“Short article” Serological and molecular survey on camel brucellosis in Najaf Abad

 Introduction: Brucellosis which is an important zoonotic disease, exists in our country. Camel is an animal that is frequently imported to Iran and doesn't have any inspection for its brucellosis. The objective of this study was determination of active and passive infection b...

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Main Authors: mohamadreza Mahzounieh, mahdi salimi
Format: Article
Language:English
Published: University of Isfahan 2015-09-01
Series:Biological Journal of Microorganism
Subjects:
PCR
Online Access:http://uijs.ui.ac.ir/bjm//browse.php?a_code=A-10-453-1&slc_lang=en&sid=1
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spelling doaj-281f495cc2814933ae7b7b867e3692b82020-11-24T23:58:38ZengUniversity of IsfahanBiological Journal of Microorganism2322-51732322-51812015-09-01414167174“Short article” Serological and molecular survey on camel brucellosis in Najaf Abadmohamadreza Mahzounieh0mahdi salimi1 Associate Professor of Microbiology, Member of Research Institute of Zoonotic Diseases, University of Shahrekord, Iran D.V.M. Student, Member of Research Institute of Zoonotic Diseases, University of Shahrekord, Iran  Introduction: Brucellosis which is an important zoonotic disease, exists in our country. Camel is an animal that is frequently imported to Iran and doesn't have any inspection for its brucellosis. The objective of this study was determination of active and passive infection by serologic and genomic detection of brucellosis in one-humped camel that was slaughtered in central part of Iran during 2012- 2013. Materials and methods: For this purpose, 150 blood samples were collected from camels that were slaughtered in Najaf-Abad abattoir and they transported to laboratory in cool box. Initially, Samples were tested by serological methods include: Rose Bengal plat test, tube agglutination test and 2-mercaptoethanol test. Samples which showed anti-brucella antibodies titer equal or more than 1/80 in Wright test and equal or more than 1/40 in 2-ME test were considered as positive. Nucleic acid of samples were extracted and tested by polymerase chain reaction. Results: Results showed that the infection rates were12, 8 and 6 % in RBPT, tube agglutination and 2-ME tests respectively. However 1.3 % of samples were positive in PCR test. Discussion and conclusion: According to 2ME titers, results of serological tests indicated that animals were chronically infected. In present study sequence of pb26 gene was detected, that is common in most brucella species. Present study shows that camel can be a potential carrier; therefore importing camel to the country is a way of bacterial spread to central part of Iran. http://uijs.ui.ac.ir/bjm//browse.php?a_code=A-10-453-1&slc_lang=en&sid=1PCR Serology Brucella Camel Iran
collection DOAJ
language English
format Article
sources DOAJ
author mohamadreza Mahzounieh
mahdi salimi
spellingShingle mohamadreza Mahzounieh
mahdi salimi
“Short article” Serological and molecular survey on camel brucellosis in Najaf Abad
Biological Journal of Microorganism
PCR
Serology
Brucella
Camel
Iran
author_facet mohamadreza Mahzounieh
mahdi salimi
author_sort mohamadreza Mahzounieh
title “Short article” Serological and molecular survey on camel brucellosis in Najaf Abad
title_short “Short article” Serological and molecular survey on camel brucellosis in Najaf Abad
title_full “Short article” Serological and molecular survey on camel brucellosis in Najaf Abad
title_fullStr “Short article” Serological and molecular survey on camel brucellosis in Najaf Abad
title_full_unstemmed “Short article” Serological and molecular survey on camel brucellosis in Najaf Abad
title_sort “short article” serological and molecular survey on camel brucellosis in najaf abad
publisher University of Isfahan
series Biological Journal of Microorganism
issn 2322-5173
2322-5181
publishDate 2015-09-01
description  Introduction: Brucellosis which is an important zoonotic disease, exists in our country. Camel is an animal that is frequently imported to Iran and doesn't have any inspection for its brucellosis. The objective of this study was determination of active and passive infection by serologic and genomic detection of brucellosis in one-humped camel that was slaughtered in central part of Iran during 2012- 2013. Materials and methods: For this purpose, 150 blood samples were collected from camels that were slaughtered in Najaf-Abad abattoir and they transported to laboratory in cool box. Initially, Samples were tested by serological methods include: Rose Bengal plat test, tube agglutination test and 2-mercaptoethanol test. Samples which showed anti-brucella antibodies titer equal or more than 1/80 in Wright test and equal or more than 1/40 in 2-ME test were considered as positive. Nucleic acid of samples were extracted and tested by polymerase chain reaction. Results: Results showed that the infection rates were12, 8 and 6 % in RBPT, tube agglutination and 2-ME tests respectively. However 1.3 % of samples were positive in PCR test. Discussion and conclusion: According to 2ME titers, results of serological tests indicated that animals were chronically infected. In present study sequence of pb26 gene was detected, that is common in most brucella species. Present study shows that camel can be a potential carrier; therefore importing camel to the country is a way of bacterial spread to central part of Iran. 
topic PCR
Serology
Brucella
Camel
Iran
url http://uijs.ui.ac.ir/bjm//browse.php?a_code=A-10-453-1&slc_lang=en&sid=1
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