Comparison of diagnostic performance among Abbott RealTime HCV Genotyping II, Abbott HCV Genotype plus RUO, and Roche Cobas HCV Genotyping assays for hepatitis C virus genotyping

Author:

Chang Yu‐Ping1,Huang Chiuan‐Bo1,Su Tung‐Hung12,Liu Chun‐Jen123,Tseng Tai‐Chung124,Huang Shang‐Chin25,Chen Pei‐Jer123,Kao Jia‐Horng1234,Liu Chen‐Hua126ORCID

Affiliation:

1. Department of Internal Medicine National Taiwan University Hospital Taipei Taiwan

2. Hepatitis Research Center National Taiwan University Hospital Taipei Taiwan

3. Graduate Institute of Clinical Medicine National Taiwan University College of Medicine Taipei Taiwan

4. Department of Medical Research National Taiwan University Hospital Taipei Taiwan

5. Department of Internal Medicine National Taiwan University Hospital Bei‐Hu Branch Taipei Taiwan

6. Department of Internal Medicine National Taiwan University Hospital, Yun‐Lin Branch Douliou Taiwan

Abstract

AbstractComparison of diagnostic accuracy for commercial hepatitis C virus (HCV) genotyping (Abbott RealTime HCV Genotyping II, Roche Cobas Genotyping) and investigational Abbott HCV Genotype plus RUO assays designed to discriminate genotype (GT)‐1a, 1b or 6 in cases of ambiguous GT from the Abbott commercial assay remains limited. 743 HCV‐viremic samples were subjected to analysis using Abbott and Roche commercial as well as Abbott HCV Genotype plus RUO assays. Next‐generation sequencing (NGS) targeting core region was employed as the reference standard. Diagnostic accuracy was reported as the number of participants (percentages) along with 95% confidence intervals (CIs). Using NGS, 741 samples (99.7%) yielded valid genotyping results. The diagnostic accuracies were 97.6% (95% CI: 96.1%–98.5%) and 95.3% (95% CI: 93.4%–96.6%) using Abbott and Roche commercial assays (p = 0.0174). Abbott commercial assay accurately diagnosed HCV GT‐6a and 6w, whereas Roche commercial assay accurately diagnosed HCV GT‐6a. Both assays demonstrated low accuracies for HCV GT‐6b, 6e, 6g, and 6n. Abbott HCV Genotype plus RUO assay discriminated 13 of the 14 samples (92.9%; 95% CI: 64.2%–99.6%) that yielded ambiguous GT. Both assays were capable of diagnosing mixed HCV infections when the minor genotype comprised >8.4% of the viral load. The diagnostic performance of commercial HCV genotyping assays is commendable. Abbott assay demonstrated superior performance compared to Roche assay in diagnosing HCV GT‐6. Abbott HCV Genotype plus RUO assay aids in discriminating ambiguous GT. Both commercial assays are proficient in diagnosing mixed HCV infections at a cut‐off viral load of 8.4% in minor genotype.

Funder

Ministry of Science and Technology, Taiwan

Publisher

Wiley

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