» Articles » PMID: 36687645

Pan-genome Association Study of Lineage-4 Revealed Specific Genes Related to the High and Low Prevalence of the Disease in Patients from the North-Eastern Area of Medellín, Colombia

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2023 Jan 23
PMID 36687645
Authors
Affiliations
Soon will be listed here.
Abstract

() lineage 4 is responsible for the highest burden of tuberculosis (TB) worldwide. This lineage has been the most prevalent lineage in Colombia, especially in the North-Eastern (NE) area of Medellin, where it has been shown to have a high prevalence of LAM9 SIT42 and Haarlem1 SIT62 sublineages. There is evidence that regardless of environmental factors and host genetics, differences among sublineages of strains play an important role in the course of infection and disease. Nevertheless, the genetic basis of the success of a sublineage in a specific geographic area remains uncertain. We used a pan-genome-wide association study (pan-GWAS) of 47 strains isolated from NE Medellin between 2005 and 2008 to identify the genes responsible for the phenotypic differences among high and low prevalence sublineages. Our results allowed the identification of 12 variants in 11 genes, of which 4 genes showed the strongest association to low prevalence (, , , and ). The first three have been described as necessary for invasion and intracellular survival. Polymorphisms identified in low prevalence isolates may suggest related to a fitness cost of , which might reflect a decrease in their capacity to be transmitted or to cause an active infection. These results contribute to understanding the success of some sublineages of lineage-4 in a specific geographical area.

Citing Articles

High Prevalence of atpE Mutations in Bedaquiline-Resistant Mycobacterium tuberculosis Isolates, Russia.

Zimenkov D, Ushtanit A, Gordeeva E, Guselnikova E, Schwartz Y, Stavitskaya N Emerg Infect Dis. 2025; 31(3):525-536.

PMID: 40023803 PMC: 11878324. DOI: 10.3201/eid3103.241488.


Decoding Ecuadorian Isolates: Unveiling Lineage-Associated Signatures in Beta-Lactamase Resistance via Pangenome Analysis.

Morey-Leon G, Fernandez-Cadena J, Andrade-Molina D, Berna L Biomedicines. 2025; 13(2).

PMID: 40002726 PMC: 11853040. DOI: 10.3390/biomedicines13020313.


Pangenome and genomic signatures linked to the dominance of the lineage-4 of Mycobacterium tuberculosis isolated from extrapulmonary tuberculosis patients in western Ethiopia.

Chekesa B, Singh H, Gonzalez-Juarbe N, Vashee S, Wiscovitch-Russo R, Dupont C PLoS One. 2024; 19(7):e0304060.

PMID: 39052555 PMC: 11271921. DOI: 10.1371/journal.pone.0304060.


Genome-Wide Association Studies (GWAS) Approaches for the Detection of Genetic Variants Associated with Antibiotic Resistance: A Systematic Review.

Mosquera-Rendon J, Moreno-Herrera C, Robledo J, Hurtado-Paez U Microorganisms. 2023; 11(12).

PMID: 38138010 PMC: 10745584. DOI: 10.3390/microorganisms11122866.


Pangenome Reconstruction of as a Guide to Reveal Genomic Features Associated with Strain Clinical Phenotype.

Negrete-Paz A, Vazquez-Marrufo G, Gutierrez-Moraga A, Vazquez-Garciduenas M Microorganisms. 2023; 11(6).

PMID: 37374997 PMC: 10300688. DOI: 10.3390/microorganisms11061495.

References
1.
Buu T, van Soolingen D, Huyen M, Lan N, Quy H, Tiemersma E . Increased transmission of Mycobacterium tuberculosis Beijing genotype strains associated with resistance to streptomycin: a population-based study. PLoS One. 2012; 7(8):e42323. PMC: 3418256. DOI: 10.1371/journal.pone.0042323. View

2.
Gey van Pittius N, Sampson S, Lee H, Kim Y, van Helden P, Warren R . Evolution and expansion of the Mycobacterium tuberculosis PE and PPE multigene families and their association with the duplication of the ESAT-6 (esx) gene cluster regions. BMC Evol Biol. 2006; 6:95. PMC: 1660551. DOI: 10.1186/1471-2148-6-95. View

3.
Contreras-Moreira B, Vinuesa P . GET_HOMOLOGUES, a versatile software package for scalable and robust microbial pangenome analysis. Appl Environ Microbiol. 2013; 79(24):7696-701. PMC: 3837814. DOI: 10.1128/AEM.02411-13. View

4.
Jou R, Chiang C, Huang W . Distribution of the Beijing family genotypes of Mycobacterium tuberculosis in Taiwan. J Clin Microbiol. 2005; 43(1):95-100. PMC: 540113. DOI: 10.1128/JCM.43.1.95-100.2005. View

5.
Brynildsrud O, Bohlin J, Scheffer L, Eldholm V . Rapid scoring of genes in microbial pan-genome-wide association studies with Scoary. Genome Biol. 2016; 17(1):238. PMC: 5124306. DOI: 10.1186/s13059-016-1108-8. View