Literature DB >> 15244055

The development of random DNA probes specific for Aeromonas salmonicida.

H J Oakey1, J T Ellis, L F Gibson.   

Abstract

RAPD-PCR has been used to produce DNA probes for Aeromonas salmonicida. DNA hybridization studies showed that RAPD-PCR fragments of the same size did not necessarily hybridize to each other and therefore these sequences were not always homologous. However, a single RAPD-PCR fragment (designated 15e) was identified as being common to Aer. salmonicida. Subsequently, 15e was found to comprise five DNA fragments of similar size which differed in their nucleotide sequences. All five fragments were evaluated as DNA probes for the specific detection of Aer. salmonicida DNA: two hybridized specifically to DNA of all Aer. salmonicida isolates tested, including the four current subspecies and atypical isolates; one hybridized to subspecies salmonicida, achromogenes and masoucida, but not subspecies smithia; one hybridized to subspecies salmonicida and achromogenes, but not subspecies masoucida or smithia; and one hybridized to subspecies salmonicida, achromogenes and smithia, but not subspecies masoucida. It is believed that these fragments could be useful as non-radioactive probes for the safe and rapid diagnosis of these fish pathogens.

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Year:  1998        PMID: 15244055     DOI: 10.1046/j.1365-2672.1997.00304.x

Source DB:  PubMed          Journal:  J Appl Microbiol        ISSN: 1364-5072            Impact factor:   3.772


  3 in total

1.  DNA fingerprinting of Flavobacterium columnare using RAPD-PCR.

Authors:  Lopamudra Sahoo; B K Das; J Parhi; S C Mukherjee
Journal:  Indian J Microbiol       Date:  2010-11-25       Impact factor: 2.461

2.  Molecular fingerprinting of fish-pathogenic Lactococcus garvieae strains by random amplified polymorphic DNA analysis.

Authors:  Carmen Ravelo; Beatriz Magariños; Sonia López-Romalde; Alicia E Toranzo; Jesús L Romalde
Journal:  J Clin Microbiol       Date:  2003-02       Impact factor: 5.948

3.  Inter- and intraspecific identification of the screwworm, Cochliomyia hominivorax, using random amplified polymorphic DNA-polymerase chain reaction.

Authors:  Steven R Skoda; James L Figarola; Saowaluck Pornkulwat; John E Foster
Journal:  J Insect Sci       Date:  2013       Impact factor: 1.857

  3 in total

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