Molecular Characterization of Mycoplasma gallisepticum Isolates from Jordan

Two groups of Mycoplasma gallisepticum (MG) isolates (n  =  24) from Jordan were analyzed by molecular methods and compared with other Middle Eastern isolates, related international isolates, and reference strains. The first group (n  =  19) was isolated from July 2004 to January 2005 (isolation per...

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Veröffentlicht in:Avian diseases 2011-06, Vol.55 (2), p.212-216
Hauptverfasser: Gharaibeh, Saad, Laibinis, Victoria, Wooten, Ruth, Stabler, Lisa, Ferguson-Noel, Naola
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Sprache:eng
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Zusammenfassung:Two groups of Mycoplasma gallisepticum (MG) isolates (n  =  24) from Jordan were analyzed by molecular methods and compared with other Middle Eastern isolates, related international isolates, and reference strains. The first group (n  =  19) was isolated from July 2004 to January 2005 (isolation period A), and the newer group (n  =  5) from June 2007 to April 2008 (isolation period B). The groups of isolates are from chicken flocks from northern Jordan, but are not from the same farms. None of the flocks were vaccinated for MG. Random amplified polymorphic DNA analysis, targeted sequencing of the partial MG cytadhesin 2 (mgc2), and the MG 16S–23S rRNA intergenic spacer region (IGSR) divided the Jordanian isolates into two groups. All of the 19 isolates from time period A, in addition to two isolates from time period B, were indistinguishable from the F strain. Three of five isolates from time period B were characterized as wild types and were indistinguishable from each other. The wild-type field strain was readily distinguished from the F strain. It was 91% and 96.4% similar to the F strain based on Clustal-W alignments of sequences of mgc2 and IGSR, respectively. Sequence similarity of mgc2 gene of the Jordan wild-type strain to isolates from Israel and Egypt ranged from 96.5% to 100%, whereas for IGSR it was 99.4%–100%. We theorize that the F-strain live MG vaccine, commonly used in Jordan prior to 2007, was transmitted to nonvaccinated poultry in the region and was a predominant genotype during time period A.
ISSN:0005-2086
1938-4351
DOI:10.1637/9526-091510-Reg.1