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2010 | 66 | 01 |

Tytuł artykułu

Wykrywanie Pasteurella multocida i Bordetella bronchiseptica - czynnikow etiologicznych zakaznego zanikowego zapalenia nosa swin przy pomocy testow PCR

Warianty tytułu

EN
Detection of Pasteurella multocida and Bordetella bronchiseptica - etiological agents of atrophic rhinitis, by means of PCR tests

Języki publikacji

PL

Abstrakty

EN
Dermonecrotoxigenic (DNT) strains of Pasteurella multocida (Pm) and Bordetella bronchiseptica (Bbr), etiological agents of atrophic rhinitis (AR) of swine, are usually detected by conventional microbiological methods. Currently the main tasks in the diagnosis of infectious diseases is to detect the specific genes of pathogens directly from clinical samples within the shortest possible period of time by using sufficiently specific and sensitive methods. In this study two PCR tests were developed for the detection of genes encoding DNT in Pm and Bbr directly in nasal swabs. They were used for examining 481 nasal swabs collected from pigs raised in 56 farms, suspected of AR or displaying clinical symptoms of PAR. Additionally, the usefulness of PCR in the routine diagnosis of AR was compared with standard microbiological and serological methods. DNT+ Pm were directly evidenced in 74 samples (15.4%) from 27 tested herds (48.2%) while DNT+ Bbr were detected in 196 swabs (40.7%) from 41 farms (73.2%). Using the standard microbiological examination, the presence of bacterial cultures of the morphology typical of Pm was observed in 114 tested samples (23.7%) and those typical of Bbr, in 156 samples (32.45%). In the PCR test performed to confirm the presence of the DNT- -encoding gene in Pm isolates, positive results were obtained in 26 samples (22.8%), while among isolated Bbr strains, 95 out of 156 (60.1%) possessed the gene encoding DNT. In the ELISA test, 22 out of 26 isolates (84.6%) were DNT+. In the case of DNT- isolates of PM, the results of ELISA were in full agreement with PCR results. In total, PAR was detected in 27 farms (48.2%), NPAR in 21 farms (37.5%), and 8 farms (14.8%) were diagnosed as free from AR since no positive results were obtained by either method. Summarizing, the results of serological, bacteriological and molecular examinations clearly demonstrated the usefulness of PCR in the routine diagnosis of AR directly from clinical material.

Wydawca

-

Rocznik

Tom

66

Numer

01

Opis fizyczny

s.45-50,fot.,tab.,bibliogr.

Twórcy

  • Panstwowy Instytut Weterynaryjny - Panstwowy Instytut Badawczy, Al.Partyzantow 57, 24-100 Pulawy
autor

Bibliografia

  • 1.Amigot J. A., Torremorell M., Pijoan C.: Evaluation of techniques for the detection of toxigenic Pasteurella multocida strains from pigs. J. Vet. Diagn. Invest. 1998, 10, 169-173.
  • 2.Anon.: Atrophic rhinitis of swine, [w:] OIE Terrestrial Manual. Paryż, Francja 2008, 1083-1091.
  • 3.Bowersock T. L., Hooper T., Pottenger R.: Use of ELISA to detect toxigenic Pasteurella multocida in atrophic rhinitis in swine. J. Vet. Diagn. Invest. 1992, 4, 419-422.
  • 4.Brockmeier S. L., Register K. B., Magyar T., Lax A. J., Pullinger G. D., Kunkle R. A.: Role of the dermonecrotic toxin of Bordetella bronchiseptica in pathogenesis of respiratory disease in swine. Inf. Immun. 2002, 70, 481-490.
  • 5.Choi C., Chae C.: Enhanced detection of toxigenic Pasteurella multocida directly from nasal swabs using a nested polymerase chain reaction. Vet. J. 2001, 162, 255-258.
  • 6.Done J. T., Upcott D. H., Frewin D., Herbert C. N.: Atrophic rhinitis snout morphometry for quantitative assessment of conchal atrophy. Vet. Rec. 1984, 114, 33-35.
  • 7.Hozbor D., Fouque F., Guiso N.: Detection of Bordetella bronchiseptica by the polymerase chain reaction. Res. Microbiol. 1999, 150, 333-431.
  • 8.Janda W. M., Mutters R.: Pasteurella, Mannheimia, Actinobacillus, Eikenella, Kingella, Capnocytophaga and other miscellaneous gram-negative rods, [w:] Borriello S. P., Murray P. R., Funke G.: Topley and Wilson's Mircrobiology, Vol. 2. Bacteriology. Hodder Education, Londyn, Wielka Brytania 2005, 1650-1655.
  • 9.Jong-de M. F.: Progressive and nonprogressive atrophic rhinitis, [w:] Straw B. E., Zimmerman J. J., D'Allaire S., Taylor D. J.: Diseases of Swine. Blackwell Publishing, Ames, Iowa, USA 2006, 577-602.
  • 10.Lariviere S., Leblanc L., Mittal K. R., Martineau G. P.: Comparison of isolation methods for the recovery of Bordetella bronchiseptica and Pasteurella multocida from the nasal cavities of piglets. J. Clin. Microbiol. 1993, 31, 364-367.
  • 11.Lichtensteiger C. A., Steenbergen S. M., Lee R. M., Polson D. D., Vimr E. R.: Direct PCR analysis for toxigenic Pasteurella multocida. J. Clin. Microbiol. 1996, 34, 3035-3039.
  • 12.Markowska-Daniel I., Jabłoński A., Nowak A., Stępniewska K., Pejsak Z.: Opracowanie testu PCR do wykrywania genu kodującego dermonekrotoksynę Pasteurella multocida w wymazach z nosa świń. Medycyna Wet. 2009, 65, 542-545.
  • 13.Nagai S., Someno S., Yagihashi T.: Differentation of toxigenic from nontoxigenic isolates of Pasteurella multocida by PCR. J. Clin. Microbiol. 1994, 32, 1004-1010.
  • 14.Parton R.: Bordetella, [w:] Borriello S. P., Murray P. R., Funke G.: Topley and Wilson's Mircrobiology, Vol. 2. Bacteriology. Hodder Education, Londyn, Wielka Brytania 2005, 1786-1817.
  • 15.Pejsak Z.: Pastereloza, Zakaźne zanikowe zapalenie nosa, Nieprogresywne zakaźne zanikowe zapalenie nosa (bordeteloza), [w:] Ochrona zdrowia świń. PWR, Poznań 2007, 287-297.
  • 16.Register K. B., DeJong K. D.: Analitical verification of a multiplex PCR for identification of Bordetella bronchiseptica and Pasteurella multocida from swine. Vet. Microbiol. 2006, 117, 201-210.
  • 17.Roop R. M., Veit H. P., Sinsky R. J., Veit S. P., Hewlett E. L., Kornegay E. T.: Virulence factors of Bordetella bronchiseptica associated with the production of infectious atrophic rhinitis and pneumonia in experimentally infected neonatal swine. Inf. Immun. 1987, 55, 217-222.
  • 18.Stępniewska K., Markowska-Daniel I.: Elaboration of PCR test for detection of dermonecrotoxin in Bordetella bronchiseptica isolates. Bull. Vet. Ins. Pulawy - w druku.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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