulcerans being detected was indistinguishable from the strain causing disease in humans in that region. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
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