scholarly journals Evolution of the Extensively Drug-Resistant F15/LAM4/KZN Strain of Mycobacterium tuberculosis in KwaZulu-Natal, South Africa

2007 ◽  
Vol 45 (11) ◽  
pp. 1409-1414 ◽  
Author(s):  
M. Pillay ◽  
A. W. Sturm
PLoS ONE ◽  
2009 ◽  
Vol 4 (11) ◽  
pp. e7778 ◽  
Author(s):  
Thomas R. Ioerger ◽  
Sunwoo Koo ◽  
Eun-Gyu No ◽  
Xiaohua Chen ◽  
Michelle H. Larsen ◽  
...  

2018 ◽  
Vol 52 (4) ◽  
pp. 1800246 ◽  
Author(s):  
Sara C. Auld ◽  
N. Sarita Shah ◽  
Barun Mathema ◽  
Tyler S. Brown ◽  
Nazir Ismail ◽  
...  

Despite evidence that transmission is driving an extensively drug-resistant TB (XDR-TB) epidemic, our understanding of where and between whom transmission occurs is limited. We sought to determine whether there was genomic evidence of transmission between individuals without an epidemiologic connection.We conducted a prospective study of XDR-TB patients in KwaZulu-Natal, South Africa, during the 2011–2014 period. We collected sociodemographic and clinical data, and identified epidemiologic links based on person-to-person or hospital-based connections. We performed whole-genome sequencing (WGS) on theMycobacterium tuberculosisisolates and determined pairwise single nucleotide polymorphism (SNP) differences.Among 404 participants, 123 (30%) had person-to-person or hospital-based links, leaving 281 (70%) epidemiologically unlinked. The median SNP difference between participants with person-to-person and hospital-based links was 10 (interquartile range (IQR) 8–24) and 16 (IQR 10–23), respectively. The median SNP difference between unlinked participants and their closest genomic link was 5 (IQR 3–9) and half of unlinked participants were within 7 SNPs of at least five participants.The majority of epidemiologically-unlinked XDR-TB patients had low pairwise SNP differences with at least one other participant, consistent with transmission. These data suggest that much of transmission may result from casual contact in community settings between individuals not known to one another.


PLoS ONE ◽  
2017 ◽  
Vol 12 (10) ◽  
pp. e0181797 ◽  
Author(s):  
Thandi Kapwata ◽  
Natashia Morris ◽  
Angela Campbell ◽  
Thuli Mthiyane ◽  
Primrose Mpangase ◽  
...  

2011 ◽  
Vol 17 (10) ◽  
pp. 1942-1945 ◽  
Author(s):  
Max R. O’Donnell ◽  
Jennifer Zelnick ◽  
Lise Werner ◽  
Iqbal Master ◽  
Marian Loveday ◽  
...  

2020 ◽  
Vol 189 (7) ◽  
pp. 735-745
Author(s):  
Kristin N Nelson ◽  
Neel R Gandhi ◽  
Barun Mathema ◽  
Benjamin A Lopman ◽  
James C M Brust ◽  
...  

Abstract Patterns of transmission of drug-resistant tuberculosis (TB) remain poorly understood, despite over half a million incident cases worldwide in 2017. Modeling TB transmission networks can provide insight into drivers of transmission, but incomplete sampling of TB cases can pose challenges for inference from individual epidemiologic and molecular data. We assessed the effect of missing cases on a transmission network inferred from Mycobacterium tuberculosis sequencing data on extensively drug-resistant TB cases in KwaZulu-Natal, South Africa, diagnosed in 2011–2014. We tested scenarios in which cases were missing at random, missing differentially by clinical characteristics, or missing differentially by transmission (i.e., cases with many links were under- or oversampled). Under the assumption that cases were missing randomly, the mean number of transmissions per case in the complete network needed to be larger than 20, far higher than expected, to reproduce the observed network. Instead, the most likely scenario involved undersampling of high-transmitting cases, and models provided evidence for super-spreading. To our knowledge, this is the first analysis to have assessed support for different mechanisms of missingness in a TB transmission study, but our results are subject to the distributional assumptions of the network models we used. Transmission studies should consider the potential biases introduced by incomplete sampling and identify host, pathogen, or environmental factors driving super-spreading.


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