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本文引用的文献

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Genomic characterization of Haemophilus influenzae: a focus on the capsule locus.流感嗜血杆菌的基因组特征:关注荚膜基因座。
BMC Genomics. 2019 Oct 12;20(1):733. doi: 10.1186/s12864-019-6145-8.
2
Triplex real-time PCR assay for the detection of Streptococcus pneumoniae, Neisseria meningitidis and Haemophilus influenzae directly from clinical specimens without extraction of DNA.用于直接从临床标本中检测肺炎链球菌、脑膜炎奈瑟菌和流感嗜血杆菌而无需提取DNA的三重实时PCR检测法。
Diagn Microbiol Infect Dis. 2019 Mar;93(3):188-190. doi: 10.1016/j.diagmicrobio.2018.10.008. Epub 2018 Oct 16.
3
Triplex Real-Time PCR without DNA Extraction for the Monitoring of Meningococcal Disease.无需DNA提取的三重实时荧光定量PCR用于监测脑膜炎球菌病
Diagnostics (Basel). 2018 Aug 30;8(3):58. doi: 10.3390/diagnostics8030058.
4
BMScan: using whole genome similarity to rapidly and accurately identify bacterial meningitis causing species.BMScan:利用全基因组相似度快速准确地鉴定细菌性脑膜炎致病菌种。
BMC Infect Dis. 2018 Aug 15;18(1):405. doi: 10.1186/s12879-018-3324-1.
5
Current Epidemiology and Trends in Invasive Haemophilus influenzae Disease-United States, 2009-2015.2009-2015 年美国侵袭性流感嗜血杆菌病的流行现状和趋势。
Clin Infect Dis. 2018 Aug 31;67(6):881-889. doi: 10.1093/cid/ciy187.
6
The changing epidemiology of invasive Haemophilus influenzae disease: Emergence and global presence of serotype a strains that may require a new vaccine for control.侵袭性流感嗜血杆菌疾病不断变化的流行病学:a 型菌株的出现及全球分布,可能需要新型疫苗来进行防控。
Vaccine. 2017 Jul 24;35(33):4270-4275. doi: 10.1016/j.vaccine.2017.06.001. Epub 2017 Jun 27.
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Epidemiology of Invasive Haemophilus influenzae Disease, Europe, 2007-2014.2007 - 2014年欧洲侵袭性流感嗜血杆菌病流行病学
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Duplex Quantitative PCR Assay for Detection of Haemophilus influenzae That Distinguishes Fucose- and Protein D-Negative Strains.用于检测区分岩藻糖和蛋白D阴性菌株的流感嗜血杆菌的双重定量PCR检测法。
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10
Development of Real-Time PCR Methods for the Detection of Bacterial Meningitis Pathogens without DNA Extraction.无需DNA提取的用于检测细菌性脑膜炎病原体的实时PCR方法的开发
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无需 DNA 提取的直接实时 PCR 检测和流感嗜血杆菌血清分型。

Direct Real-Time PCR for the Detection and Serotyping of Haemophilus influenzae without DNA Extraction.

机构信息

Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Preventiongrid.416738.f, Atlanta, Georgia, USA.

IHRC Inc., Contractor to Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Preventiongrid.416738.f, Atlanta, Georgia, USA.

出版信息

J Clin Microbiol. 2022 Apr 20;60(4):e0211121. doi: 10.1128/jcm.02111-21. Epub 2022 Mar 21.

DOI:10.1128/jcm.02111-21
PMID:35306833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9020362/
Abstract

To monitor the burden and changes in Haemophilus influenzae (Hi) disease, direct real-time PCR (drt-PCR) assays have been developed for Hi detection in monoplex form and its six serotypes in triplex form, directly from cerebrospinal fluid (CSF) specimens. These assays target the gene for the species detection (Hi-) and serotype-specific genes in region II of the capsule biosynthesis locus (Hi-abf and Hi-cde), identified through comparative analysis of Hi and non-Hi whole-genome sequences. The lower limit of detection (LLD) is 293 CFU/mL for the Hi- assay and ranged from 11 to 130 CFU/mL for the triplex serotyping assays. Using culture as a reference method, the sensitivity and specificity of Hi-, Hi-abf, and Hi-cde were 100%. Triplex serotyping assays also showed 100% agreement for each serotype compared to their corresponding monoplex serotyping assay. These highly sensitive and specific drt-PCR assays do not require DNA extraction and thereby reduce the time, cost, and handling required to process CSF specimens. Furthermore, triplex drt-PCR assays combine the detection of three serotypes in a single reaction, further improving testing efficiency, which is critical for laboratories that process high volumes of Hi specimens for surveillance and diagnostic purposes.

摘要

为了监测流感嗜血杆菌(Hi)疾病的负担和变化,已经开发了直接实时 PCR(drt-PCR)检测方法,用于从脑脊液(CSF)标本中单重形式和三重形式直接检测 Hi 及其六个血清型。这些检测方法针对种属检测(Hi-)和荚膜生物合成基因座区域 II 中血清型特异性基因(Hi-abf 和 Hi-cde)的基因,通过对 Hi 和非 Hi 全基因组序列的比较分析确定。Hi-检测的最低检测限(LLD)为 293 CFU/mL,三重血清分型检测的范围为 11 至 130 CFU/mL。使用培养作为参考方法,Hi-、Hi-abf 和 Hi-cde 的敏感性和特异性均为 100%。与相应的单重血清分型检测相比,三重血清分型检测对于每个血清型也显示出 100%的一致性。这些高度敏感和特异性的 drt-PCR 检测方法不需要 DNA 提取,从而减少了处理 CSF 标本所需的时间、成本和处理。此外,三重 drt-PCR 检测方法将三种血清型的检测结合在一个反应中,进一步提高了检测效率,这对于处理大量 Hi 标本进行监测和诊断目的的实验室至关重要。