type ii heat-labile enterotoxins from 50 diverse escherichia coli isolates belong almost exclusively to the lt-iic family and may be prophage encodedii型heat-labile肠毒素来自50个不同的大肠杆菌分离株几乎只属于lt-iic家族,可能是前噬菌体编码的.pdfVIP
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type ii heat-labile enterotoxins from 50 diverse escherichia coli isolates belong almost exclusively to the lt-iic family and may be prophage encodedii型heat-labile肠毒素来自50个不同的大肠杆菌分离株几乎只属于lt-iic家族,可能是前噬菌体编码的
Type II Heat-Labile Enterotoxins from 50 Diverse
Escherichia coli Isolates Belong Almost Exclusively to the
LT-IIc Family and May Be Prophage Encoded
Michael G. Jobling*, Randall K. Holmes
Department of Microbiology, University of Colorado School of Medicine, Aurora, Colorado, United States of America
Abstract
Some enterotoxigenic Escherichia coli (ETEC) produce a type II heat-labile enterotoxin (LT-II) that activates adenylate cyclase
in susceptible cells but is not neutralized by antisera against cholera toxin or type I heat-labile enterotoxin (LT-I). LT-I
variants encoded by plasmids in ETEC from humans and pigs have amino acid sequences that are $95% identical. In
contrast, LT-II toxins are chromosomally encoded and are much more diverse. Early studies characterized LT-IIa and LT-IIb
variants, but a novel LT-IIc was reported recently. Here we characterized the LT-II encoding loci from 48 additional ETEC
isolates. Two encoded LT-IIa, none encoded LT-IIb, and 46 encoded highly related variants of LT-IIc. Phylogenetic analysis
indicated that the predicted LT-IIc toxins encoded by these loci could be assigned to 6 subgroups. The loci corresponding to
individual toxins within each subgroup had DNA sequences that were more than 99% identical. The LT-IIc subgroups
appear to have arisen by multiple recombinational events between progenitor loci encoding LT-IIc1- and LT-IIc3-like
variants. All loci from representative isolates encoding the LT-IIa, LT-IIb, and each subgroup of LT-IIc enterotoxins are
preceded by highly-related genes that are between 80 and 93% identical to predicted phage lysozyme genes. DNA
sequences immediately following the B genes differ considerably between toxin subgroups, but all are most closely related
to genomic sequences found in predicted prophages. Tog
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