tetano
Editor, Senior Moderator
J Virol Methods. 2012 Jun 1. [Epub ahead of print]
Multiplex RT-PCR assay for differentiating European swine influenza virus subtypes H1N1, H1N2 and H3N2.
Chiapponi C, Moreno A, Barbieri I, Merenda M, Foni E.
Source
Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna "Bruno Ubertini", Sezione Diagnostica di Parma, via dei Mercati 13/A, 43126 Parma, Italy.
Abstract
In Europe, three major swine influenza viral (SIV) subtypes (H1N1, H1N2 and H3N2) have been isolated in pigs. Developing a test that is able to detect and identify the subtype of the circulating strain rapidly during an outbreak of respiratory disease in the pig population is of essential importance. This study describes two multiplex RT-PCRs which distinguish the haemagglutinin (HA) gene and the neuraminidase (NA) gene of the three major subtypes of SIV circulating in Europe. The HA PCR was able to identify the lineage (avian or human) of the HA of H1 subtypes. The analytical sensitivity of the test, considered to be unique, was assessed using three reference viruses. The detection limit corresponded to 1?10(-1) TCID(50)/200μl for avian-like H1N1, 1?10(0) TCID(50)/200μl for human-like H1N2 and 1?10(1) TCID(50)/200μl for H3N2 SIV. The multiplex RT-PCR was first carried out on a collection of 70 isolated viruses showing 100% specificity and then on clinical samples, from which viruses had previously been isolated, resulting in an 89% positive specificity of the viral subtype. Finally, the test was able to identify the viral subtype correctly in 56% of influenza A positive samples, from which SIV had not been isolated previously. It was also possible to identify mixed viral infections and the circulation of a reassortant strain before performing genomic studies.
Copyright ? 2012. Published by Elsevier B.V.
PMID:
22664185
[PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/22664185
Multiplex RT-PCR assay for differentiating European swine influenza virus subtypes H1N1, H1N2 and H3N2.
Chiapponi C, Moreno A, Barbieri I, Merenda M, Foni E.
Source
Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna "Bruno Ubertini", Sezione Diagnostica di Parma, via dei Mercati 13/A, 43126 Parma, Italy.
Abstract
In Europe, three major swine influenza viral (SIV) subtypes (H1N1, H1N2 and H3N2) have been isolated in pigs. Developing a test that is able to detect and identify the subtype of the circulating strain rapidly during an outbreak of respiratory disease in the pig population is of essential importance. This study describes two multiplex RT-PCRs which distinguish the haemagglutinin (HA) gene and the neuraminidase (NA) gene of the three major subtypes of SIV circulating in Europe. The HA PCR was able to identify the lineage (avian or human) of the HA of H1 subtypes. The analytical sensitivity of the test, considered to be unique, was assessed using three reference viruses. The detection limit corresponded to 1?10(-1) TCID(50)/200μl for avian-like H1N1, 1?10(0) TCID(50)/200μl for human-like H1N2 and 1?10(1) TCID(50)/200μl for H3N2 SIV. The multiplex RT-PCR was first carried out on a collection of 70 isolated viruses showing 100% specificity and then on clinical samples, from which viruses had previously been isolated, resulting in an 89% positive specificity of the viral subtype. Finally, the test was able to identify the viral subtype correctly in 56% of influenza A positive samples, from which SIV had not been isolated previously. It was also possible to identify mixed viral infections and the circulation of a reassortant strain before performing genomic studies.
Copyright ? 2012. Published by Elsevier B.V.
PMID:
22664185
[PubMed - as supplied by publisher]
http://www.ncbi.nlm.nih.gov/pubmed/22664185