Viral Interference as a Factor of False-Negative in the Infectious Adenovirus Detection Using Integrated Cell Culture-PCR with a BGM Cell Line

被引:2
作者
Sano, Daisuke [1 ,2 ]
Watanabe, Ryosuke [3 ]
Oishi, Wakana [2 ]
Amarasiri, Mohan [4 ]
Kitajima, Masaaki [3 ]
Okabe, Satoshi [3 ]
机构
[1] Tohoku Univ, Grad Sch Environm Studies, Dept Frontier Sci Adv Environm, Aoba Ku, Aoba 6-6-06, Sendai, Miyagi 9808579, Japan
[2] Tohoku Univ, Grad Sch Engn, Dept Civil & Environm Engn, Aoba Ku, Aoba 6-6-06, Sendai, Miyagi 9808579, Japan
[3] Hokkaido Univ, Div Environm Engn, Fac Engn, Kita Ku, North 13,West 8, Sapporo, Hokkaido 0608628, Japan
[4] Kitasato Univ, Sch Allied Hlth Sci, Dept Hlth Sci, Minami Ku, A1-505,1-15-1 Kitasato, Sagamihara, Kanagawa A1505, Japan
基金
日本学术振兴会;
关键词
ICC-PCR; Adenovirus; Enterovirus; Virus interference; BGM cell line; Environmental samples; NESTED-PCR; DRINKING-WATER; ENTEROVIRUSES; VIRUS; QUANTIFICATION; SAMPLES; IDENTIFICATION; POLYOMAVIRUS; INACTIVATION; NOROVIRUSES;
D O I
10.1007/s12560-020-09453-x
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study investigated the influence of viral interference on the detection of enteric viruses using the integrated cell culture (ICC)-PCR with a BGM cell line. It was possible to detect 10(2) plaque-forming units (PFU)/flask of enterovirus 71 (EV71) in spite of the presence of 10(4) PFU/flask of adenovirus 40 (AdV40). Meanwhile, 10(4) PFU/flask of AdV40 was not detected in the presence of 10(2) PFU/flask of EV71. This inhibition of AdV40 detection using ICC-PCR was attributable to the growth of EV71, because the addition of a growth inhibitor of EV71 (rupintrivir) neutralized the detection inhibition of AdV40. The growth inhibition of AdV40 under co-infection with EV71 is probably caused by the immune responses of EV71-infected cells. AdV is frequently used as a fecal contamination indicator of environmental water, but this study demonstrated that false-negative detection of infectious AdV using ICC-PCR could be caused by the co-existence of infectious EV in a water sample. The addition of rupintrivir could prevent false-negative detection of AdV using ICC-PCR. This study, therefore, emphasizes the importance of confirming the presence of multiple enteric viruses in a sample derived from environmental water prior to the application of ICC-PCR because the viral interference phenomenon may lead to the false-negative detection of target viruses.
引用
收藏
页码:84 / 92
页数:9
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