Isolation and identification of Mycoplasma agalactiae by culture and polymerase chain reaction (PCR) from affected sheep to Contagious agalactia of Khuzestan province, Iran

Mycoplasma agalactiae (M. agalactiae) is one of the main causes of contagious agalactia, an infectious syndrome of sheep and goats in Khuzestan province –southwest of Iran that is characterized by mastitis and subsequent failure of milk production, arthritis, abortion and keratoconjunctivitis. This...

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Main Authors: Pooladgar, A.R., Looni, R., Ghaemmaghami, Sh., Pourbakhsh, A., Ashtari, A., Ali Shirudi, A.
Format: Article
Language:English
Published: Razi Vaccine and Serum Research Institute 2015-04-01
Series:Archives of Razi Institute
Subjects:
PCR
Online Access:http://www.archrazi.com/browse.php?a_id=539&sid=1&slc_lang=en
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spelling doaj-8c2161f3b09b476c8803eeb316712b102020-11-24T22:16:30Zeng Razi Vaccine and Serum Research InstituteArchives of Razi Institute 0365-34392008-98722015-04-0170012127Isolation and identification of Mycoplasma agalactiae by culture and polymerase chain reaction (PCR) from affected sheep to Contagious agalactia of Khuzestan province, IranPooladgar, A.R.0Looni, R.,1Ghaemmaghami, Sh.2Pourbakhsh, A.3Ashtari, A.4Ali Shirudi, A.5Department of Poultry Diseases Research, Razi vaccine and Serum Research Institute, Ahwaz, IranMycoplasma Reference Laboratory, Razi vaccine and Serum Research Institute, Karaj, IranDepartment of Poultry Diseases Research, Razi vaccine and Serum Research Institute, Ahwaz, IranMycoplasma Reference Laboratory, Razi vaccine and Serum Research Institute, Karaj, IranMycoplasma Reference Laboratory, Razi vaccine and Serum Research Institute, Karaj, IranRamshir Veterinary Office, Ramshir, KhuzestanMycoplasma agalactiae (M. agalactiae) is one of the main causes of contagious agalactia, an infectious syndrome of sheep and goats in Khuzestan province –southwest of Iran that is characterized by mastitis and subsequent failure of milk production, arthritis, abortion and keratoconjunctivitis. This study was carried out to isolation and identification of M. agalactiae with culture and polymerase chain reaction (PCR) method from sheep in Khuzestan province, Iran. A total of 91 samples were collected from milk secretion, eye, ear, nose and joint exudates of sheep. All samples were cultured in PPLO broth supplemented for isolation of M. agalaciae. Extraction of the DNA of bacteria was done by phenol/chloroform method and the PCR assay was applied for detection of Mycoplasma genus in 163bp fragment of 16S rRNA gene and M. agalactiae in 375bp fragment of lipoprotein gene from culture as same as in clinical samples. Out of the 91 samples, 34(37.36%) cultures were shown positive and typical Mycoplasma colonies in PPLO agar culture diagnostic method and 47(51.65%) were scored positive by Mycoplasma genus PCR, 8(8.79%) of the samples were scored positive by using M. agalactiae PCR as diagnostic method. Out of the 91 samples, 26 samples were shown both positive in the culture and PCR, 5 samples were shown both positive in the culture, MPCR and MAPCR. 15 samples were negative in the culture and positive in PCR whereas only 3 samples were positive in culture and negative in PCR. The results showed that the more isolations of M. agalactiae were taken from eye and less in ear and nose samples. M. agalactiae was one of the main factors of contagious agalactia that was detected for the first time from sheep in Khuzestan province.http://www.archrazi.com/browse.php?a_id=539&sid=1&slc_lang=enMycoplasma agalactiaeCulturePCR16S rRNALipoprotein geneSheep
collection DOAJ
language English
format Article
sources DOAJ
author Pooladgar, A.R.
Looni, R.,
Ghaemmaghami, Sh.
Pourbakhsh, A.
Ashtari, A.
Ali Shirudi, A.
spellingShingle Pooladgar, A.R.
Looni, R.,
Ghaemmaghami, Sh.
Pourbakhsh, A.
Ashtari, A.
Ali Shirudi, A.
Isolation and identification of Mycoplasma agalactiae by culture and polymerase chain reaction (PCR) from affected sheep to Contagious agalactia of Khuzestan province, Iran
Archives of Razi Institute
Mycoplasma agalactiae
Culture
PCR
16S rRNA
Lipoprotein gene
Sheep
author_facet Pooladgar, A.R.
Looni, R.,
Ghaemmaghami, Sh.
Pourbakhsh, A.
Ashtari, A.
Ali Shirudi, A.
author_sort Pooladgar, A.R.
title Isolation and identification of Mycoplasma agalactiae by culture and polymerase chain reaction (PCR) from affected sheep to Contagious agalactia of Khuzestan province, Iran
title_short Isolation and identification of Mycoplasma agalactiae by culture and polymerase chain reaction (PCR) from affected sheep to Contagious agalactia of Khuzestan province, Iran
title_full Isolation and identification of Mycoplasma agalactiae by culture and polymerase chain reaction (PCR) from affected sheep to Contagious agalactia of Khuzestan province, Iran
title_fullStr Isolation and identification of Mycoplasma agalactiae by culture and polymerase chain reaction (PCR) from affected sheep to Contagious agalactia of Khuzestan province, Iran
title_full_unstemmed Isolation and identification of Mycoplasma agalactiae by culture and polymerase chain reaction (PCR) from affected sheep to Contagious agalactia of Khuzestan province, Iran
title_sort isolation and identification of mycoplasma agalactiae by culture and polymerase chain reaction (pcr) from affected sheep to contagious agalactia of khuzestan province, iran
publisher Razi Vaccine and Serum Research Institute
series Archives of Razi Institute
issn 0365-3439
2008-9872
publishDate 2015-04-01
description Mycoplasma agalactiae (M. agalactiae) is one of the main causes of contagious agalactia, an infectious syndrome of sheep and goats in Khuzestan province –southwest of Iran that is characterized by mastitis and subsequent failure of milk production, arthritis, abortion and keratoconjunctivitis. This study was carried out to isolation and identification of M. agalactiae with culture and polymerase chain reaction (PCR) method from sheep in Khuzestan province, Iran. A total of 91 samples were collected from milk secretion, eye, ear, nose and joint exudates of sheep. All samples were cultured in PPLO broth supplemented for isolation of M. agalaciae. Extraction of the DNA of bacteria was done by phenol/chloroform method and the PCR assay was applied for detection of Mycoplasma genus in 163bp fragment of 16S rRNA gene and M. agalactiae in 375bp fragment of lipoprotein gene from culture as same as in clinical samples. Out of the 91 samples, 34(37.36%) cultures were shown positive and typical Mycoplasma colonies in PPLO agar culture diagnostic method and 47(51.65%) were scored positive by Mycoplasma genus PCR, 8(8.79%) of the samples were scored positive by using M. agalactiae PCR as diagnostic method. Out of the 91 samples, 26 samples were shown both positive in the culture and PCR, 5 samples were shown both positive in the culture, MPCR and MAPCR. 15 samples were negative in the culture and positive in PCR whereas only 3 samples were positive in culture and negative in PCR. The results showed that the more isolations of M. agalactiae were taken from eye and less in ear and nose samples. M. agalactiae was one of the main factors of contagious agalactia that was detected for the first time from sheep in Khuzestan province.
topic Mycoplasma agalactiae
Culture
PCR
16S rRNA
Lipoprotein gene
Sheep
url http://www.archrazi.com/browse.php?a_id=539&sid=1&slc_lang=en
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