LPS-PCR typing of ovine Pasteurella multocida isolates from Iran based on (L۱ to L۸) outer core biosynthesis loci

  • سال انتشار: 1396
  • محل انتشار: مجله آرشیو رازی، دوره: 72، شماره: 3
  • کد COI اختصاصی: JR_ARCHRAZI-72-3_003
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 179
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نویسندگان

S. F. Mirhaghgoye Jalali

Pasteurella National Research Laboratory, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, Iran

A.R. Jabbari

M. Esmael Zad

assistant professor razi institute

چکیده

Pasteurella multocida isa gram-negative bacterial pathogen that is causative agent of a wide range of diseases in many animal species and humans. Lipopolysaccharides (LPS) are an important virulence factor, minor changes to structure of which can exert dramatic effects on pathogenicity of P. multocida in its host. LPS can be used for the identification and classification of strains with somatic typing systems.The aim of this study was to identify the LPS genotypes of the ovine P. multocida isolates obtained from pneumonia cases in Iran. The LPS genotype of the isolates was determined using eight specific primers for LPS outer core biosynthesis loci. The LPS genes were amplified by polymerase chain reaction (PCR), then they were sequenced and compared to the sequences registered in the GenBank. Of the ۳۲ ovine P. multocida isolates tested, ۲۱ (۶۵.۶۲%) isolates belonged to genotype L۶, ۹ (۲۸.۱۲%) isolates contained genotype L۳, ۱ (۳.۱۲%) isolate had both L۳ and L۶ loci, and ۱ (۳.۱۲%) isolate remained untypeable. The LPS-PCR was able to type ۳۱ of ۳۲ field ovine isolates from Iran. According to the phylogenetic analysis, L۳ genotype isolates were grouped into two distinct lineages. LPS gene sequences among L۶ genotypes of ovine P. multocida isolates from Iran and the related sequences in the GenBank were highly similar (> ۹۹.۵%). LPS-PCR is an accurate genotyping method that was able to classify P. multocida strains into one of the eight distinct LPS genotypes.

کلیدواژه ها

P. multocida, Sheep, LPS outer core, PCR-typing

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