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1.
Transbound Emerg Dis ; 68(4): 2229-2238, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33048439

ABSTRACT

Beijing genotype Mycobacterium tuberculosis strains associate with increased virulence, resistance and/or higher transmission rates. This study describes a specific Beijing strain predominantly identified in the Panamanian province of Colon with one of the highest incidences of tuberculosis in the country. Retrospective mycobacterial interspersed repetitive unit/variable number of tandem repeats analysis of 42 isolates collected between January and August 2018 allowed to identify a cluster (Beijing A) with 17 (40.5%) Beijing isolates. Subsequent prospective strain-specific PCR-based surveillance from September 2019 to March 2020 confirmed the predominance of the Beijing A strain (44.1%) in this province. Whole-genome sequencing revealed higher-than-expected diversity within the cluster, suggesting long-term prevalence of this strain and low number of cases caused by recent transmission. The Beijing A strain belongs to the Asian African 3 (Bmyc13, L2.2.5) branch of the modern Beijing sublineage, with their closest isolates corresponding to cases from Vietnam, probably introduced in Panama between 2000 and 2012.


Subject(s)
Mycobacterium tuberculosis , Tuberculosis/epidemiology , Animals , Beijing , Clone Cells , Genotype , Minisatellite Repeats , Mycobacterium tuberculosis/genetics , Panama/epidemiology , Prevalence , Prospective Studies , Retrospective Studies
2.
Emerg Infect Dis ; 25(3): 507-514, 2019 03.
Article in English | MEDLINE | ID: mdl-30789134

ABSTRACT

Systematic molecular/genomic epidemiology studies for tuberculosis surveillance cannot be implemented in many countries. We selected Panama as a model for an alternative strategy. Mycobacterial interspersed repetitive unit-variable-number tandem-repeat (MIRU-VNTR) analysis revealed a high proportion (50%) of Mycobacterium tuberculosis isolates included in 6 clusters (A-F) in 2 provinces (Panama and Colon). Cluster A corresponded to the Beijing sublineage. Whole-genome sequencing (WGS) differentiated clusters due to active recent transmission, with low single-nucleotide polymorphism-based diversity (cluster C), from clusters involving long-term prevalent strains with higher diversity (clusters A, B). Prospective application in Panama of 3 tailored strain-specific PCRs targeting marker single-nucleotide polymorphisms identified from WGS data revealed that 31.4% of incident cases involved strains A-C and that the Beijing strain was highly represented and restricted mainly to Colon. Rational integration of MIRU-VNTR, WGS, and tailored strain-specific PCRs could be a new model for tuberculosis surveillance in countries without molecular/genomic epidemiology programs.


Subject(s)
Models, Theoretical , Mycobacterium tuberculosis , Tuberculosis/epidemiology , Tuberculosis/transmission , Humans , Minisatellite Repeats , Molecular Epidemiology , Molecular Typing , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/genetics , Phylogeny , Polymorphism, Single Nucleotide , Population Surveillance , Tuberculosis/genetics , Tuberculosis/microbiology , Whole Genome Sequencing
3.
Lung ; 195(4): 517-521, 2017 08.
Article in English | MEDLINE | ID: mdl-28551717

ABSTRACT

The cellular immune response to Mycobacterium tuberculosis infection has been well characterized, while the humoral antibody response remains underexplored. We aimed to examine the total and anti-phospholipid IgM levels in the pleural lavage from mice with Mycobacterium bovis BCG extrapulmonary infection. We found that the levels of total and anti-phosphatidylcholine IgM antibodies remained significantly higher in infected mice as compared to non-infected mice up to day 90 after BCG infection, while the anti-cardiolipin IgM antibody levels decreased with bacteria clearance. Our findings suggest that IgM antibodies are secreted and their composition vary during early and late immune response to BCG pleurisy.


Subject(s)
Antibodies, Antiphospholipid/immunology , Immunity, Humoral , Immunoglobulin M/immunology , Mycobacterium tuberculosis/immunology , Phosphatidylcholines/immunology , Tuberculosis, Pleural/immunology , Animals , Antibodies, Anticardiolipin/immunology , Bacterial Load , Disease Models, Animal , Female , Host-Pathogen Interactions , Male , Mice, Inbred C57BL , Time Factors , Tuberculosis, Pleural/microbiology
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