Acta Medica International

ORIGINAL ARTICLE
Year
: 2015  |  Volume : 2  |  Issue : 2  |  Page : 68--71

Novel polymorphisms with in TLR4 exon1 sequences in visceral leishmaniasis and pulmonary tuberculosis patients


Hadeel Faisal Gad1, Maowia M Mukhtar2 
1 Assistant Professor, Faculty of Science, University of Princess Nora bint Abdul Rahman, Riyadh, Saudi Arabia
2 Professor, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan

Correspondence Address:
Hadeel Faisal Gad
Assistant Professor, Faculty of Science, University of Princess Nora bint Abdul Rahman, Riyadh
Saudi Arabia

Introduction: Leishmania and Mycobacterium Tuberculosis share many similarities in their pathogenesis and both pathogens are macrophage parasites. The present study was carried out to determine the diversity of TLR4 gene in VL and pulmonary TB as innate immunity marker. Materials and Method: Confirmed VL patients, pulmonary TB patients and healthy individuals DNAs were analyzedfor TLR 4 exon1 mutationsafter stimulation with live Leishmania promastigotes and BCG. PCR based sequencing was done to determine the diversity of for toll-liked receptor 4 exon-1. Results: Three polymorphisms were detected for the first time in TLR4 exon1, TLR4-35C/T and TLR4-5C/T located in the transcription factor binding site, and TLR4+18C/T located in the coding region which resulted in the change from the amino-acid Threonine (polar) to Alanine (non-polar). Conclusion: The diversity in TLR4 suggests possible variation in the innate immune responses of the two patients groups.


How to cite this article:
Gad HF, Mukhtar MM. Novel polymorphisms with in TLR4 exon1 sequences in visceral leishmaniasis and pulmonary tuberculosis patients.Acta Med Int 2015;2:68-71


How to cite this URL:
Gad HF, Mukhtar MM. Novel polymorphisms with in TLR4 exon1 sequences in visceral leishmaniasis and pulmonary tuberculosis patients. Acta Med Int [serial online] 2015 [cited 2021 Aug 4 ];2:68-71
Available from: https://www.actamedicainternational.com/article.asp?issn=2349-0578;year=2015;volume=2;issue=2;spage=68;epage=71;aulast=Gad;type=0