Czasopismo
Tytuł artykułu
Warianty tytułu
Comparison of standard PCR and Real-Time PCR in the diagnose of canine parvoviral infections
Języki publikacji
Abstrakty
The aim of this study was to compare a standard PCR and Sybr-Green HRM PCR in the diagnosis of canine parvoviral infections. A total of 22 feces samples were collected from dogs suspected of parvovirosis. The entire DNA for standard PCR and Real-Time PCR was isolated from the feces. In both methods this same pair of primers that allow the amplification of a fragment of VP 2 gene with a length of 1278 bp were used. The specificity of the obtained PCR products in the classical method were established based on the results of sequencing 8 out of 22 DNA probes and based on the comparison of their sequences with a CPV VP2 FJ 222823 sequence taken from the GeneBank. The specificity of Real-Time PCR products were established based on the analysis of their melting curve. In both standard and Real-Time PCR CPV DNA was detected in all 22 feces samples. The length of the obtained products was 1190 bp. To obtain a positive result in Real-Time PCR it was required to increase the number of the cycles from 30 to 60. The Ct values were between 43-53, and the analysis of the melting curve revealed that the Tm of Real-Time PCR products ranged between 80.5-85°C. Despite the results of this study indicating that both of these techniques are specific, sensitive, and repeated methods for detection of the CPV DNA, to shorten the time of Real-Time PCR the application of appropriate primers is required, which enables the amplification of shorter fragments of the DNA than those obtained in our study.
Wydawca
Czasopismo
Rocznik
Tom
Numer
Strony
683-686
Opis fizyczny
s.683-686,fot.,rys.,bibliogr.
Twórcy
autor
- Uniwersytet Przyrodniczy w Lublinie, ul.Gleboka 30, 20-612 Lublin
autor
autor
autor
autor
Bibliografia
- 1.Buonavoglia C., Martella V., Pratelli A., Tempesta M., Cavalli A., Buonavoglia D.: Evidence for evolution of canine parvovirus type-2 in Italy. J. Gen. Virol. 2001, 82, 3021-3025.
- 2.Cho H.-S., Kang J.-I., Park N.-Y.: Detection of canine parvovirus in fecal samples using loop-mediated isothermal amplification. J. Vet. Diagn. Invest. 2006, 18, 81-84.
- 3.Costa A. P., Leite J. P., Labarthe N. V., Garcia R. C.: Genomic typing of canine parvovirus circulating in the State of Rio de Janeiro, Brazil, from 1995 to 2001 using polymerase chain reaction assay. Vet. Res. Commun. 2005, 29, 735-743.
- 4.Decaro N. i wsp.: Molecular epidemiology of canine parvovirus, Eur. Emer. Infect. Dis. 2007, 13, 1222-1223.
- 5.Decaro N., Elia G., Desario C., Roperto S., Martella V., Campolo M., Lorusso A., Cavalli A., Buonavoglia C.: A minor groove binder probe real-time PCR assay for discrimination between type 2-based vaccines and field strains of canine parvovirus. J. Virol. Methods 2006, 136, 65-70.
- 6.Decaro N., Elia G., Martella V., Desario C., Campolo M., Trani L. D., Tarsitano E., Tempesta M., Buonavoglia C.: A real-time PCR assay for rapid detection and quantitation of canine parvovirus type 2 in the feces of dogs. Vet. Microbiol. 2005, 105, 19-28.
- 7.Desario C., Decaro N., Campolo M., Cavalli A., Cirone F., Elia G., Martella V., Lorusso E., Camero M., Buonavoglia C.: Canine parvovirus infection: which diagnostic test for virus? J. Virol. Methods 2005, 126, 179-185.
- 8.Drane D. P., Hamilton R. C., Cox J. C.: Evaluation of a novel diagnostic test for canine parvovirus. Vet. Microbiol. 1994, 41, 293-302.
- 9.Hueffer K., Parrish C. R.: Parvovirus host range, cell tropism and evolution. Current Opinion Microbiol. 2003, 6, 392-398.
- 10.Kamińska A., Dąbrowska J.: Fałszywie dodatnie i fałszywie ujemne wyniki reakcji opartych na amplifikacji kwasów nukleinowych w diagnostyce zakażeń. Przyczyny i implikacje diagnostyczne. Przegl. Epidemiol. 2004, 58, 343-349.
- 11.Manaresi E., Gallinella G., Zuffi E., Bonvicini F., Zerbini M., Musiani M.: Diagnosis and quantitative evaluation of parvovirus B19 infections by real-time PCR in the clinical laboratory. J. Med. Virol. 2002, 67, 275-281.
- 12.Mizak B., Borowski A.: Zastosowanie testu PLA do oceny namnażania wirusa nosówki, adenowirusa typu 1 oraz parwowirusa psów w hodowlach komórkowych. Medycyna Wet. 1998, 54, 753-756.
- 13.Mochizuki M., San Gabriel M. C., Nakatani H., Yoshida M.: Comparison of polymerase chain reaction with virus isolation and haemaglutination assays for the detection of canine parvoviruses in faecal samples. Res. Vet. Sci. 1993, 55, 60-63.
- 14.Ozkul A., Keles I., Karaoglu T., Cabalar M., Burgu I.: Detection and RFLP analysis of canine parvovirus (CPV) DNA by polymerase chain reaction (PCR) in a dog. Turkish J. Vet. Anim. Sci. 2002, 26, 1201-1203.
- 15.Salwa A., Kopczewski A., Wolañczyk-Rutkowiak K.: Badania serologiczne i molekularne psów uodpornionych przeciw parwowirozie. Medycyna Wet. 2006, 62, 1261-1264.
- 16.Słomski R.: Przykłady analiz DNA. Wyd. AR, Poznań 2004, 13-18.
- 17.Stadejek T.: Postęp w rozwoju techniki cyklicznej polimeryzacji DNA in vitro - Real-Time PCR. Medycyna Wet. 2006, 62, 390-394.
- 18.Wilhelm S., Zimmermann P., Selbitz H. J., Truyen U.: Real-time PCR protocol for the detection of porcine parvovirus in field samples. J. Virol. Methods 2006, 134, 257-260.
- 19.Zipper H., Brunner H., Bernhagen J., Vitzthum F.: Investigations on DNA intercalation and surface binding by SYBR Green I, its structure determination and methodological implications. Nucleic Acids Res. 2004, 32, 1-10.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.agro-article-08665e32-e751-48ea-b9d7-1a5680f3d7ef