Modeling Missing Cases and Transmission Links in Networks of Extensively Drug-Resistant Tuberculosis in KwaZulu-Natal, South Africa

Author:

Nelson Kristin N1,Gandhi Neel R12,Mathema Barun3,Lopman Benjamin A1,Brust James C M4,Auld Sara C12,Ismail Nazir56,Omar Shaheed Vally5,Brown Tyler S7,Allana Salim1,Campbell Angie1,Moodley Pravi89,Mlisana Koleka89,Shah N Sarita10,Jenness Samuel M1

Affiliation:

1. Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia

2. School of Medicine, Emory University, Atlanta, Georgia

3. Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York

4. Albert Einstein College of Medicine and Montefiore Medical Center, New York, New York

5. National Institute for Communicable Diseases, Johannesburg, South Africa

6. Department of Medical Microbiology, School of Medicine, University of Pretoria, Pretoria, South Africa

7. Infectious Diseases Division, Massachusetts General Hospital, Boston, Massachusetts

8. National Health Laboratory Service, Johannesburg, South Africa

9. School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa

10. Centers for Disease Control and Prevention, Atlanta, Georgia

Abstract

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.

Funder

National Institutes of Health

National Institute of Allergy and Infectious Diseases

Center for AIDS Research, Emory University

Institute for Clinical and Translational Research

Publisher

Oxford University Press (OUP)

Subject

Epidemiology

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