Araştırma Makalesi

Norovirüs enfeksiyonlarının Çanakkale'de ELİSA ve RT-PCR ile saptanması

Cilt: 41 Sayı: 3 30 Eylül 2016
Arif Aksu , Alper Akçalı
PDF İndir
EN TR

Detection of norovirus infections in Canakkale with ELISA and RT-PCR

Abstract

Purpose: Noroviruses are important agents of gastroenteritis worldwide in every age group. There is no large countrywide dataset available for norovirus infections in Turkey. This is the first investigation of noroviruses in Çanakkale, and we aimed to compare commercial ELISA and real time RT-PCR assays in clinical use. 

Material and Methods: Fecal samples from 92 clinical gastroenteritis cases were collected and stored at -20°C. Norovirus antigen was investigated using RidaScreen ELISA and norovirus GI and GII molecular detection made with RealStar Norovirus RT-PCR kit 2.0. 

Results: We found that 16 (17.4%) samples were positive for norovirus in our study group. Using ELISA, 10 samples were positive from 92 samples. In PCR analysis, internal control amplification failed for four samples. We found 15 of 88 samples positive for real time RT-PCR analysis; of these one was GI and 14 were GII. When we accepted PCR as the reference test, the sensitivity and specificity of ELISA were calculated as 60% and 98% respectively. 

Conclusion: Single cases of norovirus infection can be seen even in rural cities like Çanakkale. There is a need to set up diagnostic capabilities for norovirus infections. ELISA has a low sensitivity, but this method is cheaper than RT-PCR and is not affected by PCR inhibitors.

Keywords

Norovirus,ishal,ELISA

Kaynakça

  1. Zheng DP, Ando T, Fankhauser RL, Beard RS, Glass RI, Monroe SS. Norovirus classification and proposed 2006;346:312–23. A, Virology. 2. Kirby
  2. Turriza-Gómara MI. applications diagnostics :
  3. interpretations. Expert Rev Anti-infective Ther.
  4. ;10:423–33. and
  5. Hoa Tran TN, Trainor E, Nakagomi T, Cunliffe NA, Nakagomi O. Molecular epidemiology of noroviruses associated with acute sporadic gastroenteritis in children: Global distribution of genogroups, genotypes and GII.4 variants. J Clin Virol. 2013;56:185–93.
  6. Patel MM, Hall AJ, Vinjé J, Umesh DP. Noroviruses: a comprehensive review. J Clin Virol. 2009;44:1–8.
  7. Uyar Y, Carhan A, Ozkaya E, Ertek M. Evaluation of laboratory diagnosis of the first norovirus outbreak in Turkey in 2008. Mikrobiyol Bul. 2008;42:607–15.
  8. Albayrak N, Yagci-Caglayik D, Altaş AB, Korukluoglu G, Ertek M. Refik Saydam Hıfzıssıhha Merkezi Başkanlığı, Viroloji Referans ve Araştırma Laboratuvarı, 2009 yılı akut viral gastroenterit verilerinin değerlendirilmesi. Turk Hij ve Deney Biyol Derg. 2011;68:9–15.
  9. Inan N, Kabakoğlu Ünsür E, Demirel A, Mamçu D, Sönmez E et al. Akut viral gastroenterit öntanılı vakalarda rotavirus, adenovirus ve norovirus sıklığının araştırılması. Ankem Derg. 2014;28:14–19.
  10. Altindis M, Bányai K, Kalayci R, Gulamber C, Koken R, Yoldas Y et al. Frequency of norovirus in stool samples from hospitalized children due to acute gastroenteritis in Anatolia, Turkey, 2006-2007. Scand J Infect Dis. 2009;41:685–88.

Kaynak Göster

MLA
Aksu, Arif, ve Alper Akçalı. “Detection of norovirus infections in Canakkale with ELISA and RT-PCR”. Cukurova Medical Journal, c. 41, sy 3, Eylül 2016, ss. 533-8, doi:10.17826/cukmedj.237508.