Yoon Jung, Yun Seung Gyu, Nam Jeonghun, Choi Sung-Hyuk, Lim Chae Seung
Department of Laboratory Medicine, Korea University College of Medicine, Seoul, Republic of Korea.
Department of Emergency Medicine, Korea University College of Medicine, Seoul, Republic of Korea.
J Virol Methods. 2017 May;243:15-19. doi: 10.1016/j.jviromet.2017.01.013. Epub 2017 Jan 19.
Diagnostic tests for influenza infection commonly use nasopharyngeal swabs (NPS) even though these are invasive to obtain. As an alternative specimen, we evaluated the diagnostic usefulness of saliva samples with rapid influenza diagnostic tests (RIDTs).
Both NPS and saliva samples were collected from 385 influenza suspected patients and analyzed using Sofia Influenza A+B Fluorescence Immunoassay (Quidel Corporation, San Diego, CA, USA), ichroma TRIAS Influenza A+B (Boditech, Chuncheon, Korea), SD Bioline Influenza Ag (Standard Diagnostic, Yonggin, Korea), BinaxNOW Influenza A/B antigen kit (Alere Inc., Waltham, MA, USA), and real-time reverse transcriptase PCR (RT-PCR).
Of the 385 patients, 31.2% (120/385) were positive for influenza A, and 7.5% (29/385) were positive for influenza B virus with saliva or NPS by RT-PCR. The diagnostic sensitivity was slightly higher in NPS than in saliva samples for both influenza A and B by all of the four RIDTs. The diagnostic sensitivities of Sofia and ichroma TRIAS were significantly superior to those of the other conventional influenza RIDTs with both types of sample. The sensitivities of Sofia and ichroma TRIAS with saliva specimens were comparable to the sensitivities of the other two conventional RIDTs with NPS specimens. The simultaneous use of saliva and NPS samples exhibited improved sensitivity from 10.0% to 13.3% for influenza A and from 10.3% to 17.2% for influenza B compared to using NPS alone.
This study demonstrates that saliva is a useful specimen for influenza detection, and that the combination of saliva and NPS could improve the sensitivities of influenza RIDTs.
尽管鼻咽拭子(NPS)获取时具有侵入性,但流感感染的诊断测试通常仍使用它。作为一种替代样本,我们评估了唾液样本在快速流感诊断测试(RIDTs)中的诊断效用。
从385名疑似流感患者中采集了NPS和唾液样本,并使用索非亚甲型和乙型流感荧光免疫测定法(美国加利福尼亚州圣地亚哥的Quidel公司)、ichroma TRIAS甲型和乙型流感检测试剂(韩国春川的Boditech公司)、SD生物线流感抗原检测试剂(韩国龙仁的Standard Diagnostic公司)、BinaxNOW甲型/乙型流感抗原检测试剂盒(美国马萨诸塞州沃尔瑟姆的Alere公司)以及实时逆转录聚合酶链反应(RT-PCR)进行分析。
在这385名患者中,通过RT-PCR检测,120例(31.2%)甲型流感呈阳性,29例(7.5%)乙型流感病毒呈阳性,样本为唾液或NPS。对于甲型和乙型流感,在所有四种RIDTs检测中,NPS的诊断敏感性略高于唾液样本。索非亚和ichroma TRIAS的诊断敏感性明显优于其他两种传统的流感RIDTs,两种样本类型均如此。索非亚和ichroma TRIAS对唾液样本的敏感性与其他两种传统RIDTs对NPS样本的敏感性相当。与单独使用NPS相比,同时使用唾液和NPS样本时,甲型流感的敏感性从10.0%提高到13.3%,乙型流感的敏感性从10.3%提高到17.2%。
本研究表明唾液是流感检测的有用样本,唾液和NPS联合使用可提高流感RIDTs的敏感性。