首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Evaluation of Methodology for Serotyping Invasive and Nasopharyngeal Isolates of Haemophilus influenzae in the Ongoing Surveillance in Brazil
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Evaluation of Methodology for Serotyping Invasive and Nasopharyngeal Isolates of Haemophilus influenzae in the Ongoing Surveillance in Brazil

机译:在巴西进行的持续监测中对流感嗜血杆菌的侵袭性鼻咽分离物进行血清分型的方法学评价

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摘要

To assess the magnitude of discrepant results obtained by routine Haemophilus influenzae serotyping, 258 isolates, collected by the epidemiological surveillance system in Brazil from individuals with invasive diseases or carriage, were evaluated by two slide agglutination (SlAg) methods: SlAg method 1, by which strains were initially screened with a serotype b-specific antiserum, and SlAg method 2, by which strains were tested against all serotype-specific antisera in parallel. Investigators comparing results of the two SlAg methods with those obtained by capsule type-specific PCR were blinded to the method used. The serotype prevalence rates found by the three methods were significantly different, involving discrepancies mainly between serotype b and noncapsulated (NC) isolates. For invasive isolates (n = 131), the overall agreement rate between SlAg method 1 or 2 and PCR was 68.0 or 88.3%, respectively, whereas for colonizing isolates (n = 127) the corresponding rate was 46.5 or 94.2%, respectively. SlAg method 2 improved the ascertainment of serotypes over that obtained with SlAg method 1, demonstrating good correlation with PCR. Use of the polyvalent antiserum as a screening reagent for SlAg for invasive and colonizing isolates showed poor discriminatory power, with a sensitivity of 65.8% and a specificity of 91.7%. We stress the importance of using a well-standardized SlAg methodology and suggest that reference laboratories should utilize PCR routinely to confirm SlAg results and to check all nonspecific SlAg reactions and apparent NC isolates by SlAg in order to provide reliable data on the prevalence of H. influenzae serotypes in the H. influenzae type b vaccine era.
机译:为了评估常规流感嗜血杆菌血清分型所获得的差异结果的严重程度,采用两种玻片凝集(SlAg)方法(SlAg方法1),通过流行病学监测系统在巴西的流行病学监测系统从侵袭性疾病或携带疾病的个体中收集了258个分离株,以评估这些结果。首先用血清型b特异性抗血清和SlAg方法2筛选菌株,通过平行测试针对所有血清型特异性抗血清测试菌株。研究人员将两种SlAg方法的结果与通过胶囊类型特异性PCR获得的结果进行比较,对所使用的方法不了解。通过三种方法发现的血清型流行率存在显着差异,主要涉及血清型b和未包囊(NC)分离株之间的差异。对于侵入性分离株(n = 131),SlAg方法1或2与PCR之间的总体符合率分别为68.0或88.3%,而对于定居分离株(n = 127),对应率分别为46.5或94.2%。与用SlAg方法1获得的血清型相比,SlAg方法2改善了血清型的确定性,表明与PCR的相关性很好。使用多价抗血清作为针对侵袭性和定殖性分离株的SlAg的筛选试剂显示出差的鉴别能力,灵敏度为65.8%,特异性为91.7%。我们强调使用标准化的SlAg方法的重要性,并建议参考实验室应常规使用PCR来确认SlAg结果并检查SlAg的所有非特异性SlAg反应和明显的NC分离株,以便提供有关H流行率的可靠数据。乙型流感嗜血杆菌疫苗时代的流感血清型。

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