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2009 | 53 | 3 |

Tytuł artykułu

Detection and subtyping of swine influenza viruses in clinical samples by the mean of developed multiplex polymerase chain reaction assays

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Multiplex PCR assays that can detect and identify three haemagglutinins and two neuraminidases of three main subtypes: H1N1, H1N2, and H3N2 of swine influenza virus (SIV), circulating in a pig population, were developed. Three oligonucleotide primer sets were evaluated based on the published sequences, with unique sizes characteristic for each subtype. The sequences of each primers were demonstrated to be specific for every subtype of SIV with the cDNA of reference viruses. Furthermore, the assays could detect and subtype up to 10⁻¹ dilution of 10⁴ EID₅₀/0.2 mL of H1N1 and 10⁻¹ dilution of 10² EID₅₀ /0.2 mL of H1N2. For the H3N2 mPCR test, sensitivity was observed in a dilution as low as 10⁻³, which equals 10 EID₅₀/0.2 mL. Conditions for the reactions and reagents concentrations were optimised. The optimal temperature was also ensemble. For all RNA positive samples in the RT- nested-PCR test for influenza A viruses, the mPCR agreed completely. In 19 farms (95% of cases) the H1N1 subtype was determined, and in one farm H3N2 subtype was confirmed. Therefore, these methods could facilitate the rapid and accurate subtyping of influenza A viruses directly from field specimens.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

53

Numer

3

Opis fizyczny

p.319-325,fig.,ref.

Twórcy

  • Department of Swine Diseases, National Veterinary Research Institute, 24-100 Pulawy, Poland
  • Department of Swine Diseases, National Veterinary Research Institute, 24-100 Pulawy, Poland

Bibliografia

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  • 2. Chang H.K., Park J.H., Song M.S., Oh T.K., Kim S.Y.: Development of multiplex RT-PCR assays for rapid detection and subtyping of influenza type A viruses from clinical specimens. J Microbiol Biotechnol 2008, 18, 1164-1169.
  • 3. Daum L.T., Canas L.C., Schadler C.A., Ujimori V.A., Huff W.B.: A rapid, single-step multiplex reverse transcription-PCR assay for the detection of human H1N1, H3N2, and B influenza viruses. J Clin Virol 2002, 25, 345-350.
  • 4. Dieffenbach C.W., Dveksler G.S.: PCR Primer: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 1995.
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  • 6. Edward M.C., Gibbs R.A.: Multiplex PCR. In: PCR Primer: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 1995, pp. 157-171.
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  • 8. Giammarioli M., Pellegrini C., Casciari C., De Mia G.M.: Development of a novel hot-start multiplex PCR for simultaneous detection of classical swine fever virus, African swine fever virus, porcine circovirus type 2, porcine reproductive and respiratory syndrome virus and porcine parvovirus. Vet Res Commun 2008, 32, 255-262.
  • 9. Kiss I., Germán P., Sámi L., Antal M., Farkas T., Kardos Kecskeméti S., Dán A., Belák S.: Application of realtime RT-PCR utilising lux (light upon extension) fluorogenic primer for the rapid detection of avian influenza viruses. Acta Vet Hung 2006, 54, 525-533.
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  • 13. Olsen C.W., Brammer L., Easterday B.C., Arden N., Belay E., Baker I., Cox N.J.: Serologic evidence of H1 swine influenza virus infection in swine farm residents and employees. Emerg Infect Dis 2002, 8, 814-819.
  • 14. Poddar S.K.: Influenza virus types and subtypes detection by single step single tube multiplex reverse transcription- polymerase chain reaction (RT-PCR) and agarose gel electrophoresis. J Virol Methods 2002, 99, 63-70.
  • 15. Van Reeth K: Avian and swine influenza viruses: our current understanding of the zoonotic risk. Vet Res 2007, 38, 243-260.
  • 16. Schorr E., Wentworth D., Hinshaw V.S.: Use of polymerase chain reaction to detect swine influenza virus in nasal swab specimens. Am J Vet Res 1994, 55, 952- 956.
  • 17. Stockton J., Ellis J.S., Saville M., Clewley J.P., Zambon M.C.: Multiplex PCR for typing and subtyping influenza and respiratory syncytial viruses. J Clin Microbiol 1998, 36, 2990-2995.
  • 18. Subramanian B.M., Raj G.D., Kumanan K., Nachimuthu K., Nainar A.M.: Interaction between genomes of infectious bronchitis and Newcastle disease viruses studied by reverse transcription-polymerase chain reaction. Acta Virol 2004, 48, 123-129.
  • 19. Yang I., Kim Y.H., Byun J.Y., Park S.R.: Use of multiplex polymerase chain reactions to indicate the accuracy of the annealing temperature of thermal cycling. Anal Biochem 2005, 338, 192-200.

Typ dokumentu

Bibliografia

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