IS 1414 , an Escherichia coli Insertion Sequence with a Heat-Stable Enterotoxin Gene Embedded in a Transposase-Like Gene

Author:

McVeigh Annette12,Fasano Alessio3,Scott Daniel A.1,Jelacic Sandra4,Moseley Steve L.4,Robertson Donald C.5,Savarino Stephen J.1

Affiliation:

1. Enteric Diseases Department, Naval Medical Research Center, Silver Spring,1

2. Henry M. Jackson Foundation for the Advancement of Military Medicine, Rockville,2 and

3. Center for Vaccine Development and Department of Pediatrics, University of Maryland School of Medicine, Baltimore,3 Maryland;

4. Department of Microbiology, University of Washington, Seattle, Washington4; and

5. Department of Molecular Biology, Biochemistry and Microbiology, University of Idaho, Moscow, Idaho5

Abstract

ABSTRACT Enteroaggregative Escherichia coli (EAEC) heat-stable enterotoxin 1 (EAST1) was originally discovered in EAEC but has also been associated with enterotoxigenic E. coli (ETEC). Multiple genomic restriction fragments from each of three ETEC strains of human origin showed homology with an EAST1 gene probe. A single hybridizing fragment was detected on the plasmid of ETEC strain 27D that also encodes heat-stable enterotoxin Ib and colonization factor antigen I. We isolated and characterized this fragment, showing that it (i) carries an allele of astA nearly identical to that originally reported from EAEC 17-2 and (ii) expressed enterotoxic activity. Sequence analysis of the toxin coding region revealed that astA is completely embedded within a 1,209-bp open reading frame (ORF1), whose coding sequence is on the same strand but in the −1 reading frame in reference to the toxin gene. In vitro expression of the predicted M r -∼46,000 protein product of ORF1 was demonstrated. ORF1 is highly similar to transposase genes of IS 285 from Yersinia pestis , IS 1356 from Burkholderia cepacia , and IS Rm3 from Rhizobium meliloti . It is bounded by 30-bp imperfect inverted repeat sequences and flanked by 8-bp direct repeats. Based on these structural features, pathognomonic of a regular insertion sequence, this element was designated IS 1414 . Preliminary experiments to show IS 1414 translocation were unsuccessful. Overlapping genes of the type suggested by the IS 1414 core region have heretofore not been described in bacteria. It seems to offer a most efficient mechanism for intragenomic and horizontal dissemination of EAST1.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference49 articles.

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