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 J. Garton,
Helen M. O’Hare
Affiliations
Robeena Farzand
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Richard D. Haigh
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Philip Monk
Public Health England, Department of Health and Social Care in England, Government Agency, East Midlands, UK
Pranabashis Haldar
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Hemu Patel
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Manish Pareek
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Raman Verma
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Michael R. Barer
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Gerrit Woltmann
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Lauren Ahyow
National TB Unit, UK Health Security Agency, Government Agency, London, UK
Heena Jagatia
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Jonathan Decker
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Galina V. Mukamolova
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Andrea M. Cooper
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Natalie J. Garton
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
Helen M. O’Hare
Leicester TB Research Group, Department of Respiratory Sciences, University of Leicester, Leicester, UK
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. IMPORTANCE Tuberculosis (TB) killed 1.5 million people in 2020 and affects every country. The extent to which the natural genetic diversity of Mycobacterium tuberculosis influences disease manifestation at both the individual and epidemiological levels remains poorly understood. Insights into how pathogen polymorphisms affect patterns of TB have the potential to translate into clinical and public health practice. Two distinct lineage 3 strains isolated from local TB outbreaks, one of which (CH) was rapidly terminated and the other of which (Lro) persistently transmitted for over a decade, provided us with an opportunity to study these issues. We compared genome sequences, microbiological characteristics, and early immune responses that were evoked upon infection. Our results indicate that the natural lack of fadB4 in the Lro strain contributes to its unique features.
