应用聚合酶链反应和杂交技术检测婴儿呼吸道合胞病毒、副流感病毒3、腺病毒和鼻病毒序列

François Freymuth , Astrid Vabret , Françoise Galateau-Salle , Janine Ferey , Geneviève Eugene , Joelle Petitjean , Evelyne Gennetay , Jacques Brouard , Mikael Jokik , Jean-François Duhamel , Bernard Guillois
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Using the two techniques, IFA and VIT, a significant number of specimens remain negative in spite of clinical and epidemiological presumptions of viral infection.</p><p><strong>Objectives and study design:</strong> The polymerase chain reaction (PCR) should improve the sensitivity of viral detection in clinical specimens. From October 1995 to March 1996, 277 nasal aspirates from hospitalized infants were tested simultaneously by IFA, VIT, polymerase chain reaction and hybridization with a DNA enzyme immunoassay (PCR-EIA) for RSV, PIV-3, AdV and RV.</p><p><strong>Results:</strong> RSV were detected in 177 (64%) samples, PIV-3 in 23 (8%), RV in 40 (14%), and AdV in 30 (10%). PCR-EIA detected RSV in more samples 173 (62%) than <span><math><mtext>IFA</mtext><mtext>VIT</mtext></math></span>: 109 (39%) (<em>P</em> &lt; 10<sup>−7</sup>). In most cases (79%), RSV-infected infants had lower respiratory tract disease, and routine and PCR techniques were positive. 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引用次数: 120

摘要

背景:鼻吸液中病毒抗原的免疫荧光检测(IFA)主要用于呼吸道合胞病毒(RSV)、副流感病毒(PIV) 3型和腺病毒(AdV)感染的诊断,而鼻病毒(RV)仅通过病毒分离技术(VIT)检测。使用IFA和VIT两种技术,尽管临床和流行病学推测病毒感染,但仍有大量标本呈阴性。目的与研究设计:聚合酶链反应(PCR)可提高临床标本中病毒检测的敏感性。1995年10月至1996年3月,对277例住院患儿鼻吸液进行了呼吸道合胞病毒(RSV)、呼吸道合胞病毒(PIV-3)、呼吸道合胞病毒(AdV)和呼吸道合胞病毒(RV)的IFA、VIT、聚合酶链反应和DNA酶免疫杂交(PCR-EIA)检测。结果:共检出RSV 177例(64%),PIV-3 23例(8%),RV 40例(14%),AdV 30例(10%)。PCR-EIA检出RSV的样本173份(62%)高于IFAVIT检出的样本109份(39%)(P <10−7)。在大多数病例中(79%),感染rsv的婴儿患有下呼吸道疾病,常规和PCR技术均为阳性。在23例PIV-3感染中,12例为IFAVIT和pcr - eia阳性,11例为IFAVIT阴性和pcr - eia阳性。RV 35例(87%)PCR eia阳性,11例(27%)培养阳性;AdV的pcr - eia阳性30份,培养阳性4份。同时病毒感染的比例明显高于传统技术:18%(50277)对2.5% (7277);P & lt;10−7。四分之一的RSV感染与另一种病毒的存在有关,主要是PIV-3(16例)和AdV(13例)。结论:PCR-EIA检出率高于IFAVIT, RSV检出率为1.5倍,PIV-3检出率为1.9倍,RV检出率为4倍,AdV检出率为10倍。与IFAVIT相比,PCR-EIA检测病毒的灵敏度增加,可能表明常规方法IFAVIT遗漏了含有低水平病毒的样本,因此,RSV或PIV-3,尤其是RV或AdV被忽视为呼吸道疾病的病原体。然而,除了不能错过病毒诊断的经济和方便方面的事实外,很难回答以下问题:在婴儿鼻吸液中检测病毒序列的意义是什么?或者聚合酶链反应可能在不会发病的患者身上检测到病毒?
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Detection of respiratory syncytial virus, parainfluenzavirus 3, adenovirus and rhinovirus sequences in respiratory tract of infants by polymerase chain reaction and hybridization

Background: Immunofluorescence assay (IFA) of viral antigens in nasal aspirates is largely used for the diagnosis of respiratory syncytial virus (RSV), parainfluenzavirus (PIV) type 3 and adenovirus (AdV) infections, whilst rhinovirus (RV) are detected by virus isolation technique (VIT) only. Using the two techniques, IFA and VIT, a significant number of specimens remain negative in spite of clinical and epidemiological presumptions of viral infection.

Objectives and study design: The polymerase chain reaction (PCR) should improve the sensitivity of viral detection in clinical specimens. From October 1995 to March 1996, 277 nasal aspirates from hospitalized infants were tested simultaneously by IFA, VIT, polymerase chain reaction and hybridization with a DNA enzyme immunoassay (PCR-EIA) for RSV, PIV-3, AdV and RV.

Results: RSV were detected in 177 (64%) samples, PIV-3 in 23 (8%), RV in 40 (14%), and AdV in 30 (10%). PCR-EIA detected RSV in more samples 173 (62%) than IFAVIT: 109 (39%) (P < 10−7). In most cases (79%), RSV-infected infants had lower respiratory tract disease, and routine and PCR techniques were positive. Out of the 23 PIV-3 infections, 12 were IFAVIT- and PCR-EIA-positive, and 11 IFAVIT-negative and PCR-EIA-positive. For RV, 35 (87%) specimens were PCR EIA-positive and 11 (27%) culture-positive; for AdV 30 samples were PCR-EIA-positive and four were culture-positive. Simultaneous viral infections were revealed in a significantly higher proportion than in conventional techniques: 18% (50277) versus 2.5% (7277); P < 10−7. One RSV infection in four was associated with the presence of another virus, mainly PIV-3 (16 cases) and AdV (13 cases).

Conclusions: PCR-EIA detects more positive-specimens than IFAVIT, 1.5 times more for RSV, 1.9 for PIV-3, 4 for RV and 10 for AdV, respectively. This increased sensitivity of viral detection by PCR-EIA compared to the IFAVIT could suggest that samples containing low levels of virus are missed by routine methods IFAVIT, and consequently, RSV or PIV-3, and above all RV or AdV are overlooked as agents of respiratory diseases. However, apart from the fact that the economic and convenient aspects of virus diagnostic cannot be missed, it is difficult to answer the following questions: what is the meaning of the detection of a viral sequences in nasal aspirates of infants. or may PCR have detected virus in patients who would not developed disease?

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