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Liczba wyników
2010 | 62 | 1 | 85-92
Tytuł artykułu

Zastosowanie techniki real-time PCR do wykrywania DNA ludzkiego wirusa opryszczki typu 1

Warianty tytułu
EN
Application of real-time PCR assay for investigating the presence of herpes simplex virus type 1 DNA
Języki publikacji
PL
Abstrakty
PL
Celem pracy było zaprojektowanie i zbadanie użyteczności metody real-time PCR do diagnostyki zakażeń ludzkim wirusem opryszczki typu 1, zwłaszcza u pacjentów poddanych immunosupresji oraz z zakażeniami ośrodkowego układu nerwowego.
EN
Herpes simplex virus type 1 is a member of the Alphaherpesviridae subfamily, as it can infect both skin and nerves and develop latent infection within the dorsal root and trigeminal ganglia. Infection with this virus is common and causes a wide range of clinical syndromes. Although HSV-1infect healthy children and adults, disease is more severe and extensive in the immunocompromised individuals. The goal of the study was development of real-time PCR assay for detection of herpes simplex virus type 1 DNA in clinical samples, using primers targeting a conserved region of the viral DNA glycoproteine G gene and a specific TaqMan hydrolyzing probe. The analytical sensitivity of assay was tested using serial dilutions of HSV-1 DNA in range between 10° and 10-6 (4,35x105 - 4,00x101 copies/ml). Fifteen cell line isolates and twenty plasma samples taken from a group of adult recipients of allogeneic HSCT were tested for the presence of HSV-1 DNA in the LightCycler® system. For comparison commercial quantitative HSV-1/2 LC PCR Kit (Artus/Qiagen) was used, according to the manufacturer's instructions. Both LightCycler® assays, including in-house real-time PCR, detected HSV-1 DNA in 23 specimens. The conclusion is that developed TaqMan-based probe real-time PCR test is very reliable and valuable for detection of HSV-1 viremia in different kind of samples. The high level of sensitivity and accuracy provided by the LightCycler® instrument is favorable for the use of this method in the detection of herpes simplex virus 1 DNA also in clinical specimens.
Wydawca
-
Rocznik
Tom
62
Numer
1
Strony
85-92
Opis fizyczny
s.85-92,tab.,wykr.,bibliogr.
Twórcy
  • Katedra i Zaklad Mikrobiologii Lekarskiej, Warszawski Uniwersytet Medyczny, ul.Chalubinskiego 5, 02-004 Warszawa
autor
autor
autor
autor
Bibliografia
  • 1. Bilichodmath S, Mangalekar SB, Sharma DC i inni. Herpesviruses in chronic and aggressive periodontitis patients in an Indian population. J Oral Sci; 2009; 51: 79-86.
  • 2. Davison A, Eberle R, Hayward GS i inni. Herpesviruses. W: Virus taxonomy - classification and nomenclature of viruses. VHIth report of the International Committee on Taxonomy of Viruses. Red. C.M. Fauquet, M.A. Mayo, J. Maniloff i inni, Elsevier Academic Press, San Diego 2005, 193-212.
  • 3. Herget GW, Riede UN, Schmitt-Gräff A i inni. Generalized herpes simplex virus infection in immunocompromised patient - report of a case and review of the literature. Pathol Res Pract; 2005; 201: 123-9.
  • 4. Huppatz C, Durrheim DN, Levi C i inni. Etiology of encephalitis in Australia, 1990-2007. Emerg Infect Dis; 2009; 15: 1359-65.
  • 5. Kapranos NC, Kotronias DC. Detection of herpes simplex virus in first trimetr pregnancy loss using molecular techniques. In Vivo; 2009; ;23: 839-42
  • 6. Li JZ, Sax PE. HSV-1 encephalitis complicated by cerebral hemorrhage in an HIV-positive person. AIDS Read; 2009; 19: 153-5.
  • 7. Madhavan HN, Priya K, Anand AR i inni. Detection of Herpes simplex virus (HSV) genome using polymerase chain reaction (PCR) in clinical samples. Comparison of PCR with standard laboratory methods for the detection of HSV. J Clin Virol; 1999; 14: 145-51.
  • 8. Majewska A, Kilijańczyk M, Gajewska M i inni. Identyfikacja wirusów opryszczki pospolitej w materiale pobranym z błony śluzowej narządów płciowych od pacjentek poradni ginekologicznej przy I Katedrze i Klinice Położnictwa i Ginekologii WUM w Warszawie. Gin Prakt; 2009; 17: 17-20.
  • 9. Miller GG, Dummer JS. Herpes simplex and varicella zoster viruses: forgotten but not gone. Am J Transpl; 2007; 7: 741-7.
  • 10. Puchhammer-Stöckl E, Popow-Kraupp T, Heinz FX i inni. Establishment of PCR for the early diagnosis of herpes simplex encephalitis. J Med Virol; 1990; 32: 77-82.
  • 11. Powell HR, Almeyda J. An immunocompetent patient presenting with severe nasal herpes simplex: a case report. Cases J; 2009; 23: 9079.
  • 12. ReboraA. Life-threatening cutaneous viral diseases. Clin Dermatol; 2005; 23: 157-63.
  • 13. Schloss L, Falk KI, Skoog E i inni. Monitoring of herpes simplex virus DNA types 1 and 2 viral load in cerebrospinal fluid by real-time PCR in patients with herpes simplex encephalitis. J Med Virol; 2009; 81: 1432-7.
  • 14. Watzinger F, Suda M, Preuner S i inni. Real-time quantitative PCR assays for detection and monitoring of pathogenic human viruses in immunosuppressed pediatric patients. J Clin Microbiol; 2004; 42: 189-98.
  • 15. Weidmann M, Meyer-König U, Hufert FT. Rapid detection of herpes simplex virus and varicellazoster virus infections by real-time PCR. J Clin Microbiol; 2003; 41: 1565-8.
  • 16. Whitley RJ, Roizman B. Herpes simplex virus infections. Lancet; 2001; 357: 1513-18.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
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