Evaluation of a commercial real-time PCR kit for the detection of the Q80K polymorphism in plasma from HCV genotype 1a infected patients
| Autor: | Bianca Bruzzone, Ilaria Vicenti, Ombretta Turriziani, Maurizio Zazzi, Laura Sticchi, Francesca Falasca |
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| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
Simeprevir Drug resistance assay HCV Natural polymorphisms Q80K Infectious Diseases Virology Genotype Hepacivirus Concordance 030106 microbiology Viral Nonstructural Proteins Real-Time Polymerase Chain Reaction Antiviral Agents Sensitivity and Specificity 03 medical and health sciences 0302 clinical medicine Genotype 1b Drug Resistance Viral Humans Polymorphism Genetic biology Wild type Hepatitis C Chronic biology.organism_classification Real-time polymerase chain reaction Italy 030211 gastroenterology & hepatology Reagent Kits Diagnostic Clinical virology |
| Zdroj: | Journal of Clinical Virology. 76:20-23 |
| ISSN: | 1386-6532 |
| DOI: | 10.1016/j.jcv.2016.01.006 |
| Popis: | Background Screening of the natural HCV NS3 polymorphism Q80K is required prior to simeprevir administration due to the reduced susceptibility of genotype 1 viruses carrying this amino acid variant. A simple, rapid and robust test for Q80K screening would be advisable in routine diagnostic laboratories. Objectives The aim of this study was to evaluate a commercial NS3 Q80K real-time PCR kit (Q80K Polymorphism Kit, Clonit srl, Milan, Italy). Study design Forty-three plasma samples obtained from untreated HCV genotype 1a-infected patients and previously sequenced at a reference laboratory, were sent to two public clinical virology laboratories for blinded Q80K screening with the kit under evaluation. The sample panel included 25 cases with the wild type 80Q, 17 with the mutant 80K and 1 with the mutant 80L. Results Laboratory 1 identified 22/25 (88.0%) 80Q and 17/17 (100.0%) 80K cases. Laboratory 2 identified 23/25 (92.0%) 80Q and 16/17 (94.2%) 80K cases. All of the unidentified cases were scored as negative, with no mutant/wild type miscalling. The 80L variant was scored as indeterminate by Laboratory 1 and as negative by Laboratory 2. Overall, sensitivity and specificity for detection of 80K were 97.1% (95% C.I., 82.9–99.8%) and 100.0% (90.2–100.0%), respectively. However, the system did not provide any result for 6/84 cases (7.1% failure rate), not including the 80L variant which is not expected to be detected as stated in the kit package insert. Global inter-laboratory concordance was 93.0%. Conclusions Despite good specificity, this Q80K detection system needs improvements in amplification success rate and robustness. |
| Databáze: | OpenAIRE |
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