ISOLATION AND MOLECULAR CHARACTERIZATION OF MYCOPLASMA SYNOVIAE FROM INFECTED CHICKENS WITH RESPIRATORY SIGNS.

The aim of this study was to investigate the presence of Mycoplasma synoviae in broiler and layer chickens infected with respiratory signs. A total of 80 samples were collected randomly from layer and broiler chickens with respiratory signs in Baghdad from the period between January to May 2017 fro...

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Main Author: Ali & et al.
Format: Article
Language:English
Published: Baghdad University 2020-10-01
Series:The Iraqi Journal of Agricultural science
Subjects:
Online Access:http://jcoagri.uobaghdad.edu.iq/index.php/intro/article/view/1157
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spelling doaj-1f9dc12b26c54c0ab45f4773e258e0732020-11-25T04:00:56ZengBaghdad UniversityThe Iraqi Journal of Agricultural science0075-05302410-08622020-10-0151510.36103/ijas.v51i5.1157ISOLATION AND MOLECULAR CHARACTERIZATION OF MYCOPLASMA SYNOVIAE FROM INFECTED CHICKENS WITH RESPIRATORY SIGNS.Ali & et al. The aim of this study was to investigate the presence of Mycoplasma synoviae in broiler and layer chickens infected with respiratory signs. A total of 80 samples were collected randomly from layer and broiler chickens with respiratory signs in Baghdad from the period between January to May 2017 from the trachea, Lung, Air sac, oviduct, tracheal swabs, conjunctiva swabs, choanal swabs, and nasal swabs and cultured in PPLO medium with supplements, then positive culture subjected to DNA extracted and Polymerase Chain Reaction assay (PCR) to detect Mycoplasma as a genus and Mycoplasma spp by using specific primers targeting16S rRNA gene. The results of culture revealed that the total rate of Mycoplasma isolates was19/80(23.75%). DNA was extracted from 19  positive isolates, all nineteen isolates were positive for Mycoplasma genus by conventional PCR assay, and a product of 270 bp was generated by amplification of the 16SrRNA gene, while a 210 bp region of 16S rRNA gene was amplified for the Mycoplasma synoviae in 19 isolates. The products of amplification of Mycoplasma synoviae16SrRNA gene was sent to MACROGEM (Korea) for sequencing, then submitted in the Gene bank database and have accession number:ID: MG846121.1. Sequencing alignment showed that local MS isolates had highly identical with standard references at gene bank, analysis the phylogenetic tree revealed the presence of 100% identity of the Iraqi isolate to the USA: West Virginia, United Kingdom, Australia, and Brazil, also had 99% identity to South Africa, China, Sweden, USA, and  VitNamHatey. This result was concluded that circulation of the Mycoplasma synoviae among birds of the flock and caused respiratory signs in chickens. http://jcoagri.uobaghdad.edu.iq/index.php/intro/article/view/1157Molicutes,salpengitis,hens,respiratorysign,MS,primers
collection DOAJ
language English
format Article
sources DOAJ
author Ali & et al.
spellingShingle Ali & et al.
ISOLATION AND MOLECULAR CHARACTERIZATION OF MYCOPLASMA SYNOVIAE FROM INFECTED CHICKENS WITH RESPIRATORY SIGNS.
The Iraqi Journal of Agricultural science
Molicutes,salpengitis,hens,respiratorysign,MS,primers
author_facet Ali & et al.
author_sort Ali & et al.
title ISOLATION AND MOLECULAR CHARACTERIZATION OF MYCOPLASMA SYNOVIAE FROM INFECTED CHICKENS WITH RESPIRATORY SIGNS.
title_short ISOLATION AND MOLECULAR CHARACTERIZATION OF MYCOPLASMA SYNOVIAE FROM INFECTED CHICKENS WITH RESPIRATORY SIGNS.
title_full ISOLATION AND MOLECULAR CHARACTERIZATION OF MYCOPLASMA SYNOVIAE FROM INFECTED CHICKENS WITH RESPIRATORY SIGNS.
title_fullStr ISOLATION AND MOLECULAR CHARACTERIZATION OF MYCOPLASMA SYNOVIAE FROM INFECTED CHICKENS WITH RESPIRATORY SIGNS.
title_full_unstemmed ISOLATION AND MOLECULAR CHARACTERIZATION OF MYCOPLASMA SYNOVIAE FROM INFECTED CHICKENS WITH RESPIRATORY SIGNS.
title_sort isolation and molecular characterization of mycoplasma synoviae from infected chickens with respiratory signs.
publisher Baghdad University
series The Iraqi Journal of Agricultural science
issn 0075-0530
2410-0862
publishDate 2020-10-01
description The aim of this study was to investigate the presence of Mycoplasma synoviae in broiler and layer chickens infected with respiratory signs. A total of 80 samples were collected randomly from layer and broiler chickens with respiratory signs in Baghdad from the period between January to May 2017 from the trachea, Lung, Air sac, oviduct, tracheal swabs, conjunctiva swabs, choanal swabs, and nasal swabs and cultured in PPLO medium with supplements, then positive culture subjected to DNA extracted and Polymerase Chain Reaction assay (PCR) to detect Mycoplasma as a genus and Mycoplasma spp by using specific primers targeting16S rRNA gene. The results of culture revealed that the total rate of Mycoplasma isolates was19/80(23.75%). DNA was extracted from 19  positive isolates, all nineteen isolates were positive for Mycoplasma genus by conventional PCR assay, and a product of 270 bp was generated by amplification of the 16SrRNA gene, while a 210 bp region of 16S rRNA gene was amplified for the Mycoplasma synoviae in 19 isolates. The products of amplification of Mycoplasma synoviae16SrRNA gene was sent to MACROGEM (Korea) for sequencing, then submitted in the Gene bank database and have accession number:ID: MG846121.1. Sequencing alignment showed that local MS isolates had highly identical with standard references at gene bank, analysis the phylogenetic tree revealed the presence of 100% identity of the Iraqi isolate to the USA: West Virginia, United Kingdom, Australia, and Brazil, also had 99% identity to South Africa, China, Sweden, USA, and  VitNamHatey. This result was concluded that circulation of the Mycoplasma synoviae among birds of the flock and caused respiratory signs in chickens.
topic Molicutes,salpengitis,hens,respiratorysign,MS,primers
url http://jcoagri.uobaghdad.edu.iq/index.php/intro/article/view/1157
work_keys_str_mv AT alietal isolationandmolecularcharacterizationofmycoplasmasynoviaefrominfectedchickenswithrespiratorysigns
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