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胞内分枝杆菌中编码免疫显性38 kDa抗原的基因重复。

Duplication of genes encoding the immunodominant 38 kDa antigen in Mycobacterium intracellulare.

作者信息

Thangaraj H S, Bull T J, De Smet K A, Hill M K, Rouse D A, Moreno C, Ivanyi J

机构信息

M.R.C. Tuberculosis and Related Infections, Unit, Hammersmith Hospital,London, UK.

出版信息

FEMS Microbiol Lett. 1996 Nov 1;144(2-3):235-40. doi: 10.1111/j.1574-6968.1996.tb08536.x.

Abstract

Mycobacterium avium is a causative agent of mycobacterioses in systemically immunocompromised individuals, whereas Mycobacterium intracellulare is responsible for causing infections in relatively immunocompetent hosts. In an attempt to identify components that could be involved in virulence, we characterised the 38 kDa-encoding gene of M intracellulare that is absent in M. avium. This antigen cross reacts immunologically with a major 38 kDa antigen of M. tuberculosis, and both antigens are homologues of the phosphate transport subunit S (PstS) of the pst complex of Escherichia coli. Unlike the M. tuberculosis complex the M. intracellulare coding gene was found to be duplicated. We also identified and characterised other pst genes that may constitute an operon. Considering that multiple isoforms of PstS are present in mycobacteria the possible role of pstS1 genes for pathogenesis is discussed.

摘要

鸟分枝杆菌是全身免疫功能低下个体发生分枝杆菌病的病原体,而胞内分枝杆菌则在免疫功能相对正常的宿主中引起感染。为了确定可能与毒力有关的成分,我们对鸟分枝杆菌中不存在的胞内分枝杆菌38 kDa编码基因进行了表征。该抗原与结核分枝杆菌的一种主要38 kDa抗原发生免疫交叉反应,并且这两种抗原都是大肠杆菌pst复合体的磷酸盐转运亚基S(PstS)的同源物。与结核分枝杆菌复合体不同,胞内分枝杆菌的编码基因被发现是重复的。我们还鉴定并表征了其他可能构成操纵子的pst基因。鉴于分枝杆菌中存在多种PstS同工型,讨论了pstS1基因在发病机制中的可能作用。

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