Quantification of Cyprinid Herpesvirus 3 in Environmental Water by Using an External Standard Virus

  • Mie N. Honjo
    Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047, Japan
  • Toshifumi Minamoto
    Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047, Japan
  • Kazuaki Matsui
    Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047, Japan
  • Kimiko Uchii
    Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047, Japan
  • Hiroki Yamanaka
    Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047, Japan
  • Alata A. Suzuki
    Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047, Japan
  • Yukihiro Kohmatsu
    Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047, Japan
  • Takaji Iida
    National Research Institute of Aquaculture, Fisheries Research Agency, Minami-Ise, Mie 516-0193, Japan
  • Zen'ichiro Kawabata
    Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047, Japan

説明

<jats:title>ABSTRACT</jats:title><jats:p>Cyprinid herpesvirus 3 (CyHV-3), a lethal DNA virus that spreads in natural lakes and rivers, infects common carp and koi. We established a quantification method for CyHV-3 that includes a viral concentration method and quantitative PCR combined with an external standard virus. Viral concentration methods were compared using the cation-coated filter and ultrafiltration methods. The recovery of virus-like particles was similar for the two methods (cation-coated filter method, 44% ± 19%,<jats:italic>n</jats:italic>= 3; ultrafiltration method, 50% ± 3%,<jats:italic>n</jats:italic>= 3); however, the former method was faster and more suitable for routine determinations. The recovery of seeded CyHV-3 based on the cation-coated filter method varied by more than 3 orders of magnitude among the water samples. The recovery yield of CyHV-3 was significantly correlated with that of the seeded λ phage, and the average ratio of λ to the CyHV-3 recovery yield was 1.4, indicating that λ is useful as an external standard virus for determining the recovery yield of CyHV-3. Therefore, to quantify CyHV-3 in environmental water, a known amount of λ was added as an external standard virus to each water sample. Using this method, CyHV-3 DNA was detected in 6 of the 10 (60%) types of environmental water tested; the highest concentration of CyHV-3 DNA was 2 × 10<jats:sup>5</jats:sup>copies liter<jats:sup>−1</jats:sup>. The lowest recovery limit of CyHV-3 DNA was 60 copies liter<jats:sup>−1</jats:sup>. This method is practical for monitoring CyHV-3 abundance in environmental water.</jats:p>

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