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Innate immune response to Mycobacterium tuberculosis Beijing and other genotypes

Authors :
Wang, C.
Peyron, P.
Mestre, O.
Kaplan, G.
Soolingen, D. van
Gao, Q.
Gicquel, B.
Neyrolles, O.
Wang, C.
Peyron, P.
Mestre, O.
Kaplan, G.
Soolingen, D. van
Gao, Q.
Gicquel, B.
Neyrolles, O.
Source :
PLoS One; 1932-6203; 10; vol. 5; e13594; ~PLoS One~~~~~1932-6203~10~5~~e13594
Publication Year :
2010

Abstract

Contains fulltext : 124335.pdf (publisher's version ) (Open Access)<br />BACKGROUND: As a species, Mycobacterium tuberculosis is more diverse than previously thought. In particular, the Beijing family of M. tuberculosis strains is spreading and evaluating throughout the world and this is giving rise to public health concerns. Genetic diversity within this family has recently been delineated further and a specific genotype, called Bmyc10, has been shown to represent over 60% of all Beijing clinical isolates in several parts of the world. How the host immune system senses and responds to various M. tuberculosis strains may profoundly influence clinical outcome and the relative epidemiological success of the different mycobacterial lineages. We hypothesised that the success of the Bmyc10 group may, at least in part, rely upon its ability to alter innate immune responses and the secretion of cytokines and chemokines by host phagocytes. METHODOLOGY/PRINCIPAL FINDINGS: We infected human macrophages and dendritic cells with a collection of genetically well-defined M. tuberculosis clinical isolates belonging to various mycobacterial families, including Beijing. We analyzed cytokine and chemokine secretion on a semi-global level using antibody arrays allowing the detection of sixty-five immunity-related soluble molecules. Our data indicate that Beijing strains induce significantly less interleukin (IL)-6, tumor necrosis factor (TNF), IL-10 and GRO-alpha than the H37Rv reference strain, a feature that is variously shared by other modern and ancient M. tuberculosis families and which constitutes a signature of the Beijing family as a whole. However, Beijing strains did not differ relative to each other in their ability to modulate cytokine secretion. CONCLUSIONS/SIGNIFICANCE: Our results confirm and expand upon previous reports showing that M. tuberculosis Beijing strains in general are poor in vitro cytokine inducers in human phagocytes. The results suggest that the epidemiological success of the Beijing Bmyc10 is unlikely to rely upon any specifi

Details

Database :
OAIster
Journal :
PLoS One; 1932-6203; 10; vol. 5; e13594; ~PLoS One~~~~~1932-6203~10~5~~e13594
Publication Type :
Electronic Resource
Accession number :
edsoai.on1284090538
Document Type :
Electronic Resource