Affiliation:
1. Laboratoire de Pathologie Infectieuse et Immunologie, Institut National de la Recherche Agronomique, 37380 Nouzilly, France
Abstract
ABSTRACT
DNA polymorphism of the
bp26
gene, coding for a diagnostic protein antigen for brucellosis, was assessed by PCR and restriction fragment length polymorphism analysis using primers to amplify the
bp26
gene with its flanking regions. Surprisingly, whereas PCR performed on DNA of the reference strains of the six recognized
Brucella
species produced a product of the expected size (1,029 bp), PCR performed on DNA of three representative strains from marine mammals (from a seal, a dolphin, and a porpoise) produced a larger product, of about 1,900 bp. Nucleotide sequencing of the 1,900-bp PCR products revealed the presence of an insertion sequence, IS
711
, downstream of the
bp26
gene and adjacent to a Bru-RS1 element previously described as being a hot spot for IS
711
insertion. PCR performed on a large number of field strains from different geographic origins and from marine mammal isolates indicated that the occurrence of an IS
711
element downstream of the
bp26
gene was a feature specific to the marine mammal
Brucella
strains. Thus, this PCR assay is able to differentiate
Brucella
terrestrial isolates from marine mammal isolates and could be applied for diagnostic purposes.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
Cited by
87 articles.
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