Volume 84, Issue 3 pp. 164-169

Heat sensitivity of human parvovirus B19

M. Yunoki

Corresponding Author

M. Yunoki

Department of Virology, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

Protein Research Laboratory, Pharmaceutical Research Division, Mitsubishi Pharma Corporation, Osaka, Japan

: Mikihiro Yunoki, Department of Virology, Research Institute for Microbial Diseases, Osaka University, Yamadaoka 3–1, Suita, Osaka 565–0871, Japan
E-mail: [email protected]Search for more papers by this author
M. Tsujikawa

M. Tsujikawa

Protein Research Laboratory, Pharmaceutical Research Division, Mitsubishi Pharma Corporation, Osaka, Japan

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T. Urayama

T. Urayama

Department of Virology, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

Protein Research Laboratory, Pharmaceutical Research Division, Mitsubishi Pharma Corporation, Osaka, Japan

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Y. Sasaki

Y. Sasaki

Protein Research Laboratory, Pharmaceutical Research Division, Mitsubishi Pharma Corporation, Osaka, Japan

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M. Morita

M. Morita

Protein Research Laboratory, Pharmaceutical Research Division, Mitsubishi Pharma Corporation, Osaka, Japan

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H. Tanaka

H. Tanaka

Protein Research Laboratory, Pharmaceutical Research Division, Mitsubishi Pharma Corporation, Osaka, Japan

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S. Hattori

S. Hattori

Protein Research Laboratory, Pharmaceutical Research Division, Mitsubishi Pharma Corporation, Osaka, Japan

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K. Takechi

K. Takechi

Protein Research Laboratory, Pharmaceutical Research Division, Mitsubishi Pharma Corporation, Osaka, Japan

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K. Ikuta

K. Ikuta

Department of Virology, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

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First published: 02 April 2003
Citations: 40

Abstract

Background and Objectives To date there has been no published report on a systematic evaluation of the heat sensitivity of human parvovirus B19 (B19) and the related safety of the plasma-derived fractionated products. In this study, we examined the heat sensitivity of B19 by using the infectivity assay with cultured cells.

Materials and Methods The heat sensitivity of B19 was examined by measuring the reduction in viral infectivity titres after heating liquid containing B19 at 60 °C. Viral infectivity was assayed by detection of viral antigens or viral mRNA in infected cells. As a control, canine parvovirus (CPV) was also heat-treated.

Results B19 displayed quite different inactivation kinetics to CPV when both were heated in liquid at 60 °C. In sharp contrast to the latter, B19 was rapidly inactivated within 1 h when the virus was suspended in 5% or 25% human serum albumin solution, phosphate-buffered saline, or complete medium. However, B19 appeared to be resistant to heat inactivation in liquid containing 60% sucrose.

Conclusions The heat sensitivity of B19 in liquid was clearly different from that of CPV. Significantly, the efficiency to inactivate B19 and reduce its infectivity following heating in liquid was mainly affected by the composition of the solutions used for virus suspension.

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