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Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing

BACKGROUND: Understanding the emergence and spread of multidrug-resistant tuberculosis (MDR-TB) is crucial for its control. MDR-TB in previously treated patients is generally attributed to the selection of drug resistant mutants during inadequate therapy rather than transmission of a resistant strai...

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Autores principales: Clark, Taane G., Mallard, Kim, Coll, Francesc, Preston, Mark, Assefa, Samuel, Harris, David, Ogwang, Sam, Mumbowa, Francis, Kirenga, Bruce, O’Sullivan, Denise M., Okwera, Alphonse, Eisenach, Kathleen D., Joloba, Moses, Bentley, Stephen D., Ellner, Jerrold J., Parkhill, Julian, Jones-López, Edward C., McNerney, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859632/
https://www.ncbi.nlm.nih.gov/pubmed/24349420
http://dx.doi.org/10.1371/journal.pone.0083012
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author Clark, Taane G.
Mallard, Kim
Coll, Francesc
Preston, Mark
Assefa, Samuel
Harris, David
Ogwang, Sam
Mumbowa, Francis
Kirenga, Bruce
O’Sullivan, Denise M.
Okwera, Alphonse
Eisenach, Kathleen D.
Joloba, Moses
Bentley, Stephen D.
Ellner, Jerrold J.
Parkhill, Julian
Jones-López, Edward C.
McNerney, Ruth
author_facet Clark, Taane G.
Mallard, Kim
Coll, Francesc
Preston, Mark
Assefa, Samuel
Harris, David
Ogwang, Sam
Mumbowa, Francis
Kirenga, Bruce
O’Sullivan, Denise M.
Okwera, Alphonse
Eisenach, Kathleen D.
Joloba, Moses
Bentley, Stephen D.
Ellner, Jerrold J.
Parkhill, Julian
Jones-López, Edward C.
McNerney, Ruth
author_sort Clark, Taane G.
collection PubMed
description BACKGROUND: Understanding the emergence and spread of multidrug-resistant tuberculosis (MDR-TB) is crucial for its control. MDR-TB in previously treated patients is generally attributed to the selection of drug resistant mutants during inadequate therapy rather than transmission of a resistant strain. Traditional genotyping methods are not sufficient to distinguish strains in populations with a high burden of tuberculosis and it has previously been difficult to assess the degree of transmission in these settings. We have used whole genome analysis to investigate M. tuberculosis strains isolated from treatment experienced patients with MDR-TB in Uganda over a period of four years. METHODS AND FINDINGS: We used high throughput genome sequencing technology to investigate small polymorphisms and large deletions in 51 Mycobacterium tuberculosis samples from 41 treatment-experienced TB patients attending a TB referral and treatment clinic in Kampala. This was a convenience sample representing 69% of MDR-TB cases identified over the four year period. Low polymorphism was observed in longitudinal samples from individual patients (2-15 SNPs). Clusters of samples with less than 50 SNPs variation were examined. Three clusters comprising a total of 8 patients were found with almost identical genetic profiles, including mutations predictive for resistance to rifampicin and isoniazid, suggesting transmission of MDR-TB. Two patients with previous drug susceptible disease were found to have acquired MDR strains, one of which shared its genotype with an isolate from another patient in the cohort. CONCLUSIONS: Whole genome sequence analysis identified MDR-TB strains that were shared by more than one patient. The transmission of multidrug-resistant disease in this cohort of retreatment patients emphasises the importance of early detection and need for infection control. Consideration should be given to rapid testing for drug resistance in patients undergoing treatment to monitor the emergence of resistance and permit early intervention to avoid onward transmission.
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spelling pubmed-38596322013-12-13 Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing Clark, Taane G. Mallard, Kim Coll, Francesc Preston, Mark Assefa, Samuel Harris, David Ogwang, Sam Mumbowa, Francis Kirenga, Bruce O’Sullivan, Denise M. Okwera, Alphonse Eisenach, Kathleen D. Joloba, Moses Bentley, Stephen D. Ellner, Jerrold J. Parkhill, Julian Jones-López, Edward C. McNerney, Ruth PLoS One Research Article BACKGROUND: Understanding the emergence and spread of multidrug-resistant tuberculosis (MDR-TB) is crucial for its control. MDR-TB in previously treated patients is generally attributed to the selection of drug resistant mutants during inadequate therapy rather than transmission of a resistant strain. Traditional genotyping methods are not sufficient to distinguish strains in populations with a high burden of tuberculosis and it has previously been difficult to assess the degree of transmission in these settings. We have used whole genome analysis to investigate M. tuberculosis strains isolated from treatment experienced patients with MDR-TB in Uganda over a period of four years. METHODS AND FINDINGS: We used high throughput genome sequencing technology to investigate small polymorphisms and large deletions in 51 Mycobacterium tuberculosis samples from 41 treatment-experienced TB patients attending a TB referral and treatment clinic in Kampala. This was a convenience sample representing 69% of MDR-TB cases identified over the four year period. Low polymorphism was observed in longitudinal samples from individual patients (2-15 SNPs). Clusters of samples with less than 50 SNPs variation were examined. Three clusters comprising a total of 8 patients were found with almost identical genetic profiles, including mutations predictive for resistance to rifampicin and isoniazid, suggesting transmission of MDR-TB. Two patients with previous drug susceptible disease were found to have acquired MDR strains, one of which shared its genotype with an isolate from another patient in the cohort. CONCLUSIONS: Whole genome sequence analysis identified MDR-TB strains that were shared by more than one patient. The transmission of multidrug-resistant disease in this cohort of retreatment patients emphasises the importance of early detection and need for infection control. Consideration should be given to rapid testing for drug resistance in patients undergoing treatment to monitor the emergence of resistance and permit early intervention to avoid onward transmission. Public Library of Science 2013-12-11 /pmc/articles/PMC3859632/ /pubmed/24349420 http://dx.doi.org/10.1371/journal.pone.0083012 Text en © 2013 Clark et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Clark, Taane G.
Mallard, Kim
Coll, Francesc
Preston, Mark
Assefa, Samuel
Harris, David
Ogwang, Sam
Mumbowa, Francis
Kirenga, Bruce
O’Sullivan, Denise M.
Okwera, Alphonse
Eisenach, Kathleen D.
Joloba, Moses
Bentley, Stephen D.
Ellner, Jerrold J.
Parkhill, Julian
Jones-López, Edward C.
McNerney, Ruth
Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing
title Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing
title_full Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing
title_fullStr Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing
title_full_unstemmed Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing
title_short Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing
title_sort elucidating emergence and transmission of multidrug-resistant tuberculosis in treatment experienced patients by whole genome sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859632/
https://www.ncbi.nlm.nih.gov/pubmed/24349420
http://dx.doi.org/10.1371/journal.pone.0083012
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