Veterinary Research Forum

Abstract Infectious coryza, caused by Avibacterium paragallinarum, poses a significant economic threat to the global poultry industry. Although infectious coryza is present in Iran, there is limited molecular data characterizing the circulating strains, particularly regarding key hemagglutinin genes such as hagA. This study aimed to investigate the genetic diversity and phylogenetic relationships of the Av. paragallinarum isolates recovered from commercial and backyard poultry in Iran by sequencing the hagA gene and comparing the findings with those of global strains. Twenty-three Av. paragallinarum isolates collected from Iranian poultry farms underwent PCR amplification and sequencing of the hagA gene. Nucleotide and deduced amino acid sequences were analyzed for homology, subjected to BLAST searches, and used for phylogenetic reconstruction. The isolates showed high sequence identity, ranging from 94.10 - 99.90% at the nucleotide level and 92.10 - 100% at the protein level. Phylogenetic analysis classified the isolates into five distinct clusters (Iran-1 to Iran-5). The largest cluster (Iran-1) showed a strong affiliation with strains from China and India, whereas the other isolates clustered with strains from South Korea, Germany, and Japan. Notably, the Iran-5 group exhibited high similarity to a non-typable strain from USA. Additionally, eight isolates encoded truncated HagA proteins, each consisting of 344 rather than 345 amino acids. This study demonstrates the circulation of genetically diverse Av. paragallinarum strains in Iran. These findings highlight the need for further molecular investigations to improve control measures and assess the efficacy of the vaccines currently used in the country.

Abstract The aim of this study was to provide information on the molecular characteristic and the phylogenic relationship of infectious bronchitis viruses (IBV) strains in Bushehr province in comparison to other strains reported in the Middle East. Samples were collected from broiler flocks in Bushehr province during 2014 - 2015. These flocks had respiratory problems such as gasping, sneezing and bronchial rales. A number of 135 tracheal swabs were taken from fifteen flocks (nine swabs per flock). Each three swabs collected from each flock were pooled in one tube (finally, we had three tubes for each flock). The samples were subjected to reverse transcription polymerase chain reaction (RT-PCR). The PCR products of positive samples were analyzed by sequencing of a (392 bp) segment of the spike gene and the related results were compared with the other IBV sequences in GenBank database. Samples from twelve farms (80.0%) were found to be positive. The viruses from seven farms (46.6%) were identified as field viruses closely related to variant 2. The viruses from three farms (20.0%) were characterized as Mass type and were related to vaccine strains. Two different IB viruses (variant 2 and Mass) were detected in samples from two farms (13.3%). The variant 2 genotype detected in Bushehr had high similarity to variant 2 reported from the Middle East.These variants displayed homologies ranging from 72.9% to 76.5%, and 78.8% to 80.0% with H120 and 4/91, respectively. It is necessary to design vaccination program of poultry farms using IBV strains circulating in the region.