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1. Inter-species gene flow drives ongoing evolution of Streptococcus pyogenes and Streptococcus dysgalactiae subsp. equisimilis

Author

Xie, Ouli, Morris, Jacqueline M., Hayes, Andrew J., Towers, Rebecca J., Jespersen, Magnus G., Lees, John A., Ben Zakour, Nouri L., Berking, Olga, Baines, Sarah L., Carter, Glen P., Tonkin-Hill, Gerry, Schrieber, Layla, McIntyre, Liam, Lacey, Jake A., James, Taylah B., Sriprakash, Kadaba S., Beatson, Scott A., Hasegawa, Tadao, Giffard, Phil, Steer, Andrew C., Batzloff, Michael R., Beall, Bernard W., Pinho, Marcos D., Ramirez, Mario, Bessen, Debra E., Dougan, Gordon, Bentley, Stephen D., Walker, Mark J., Currie, Bart J., Tong, Steven Y. C., McMillan, David J., and Davies, Mark R.

Published
2024
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2. A convergent evolutionary pathway attenuating cellulose production drives enhanced virulence of some bacteria

Author

Nhu, Nguyen Thi Khanh, Rahman, M. Arifur, Goh, Kelvin G. K., Kim, Seung Jae, Phan, Minh-Duy, Peters, Kate M., Alvarez-Fraga, Laura, Hancock, Steven J., Ravi, Chitra, Kidd, Timothy J., Sullivan, Matthew J., Irvine, Katharine M., Beatson, Scott A., Sweet, Matthew J., Irwin, Adam D., Vukovic, Jana, Ulett, Glen C., Hasnain, Sumaira Z., and Schembri, Mark A.

Published
2024
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5. Integrative omics identifies conserved and pathogen-specific responses of sepsis-causing bacteria

Author

Mu, Andre, Klare, William P., Baines, Sarah L., Ignatius Pang, C. N., Guérillot, Romain, Harbison-Price, Nichaela, Keller, Nadia, Wilksch, Jonathan, Nhu, Nguyen Thi Khanh, Phan, Minh-Duy, Keller, Bernhard, Nijagal, Brunda, Tull, Dedreia, Dayalan, Saravanan, Chua, Hwa Huat Charlie, Skoneczny, Dominik, Koval, Jason, Hachani, Abderrahman, Shah, Anup D., Neha, Nitika, Jadhav, Snehal, Partridge, Sally R., Cork, Amanda J., Peters, Kate, Bertolla, Olivia, Brouwer, Stephan, Hancock, Steven J., Álvarez-Fraga, Laura, De Oliveira, David M. P., Forde, Brian, Dale, Ashleigh, Mujchariyakul, Warasinee, Walsh, Calum J., Monk, Ian, Fitzgerald, Anna, Lum, Mabel, Correa-Ospina, Carolina, Roy Chowdhury, Piklu, Parton, Robert G., De Voss, James, Beckett, James, Monty, Francois, McKinnon, Jessica, Song, Xiaomin, Stephen, John R., Everest, Marie, Bellgard, Matt I., Tinning, Matthew, Leeming, Michael, Hocking, Dianna, Jebeli, Leila, Wang, Nancy, Ben Zakour, Nouri, Yasar, Serhat A., Vecchiarelli, Stefano, Russell, Tonia, Zaw, Thiri, Chen, Tyrone, Teng, Don, Kassir, Zena, Lithgow, Trevor, Jenney, Adam, Cole, Jason N., Nizet, Victor, Sorrell, Tania C., Peleg, Anton Y., Paterson, David L., Beatson, Scott A., Wu, Jemma, Molloy, Mark P., Syme, Anna E., Goode, Robert J. A., Hunter, Adam A., Bowland, Grahame, West, Nicholas P., Wilkins, Marc R., Djordjevic, Steven P., Davies, Mark R., Seemann, Torsten, Howden, Benjamin P., Pascovici, Dana, Tyagi, Sonika, Schittenhelm, Ralf B., De Souza, David P., McConville, Malcolm J., Iredell, Jonathan R., Cordwell, Stuart J., Strugnell, Richard A., Stinear, Timothy P., Schembri, Mark A., and Walker, Mark J.

Published
2023
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7. Evolution of the pheV-tRNA integrated genomic island in Escherichia coli.

Author

Nhu, Nguyen Thi Khanh, Forde, Brian M., Ben Zakour, Nouri L., Phan, Minh-Duy, Roberts, Leah W., Beatson, Scott A., and Schembri, Mark A.

Subjects
ESCHERICHIA coli, GENETIC variation, GENE regulatory networks, MOLECULAR cloning, GENOMES
Abstract

Escherichia coli exhibit extensive genetic diversity at the genome level, particularly within their accessory genome. The tRNA integrated genomic islands (GIs), a part of the E. coli accessory genome, play an important role in pathogenicity. However, studies examining the evolution of GIs have been challenging due to their large size, considerable gene content variation and fragmented assembly in draft genomes. Here we examined the evolution of the GI integrated at pheV-tRNA (GI-pheV), with a primary focus on uropathogenic E. coli (UPEC) and the globally disseminated multidrug resistant ST131 clone. We show the gene content of GI-pheV is highly diverse and arranged in a modular configuration, with the P4 integrase encoding gene intP4 the only conserved gene. Despite this diversity, the GI-pheV gene content displayed conserved features among strains from the same pathotype. In ST131, GI-pheV corresponding to the reference strain EC958 (EC958_GI-pheV) was found in ~90% of strains. Phylogenetic analyses suggested that GI-pheV in ST131 has evolved together with the core genome, with the loss/gain of specific modules (or the entire GI) linked to strain specific events. Overall, we show GI-pheV exhibits a dynamic evolutionary pathway, in which modules and genes have evolved through multiple events including insertions, deletions and recombination. Author summary: Genomic islands (GIs) are key contributors to E. coli pathogenesis. However, studies on the evolution of GIs are limited, mostly due to their large size, variation, and fragmented assembly in draft genomes. Here we investigated the evolution of the GI-pheV genomic island. We showed that the presence of GI-pheV is primarily associated with pathogenic E. coli, with the greatest diversity in gene content observed among strains from different pathotypes. The GI-pheV in UPEC contains uropathogenicity-associated virulence and fitness encoding modules, which have either co-evolved with the island or evolved independently, possibly due to different selective pressures. Focused investigation of GI-pheV in ST131, the most globally dominant antibiotic resistant UPEC clone, revealed loss or gain of genes and modules via recombination during its evolution. [ABSTRACT FROM AUTHOR]

Published
2024
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10. High-risk Escherichia coli clones that cause neonatal meningitis and association with recrudescent infection

Author

Nhu, Nguyen Thi Khanh, primary, Phan, Minh-Duy, additional, Hancock, Steven J, additional, Peters, Kate M, additional, Alvarez-Fraga, Laura, additional, Forde, Brian M, additional, Andersen, Stacey B, additional, Miliya, Thyl, additional, Harris, Patrick NA, additional, Beatson, Scott A, additional, Schlebusch, Sanmarie, additional, Bergh, Haakon, additional, Turner, Paul, additional, Brauner, Annelie, additional, Westerlund-Wikström, Benita, additional, Irwin, Adam D, additional, and Schembri, Mark A, additional

Published
2024
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11. Author response: High-risk Escherichia coli clones that cause neonatal meningitis and association with recrudescent infection

Author

Nguyen, Nhu, primary, Phan, Minh-Duy, additional, Hancock, Steven J, additional, Peters, Kate M, additional, Alvarez-Fraga, Laura, additional, Forde, Brian M, additional, Andersen, Stacey B, additional, Miliya, Thyl, additional, Harris, Patrick, additional, Beatson, Scott, additional, Schlebusch, Sanmarie, additional, Bergh, Haakon, additional, Turner, Paul, additional, Brauner, Annelie, additional, Westerlund-Wikström, Benita, additional, Irwin, Adam D, additional, and Schembri, Mark A, additional

Published
2024
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12. The complete genome sequence of five historical Escherichia coli sequence type (ST)1193 strains reveals insights into an emerging pathogen

Author

White, Rhys T., Ashcroft, Melinda A., Bauer, Michelle J., Bell, Jan, Butkiewicz, Dominika, Alvarez-Fraga, Laura, Gibson, Justine S., Kidsley, Amanda K., Mollinger, Joanne L., Peters, Kate M., Phan, Minh-Duy, Roberts, Leah W., Rogers, Benjamin A., Schembri, Mark A., Trott, Darren J., Turnidge, John, Forde, Brian M., Beatson, Scott A., White, Rhys T., Ashcroft, Melinda A., Bauer, Michelle J., Bell, Jan, Butkiewicz, Dominika, Alvarez-Fraga, Laura, Gibson, Justine S., Kidsley, Amanda K., Mollinger, Joanne L., Peters, Kate M., Phan, Minh-Duy, Roberts, Leah W., Rogers, Benjamin A., Schembri, Mark A., Trott, Darren J., Turnidge, John, Forde, Brian M., and Beatson, Scott A.

Abstract

Fluoroquinolone-resistant Escherichia coli sequence type (ST)1193 is a profound, emerging lineage associated with systemic, urinary tract, and neonatal infections. Humans, companion animals, and the environment are reservoirs for ST1193, which has been disseminated globally. Following its detection in 2007, ST1193 has been identified repeatedly amongst fluoroquinolone-resistant clones in Australia. However, despite the growing importance of ST1193, only three complete genomes are published in the literature, none of which are from Australia. Here we expand on the available ST1193 resources with the complete genomes of five ST1193 strains sequenced using Oxford Nanopore Technologies and Illumina. Using in silico genotyping, we found that all strains were multi-drug resistant, including resistances to fluoroquinolones and cephalosporins. In vitro antibiotic susceptibility testing mostly correlated with individual genotypes. The exception was MS8320, which had additional in vitro resistance to piperacillin/tazobactam, ampicillin/sulbactam, cefazolin and doripenem (carbapenem). Further investigation identified seven additional copies of an IS26 transposable unit carrying a blaTEM-1B beta-lactamase gene, suggesting this tandem amplification is associated with extended resistance phenotypes. Uropathogenicity factors, including three separate siderophore-encoding loci, were conserved in chromosomal and plasmid regions. Using all complete genomes, we further elucidated the recombination events surrounding the previously described K5/K1 capsular loci switch. Phenotypic confirmation of differing capsules in Australian ST1193 strains, coupled with genetic analysis revealing insertions downstream of the capsular locus, underscored the genetic distinctions between K5 and K1 capsule encoding strains. This study provides five new reference ST1193 genomes from Australia. These include the earliest complete K5-capsule ST1193 genomes on record (collected 2007), alongside our referenc

Published
2024

14. Complete genome sequence of the haloalkaliphilic, obligately chemolithoautotrophic thiosulfate and sulfide-oxidizing γ-proteobacterium Thioalkalimicrobium cyclicum type strain ALM 1 (DSM 14477T)

Author

Kappler, Ulrike, Davenport, Karen, Beatson, Scott, Lapidus, Alla, Pan, Chongle, Han, Cliff, Montero-Calasanz, Maria del Carmen, Land, Miriam, Hauser, Loren, Rohde, Manfred, Göker, Markus, Ivanova, Natalia, Woyke, Tanja, Klenk, Hans-Peter, and Kyrpides, Nikos C

Subjects
Microbiology, Biological Sciences, Genetics, Biotechnology, Human Genome, Aerobic, Obligate chemolithoautotroph, Sulfur oxidizer, Gram-negative, Mono Lake, Piscirickettsiaceae, CSP 2008
Abstract

Thioalkalimicrobium cyclicum Sorokin et al. 2002 is a member of the family Piscirickettsiaceae in the order Thiotrichales. The γ-proteobacterium belongs to the colourless sulfur-oxidizing bacteria isolated from saline soda lakes with stable alkaline pH, such as Lake Mono (California) and Soap Lake (Washington State). Strain ALM 1(T) is characterized by its adaptation to life in the oxic/anoxic interface towards the less saline aerobic waters (mixolimnion) of the stable stratified alkaline salt lakes. Strain ALM 1(T) is the first representative of the genus Thioalkalimicrobium whose genome sequence has been deciphered and the fourth genome sequence of a type strain of the Piscirickettsiaceae to be published. The 1,932,455 bp long chromosome with its 1,684 protein-coding and 50 RNA genes was sequenced as part of the DOE Joint Genome Institute Community Sequencing Program (CSP) 2008.

Published
2016

16. High-risk Escherichia coli clones that cause neonatal meningitis and association with recrudescent infection

Author

Nhu, Nguyen Thi Khanh, primary, Phan, Minh-Duy, additional, Hancock, Steven J., additional, Peters, Kate M., additional, Alvarez-Fraga, Laura, additional, Forde, Brian M., additional, Andersen, Stacey B., additional, Miliya, Thyl, additional, Harris, Patrick N.A., additional, Beatson, Scott A., additional, Schlebusch, Sanmarie, additional, Bergh, Haakon, additional, Turner, Paul, additional, Brauner, Annelie, additional, Westerlund-Wikström, Benita, additional, Irwin, Adam D., additional, and Schembri, Mark A., additional

Published
2023
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17. Author Response: High-risk Escherichia coli clones that cause neonatal meningitis and association with recrudescent infection

Author

Nhu, Nguyen Thi Khanh, primary, Phan, Minh-Duy, additional, Hancock, Steven J., additional, Peters, Kate M., additional, Alvarez-Fraga, Laura, additional, Forde, Brian M., additional, Andersen, Stacey B., additional, Miliya, Thyl, additional, Harris, Patrick N.A., additional, Beatson, Scott A., additional, Schlebusch, Sanmarie, additional, Bergh, Haakon, additional, Turner, Paul, additional, Brauner, Annelie, additional, Westerlund-Wikström, Benita, additional, Irwin, Adam D., additional, and Schembri, Mark A., additional

Published
2023
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20. Mutual Exclusivity of Hyaluronan and Hyaluronidase in Invasive Group A Streptococcus *

Author

Henningham, Anna, Yamaguchi, Masaya, Aziz, Ramy K, Kuipers, Kirsten, Buffalo, Cosmo Z, Dahesh, Samira, Choudhury, Biswa, Van Vleet, Jeremy, Yamaguchi, Yuka, Seymour, Lisa M, Zakour, Nouri L Ben, He, Lingjun, Smith, Helen V, Grimwood, Keith, Beatson, Scott A, Ghosh, Partho, Walker, Mark J, Nizet, Victor, and Cole, Jason N

Subjects
Microbiology, Biological Sciences, Biomedical and Clinical Sciences, Clinical Sciences, Infectious Diseases, Genetics, Emerging Infectious Diseases, 2.2 Factors relating to the physical environment, Infection, Animals, Bacterial Proteins, Base Sequence, Cell Membrane, Computational Biology, Exotoxins, Female, Genetic Complementation Test, Histidine Kinase, Humans, Hyaluronic Acid, Hyaluronoglucosaminidase, Intracellular Signaling Peptides and Proteins, Mice, Molecular Sequence Data, Neutrophils, Point Mutation, Polysaccharide-Lyases, Polysaccharides, Recombinant Proteins, Repressor Proteins, Streptococcal Infections, Streptococcus pyogenes, Virulence, Bacterial Pathogenesis, Hyaluronan, Hyaluronate, Infectious Disease, Streptococcus Pyogenes (S, Pyogenes), Group A Streptococcus, Hyaluronate Lyase, Hyaluronic acid Capsule, Invasive Disease, Nonencapsulated, Streptococcus Pyogenes, Chemical Sciences, Medical and Health Sciences, Biochemistry & Molecular Biology, Biological sciences, Biomedical and clinical sciences, Chemical sciences
Abstract

A recent analysis of group A Streptococcus (GAS) invasive infections in Australia has shown a predominance of M4 GAS, a serotype recently reported to lack the antiphagocytic hyaluronic acid (HA) capsule. Here, we use molecular genetics and bioinformatics techniques to characterize 17 clinical M4 isolates associated with invasive disease in children during this recent epidemiology. All M4 isolates lacked HA capsule, and whole genome sequence analysis of two isolates revealed the complete absence of the hasABC capsule biosynthesis operon. Conversely, M4 isolates possess a functional HA-degrading hyaluronate lyase (HylA) enzyme that is rendered nonfunctional in other GAS through a point mutation. Transformation with a plasmid expressing hasABC restored partial encapsulation in wild-type (WT) M4 GAS, and full encapsulation in an isogenic M4 mutant lacking HylA. However, partial encapsulation reduced binding to human complement regulatory protein C4BP, did not enhance survival in whole human blood, and did not increase virulence of WT M4 GAS in a mouse model of systemic infection. Bioinformatics analysis found no hasABC homologs in closely related species, suggesting that this operon was a recent acquisition. These data showcase a mutually exclusive interaction of HA capsule and active HylA among strains of this leading human pathogen.

Published
2014

22. High-riskEscherichia coliclones that cause neonatal meningitis and association with recrudescent infection

Author

Nhu, Nguyen Thi Khanh, primary, Phan, Minh-Duy, additional, Hancock, Steven J., additional, Peters, Kate M., additional, Alvarez-Fraga, Laura, additional, Forde, Brian M., additional, Andersen, Stacey B., additional, Miliya, Thyl, additional, Harris, Patrick N.A., additional, Beatson, Scott A., additional, Schlebusch, Sanmarie, additional, Bergh, Haakon, additional, Turner, Paul, additional, Brauner, Annelie, additional, Westerlund-Wikström, Benita, additional, Irwin, Adam D., additional, and Schembri, Mark A., additional

Published
2023
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24. Inter-species gene flow drives ongoing evolution ofStreptococcus pyogenesandStreptococcus dysgalactiaesubsp.equisimilis

Author

Xie, Ouli, primary, Morris, Jacqueline M., additional, Hayes, Andrew J., additional, Towers, Rebecca J., additional, Jespersen, Magnus G., additional, Lees, John A., additional, Ben Zakour, Nouri L., additional, Berking, Olga, additional, Baines, Sarah L., additional, Carter, Glen P., additional, Tonkin-Hill, Gerry, additional, Schrieber, Layla, additional, McIntyre, Liam, additional, Lacey, Jake A., additional, James, Taylah B., additional, Sriprakash, Kadaba S., additional, Beatson, Scott A., additional, Hasegawa, Tadao, additional, Giffard, Phil, additional, Steer, Andrew C., additional, Batzloff, Michael R., additional, Beall, Bernie W., additional, Pinho, Marcos D., additional, Ramirez, Mario, additional, Bessen, Debra E., additional, Dougan, Gordon, additional, Bentley, Stephen D., additional, Walker, Mark J., additional, Currie, Bart J., additional, Tong, Steven Y. C., additional, McMillan, David J., additional, and Davies, Mark R., additional

Published
2023
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26. Integrating multiple genomic technologies to investigate an outbreak of carbapenemase-producing Enterobacter hormaechei

Author

Roberts, Leah W., Harris, Patrick N. A., Forde, Brian M., Ben Zakour, Nouri L., Catchpoole, Elizabeth, Stanton-Cook, Mitchell, Phan, Minh-Duy, Sidjabat, Hanna E., Bergh, Haakon, Heney, Claire, Gawthorne, Jayde A., Lipman, Jeffrey, Allworth, Anthony, Chan, Kok-Gan, Chong, Teik Min, Yin, Wai-Fong, Schembri, Mark A., Paterson, David L., and Beatson, Scott A.

Published
2020
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33. Clinical Implementation of Routine Whole-genome Sequencing for Hospital Infection Control of Multi-drug Resistant Pathogens

Author

Forde, Brian M, primary, Bergh, Haakon, additional, Cuddihy, Thom, additional, Hajkowicz, Krispin, additional, Hurst, Trish, additional, Playford, E Geoffrey, additional, Henderson, Belinda C, additional, Runnegar, Naomi, additional, Clark, Julia, additional, Jennison, Amy V, additional, Moss, Susan, additional, Hume, Anna, additional, Leroux, Hugo, additional, Beatson, Scott A, additional, Paterson, David L, additional, and Harris, Patrick N A, additional

Published
2022
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36. Global dissemination of a multidrug resistant Escherichia coli clone

Author

Petty, Nicola K., Zakour, Nouri L. Ben, Stanton-Cook, Mitchell, Skippington, Elizabeth, Totsika, Makrina, Forde, Brian M., Phan, Minh-Duy, Moriel, Danilo Gomes, Peters, Kate M., Davies, Mark, Rogers, Benjamin A., Dougan, Gordon, Rodriguez-Baño, Jesús, Pascual, Alvaro, Pitout, Johann D. D., Upton, Mathew, Paterson, David L., Walsh, Timothy R., Schembri, Mark A., and Beatson, Scott A.

Published
2014

38. Ucl fimbriae regulation and glycan receptor specificity contribute to gut colonisation by extra-intestinal pathogenic Escherichia coli

Author

Hancock, Steven J., primary, Lo, Alvin W., additional, Ve, Thomas, additional, Day, Christopher J., additional, Tan, Lendl, additional, Mendez, Alejandra A., additional, Phan, Minh-Duy, additional, Nhu, Nguyen Thi Khanh, additional, Peters, Kate M., additional, Richards, Amanda C., additional, Fleming, Brittany A., additional, Chang, Chyden, additional, Ngu, Dalton H. Y., additional, Forde, Brian M., additional, Haselhorst, Thomas, additional, Goh, Kelvin G. K., additional, Beatson, Scott A., additional, Jennings, Michael P., additional, Mulvey, Matthew A., additional, Kobe, Bostjan, additional, and Schembri, Mark A., additional

Published
2022
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40. Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone

Author

Alvarez-Fraga, Laura, Phan, Minh Duy, Goh, Kelvin G.K., Nhu, Nguyen Thi Khanh, Hancock, Steven J., Allsopp, Luke P., Peters, Kate M., Forde, Brian M., Roberts, Leah W., Sullivan, Matthew J., Totsika, Makrina, Beatson, Scott A., Ulett, Glen C., Schembri, Mark A., Alvarez-Fraga, Laura, Phan, Minh Duy, Goh, Kelvin G.K., Nhu, Nguyen Thi Khanh, Hancock, Steven J., Allsopp, Luke P., Peters, Kate M., Forde, Brian M., Roberts, Leah W., Sullivan, Matthew J., Totsika, Makrina, Beatson, Scott A., Ulett, Glen C., and Schembri, Mark A.

Abstract

Many antibiotic resistant uropathogenic Escherichia coli (UPEC) strains belong to clones defined by their multilocus sequence type (ST), with ST131 being the most dominant. Although we have a good understanding of resistance development to fluoroquinolones and third-generation cephalosporins by ST131, our understanding of the virulence repertoire that has contributed to its global dissemination is limited. Here we show that the genes encoding Afa/Dr fimbriae, a group of adhesins strongly associated with UPEC that cause gestational pyelonephritis and recurrent cystitis, are found in approximately one third of all ST131 strains. Sequence comparison of the AfaE adhesin protein revealed a unique allelic variant carried by 82.9% of afa-positive ST131 strains. We identify the afa regulatory region as a hotspot for the integration of insertion sequence (IS) elements, all but one of which alter afa transcription. Close investigation demonstrated that the integration of an IS1 element in the afa regulatory region leads to increased expression of Afa/Dr fimbriae, promoting enhanced adhesion to kidney epithelial cells and suggesting a mechanism for altered virulence. Finally, we provide evidence for a more widespread impact of IS1 on ST131 genome evolution, suggesting that IS dynamics contribute to strain level microevolution that impacts ST131 fitness. IMPORTANCE E. coli ST131 is the most common antibiotic resistant UPEC clone associated with human urinary tract and bloodstream infections. Understanding the features of ST131 that have driven its global dissemination remains a critical priority if we are to counter its increasing antibiotic resistance. Here, we utilized a large collection of ST131 isolates to investigate the prevalence, regulation, and function of Afa/ Dr fimbriae, a well-characterized UPEC colonization and virulence factor. We show that the afa genes are found frequently in ST131 and demonstrate how the integration of IS elements in the afa regulatory regi

Published
2022

46. Rescuing Tetracycline Class Antibiotics for the Treatment of Multidrug-Resistant Acinetobacter baumannii Pulmonary Infection

Author

De Oliveira, David M. P., primary, Forde, Brian M., additional, Phan, Minh-Duy, additional, Steiner, Bernhard, additional, Zhang, Bing, additional, Zuegg, Johannes, additional, El-deeb, Ibrahim M., additional, Li, Gen, additional, Keller, Nadia, additional, Brouwer, Stephan, additional, Harbison-Price, Nichaela, additional, Cork, Amanda J., additional, Bauer, Michelle J., additional, Alquethamy, Saleh F., additional, Beatson, Scott A., additional, Roberts, Jason A., additional, Paterson, David L., additional, McEwan, Alastair G., additional, Blaskovich, Mark A. T., additional, Schembri, Mark A., additional, McDevitt, Christopher A., additional, von Itzstein, Mark, additional, and Walker, Mark J., additional

Published
2022
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47. Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone

Author

Alvarez-Fraga, Laura, primary, Phan, Minh-Duy, additional, Goh, Kelvin G. K., additional, Nhu, Nguyen Thi Khanh, additional, Hancock, Steven J., additional, Allsopp, Luke P., additional, Peters, Kate M., additional, Forde, Brian M., additional, Roberts, Leah W., additional, Sullivan, Matthew J., additional, Totsika, Makrina, additional, Beatson, Scott A., additional, Ulett, Glen C., additional, and Schembri, Mark A., additional

Published
2022
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48. Plasmid-Mediated Ciprofloxacin Resistance Imparts a Selective Advantage on Escherichia coli ST131

Author

Phan, Minh-Duy, primary, Peters, Kate M., additional, Alvarez Fraga, Laura, additional, Wallis, Steven C., additional, Hancock, Steven J., additional, Nhu, Nguyen Thi Khanh, additional, Forde, Brian M., additional, Bauer, Michelle J., additional, Paterson, David L., additional, Beatson, Scott A., additional, Lipman, Jeffrey, additional, and Schembri, Mark A., additional

Published
2022
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