https://doi.org/10.5812/jjm.19262

Isolation and Identification of Mycoplasma synoviae From Suspected Ostriches by Polymerase Chain Reaction, in Kerman Province, Iran

authors:

avatar Hamid Tebyanian 1 , avatar Seyed Hanif Mirhosseiny 1 , avatar Babak Kheirkhah ORCID 1 , * , avatar Mehdi Hassanshahian 2 , avatar Hamze farhadian 1

Department of Microbiology, Kerman Science and Research Branch, Islamic Azad University, Kerman, IR Iran
Department of Biology, Faculty of Science, Shahid Bahonar University of Kerman, Kerman, IR Iran
Jundishapur Journal of Microbiology: Vol.7, issue 9; 19262
published online: August 31, 2014
article type: Research Article
received: April 5, 2014
accepted: June 20, 2014

how to cite: Tebyanian H, Mirhosseiny S H, Kheirkhah B, Hassanshahian M, farhadian H. Isolation and Identification of Mycoplasma synoviae From Suspected Ostriches by Polymerase Chain Reaction, in Kerman Province, Iran. Jundishapur J Microbiol. 2014;7(9):19262. https://doi.org/10.5812/jjm.19262.

Abstract

Background:

Mycoplasma synoviae is an important avian pathogen which can cause both respiratory disease and synovial joint inflammation (synovitis) in poultry. Mycoplasmas spp. may cause the respiratory system infection in ostriches with symptoms such as inflammation of the nose, trachea and also damages of lungs.

Objectives:

The current study aimed to use the M. synoviae specific Polymerase Chain Reaction (PCR) and microbiological methods in order to isolate and identify M. synoviae from suspected ostriches in Kerman Province, Iran, and compare the two methods (microbiological and PCR) employed to confirm Mycoplasmal contamination of ostrich lungs.

Materials and Methods:

Fifty three samples of different parts of lung and trachea were immediately collected after slaughtering the ostriches in Kerman Province six months. Samples were cultured in the same conditions in pleuropneumonia-like organism (PPLO) broth and to isolate and identify M. synoviae, PCR and microbiological methods were conducted. The identified isolates were confirmed by specific amplification of 16S rRNA gene (163 and 207 base pair).

Results:

In the current study, 25 and 17 out of 53 ostrich samples were identified as Mycoplasma-positive in the PCR and microbiological methods, respectively; and 13 out of 25 the mentioned Mycoplasma-positive samples were also confirmed by PCR method.

Conclusions:

The current study showed that PCR method is time consuming, effective, and efficient method to detect M. synoviae infection in ostriches. PCR method could be recommended as an alternative for culturing; M. synoviae was isolated from ostriches for first time in Kerman Province, Iran.

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