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Detecting Mutations in the Mycobacterium tuberculosis Pyrazinamidase Gene pncA to Improve Infection Control and Decrease Drug Resistance Rates in Human Immunodeficiency Virus Coinfection.

Dudley, MZ; Sheen, P; Gilman, RH; Ticona, E; Friedland, JS; Kirwan, DE; Caviedes, L; Rodriguez, R; Cabrera, LZ; Coronel, J; et al. Dudley, MZ; Sheen, P; Gilman, RH; Ticona, E; Friedland, JS; Kirwan, DE; Caviedes, L; Rodriguez, R; Cabrera, LZ; Coronel, J; Grandjean, L; Moore, DAJ; Evans, CA; Huaroto, L; Chávez-Pérez, V; Zimic, M (2016) Detecting Mutations in the Mycobacterium tuberculosis Pyrazinamidase Gene pncA to Improve Infection Control and Decrease Drug Resistance Rates in Human Immunodeficiency Virus Coinfection. Am J Trop Med Hyg, 95 (6). pp. 1239-1246. ISSN 1476-1645 https://doi.org/10.4269/ajtmh.15-0711
SGUL Authors: Friedland, Jonathan Samuel

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Abstract

Hospital infection control measures are crucial to tuberculosis (TB) control strategies within settings caring for human immunodeficiency virus (HIV)-positive patients, as these patients are at heightened risk of developing TB. Pyrazinamide (PZA) is a potent drug that effectively sterilizes persistent Mycobacterium tuberculosis bacilli. However, PZA resistance associated with mutations in the nicotinamidase/pyrazinamidase coding gene, pncA, is increasing. A total of 794 patient isolates obtained from four sites in Lima, Peru, underwent spoligotyping and drug resistance testing. In one of these sites, the HIV unit of Hospital Dos de Mayo (HDM), an isolation ward for HIV/TB coinfected patients opened during the study as an infection control intervention: circulating genotypes and drug resistance pre- and postintervention were compared. All other sites cared for HIV-negative outpatients: genotypes and drug resistance rates from these sites were compared with those from HDM. HDM patients showed high concordance between multidrug resistance, PZA resistance according to the Wayne method, the two most common genotypes (spoligotype international type [SIT] 42 of the Latino American-Mediterranean (LAM)-9 clade and SIT 53 of the T1 clade), and the two most common pncA mutations (G145A and A403C). These associations were absent among community isolates. The infection control intervention was associated with 58-92% reductions in TB caused by SIT 42 or SIT 53 genotypes (odds ratio [OR] = 0.420, P = 0.003); multidrug-resistant TB (OR = 0.349, P < 0.001); and PZA-resistant TB (OR = 0.076, P < 0.001). In conclusion, pncA mutation typing, with resistance testing and spoligotyping, was useful in identifying a nosocomial TB outbreak and demonstrating its resolution after implementation of infection control measures.

Item Type: Article
Additional Information: © The American Society of Tropical Medicine and Hygiene [open-access] This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Keywords: Adolescent, Adult, Aged, Amidohydrolases, Antitubercular Agents, Case-Control Studies, Drug Resistance, Bacterial, Female, Gene Expression Regulation, Bacterial, Gene Expression Regulation, Enzymologic, Genotype, HIV Infections, Humans, Male, Middle Aged, Mutation, Mycobacterium tuberculosis, Tuberculosis, Young Adult, Humans, Mycobacterium tuberculosis, Tuberculosis, HIV Infections, Amidohydrolases, Antitubercular Agents, Case-Control Studies, Drug Resistance, Bacterial, Gene Expression Regulation, Bacterial, Gene Expression Regulation, Enzymologic, Genotype, Mutation, Adolescent, Adult, Aged, Middle Aged, Female, Male, Young Adult, Science & Technology, Life Sciences & Biomedicine, Public, Environmental & Occupational Health, Tropical Medicine, MICROSCOPIC-OBSERVATION, SUSCEPTIBILITY ASSAY, HIV-INFECTION, CHEMOTHERAPY, TRANSMISSION, PERU, TB, 11 Medical And Health Sciences, Tropical Medicine
Journal or Publication Title: Am J Trop Med Hyg
ISSN: 1476-1645
Language: eng
Dates:
DateEvent
7 December 2016Published
24 August 2016Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
R01 TW008669FIC NIH HHSUNSPECIFIED
057434/Z/99/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
070005/Z/02/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
078340/Z/05/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
099805/Z/12/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
105788/Z/14/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
201251/Z/16/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
MR/K007467/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/K007467/1Department for International Developmenthttp://dx.doi.org/10.13039/501100000278
MR/K007467/1Wellcome Trusthttp://dx.doi.org/10.13039/100004440
OPP1118545Bill and Melinda Gates Foundationhttp://dx.doi.org/10.13039/100000865
PubMed ID: 27928075
Web of Science ID: WOS:000400206900005
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/110664
Publisher's version: https://doi.org/10.4269/ajtmh.15-0711

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