- Author:
Yuan GAO
1
,
2
,
3
;
Yan Qing TIE
3
;
Lin Qing ZHAO
4
;
He TAN
1
,
3
;
Nan DING
3
;
Ya Xin DING
4
;
Qi GUO
4
;
Rui Qing ZHANG
5
;
Jin Rong WANG
1
,
5
;
Zi Wei CHEN
2
,
6
;
Guo Hao FAN
5
;
Xin Xin SHEN
5
;
Zhi Shan FENG
3
;
Xue Jun MA
2
,
7
Author Information
- Publication Type:Letter
- Keywords: Cytomegalovirus; Epstein-Barr virus; Isothermal nucleic acid detection; Recombinase-aided amplification
- MeSH: Adolescent; Adult; Child; Child, Preschool; Cytomegalovirus/genetics*; Cytomegalovirus Infections/virology*; DNA, Viral/analysis*; Epstein-Barr Virus Infections/virology*; Female; Herpesvirus 4, Human/genetics*; Humans; Infant; Infant, Newborn; Male; Middle Aged; Nucleic Acid Amplification Techniques; Recombinases/genetics*; Young Adult
- From: Biomedical and Environmental Sciences 2021;34(8):650-655
- CountryChina
- Language:English
- Abstract: Epstein-Barr virus (EBV) and cytomegalovirus (CMV), two of the most prevalent human herpesviruses, cause a wide spectrum of diseases and symptoms and are associated with serious health problem. In this study, we developed an internal control reference recombinase-aided amplification (ICR-RAA) assay for the rapid detection of EBV and CMV within 30 min. The assay had a sensitivity of 5 and 1 copies/test for EBV and CMV, respectively, with no cross reaction with other pathogens. In comparison with those of the commercial quantitative polymerase chain reaction (qPCR), the sensitivity of the EBV and CMV ICR-RAAs using extracted DNA was 93.33% and 84.84%, respectively; the specificity was 98.75% and 100.00%, respectively; and the Kappa values were 0.930 and 0.892 (