Characterization of Ornithobacterium rhinotracheale field isolates from Hungary

• Published in: Avian pathology 2017-10, Vol.46 (5), p.506-514
• Main Authors: Szabó, Réka, Wehmann, Enikő, Makrai, László, Nemes, Csaba, Gyuris, Éva, Thuma, Ákos, Magyar, Tibor
• Format: Article
• Language: English
• Subjects: Animal diseases; Animals; Antisera; Assaying; Chickens; Deoxyribonucleic acid; DNA; Economic conditions; Economic impact; Egg production; ERIC-PCR; Flavobacteriaceae Infections - epidemiology; Flavobacteriaceae Infections - microbiology; Flavobacteriaceae Infections - veterinary; Gene sequencing; Genetic diversity; Genetic Variation; genotyping; Geographical variations; Growth rate; Hungary - epidemiology; Identification; Industry; Nucleotide sequence; Ornithobacterium - genetics; Ornithobacterium rhinotracheale; Pathology; PCR; Phylogeny; Polymerase chain reaction; Poultry; Poultry Diseases - epidemiology; Poultry Diseases - microbiology; Primers; Random amplified polymorphic DNA; RAPD assay; RNA, Bacterial - genetics; RNA, Ribosomal, 16S - genetics; rRNA 16S; Serotypes; serotyping; Turkeys
• ISSN: 0307-9457; 1465-3338
• DOI: 10.1080/03079457.2017.1321104

Ornithobacterium rhinotracheale is a widely distributed rod-shaped Gram-negative bacterium that infects several avian species including chickens and turkeys. It is associated with respiratory signs, growth retardation, mortality, and reduced egg production, thus causing severe economic losses to the poultry industries. In this study, 37 field isolates of O. rhinotracheale, collected from various locations in Hungary between 1997 and 2015, were identified and characterized by the analysis of partial 16S rRNA gene sequences, enterobacterial repetitive intergenic consensus (ERIC)-PCR, and random amplified polymorphic DNA (RAPD) PCR assays with the OPG11, OPH19, and M13 primers. Most of the field isolates were serotype A, one was serotype B, and four were serotype D. One isolate could not be typed with antisera against serotypes A-E. In a phylogenetic analysis of the 16S rRNA sequences, the isolates formed two clusters. Thirteen distinct patterns were identified with ERIC-PCR, and the RAPD assay with the M13 primer assigned the isolates to 10 different patterns. The other two RAPD assays were unsuitable for distinguishing and grouping the isolates. Neither ERIC type nor RAPD pattern correlated with the place or year of isolation. However, the strains isolated from chickens were more heterogeneous on ERIC-PCR than the isolates recovered from turkeys. In this study, ERIC-PCR was the most discriminatory method for investigating the genetic diversity of O. rhinotracheale isolates.