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产肠毒素大肠杆菌中的定居因子抗原I和II以及1型菌毛:与肠毒素类型的关系

Colonization factor antigens I and II and type 1 somatic pili in enterotoxigenic Escherichia coli: relation to enterotoxin type.

作者信息

Levine M M, Ristaino P, Sack R B, Kaper J B, Orskov F, Orskov I

出版信息

Infect Immun. 1983 Feb;39(2):889-97. doi: 10.1128/iai.39.2.889-897.1983.

Abstract

Enterotoxigenic Escherichia coli (ETEC) isolates from 36 persons with acute traveler's diarrhea from whom no other pathogens were recovered were tested (after no more than three subcultures) for the presence of colonization factor antigens I and II (CFA/I and CFA/II) and type 1 somatic pili. CFA/I or CFA/II was identified in 7 of 10 strains with heat-labile and heat-stable enterotoxins (LT+/ST+), but in only 2 of 12 LT-/ST+ (P less than 0.05) and 0 of 14 LT+/ST- (P less than 0.02) strains. CFA pili were not found among 74 non-enterotoxigenic E. coli strains. Type 1 somatic pili were demonstrable in 42% of the 36 ETEC and in 49% of the 74 non-enterotoxigenic E. coli isolates. The nine ETEC isolates bearing a CFA were serially subcultured on 10 consecutive days and retested for CFA and toxin. After five subcultures only one strain had lost a CFA, but after 10 passages three strains were negative: two lost CFA/I and one lost CFA/II. The strain that lost CFA/II became negative for both LT and ST as well and was found to lack a 48- and a 60-megadalton plasmid. The two strains that lost CFA/I also became negative for ST, but plasmid analysis revealed no plasmid loss. Disappearance of the CFA/I phenotype without loss of a plasmid can be explained by phase variation, as exhibited by type 1 somatic pili, or by rearrangement of base sequences in the CFA/I plasmid genome. If purified pili vaccines are to provide broad-spectrum protection against ETEC diarrhea, the search must be intensified to identify the antigens responsible for adhesion to intestinal mucosa in the many ETEC strains that lack CFA/I and CFA/II.

摘要

对从36例急性旅行者腹泻患者中分离出的产肠毒素大肠杆菌(ETEC)菌株(在不超过三次传代培养后)进行检测,这些患者未检出其他病原体,检测内容包括定居因子抗原I和II(CFA/I和CFA/II)以及1型菌毛的存在情况。在10株同时产生不耐热和耐热肠毒素(LT+/ST+)的菌株中,7株鉴定出CFA/I或CFA/II,但在12株LT-/ST+菌株中只有2株(P<0.05),在14株LT+/ST-菌株中无一株(P<0.02)鉴定出CFA/I或CFA/II。在74株非产肠毒素大肠杆菌菌株中未发现CFA菌毛。1型菌毛在36株ETEC菌株中的42%以及74株非产肠毒素大肠杆菌菌株中的49%可检测到。对9株携带CFA的ETEC菌株连续传代培养10天,并重新检测CFA和毒素。传代培养5次后只有1株菌株失去了CFA,但传代培养10次后有3株菌株呈阴性:2株失去了CFA/I,1株失去了CFA/II。失去CFA/II的菌株同时也变为LT和ST阴性,并且发现其缺少一个48和一个60兆道尔顿的质粒。失去CFA/I的2株菌株也变为ST阴性,但质粒分析显示没有质粒丢失。CFA/I表型的消失而没有质粒丢失可以用相变来解释,就像1型菌毛所表现的那样,或者是CFA/I质粒基因组中碱基序列的重排。如果纯化的菌毛疫苗要提供针对ETEC腹泻的广谱保护,就必须加强寻找负责在许多缺乏CFA/I和CFA/II的ETEC菌株中黏附于肠黏膜的抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa50/348031/dfdbd13b85b3/iai00143-0414-a.jpg

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