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PMID: 2453464 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Nucleotide sequences and comparison of the hemolysin determinants of Vibrio cholerae El Tor RV79(Hly+) and RV79(Hly-) and classical 569B(Hly-).

Infection and immunity ·Vol. 56 ·No. 6 ·1988-06-00 ·Pages 1414-9

Rader AE, Murphy JR

Abstract

We determined the nucleotide sequences of the hemolysin structural gene, hlyA, of Vibrio cholerae El Tor biotype strains RV79(Hly+) and RV79(Hly-) and the hly determinant of the nonhemolytic classical biotype strain 569B(Hly-). The sequences of the hlyA gene from El Tor strains RV79(Hly+) and RV79(Hly-) have an identical 2,223-base open reading frame which is predicted to encode an 81,977-dalton precursor form of hemolysin. This value is in excellent agreement with the 84,000-Mr hemolysin described in the earlier report of Goldberg and Murphy (S. L. Goldberg and J. R. Murphy, J. Bacteriol. 162:35-41, 1985). In contrast, the sequence of the hly determinant of the classical 569B(Hly-) strain has an 11-base-pair deletion within the hlyA structural gene. In this instance the hly determinant is predicted to encode a 26,765-dalton precursor form of a truncated hemolysin. In each case, the regulatory region encoding the putative hlyA promoter and the predicted 25-amino-acid signal sequence are identical.

MeSH Terms
Amino Acid Sequence Base Sequence Cloning, Molecular Epitopes/genetics,isolation & purification Genes Genes, Bacterial Hemolysin Proteins/genetics,immunology Molecular Sequence Data Sequence Homology, Nucleic Acid Vibrio cholerae/genetics,immunology
Chemicals
Epitopes Hemolysin Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Rader A E
Evans Department of Clinical Research, University Hospital, Boston, Massachusetts 02118-2393.
Murphy J R
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15 references, click to expand
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1988-06-00
Pages
1414-9
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC259414
Subset
IM
Grants
NIAID NIH HHS · R22 AI-22661 · United States
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