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Development of a one-run real-time PCR detection system for pathogens associated with porcine respiratory diseases

Identifieur interne : 000664 ( Main/Exploration ); précédent : 000663; suivant : 000665

Development of a one-run real-time PCR detection system for pathogens associated with porcine respiratory diseases

Auteurs : Fujiko Sunaga ; Shinobu Tsuchiaka ; Mai Kishimoto ; Hiroshi Aoki ; Mari Kakinoki ; Katsumasa Kure ; Hanako Okumura ; Maho Okumura ; Atsushi Okumura ; Makoto Nagai ; Tsutomu Omatsu ; Tetsuya Mizutani

Source :

RBID : PMC:7041981

Abstract

The etiology of Porcine respiratory disease complex is complicated by infections with multiple pathogens, and multiple infections increase the difficulty in identifying the causal pathogen. In this present study, we developed a detection system of microbes from porcine respiratory by using TaqMan real-time PCR (referred to as Dempo-PCR) to screen a broad range of pathogens associated with porcine respiratory diseases in a single run. We selected 17 porcine respiratory pathogens (Actinobacillus pleuropneumoniae, Boldetella bronchiseptica, Haemophilus parasuis, Pasteurella multocida, Pasteurella multocida toxin, Streptococcus suis, Mycoplasma hyopneumoniae, Mycoplasma hyorhinis, Mycoplasma hyosynovie, porcine circovirus 2, pseudorabies virus, porcine cytomegalovirus, swine influenza A virus, porcine reproductive and respiratory virus US strain, EU strain, porcine respiratory coronavirus and porcine hemagglutinating encephalomyelitis virus) as detection targets and designed novel specific primer-probe sets for seven of them. In sensitivity test by using standard curves from synthesized DNA, all primer-probe sets showed high sensitivity. However, porcine reproductive and respiratory virus is known to have a high frequency of genetic mutations, and the primer and probe sequences will need to be checked at a considerable frequency when performing Dempo-PCR from field samples. A total of 30 lung samples from swine showing respiratory symptoms on six farms were tested by the Dempo-PCR to validate the assay’s clinical performance. As the results, 12 pathogens (5 virus and 7 bacteria) were detected and porcine reproductive and respiratory virus US strain, Mycoplasma hyorhinis, Haemophilus parasuis, and porcine cytomegalovirus were detected at high frequency. These results suggest that Dempo-PCR assay can be applied as a screening system with wide detection targets.


Url:
DOI: 10.1292/jvms.19-0063
PubMed: 31866601
PubMed Central: 7041981


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>The etiology of Porcine respiratory disease complex is complicated by infections with multiple pathogens, and multiple infections increase the difficulty in identifying the causal pathogen. In this present study, we developed a detection system of microbes from porcine respiratory by using TaqMan real-time PCR (referred to as Dempo-PCR) to screen a broad range of pathogens associated with porcine respiratory diseases in a single run. We selected 17 porcine respiratory pathogens (
<italic>Actinobacillus pleuropneumoniae</italic>
,
<italic>Boldetella bronchiseptica</italic>
,
<italic>Haemophilus parasuis</italic>
,
<italic>Pasteurella multocida</italic>
,
<italic>Pasteurella multocid</italic>
a toxin,
<italic>Streptococcus suis</italic>
,
<italic>Mycoplasma hyopneumoniae</italic>
,
<italic>Mycoplasma hyorhinis</italic>
,
<italic>Mycoplasma hyosynovie</italic>
, porcine circovirus 2, pseudorabies virus, porcine cytomegalovirus, swine influenza A virus, porcine reproductive and respiratory virus US strain, EU strain, porcine respiratory coronavirus and porcine hemagglutinating encephalomyelitis virus) as detection targets and designed novel specific primer-probe sets for seven of them. In sensitivity test by using standard curves from synthesized DNA, all primer-probe sets showed high sensitivity. However, porcine reproductive and respiratory virus is known to have a high frequency of genetic mutations, and the primer and probe sequences will need to be checked at a considerable frequency when performing Dempo-PCR from field samples. A total of 30 lung samples from swine showing respiratory symptoms on six farms were tested by the Dempo-PCR to validate the assay’s clinical performance. As the results, 12 pathogens (5 virus and 7 bacteria) were detected and porcine reproductive and respiratory virus US strain,
<italic>Mycoplasma hyorhinis</italic>
,
<italic>Haemophilus parasuis</italic>
, and porcine cytomegalovirus were detected at high frequency. These results suggest that Dempo-PCR assay can be applied as a screening system with wide detection targets.</p>
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<list></list>
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<name sortKey="Aoki, Hiroshi" sort="Aoki, Hiroshi" uniqKey="Aoki H" first="Hiroshi" last="Aoki">Hiroshi Aoki</name>
<name sortKey="Kakinoki, Mari" sort="Kakinoki, Mari" uniqKey="Kakinoki M" first="Mari" last="Kakinoki">Mari Kakinoki</name>
<name sortKey="Kishimoto, Mai" sort="Kishimoto, Mai" uniqKey="Kishimoto M" first="Mai" last="Kishimoto">Mai Kishimoto</name>
<name sortKey="Kure, Katsumasa" sort="Kure, Katsumasa" uniqKey="Kure K" first="Katsumasa" last="Kure">Katsumasa Kure</name>
<name sortKey="Mizutani, Tetsuya" sort="Mizutani, Tetsuya" uniqKey="Mizutani T" first="Tetsuya" last="Mizutani">Tetsuya Mizutani</name>
<name sortKey="Nagai, Makoto" sort="Nagai, Makoto" uniqKey="Nagai M" first="Makoto" last="Nagai">Makoto Nagai</name>
<name sortKey="Okumura, Atsushi" sort="Okumura, Atsushi" uniqKey="Okumura A" first="Atsushi" last="Okumura">Atsushi Okumura</name>
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<name sortKey="Okumura, Maho" sort="Okumura, Maho" uniqKey="Okumura M" first="Maho" last="Okumura">Maho Okumura</name>
<name sortKey="Omatsu, Tsutomu" sort="Omatsu, Tsutomu" uniqKey="Omatsu T" first="Tsutomu" last="Omatsu">Tsutomu Omatsu</name>
<name sortKey="Sunaga, Fujiko" sort="Sunaga, Fujiko" uniqKey="Sunaga F" first="Fujiko" last="Sunaga">Fujiko Sunaga</name>
<name sortKey="Tsuchiaka, Shinobu" sort="Tsuchiaka, Shinobu" uniqKey="Tsuchiaka S" first="Shinobu" last="Tsuchiaka">Shinobu Tsuchiaka</name>
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</record>

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