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POSTER PRESENTATION Open Access Association of GT microsatellite polymorphism in TLR 2 gene with leprosy NC Suryadevara 1 , NV Sanjeev 1 , Vijaya Lakshmi Valluri 1 , Suman Jain 2 , MPJS Anandraj 1* From First International Science Symposium on HIV and Infectious Diseases (HIV SCIENCE 2012) Chennai, India. 20-22 January 2012 Background Toll-like receptor 2 (TLR2) is critical in bringing up immune responses to mycobacterial infections. The mutations in TLR2 are known to confer susceptibility for severe infection with mycobacteria. TLR2 may diminish response to mycobacterial proteins and place individuals at risk of developing leprosy. We investi- gated the association of GT repeat polymorphism in intron2 of TLR2 gene with leprosy in south Indian patients. Methods A total of 20 leprosy patients and 45 contacts were enrolled in the study. Primers were designed using Pri- mer3 software for PCR amplification of the TLR2 gene. The number of GT repeats was confirmed by sequen- cing. Two-tailed Chi-Square test was performed to check the association. p less than 0.05 was considered to be statistically significant. Results The number of GT repeats varied from 13 to 24 in both the groups studied. The frequency of patients with (GT) 13 repeats was significantly low (p=0.04, OR=0.318) and that of (GT) 14 repeats (p=0.04, OR=7.76) was signifi- cantly high. Conclusion Our results suggest that an individual with (GT) 13 repeats may be resistant and those with (GT) 14 repeats may be susceptible to leprosy. Furthermore, elucidation of functional relevance studies such as gene expression and proteomics may reveal the influence and role of these repeat number variations in leprosy. Author details 1 LEPRA India Blue Peter Public Health & Research Centre, Cherlapally, Hyderabad, India. 2 Thalasemmia and Sickle Cell Anaemia Society TSCS, Hyderabad, India. Published: 4 May 2012 doi:10.1186/1471-2334-12-S1-P12 Cite this article as: Suryadevara et al.: Association of GT microsatellite polymorphism in TLR 2 gene with leprosy. BMC Infectious Diseases 2012 12(Suppl 1):P12. Submit your next manuscript to BioMed Central and take full advantage of: Convenient online submission Thorough peer review No space constraints or color figure charges Immediate publication on acceptance Inclusion in PubMed, CAS, Scopus and Google Scholar Research which is freely available for redistribution Submit your manuscript at www.biomedcentral.com/submit * Correspondence: [email protected] 1 LEPRA India Blue Peter Public Health & Research Centre, Cherlapally, Hyderabad, India Full list of author information is available at the end of the article Suryadevara et al. BMC Infectious Diseases 2012, 12(Suppl 1):P12 http://www.biomedcentral.com/1471-2334/12/S1/P12 © 2012 Suryadevara et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Association of GT microsatellite polymorphism in TLR 2 gene with leprosy

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POSTER PRESENTATION Open Access

Association of GT microsatellite polymorphism inTLR 2 gene with leprosyNC Suryadevara1, NV Sanjeev1, Vijaya Lakshmi Valluri1, Suman Jain2, MPJS Anandraj1*

From First International Science Symposium on HIV and Infectious Diseases (HIV SCIENCE 2012)Chennai, India. 20-22 January 2012

BackgroundToll-like receptor 2 (TLR2) is critical in bringing upimmune responses to mycobacterial infections. Themutations in TLR2 are known to confer susceptibilityfor severe infection with mycobacteria. TLR2 maydiminish response to mycobacterial proteins and placeindividuals at risk of developing leprosy. We investi-gated the association of GT repeat polymorphism inintron2 of TLR2 gene with leprosy in south Indianpatients.

MethodsA total of 20 leprosy patients and 45 contacts wereenrolled in the study. Primers were designed using Pri-mer3 software for PCR amplification of the TLR2 gene.The number of GT repeats was confirmed by sequen-cing. Two-tailed Chi-Square test was performed tocheck the association. p less than 0.05 was considered tobe statistically significant.

ResultsThe number of GT repeats varied from 13 to 24 in boththe groups studied. The frequency of patients with (GT)13 repeats was significantly low (p=0.04, OR=0.318) andthat of (GT) 14 repeats (p=0.04, OR=7.76) was signifi-cantly high.

ConclusionOur results suggest that an individual with (GT) 13repeats may be resistant and those with (GT) 14 repeatsmay be susceptible to leprosy. Furthermore, elucidationof functional relevance studies such as gene expression

and proteomics may reveal the influence and role ofthese repeat number variations in leprosy.

Author details1LEPRA India – Blue Peter Public Health & Research Centre, Cherlapally,Hyderabad, India. 2Thalasemmia and Sickle Cell Anaemia Society TSCS,Hyderabad, India.

Published: 4 May 2012

doi:10.1186/1471-2334-12-S1-P12Cite this article as: Suryadevara et al.: Association of GT microsatellitepolymorphism in TLR 2 gene with leprosy. BMC Infectious Diseases 201212(Suppl 1):P12.

Submit your next manuscript to BioMed Centraland take full advantage of:

• Convenient online submission

• Thorough peer review

• No space constraints or color figure charges

• Immediate publication on acceptance

• Inclusion in PubMed, CAS, Scopus and Google Scholar

• Research which is freely available for redistribution

Submit your manuscript at www.biomedcentral.com/submit

* Correspondence: [email protected] India – Blue Peter Public Health & Research Centre, Cherlapally,Hyderabad, IndiaFull list of author information is available at the end of the article

Suryadevara et al. BMC Infectious Diseases 2012, 12(Suppl 1):P12http://www.biomedcentral.com/1471-2334/12/S1/P12

© 2012 Suryadevara et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the CreativeCommons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, andreproduction in any medium, provided the original work is properly cited.