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

被引:3
|
作者
Marasini, Daya [1 ]
Whaley, Melissa J. [1 ]
Jenkins, Laurel T. [1 ]
Hu, Fang [2 ]
Jiang, Wenxin [3 ]
Topaz, Nadav [4 ]
Chen, Alex [1 ]
Schmink, Susanna [1 ]
Dolan Thomas, Jennifer [1 ]
Harcourt, Brian H. [1 ]
Marjuki, Henju [1 ]
Wang, Xin [1 ]
机构
[1] Ctr Dis Control & Prevent, Natl Ctr Immunizat & Resp Dis, Div Bacterial Dis, Atlanta, GA USA
[2] IHRC Inc, Div Bacterial Dis, Natl Ctr Immunizat & Resp Dis, Ctr Dis Control & Prevent, Atlanta, GA USA
[3] Weems Design Studio Inc, Ctr Dis Control & Prevent, Natl Ctr Immunizat & Resp Dis, Div Bacterial Dis, Atlanta, GA USA
[4] Ctr Dis Control & Prevent, Natl Ctr Immunizat & Resp Dis,Div Bacterial Dis, Meningitis & Vaccine Preventable Dis Branch, Bacterial Meningitis Lab, Atlanta, GA USA
关键词
direct real-time polymerase chain reaction; triplex; serotyping; Haemophilus influenzae; Hi-phoB; ASSAY; POLYSACCHARIDE; EPIDEMIOLOGY; MENINGITIS; DISEASE; LOCUS;
D O I
10.1128/jcm.02111-21
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 phoB gene for the species detection (Hi-phoB) 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-phoB 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-phoB, 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. 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 phoB gene for the species detection (Hi-phoB) 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.
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页数:11
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