Recovery of naked viral genomes in water by virus concentration methods

被引:40
作者
Haramoto, Eiji [1 ]
Katayama, Hiroyuki [1 ]
Oguma, Kumiko [1 ]
Ohgaki, Shinichiro [1 ]
机构
[1] Univ Tokyo, Dept Urban engn, Grad Sch Engn, Bunkyo Ku, Tokyo 1138656, Japan
关键词
poliovirus; viral genome; virion; virus concentration method; water;
D O I
10.1016/j.jviromet.2007.01.024
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The recovery efficiency of naked poliovirus-RNA in water using virus concentration methods was determined to evaluate the possibility of detecting naked viral genomes. Two conventional virus concentration methods (1 MDS-method and HA-method) and two methods developed by our research group (Mg-method and Al-method) were applied to recovery tests of poliovirus-RNA from four kinds of water sample, in parallel with recovery tests of poliovirus-virions. Mean recovery yields of poliovirus-RNA by the Mg-method were 5.7, 12, 3.4, and 17% for MilliQ water, tap water, secondary-treated sewage, and seawater, respectively. Meanwhile, mean recovery yields of poliovirus-virions by the Mg-method were 6.6-14.7 times higher than those of the RNA. Using the Al-method, poliovirus-RNA in MilliQ water and tap water was recovered at a higher recovery yield as compared to the Mg-method (69% from MilliQ water and 26% from tap water on average) in addition to the virions. The I MDS-method and the HA-method did not provide as high recovery yields of the virions as the Mg-method. From these results, the Mg-method was judged most appropriate for selective detection of virions instead of naked viral genomes in water among the four methods tested. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 173
页数:5
相关论文
共 23 条
[1]   DETECTION OF ENTEROVIRUSES IN GROUNDWATER WITH THE POLYMERASE CHAIN-REACTION [J].
ABBASZADEGAN, M ;
HUBER, MS ;
GERBA, CP ;
PEPPER, IL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (05) :1318-1324
[2]  
*AM PUBL HLTH ASS, 1995, STAND METH EX WAT WA
[3]   Vulnerability of drinking-water wells in La Crosse, Wisconsin, to enteric-virus contamination from surface water contributions [J].
Borchardt, MA ;
Haas, NL ;
Hunt, RJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (10) :5937-5946
[4]   A BLOCK IN RELEASE OF PROGENY VIRUS AND A HIGH PARTICLE-TO-INFECTIOUS UNIT RATIO CONTRIBUTE TO POOR GROWTH OF ENTERIC ADENOVIRUS TYPE-40 AND TYPE-41 IN CELL-CULTURE [J].
BROWN, M ;
WILSONFRIESEN, HL ;
DOANE, F .
JOURNAL OF VIROLOGY, 1992, 66 (05) :3198-3205
[5]   Enteric viruses of humans and animals in aquatic environments: Health risks, detection, and potential water quality assessment tools [J].
Fong, TT ;
Lipp, EK .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2005, 69 (02) :357-+
[6]   Nested multiplex PCR assay for detection of human enteric viruses in shellfish and sewage [J].
Formiga-Cruz, M ;
Hundesa, A ;
Clemente-Casares, P ;
Albiñana-Gimenez, N ;
Allard, A ;
Girones, R .
JOURNAL OF VIROLOGICAL METHODS, 2005, 125 (02) :111-118
[7]  
Grabow WOK, 2001, WATER SCI TECHNOL, V43, P1
[8]  
Griffin DW, 1999, APPL ENVIRON MICROB, V65, P4118
[9]   One-year monthly monitoring of Torque teno virus (TTV) in wastewater treatment plants in Japan [J].
Haramoto, E ;
Katayama, H ;
Oguma, K ;
Yamashita, H ;
Nakajima, E ;
Ohgaki, S .
WATER RESEARCH, 2005, 39 (10) :2008-2013
[10]   Application of cation-coated filter method to detection of noroviruses, enteroviruses, adenoviruses, and torque teno viruses in the Tamagawa River in Japan [J].
Haramoto, E ;
Katayama, H ;
Oguma, K ;
Ohgaki, S .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (05) :2403-2411