A comparative analysis of Freon substitutes in the purification of reovirus and calicivirus

被引:91
作者
Mendez, II [1 ]
Hermann, LL [1 ]
Hazelton, PR [1 ]
Coombs, KM [1 ]
机构
[1] Univ Manitoba, Dept Med Microbiol & Infect Dis, Winnipeg, MB R3E 0W3, Canada
基金
英国医学研究理事会;
关键词
comparative analysis; freon substitutes; reovirus; calicivirus;
D O I
10.1016/S0166-0934(00)00217-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Freon 113 (Freon) is an essential component used in some viral purification methods to separate virus from infected cell debris. With its environmental and toxic hazards, Freon's availability is limited and more tightly regulated. Several organic solvent substitutes were selected to identify a suitable Freon replacement for the purification of both cultivable reovirus and fastidious calicivirus. Reovirus was extracted from tissue cultured cells with each solvent tested and purified in cesium chloride gradients by standard techniques. Purified virions were analyzed for conservation of physical and biological properties by morphological examination and infectivity studies. The purification of calicivirus nucleic acid from stool samples using selected solvents was also examined. Solvent-extracted calicivirus RNA was reverse transcribed and quantified by polymerase chain reaction amplification of a standard diagnostic 117 bp amplicon. These studies indicated that Vertrel(R) XF (a newly developed environmentally friendly Freon substitute) and a 7:3 mixture of isopentane/1-chlorobutane are suitable replacements. Considerations of flammability and ease of use suggest that Vertrel(R) XF is the preferred choice as a Freon substitute for the purification of these non-enveloped viruses. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:59 / 67
页数:9
相关论文
共 32 条
[1]   DETECTION OF NORWALK VIRUS AND HEPATITIS-A VIRUS IN SHELLFISH TISSUES WITH THE PCR [J].
ATMAR, RL ;
NEILL, FH ;
ROMALDE, JL ;
LEGUYADER, F ;
WOODLEY, CM ;
METCALF, TG ;
ESTES, MK .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (08) :3014-3018
[2]   PCR AMPLIFICATION OF UP TO 35-KB DNA WITH HIGH-FIDELITY AND HIGH-YIELD FROM LAMBDA-BACTERIOPHAGE TEMPLATES [J].
BARNES, WM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2216-2220
[3]  
Barton A.F. M., 1991, CRC HDB SOLUBILITY P
[4]   A METHOD FOR RECOVERING VIRUSES FROM SLUDGES [J].
BERMAN, D ;
BERG, G ;
SAFFERMAN, RS .
JOURNAL OF VIROLOGICAL METHODS, 1981, 3 (05) :283-291
[5]   STUDIES OF THE MAJOR REOVIRUS CORE PROTEIN SIGMA-2 - REVERSION OF THE ASSEMBLY-DEFECTIVE MUTANT TSC447 IS AN INTRAGENIC PROCESS AND INVOLVES BACK MUTATION OF ASP-383 TO ASN [J].
COOMBS, KM ;
MAK, SC ;
PETRYCKYCOX, LD .
JOURNAL OF VIROLOGY, 1994, 68 (01) :177-186
[6]  
*CRC, 1977, CRC HDB CHEM PHYS
[7]  
*DUP CHEM, 1999, VERTR XF TECHN B
[8]   REOVIRUS MESSENGER-RNA CONTAINS A METHYLATED, BLOCKED 5'-TERMINAL STRUCTURE - M7G(5')PPP(5')GMPCP- [J].
FURUICHI, Y ;
MORGAN, M ;
MUTHUKRISHNAN, S ;
SHATKIN, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (01) :362-366
[9]  
GOLDSCHMIDT G, 1993, AM IND HYG ASSOC J, V54, P36, DOI 10.1202/0002-8894(1993)054<0036:AAAFRW>2.0.CO
[10]  
2