Interaction between M. tuberculosis Lineage and Human Genetic Variants Reveals Novel Pathway Associations with Severity of TB

Bibliographic Details
Title: Interaction between M. tuberculosis Lineage and Human Genetic Variants Reveals Novel Pathway Associations with Severity of TB
Authors: Michael L. McHenry, Eddie M. Wampande, Moses L. Joloba, LaShaunda L. Malone, Harriet Mayanja-Kizza, William S. Bush, W. Henry Boom, Scott M. Williams, Catherine M. Stein
Source: Pathogens, Vol 10, Iss 11, p 1487 (2021)
Publisher Information: MDPI AG, 2021.
Publication Year: 2021
Collection: LCC:Medicine
Subject Terms: tuberculosis severity, M. tuberculosis, population genetics, lineage-based GWAS, M. tuberculosis–human coevolution, Medicine
More Details: Tuberculosis (TB) remains a major public health threat globally, especially in sub-Saharan Africa. Both human and Mycobacterium tuberculosis (MTBC) genetic variation affect TB outcomes, but few studies have examined if and how the two genomes interact to affect disease. We hypothesize that long-term coexistence between human genomes and MTBC lineages modulates disease to affect its severity. We examined this hypothesis in our TB household contact study in Kampala, Uganda, in which we identified three MTBC lineages, of which one, L4.6-Uganda, is clearly derived and hence recent. We quantified TB severity using the Bandim TBscore and examined the interaction between MTBC lineage and human single-nucleotide polymorphisms (SNPs) genome-wide, in two independent cohorts of TB cases (n = 149 and n = 127). We found a significant interaction between an SNP in PPIAP2 and the Uganda lineage (combined p = 4 × 10−8). PPIAP2 is a pseudogene that is highly expressed in immune cells. Pathway and eQTL analyses indicated potential roles between coevolving SNPs and cellular replication and metabolism as well as platelet aggregation and coagulation. This finding provides further evidence that host–pathogen interactions affect clinical presentation differently than host and pathogen genetic variation independently, and that human–MTBC coevolution is likely to explain patterns of disease severity.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2076-0817
Relation: https://www.mdpi.com/2076-0817/10/11/1487; https://doaj.org/toc/2076-0817
DOI: 10.3390/pathogens10111487
Access URL: https://doaj.org/article/4ce8188910264aaebe58bdfde9f3c03f
Accession Number: edsdoj.4ce8188910264aaebe58bdfde9f3c03f
Database: Directory of Open Access Journals
More Details
ISSN:20760817
DOI:10.3390/pathogens10111487
Published in:Pathogens
Language:English