4 results on '"Duah, Mabel Sarpong"'
Search Results
2. Infection with Mansonella perstans nematodes in Buruli ulcer patients, Ghana
- Author
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Phillips, Richard O., Frimpong, Michael, Sarfo, Fred S., Kretschmer, Birte, Beissner, Marcus, Debrah, Alexander, Ampem- Amoako, Yaw, Abass, Kabiru M., Thompson, William, Duah, Mabel Sarpong, Abotsi, Justice, Adjei, Ohene, Fleischer, Bernhard, Bretzel, Gisela, Wansbrough-Jones, Mark, and Jacobsen, Marc
- Subjects
Nematoda -- Influence ,Buruli ulcer -- Complications and side effects ,Roundworm infections -- Risk factors ,Children -- Health aspects ,Health - Abstract
Buruli ulcer, caused by Mycobacterium ulcerans, is a neglected tropical disease common in rural parts of West Africa. Infection with M. ulcerans causes disfiguring skin ulcers, mainly in children. The [...]
- Published
- 2014
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3. Paradoxical reactions in Buruli ulcer after initiation of antibiotic therapy: Relationship to bacterial load.
- Author
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Frimpong, Michael, Agbavor, Bernadette, Duah, Mabel Sarpong, Loglo, Aloysius, Sarpong, Francisca N., Boakye-Appiah, Justice, Abass, Kabiru M., Dongyele, Mathias, Amofa, George, Tuah, Wilson, Frempong, Margaret, Amoako, Yaw A., Wansbrough-Jones, Mark, and Phillips, Richard O.
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BURULI ulcer ,HEALING ,ANTIBIOTICS ,NUCLEIC acids ,RIBOSOMAL RNA - Abstract
Background: We investigated the relationship between bacterial load in Buruli ulcer (BU) lesions and the development of paradoxical reaction following initiation of antibiotic treatment. Methods: This was a longitudinal study involving BU patients from June 2013 to June 2017. Fine needle aspirates (FNA) and swab samples were obtained to establish the diagnosis of BU by PCR. Additional samples were obtained at baseline, during and after treatment (if the lesion had not healed) for microscopy, culture and combined 16S rRNA reverse transcriptase/ IS2404 qPCR assay. Patients were followed up at regular intervals until complete healing. Results: Forty-seven of 354 patients (13%) with PCR confirmed BU had a PR, occurring between 2 and 42 (median 6) weeks after treatment initiation. The bacterial load, the proportion of patients with positive M. ulcerans culture (15/34 (44%) vs 29/119 (24%), p = 0.025) and the proportion with positive microscopy results (19/31 (61%) vs 28/90 (31%), p = 0.003) before initiation of treatment were significantly higher in the PR compared to the no PR group. Plaques (OR 5.12; 95% CI 2.26–11.61; p<0.001), oedematous (OR 4.23; 95% CI 1.43–12.5; p = 0.009) and category II lesions (OR 2.26; 95% CI 1.14–4.48; p = 0.02) were strongly associated with the occurrence of PR. The median time to complete healing (28 vs 13 weeks, p <0.001) was significantly longer in the PR group. Conclusions: Buruli ulcer patients who develop PR are characterized by high bacterial load in lesion samples taken at baseline and a higher rate of positive M. ulcerans culture. Occurrence of a PR was associated with delayed healing. Trial registration: ClinicalTrials.gov . [ABSTRACT FROM AUTHOR]
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- 2019
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4. IFN-γ and IL-5 whole blood response directed against mycolactone polyketide synthase domains in patients with Mycobacterium ulcerans infection.
- Author
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Loglo, Aloysius D., Frimpong, Michael, Duah, Mabel Sarpong, Sarfo, Fred, Sarpong, Francisca N., Agbavor, Bernadette, Boakye-Appiah, Justice K., Abass, Kabiru M., Dongyele, Mathias, Frempong, Margaret, Pidot, Sacha, Wansbrough-Jones, Mark, Stinear, Timothy P., Roupie, Virginie, Huygen, Kris, and Phillips, Richard O.
- Subjects
MYCOBACTERIAL diseases ,ACYL carrier protein ,POLYKETIDE synthases ,BURULI ulcer ,SOFT tissue infections ,ENZYME-linked immunosorbent assay - Abstract
Background: Buruli ulcer is a disease of the skin and soft tissues caused by infection with a slow growing pathogen, Mycobacterium ulcerans. A vaccine for this disease is not available but M. ulcerans possesses a giant plasmid pMUM001 that harbours the polyketide synthase (PKS) genes encoding a multi-enzyme complex needed for the production of its unique lipid toxin called mycolactone, which is central to the pathogenesis of Buruli ulcer. We have studied the immunogenicity of enzymatic domains in humans with M. ulcerans disease, their contacts, as well as non-endemic areas controls. Methods: Between March 2013 and August 2015, heparinized whole blood was obtained from patients confirmed with Buruli ulcer. The blood samples were diluted 1 in 10 in Roswell Park Memorial Institute (RPMI) medium and incubated for 5 days with recombinant mycolactone PKS domains and mycolyltransferase antigen 85A (Ag85A). Blood samples were obtained before and at completion of antibiotic treatment for 8 weeks and again 8 weeks after completion of treatment. Supernatants were assayed for interferon-γ (IFN-γ) and interleukin-5 (IL-5) by enzyme-linked immunosorbent assay. Responses were compared with those of contacts and non-endemic controls. Results: More than 80% of patients and contacts from endemic areas produced IFN-γ in response to all the antigens except acyl carrier protein type 3 (ACP3) to which only 47% of active Buruli ulcer cases and 71% of contacts responded. The highest proportion of responders in cases and contacts was to load module ketosynthase domain (Ksalt) (100%) and enoylreductase (100%). Lower IL-5 responses were induced in a smaller proportion of patients ranging from 54% after ketoreductase type B stimulation to only 21% with ketosynthase type C (KS C). Among endemic area contacts, the, highest proportion was 73% responding to KS C and the lowest was 40% responding to acyltransferase with acetate specificity type 2. Contacts of Buruli ulcer patients produced significantly higher IFN-γ and IL-5 responses compared with those of patients to PKS domain antigens and to mycolyltransferase Ag85A of M. ulcerans. There was low or no response to all the antigens in non-endemic areas controls. IFN-γ and IL-5 responses of patients improved after treatment when compared to baseline results. Discussion: The major response to PKS antigen stimulation was IFN-γ and the strongest responses were observed in healthy contacts of patients living in areas endemic for Buruli ulcer. Patients elicited lower responses than healthy contacts, possibly due to the immunosuppressive effect of mycolactone, but the responses were enhanced after antibiotic treatment. A vaccine made up of the most immunogenic PKS domains combined with the mycolyltransferase Ag85A warrants further investigation. [ABSTRACT FROM AUTHOR]
- Published
- 2018
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