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DOI 10.1016/j.jcv.2018.07.003

Медицинская библиотека · Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2018

Diagnostic accuracy of digital RNA quantification versus real-time PCR for the detection of respiratory syncytial virus in nasopharyngeal aspirates from children with acute respiratory infection.

Bouzas Maiara L, Oliveira Juliana R, Queiroz Artur, Fukutani Kiyoshi F, Barral Aldina, Rector Annabel, Wollants Elke, Keyaerts Els, Van der Gucht Winke, Van Ranst Marc, Beuselinck Kurt, de Oliveira Camila I, Van Weyenbergh Johan, Nascimento-Carvalho Cristiana M, Acute Respiratory Infection and Wheeze Study Group Phase I and II

Оценочное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

Virus-specific molecular assays such as real-time polymerase chain reaction (RT-PCR) are regularly used as the gold standard to diagnose viral respiratory tract infections, but simultaneous detection of multiple different pathogens is often challenging. A multiplex digital method of RNA quantification, nCounter (NanoString Technologies), can overcome this disadvantage and identify, in a single reaction, the presence of different respiratory viruses.

OBJECTIVES

To evaluate the accuracy of nCounter to identify and quantify RSV-A and RSV-B in nasopharyngeal aspirates (NPA) of children (6-23-months-old) with acute respiratory infection.

STUDY

DESIGN

NPA was collected at enrolment in a prospective cross-sectional study conducted in Salvador, Brazil. A quantitative RT-PCR with a subgroup-specific primer and probeset for RSV-A and RSV-B was performed in parallel with a customized nCounter probeset containing viral targets in NPA.

RESULTS

Of 559 NPA tested, RSV was detected by RT-PCR in 139 (24.9%), by nCounter in 122 (21.8%) and by any method in 158 (28.3%) cases. Compared to the gold standard of qRT-PCR, sensitivity of nCounter was 74.3% (95%CI:63.3%-82.9% RSV-A) and 77.6% (95%CI:66.3%-85.9% RSV-B); specificity was 98.4% (95%CI:96.8%-99.2% RSV-A) and 97.8% (95%CI:96.0%-98.8% RSV-B); positive predictive value was 87.3% (95%CI:76.9%-93.4% RSV-A) and 82.5% (95%CI:71.4%-90.0% RSV-B) and negative predictive value was 96.1% (95%CI:94.1%-97.5% RSV-A), and 96.9% (95%CI:95.1%-98.2% RSV-B). Accuracy was 95.2% (95%CI:93.1%-96.7%) for RSV-A and 95.3% (95%CI:93.3%-96.9%) for RSV-B, while both methods significantly correlated for RSV-A (r = 0.44, p = 8 × 10-5) and RSV-B (r = 0.73, p = 3 × 10-12) quantification.

CONCLUSIONS

nCounter is highly accurate in detecting RSV-A/B in NPA. Robustness and high-throughput multiplexing indicate its use in large-scale epidemiological studies.

Для цитирования: Bouzas Maiara L, Oliveira Juliana R, Queiroz Artur, Fukutani Kiyoshi F, Barral Aldina, Rector Annabel, Wollants Elke, Keyaerts Els, Van der Gucht Winke, Van Ranst Marc, Beuselinck Kurt, de Oliveira Camila I, Van Weyenbergh Johan, Nascimento-Carvalho Cristiana M, Acute Respiratory Infection and Wheeze Study Group Phase I and II. Diagnostic accuracy of digital RNA quantification versus real-time PCR for the detection of respiratory syncytial virus in nasopharyngeal aspirates from children with acute respiratory infection.. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 2018. DOI: 10.1016/j.jcv.2018.07.003.

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