Literature DB >> 1383085

Molecular cloning and sequence analysis of the gene coding for the 57-kDa major soluble antigen of the salmonid fish pathogen Renibacterium salmoninarum.

M S Chien1, T L Gilbert, C Huang, M L Landolt, P J O'Hara, J R Winton.   

Abstract

The complete sequence coding for the 57-kDa major soluble antigen of the salmonid fish pathogen, Renibacterium salmoninarum, was determined. The gene contained an opening reading frame of 1671 nucleotides coding for a protein of 557 amino acids with a calculated M(r) value of 57,190. The first 26 amino acids constituted a signal peptide. The deduced sequence for amino acid residues 27-61 was in agreement with the 35 N-terminal amino acid residues determined by microsequencing, suggesting the protein is synthesized as a 557-amino acid precursor and processed to produce a mature protein of M(r) 54,505. Two regions of the protein contained imperfect direct repeats. The first region contained two copies of an 81-residue repeat, the second contained five copies of an unrelated 25-residue repeat. Also, a perfect inverted repeat (including three in-frame UAA stop codons) was observed at the carboxyl-terminus of the gene.

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Year:  1992        PMID: 1383085     DOI: 10.1016/0378-1097(92)90414-j

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  10 in total

1.  Molecular diversity of Renibacterium salmoninarum isolates determined by randomly amplified polymorphic DNA analysis.

Authors:  T H Grayson; F A Atienzar; S M Alexander; L F Cooper; M L Gilpin
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

2.  Expression of duplicate msa genes in the salmonid pathogen Renibacterium salmoninarum.

Authors:  Linda D Rhodes; Alison M Coady; Mark S Strom
Journal:  Appl Environ Microbiol       Date:  2002-11       Impact factor: 4.792

3.  A simplified PCR-based method for the detection of Renibacterium salmoninarum utilizing preparations of rainbow trout (Oncorhynchus mykiss, Walbaum) lymphocytes.

Authors:  D McIntosh; P G Meaden; B Austin
Journal:  Appl Environ Microbiol       Date:  1996-11       Impact factor: 4.792

4.  A sensitive nested reverse transcriptase PCR assay to detect viable cells of the fish pathogen Renibacterium salmoninarum in Atlantic salmon (Salmo salar L.).

Authors:  M Cook; W H Lynch
Journal:  Appl Environ Microbiol       Date:  1999-07       Impact factor: 4.792

5.  PCR and probe-PCR assays to monitor broodstock Atlantic salmon (Salmo salar L.) ovarian fluid and kidney tissue for presence of DNA of the fish pathogen Renibacterium salmoninarum.

Authors:  A Miriam; S G Griffiths; J E Lovely; W H Lynch
Journal:  J Clin Microbiol       Date:  1997-06       Impact factor: 5.948

6.  Mapping of neutralizing epitopes on Renibacterium salmoninarum p57 by use of transposon mutagenesis and synthetic peptides.

Authors:  Gregory D Wiens; Jennifer Owen
Journal:  Appl Environ Microbiol       Date:  2005-06       Impact factor: 4.792

7.  Both msa genes in Renibacterium salmoninarum are needed for full virulence in bacterial kidney disease.

Authors:  Alison M Coady; Anthony L Murray; Diane G Elliott; Linda D Rhodes
Journal:  Appl Environ Microbiol       Date:  2006-04       Impact factor: 4.792

8.  A single Ala139-to-Glu substitution in the Renibacterium salmoninarum virulence-associated protein p57 results in antigenic variation and is associated with enhanced p57 binding to chinook salmon leukocytes.

Authors:  Gregory D Wiens; Ron Pascho; James R Winton
Journal:  Appl Environ Microbiol       Date:  2002-08       Impact factor: 4.792

9.  Specific DNA probes for the identification of the fish pathogen, Renibacterium salmoninarum.

Authors:  G León; M A Martinez; J P Etchegaray; M I Vera; J Figueroa; M Krauskopf
Journal:  World J Microbiol Biotechnol       Date:  1994-03       Impact factor: 3.312

10.  Molecular differentiation of Renibacterium salmoninarum isolates from worldwide locations.

Authors:  T H Grayson; L F Cooper; F A Atienzar; M R Knowles; M L Gilpin
Journal:  Appl Environ Microbiol       Date:  1999-03       Impact factor: 4.792

  10 in total

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