Mathematical models of drug-resistant tuberculosis lack bacterial heterogeneity: A systematic review

• Published in: PLoS pathogens Vol. 20; no. 4; p. e1011574
• Main Authors: Fuller, Naomi M, McQuaid, Christopher F, Harker, Martin J, Weerasuriya, Chathika K, McHugh, Timothy D, Knight, Gwenan M
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 10.04.2024; Public Library of Science (PLoS)
• Subjects: Antibiotic resistance; Antibiotics; Antimicrobial resistance; Antitubercular agents; Bacteria; Biology and Life Sciences; Decision making; Dosage and administration; Drug resistance; Drug resistance in microorganisms; Drug therapy; Health aspects; Heterogeneity; Inclusion; Mathematical models; Medicine and Health Sciences; Multidrug resistance; Mutation; Parameter estimation; Patient outcomes; Populations; Prevention; Public health; Research and Analysis Methods; Simulation models; Social Sciences; Systematic review; Tuberculosis; United Kingdom
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1011574

Drug-resistant tuberculosis (DR-TB) threatens progress in the control of TB. Mathematical models are increasingly being used to guide public health decisions on managing both antimicrobial resistance (AMR) and TB. It is important to consider bacterial heterogeneity in models as it can have consequences for predictions of resistance prevalence, which may affect decision-making. We conducted a systematic review of published mathematical models to determine the modelling landscape and to explore methods for including bacterial heterogeneity. Our first objective was to identify and analyse the general characteristics of mathematical models of DR-mycobacteria, including M. tuberculosis. The second objective was to analyse methods of including bacterial heterogeneity in these models. We had different definitions of heterogeneity depending on the model level. For between-host models of mycobacterium, heterogeneity was defined as any model where bacteria of the same resistance level were further differentiated. For bacterial population models, heterogeneity was defined as having multiple distinct resistant populations. The search was conducted following PRISMA guidelines in five databases, with studies included if they were mechanistic or simulation models of DR-mycobacteria. We identified 195 studies modelling DR-mycobacteria, with most being dynamic transmission models of non-treatment intervention impact in M. tuberculosis (n = 58). Studies were set in a limited number of specific countries, and 44% of models (n = 85) included only a single level of "multidrug-resistance (MDR)". Only 23 models (8 between-host) included any bacterial heterogeneity. Most of these also captured multiple antibiotic-resistant classes (n = 17), but six models included heterogeneity in bacterial populations resistant to a single antibiotic. Heterogeneity was usually represented by different fitness values for bacteria resistant to the same antibiotic (61%, n = 14). A large and growing body of mathematical models of DR-mycobacterium is being used to explore intervention impact to support policy as well as theoretical explorations of resistance dynamics. However, the majority lack bacterial heterogeneity, suggesting that important evolutionary effects may be missed.