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从动物和人类中分离出的产Ⅱ型热不稳定肠毒素大肠杆菌。

Type II heat-labile enterotoxin-producing Escherichia coli isolated from animals and humans.

作者信息

Seriwatana J, Echeverria P, Taylor D N, Rasrinaul L, Brown J E, Peiris J S, Clayton C L

机构信息

Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand.

出版信息

Infect Immun. 1988 May;56(5):1158-61. doi: 10.1128/iai.56.5.1158-1161.1988.

Abstract

Heat-labile enterotoxin (LT)-producing Escherichia coli strains, as identified by the Y1 adrenal cell assay, were examined with a DNA probe coding for type I and type II LTs. Of 236 LT-producing E. coli isolates, 60% hybridized with LT-I, 17% hybridized with LT-II, and 23% did not hybridize with either probe and no longer produced LT as determined by the Y1 adrenal cell assay. These isolates presumably lost plasmids coding for LT-I during storage. A total of 75% of LT-producing E. coli isolates (27 of 36) from cows, 64% of LT-producing E. coli isolates (7 of 11) from buffalo, 31% of LT-producing E. coli isolates (4 of 13) from beef obtained in markets, and 2% of LT-producing E. coli isolates (3 of 168) from humans contained genes coding for LT-II. Genes coding for LT-II were not found in 50 LT-I-producing and heat-stable enterotoxin-producing E. coli isolates from 11 children with diarrhea and 44 LT-nonproducing and heat-stable enterotoxin-producing E. coli isolates from 12 other children with diarrhea. A total of 9% of LT-II-producing E. coli isolates (3 of 34) from cows and buffalo hybridized with DNA probes for genes coding for verocytotoxin 2 (VT2), and 18% (6 of 34) hybridized with a DNA probe coding for enterohemorrhagic E. coli (EHEC) adhesin fimbriae. E. coli SA-53, the original isolate in which LT-II was found, contained genes coding for VT2 and EHEC adhesin fimbriae. Five VT-producing, LT-II-producing E. coli isolates that hybridized with the EHEC probe did not contain DNA sequences coding for VT1 or VT2. LT-II-producing E. coli strains were frequently isolated from cattle and buffalo but were rarely isolated from humans.

摘要

通过Y1肾上腺细胞检测鉴定出的产热不稳定肠毒素(LT)的大肠杆菌菌株,用编码I型和II型LTs的DNA探针进行检测。在236株产LT的大肠杆菌分离株中,60%与LT-I杂交,17%与LT-II杂交,23%与任何一种探针均未杂交,且通过Y1肾上腺细胞检测确定不再产生LT。这些分离株可能在储存过程中丢失了编码LT-I的质粒。来自奶牛的产LT的大肠杆菌分离株中共有75%(36株中的27株)、来自水牛的产LT的大肠杆菌分离株中64%(11株中的7株)、来自市场上牛肉的产LT的大肠杆菌分离株中31%(13株中的4株)以及来自人类的产LT的大肠杆菌分离株中2%(168株中的3株)含有编码LT-II的基因。在11例腹泻儿童的50株产LT-I和产热稳定肠毒素的大肠杆菌分离株以及12例其他腹泻儿童的44株不产LT和产热稳定肠毒素的大肠杆菌分离株中未发现编码LT-II的基因。来自奶牛和水牛的产LT-II的大肠杆菌分离株中共有9%(34株中的3株)与编码志贺毒素2(VT2)的基因的DNA探针杂交,18%(34株中的6株)与编码肠出血性大肠杆菌(EHEC)粘附性菌毛的DNA探针杂交。最初发现LT-II的分离株大肠杆菌SA-53含有编码VT2和EHEC粘附性菌毛的基因。5株与EHEC探针杂交的产VT、产LT-II的大肠杆菌分离株不含有编码VT1或VT2的DNA序列。产LT-II的大肠杆菌菌株经常从牛和水牛中分离出来,但很少从人类中分离出来。

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