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溶组织内阿米巴tRNA基因中短串联重复序列引起的等位基因变异与阿米巴病临床表型之间的关联。

Association between allelic variation due to short tandem repeats in tRNA gene of Entamoeba histolytica and clinical phenotypes of amoebiasis.

作者信息

Jaiswal Virendra, Ghoshal Ujjala, Mittal Balraj, Dhole Tapan N, Ghoshal Uday C

机构信息

Department of Microbiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.

Department of Microbiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.

出版信息

Acta Trop. 2014 May;133:1-7. doi: 10.1016/j.actatropica.2014.01.009. Epub 2014 Feb 2.

Abstract

Genotypes of Entamoeba histolytica (E. histolytica) may contribute clinical phenotypes of amoebiasis such as amoebic liver abscess (ALA), dysentery and asymptomatic cyst passers state. Hence, we evaluated allelic variation due to short tandem repeats (STRs) in tRNA gene of E. histolytica and clinical phenotypes of amoebiasis. Asymptomatic cyst passers (n=24), patients with dysentery (n=56) and ALA (n=107) were included. Extracted DNA from stool (dysentery, asymptomatic cyst passers) and liver aspirate was amplified using 6 E. histolytica specific tRNA-linked STRs (D-A, A-L, N-K2, R-R, S-Q, and S(TGA)-D) primers. PCR products were subjected to sequencing. Association between allelic variation and clinical phenotypes was analyzed. A total of 9 allelic variations were found in D-A, 8 in A-L, 4 in N-K2, 5 in R-R, 10 in S(TAG)-D and 7 in S-Q loci. A significant association was found between allelic variants and clinical phenotypes of amoebiasis. This study reveals that allelic variation due to short tandem repeats (STRs) in tRNA gene of E. histolytica is associated different clinical outcome of amoebiasis.

摘要

溶组织内阿米巴(E. histolytica)的基因型可能导致阿米巴病的临床表型,如阿米巴肝脓肿(ALA)、痢疾和无症状排包囊者状态。因此,我们评估了溶组织内阿米巴tRNA基因中短串联重复序列(STRs)引起的等位基因变异以及阿米巴病的临床表型。纳入了无症状排包囊者(n = 24)、痢疾患者(n = 56)和阿米巴肝脓肿患者(n = 107)。使用6种溶组织内阿米巴特异性tRNA连接的STR引物(D-A、A-L、N-K2、R-R、S-Q和S(TGA)-D)对从粪便(痢疾、无症状排包囊者)和肝穿刺液中提取的DNA进行扩增。对PCR产物进行测序。分析等位基因变异与临床表型之间的关联。在D-A位点共发现9种等位基因变异,A-L位点8种,N-K2位点4种,R-R位点5种,S(TAG)-D位点10种,S-Q位点7种。发现等位基因变异与阿米巴病的临床表型之间存在显著关联。本研究表明,溶组织内阿米巴tRNA基因中短串联重复序列(STRs)引起的等位基因变异与阿米巴病的不同临床结局相关。

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