A Persistent Tuberculosis Outbreak in the UK Is Characterized by Hydrophobic fadB4 -Deficient Mycobacterium tuberculosis That Replicates Rapidly in Macrophages

Robeena Farzand, Richard D Haigh, Philip Monk, Pranabashis Haldar*, Hemu Patel, Manish Pareek,, Raman Verma, Michael R. Barer, Gerrit Woltmann, Lauren Ahyow, Heena Jagatia, Jonathan Decker, Galina V Mukamolova, Andrea M. Cooper, Natalie Garton, Helen M. O’Hare*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

2 Citations (Scopus)

Abstract

The genetic diversity of Mycobacterium tuberculosis can influence disease severity and transmissibility. To better understand how this diversity influences individuals and communities, we phenotyped M. tuberculosis that was causing a persistent outbreak in the East Midlands, United Kingdom. Compared to nonoutbreak isolates, bacilli had higher lipid contents and more hydrophobic cell surfaces. In macrophage infection models, the bacteria increased more rapidly, provoked the enhanced accumulation of macrophage lipid droplets and enhanced the secretion of IL-1β. Natural deletions in fadB4, nrdB, and plcC distinguished the outbreak isolates from other lineage 3 isolates in the region. fadB4 is annotated with a putative role in cell envelope biosynthesis, so the loss of this gene has the potential to alter the interactions of bacteria with immune cells. Reintroduction of fadB4 to the outbreak strain led to a phenotype that more closely resembled those of nonoutbreak strains. The improved understanding of the microbiological characteristics and the corresponding genetic polymorphisms that associate with outbreaks have the potential to inform tuberculosis control.
Original languageEnglish
Number of pages13
JournalmBio
Volume13
Issue number6
Early online date14 Nov 2022
DOIs
Publication statusPublished - 20 Dec 2022

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© 2022 Farzand et al.

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