Assessment of Duplex PCR for the simultaneous diagnose of Mycobacterium spp. and Brucella spp. in cattle
Tuberculosis and brucellosis remain important causes of morbidity and mortality in many countries, for the detection of both diseases requires efficient and sensitive tool for effectuate the diagnosis. This study was aimed to evaluate and compare the duplex PCR versus the nested PCR, for detection o...
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Universidad Nacional de Trujillo
2013-03-01
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doaj-91bdf9596d3d43908261e708f666a01b2020-11-24T23:28:48ZengUniversidad Nacional de TrujilloScientia Agropecuaria2077-99172306-67412013-03-0141374310.17268/sci.agropecu.2013.01.04Assessment of Duplex PCR for the simultaneous diagnose of Mycobacterium spp. and Brucella spp. in cattleAriel EscobarOrly Cevallos Samir ZambranoJaime MoranteMercedes CarranzaEnrique NietoMaría CadmeEdgar PinargoteTuberculosis and brucellosis remain important causes of morbidity and mortality in many countries, for the detection of both diseases requires efficient and sensitive tool for effectuate the diagnosis. This study was aimed to evaluate and compare the duplex PCR versus the nested PCR, for detection of Brucella spp. (BR) and Mycobacterium spp. (TB). A total of 100 samples of tissues from tracheo-bronchial lymph nodes, bovine lung and bacterial isolate as positive controls were used. Were evaluated ten combinations of primers which were designed to flank the segment of the 16S rRNA sequence (RB) and antigen gen MPB70 (TB), the best result for the Duplex PCR was obtained with the primers Bru-2F/Bru-2R for BR and Tub-1F/Tub-N-R for TB. The amplification of the products was 225 and 230-bp respectively. In order to compare the results of the proposed technique, all samples were initially analyzed and compared between PCR and nested PCR (Kappa, k = 0.85) and the concordance between Duplex PCR and nested PCR (k = 0.88) for the two bacteria was very good.http://www.revistas.unitru.edu.pe/index.php/scientiaagrop/article/view/96Brucellosiscattledetectiontissuestuberculosis. |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ariel Escobar Orly Cevallos Samir Zambrano Jaime Morante Mercedes Carranza Enrique Nieto María Cadme Edgar Pinargote |
spellingShingle |
Ariel Escobar Orly Cevallos Samir Zambrano Jaime Morante Mercedes Carranza Enrique Nieto María Cadme Edgar Pinargote Assessment of Duplex PCR for the simultaneous diagnose of Mycobacterium spp. and Brucella spp. in cattle Scientia Agropecuaria Brucellosis cattle detection tissues tuberculosis. |
author_facet |
Ariel Escobar Orly Cevallos Samir Zambrano Jaime Morante Mercedes Carranza Enrique Nieto María Cadme Edgar Pinargote |
author_sort |
Ariel Escobar |
title |
Assessment of Duplex PCR for the simultaneous diagnose of Mycobacterium spp. and Brucella spp. in cattle |
title_short |
Assessment of Duplex PCR for the simultaneous diagnose of Mycobacterium spp. and Brucella spp. in cattle |
title_full |
Assessment of Duplex PCR for the simultaneous diagnose of Mycobacterium spp. and Brucella spp. in cattle |
title_fullStr |
Assessment of Duplex PCR for the simultaneous diagnose of Mycobacterium spp. and Brucella spp. in cattle |
title_full_unstemmed |
Assessment of Duplex PCR for the simultaneous diagnose of Mycobacterium spp. and Brucella spp. in cattle |
title_sort |
assessment of duplex pcr for the simultaneous diagnose of mycobacterium spp. and brucella spp. in cattle |
publisher |
Universidad Nacional de Trujillo |
series |
Scientia Agropecuaria |
issn |
2077-9917 2306-6741 |
publishDate |
2013-03-01 |
description |
Tuberculosis and brucellosis remain important causes of morbidity and mortality in many countries, for the detection of both diseases requires efficient and sensitive tool for effectuate the diagnosis. This study was aimed to evaluate and compare the duplex PCR versus the nested PCR, for detection of Brucella spp. (BR) and Mycobacterium spp. (TB). A total of 100 samples of tissues from tracheo-bronchial lymph nodes, bovine lung and bacterial isolate as positive controls were used. Were evaluated ten combinations of primers which were designed to flank the segment of the 16S rRNA sequence (RB) and antigen gen MPB70 (TB), the best result for the Duplex PCR was obtained with the primers Bru-2F/Bru-2R for BR and Tub-1F/Tub-N-R for TB. The amplification of the products was 225 and 230-bp respectively. In order to compare the results of the proposed technique, all samples were initially analyzed and compared between PCR and nested PCR (Kappa, k = 0.85) and the concordance between Duplex PCR and nested PCR (k = 0.88) for the two bacteria was very good. |
topic |
Brucellosis cattle detection tissues tuberculosis. |
url |
http://www.revistas.unitru.edu.pe/index.php/scientiaagrop/article/view/96 |
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