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肠致病性大肠杆菌中脂多糖O抗原多糖的质粒编码表达

Plasmid-encoded expression of lipopolysaccharide O-antigenic polysaccharide in enteropathogenic Escherichia coli.

作者信息

Riley L W, Junio L N, Libaek L B, Schoolnik G K

出版信息

Infect Immun. 1987 Sep;55(9):2052-6. doi: 10.1128/iai.55.9.2052-2056.1987.

Abstract

The role of a plasmid in the virulence activity of an enteropathogenic Escherichia coli (EPEC) strain belonging to serotype 0111:NM was examined. EPEC strain B171, which is resistant to chloramphenicol, streptomycin, sulfathiazole, and tetracycline, harbors a 54-megadalton plasmid, pYR111, and exhibits localized adherence (LA) with HeLa cells. Curing the plasmid yielded strain B171-4, which had lost the ability to exhibit LA, resistance to the antibiotics, and the lipopolysaccharide (LPS) O-antigenic polysaccharide. To confirm that these phenotypic characteristics were specified by pYR111, the plasmid was transferred by conjugation into a nalidixic acid-resistant strain of E. coli HB101. LA and antimicrobial resistance were expressed in most of the transconjugants examined. The O-polysaccharide side chains, antigenically reactive with O111-specific antiserum, were also expressed by the transconjugants. Although EPEC plasmids coding for both drug resistance and LA have been described, an EPEC plasmid encoding the expression of an LPS O antigen has not been previously reported. Similar findings described for some Shigella and Salmonella strains suggest that plasmid-encoded modification of the LPS in some enteric bacterial species may be more common than previously recognized and may contribute to the characteristic virulence activity of the organism.

摘要

研究了质粒在血清型为O111:NM的肠致病性大肠杆菌(EPEC)菌株毒力活性中的作用。对氯霉素、链霉素、磺胺噻唑和四环素耐药的EPEC菌株B171携带一个54兆道尔顿的质粒pYR111,并对HeLa细胞表现出局部黏附(LA)。去除该质粒得到菌株B171-4,其失去了表现LA的能力、对抗生素的耐药性以及脂多糖(LPS)O抗原多糖。为了证实这些表型特征由pYR111决定,通过接合将该质粒转移到耐萘啶酸的大肠杆菌HB101菌株中。在大多数检测的接合子中表达了LA和抗菌耐药性。接合子还表达了与O111特异性抗血清发生抗原反应的O多糖侧链。虽然已经描述了编码耐药性和LA的EPEC质粒,但此前尚未报道过编码LPS O抗原表达的EPEC质粒。一些志贺氏菌和沙门氏菌菌株的类似发现表明,某些肠道细菌物种中质粒编码的LPS修饰可能比之前认为的更为常见,并且可能有助于该生物体的特征性毒力活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8b9/260655/75ff5a1442b7/iai00093-0113-a.jpg

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