Affiliation:
1. Zentrum für Infektionsforschung, Universität Würzburg, 97070 Würzburg, Germany,1 and
2. F. Hoffmann-La Roche Ltd., Pharmaceutical Research-Gene Technology, Basel, Switzerland2
Abstract
ABSTRACT
The temperate bacteriophage K139 is highly associated with pathogenic O1
Vibrio cholerae
strains. The nucleotide sequence of the major control region of K139 was determined. The sequences of four (
cox
,
cII
,
cI
, and
int
) of the six deduced open reading frames and their gene order indicated that K139 is related to the P2 bacteriophage family. Two genes of the lysogenic transcript from the mapped promoter P
L
encode homologs to the proteins CI and Int, with deduced functions in prophage formation and maintenance. Between the
cI
and
int
genes, two additional genes were identified:
orf2
, which has no significant similarity to any other gene, and the formerly characterized gene
glo
. Further analysis revealed that Orf2 is involved in preventing superinfection. In a previous report, we described that mutations in
glo
cause an attenuation effect in the cholera mouse model (J. Reidl and J. J. Mekalanos, Mol. Microbiol. 18:685–701, 1995). In this report, we present strong evidence that Glo participates in phage exclusion. Glo was characterized to encode a 13.6-kDa periplasmic protein which inhibits phage infection at an early step, hence preventing reinfection of vibriophage K139 into K139 lysogenic cells. Immediately downstream of gene
int
, the
attP
site was identified. Upon analysis of the corresponding
attB
site within the
V. cholerae
chromosome, it became evident that phage K139 is integrated between the flagellin genes
flaA
and
flaC
of O1 El Tor and O139
V. cholerae
lysogenic strains.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
44 articles.
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