Establishment of a new cell line susceptible to Cyprinid herpesvirus 3 ( C y HV ‐3) and possible latency of C y HV ‐3 by temperature shift in the cells
A new cell line named CCF ‐ K 104 predominantly consisting of fibroblastic cells showed optimal growth at temperatures from 25 °C to 30 °C. Serial morphological changes in the cells induced by Cyprinid herpesvirus 3 ( C y HV ‐3) included cytoplasmic vacuolar formation, cell rounding and detachment....
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Veröffentlicht in: | Journal of fish diseases 2015-06, Vol.38 (6), p.507-514 |
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creator | Imajoh, M Fujioka, H Furusawa, K Tamura, K Yamasaki, K Kurihara, S Yamane, J Kawai, K Oshima, S |
description | A new cell line named
CCF
‐
K
104 predominantly consisting of fibroblastic cells showed optimal growth at temperatures from 25 °C to 30 °C. Serial morphological changes in the cells induced by Cyprinid herpesvirus 3 (
C
y
HV
‐3) included cytoplasmic vacuolar formation, cell rounding and detachment. Mature virions were purified from
C
y
HV
‐3‐infected
CCF
‐
K
104 cells by sucrose gradient ultracentrifugation and had a typical herpesvirus structure on electron microscopy. Infectious
C
y
HV
‐3 was produced stably in
CCF
‐
K
104 cells over 30 viral passages. Our findings showed that
CCF
‐
K
104 is a useful cell line for isolation and productive replication of
C
y
HV
‐3. A temperature shift from 25 °C to 15 °C or 35 °C did not allow serial morphological changes as observed at 25 °C for 14 days. Under the same conditions, real‐time
PCR
showed that
C
y
HV
‐3 was present with low viral
DNA
loads, suggesting that
C
y
HV
‐3 may establish latent infection in
CCF
‐
K
104 cells. Amplification of the left and right terminal repeat sequences of the
C
y
HV
‐3 genome arranged in a head‐to‐tail manner was detected by nested
PCR
following an upshift in temperature from 25 °C to 35 °C. The
PCR
results suggested that the circular genome may represent a latent form of
C
y
HV
‐3. |
doi_str_mv | 10.1111/jfd.12252 |
format | Article |
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CCF
‐
K
104 predominantly consisting of fibroblastic cells showed optimal growth at temperatures from 25 °C to 30 °C. Serial morphological changes in the cells induced by Cyprinid herpesvirus 3 (
C
y
HV
‐3) included cytoplasmic vacuolar formation, cell rounding and detachment. Mature virions were purified from
C
y
HV
‐3‐infected
CCF
‐
K
104 cells by sucrose gradient ultracentrifugation and had a typical herpesvirus structure on electron microscopy. Infectious
C
y
HV
‐3 was produced stably in
CCF
‐
K
104 cells over 30 viral passages. Our findings showed that
CCF
‐
K
104 is a useful cell line for isolation and productive replication of
C
y
HV
‐3. A temperature shift from 25 °C to 15 °C or 35 °C did not allow serial morphological changes as observed at 25 °C for 14 days. Under the same conditions, real‐time
PCR
showed that
C
y
HV
‐3 was present with low viral
DNA
loads, suggesting that
C
y
HV
‐3 may establish latent infection in
CCF
‐
K
104 cells. Amplification of the left and right terminal repeat sequences of the
C
y
HV
‐3 genome arranged in a head‐to‐tail manner was detected by nested
PCR
following an upshift in temperature from 25 °C to 35 °C. The
PCR
results suggested that the circular genome may represent a latent form of
C
y
HV
‐3.</description><identifier>ISSN: 0140-7775</identifier><identifier>EISSN: 1365-2761</identifier><identifier>DOI: 10.1111/jfd.12252</identifier><language>eng</language><ispartof>Journal of fish diseases, 2015-06, Vol.38 (6), p.507-514</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c742-65ffc6e00cf9c85a01241e4c4f4c82f42933780b3dea7a89692c23b8f9cadeb73</citedby><cites>FETCH-LOGICAL-c742-65ffc6e00cf9c85a01241e4c4f4c82f42933780b3dea7a89692c23b8f9cadeb73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Imajoh, M</creatorcontrib><creatorcontrib>Fujioka, H</creatorcontrib><creatorcontrib>Furusawa, K</creatorcontrib><creatorcontrib>Tamura, K</creatorcontrib><creatorcontrib>Yamasaki, K</creatorcontrib><creatorcontrib>Kurihara, S</creatorcontrib><creatorcontrib>Yamane, J</creatorcontrib><creatorcontrib>Kawai, K</creatorcontrib><creatorcontrib>Oshima, S</creatorcontrib><title>Establishment of a new cell line susceptible to Cyprinid herpesvirus 3 ( C y HV ‐3) and possible latency of C y HV ‐3 by temperature shift in the cells</title><title>Journal of fish diseases</title><description>A new cell line named
CCF
‐
K
104 predominantly consisting of fibroblastic cells showed optimal growth at temperatures from 25 °C to 30 °C. Serial morphological changes in the cells induced by Cyprinid herpesvirus 3 (
C
y
HV
‐3) included cytoplasmic vacuolar formation, cell rounding and detachment. Mature virions were purified from
C
y
HV
‐3‐infected
CCF
‐
K
104 cells by sucrose gradient ultracentrifugation and had a typical herpesvirus structure on electron microscopy. Infectious
C
y
HV
‐3 was produced stably in
CCF
‐
K
104 cells over 30 viral passages. Our findings showed that
CCF
‐
K
104 is a useful cell line for isolation and productive replication of
C
y
HV
‐3. A temperature shift from 25 °C to 15 °C or 35 °C did not allow serial morphological changes as observed at 25 °C for 14 days. Under the same conditions, real‐time
PCR
showed that
C
y
HV
‐3 was present with low viral
DNA
loads, suggesting that
C
y
HV
‐3 may establish latent infection in
CCF
‐
K
104 cells. Amplification of the left and right terminal repeat sequences of the
C
y
HV
‐3 genome arranged in a head‐to‐tail manner was detected by nested
PCR
following an upshift in temperature from 25 °C to 35 °C. The
PCR
results suggested that the circular genome may represent a latent form of
C
y
HV
‐3.</description><issn>0140-7775</issn><issn>1365-2761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNpNkD1Ow0AQhVcIJEKg4AZTksJhf2yvXSIrEKRINBGttV7PyhvZjrW7AbnjCPTcjpPgBAqmmebNe_M-Qm4ZXbJp7nemXjLOE35GZkykScRlys7JjLKYRlLK5JJceb-jlMmEpTPytfJBVa31TYd9gL0BBT2-g8a2hdb2CP7gNQ7BVi1C2EMxDs72toYG3YD-zbqDBwF3UMAI61f4_vgUC1B9DcPe-9NVqwL2ejya_xNBNULAbkCnwsFNOY01AWwPocFTvL8mF0a1Hm_-9pxsH1fbYh1tXp6ei4dNpGXMozQxRqdIqTa5zhJFGY8Zxjo2sc64iXkuhMxoJWpUUmV5mnPNRZVNalVjJcWcLH5ttZs-dmjKqWGn3FgyWh6hlhPU8gRV_ADnpGw9</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Imajoh, M</creator><creator>Fujioka, H</creator><creator>Furusawa, K</creator><creator>Tamura, K</creator><creator>Yamasaki, K</creator><creator>Kurihara, S</creator><creator>Yamane, J</creator><creator>Kawai, K</creator><creator>Oshima, S</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201506</creationdate><title>Establishment of a new cell line susceptible to Cyprinid herpesvirus 3 ( C y HV ‐3) and possible latency of C y HV ‐3 by temperature shift in the cells</title><author>Imajoh, M ; Fujioka, H ; Furusawa, K ; Tamura, K ; Yamasaki, K ; Kurihara, S ; Yamane, J ; Kawai, K ; Oshima, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c742-65ffc6e00cf9c85a01241e4c4f4c82f42933780b3dea7a89692c23b8f9cadeb73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Imajoh, M</creatorcontrib><creatorcontrib>Fujioka, H</creatorcontrib><creatorcontrib>Furusawa, K</creatorcontrib><creatorcontrib>Tamura, K</creatorcontrib><creatorcontrib>Yamasaki, K</creatorcontrib><creatorcontrib>Kurihara, S</creatorcontrib><creatorcontrib>Yamane, J</creatorcontrib><creatorcontrib>Kawai, K</creatorcontrib><creatorcontrib>Oshima, S</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of fish diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Imajoh, M</au><au>Fujioka, H</au><au>Furusawa, K</au><au>Tamura, K</au><au>Yamasaki, K</au><au>Kurihara, S</au><au>Yamane, J</au><au>Kawai, K</au><au>Oshima, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Establishment of a new cell line susceptible to Cyprinid herpesvirus 3 ( C y HV ‐3) and possible latency of C y HV ‐3 by temperature shift in the cells</atitle><jtitle>Journal of fish diseases</jtitle><date>2015-06</date><risdate>2015</risdate><volume>38</volume><issue>6</issue><spage>507</spage><epage>514</epage><pages>507-514</pages><issn>0140-7775</issn><eissn>1365-2761</eissn><abstract>A new cell line named
CCF
‐
K
104 predominantly consisting of fibroblastic cells showed optimal growth at temperatures from 25 °C to 30 °C. Serial morphological changes in the cells induced by Cyprinid herpesvirus 3 (
C
y
HV
‐3) included cytoplasmic vacuolar formation, cell rounding and detachment. Mature virions were purified from
C
y
HV
‐3‐infected
CCF
‐
K
104 cells by sucrose gradient ultracentrifugation and had a typical herpesvirus structure on electron microscopy. Infectious
C
y
HV
‐3 was produced stably in
CCF
‐
K
104 cells over 30 viral passages. Our findings showed that
CCF
‐
K
104 is a useful cell line for isolation and productive replication of
C
y
HV
‐3. A temperature shift from 25 °C to 15 °C or 35 °C did not allow serial morphological changes as observed at 25 °C for 14 days. Under the same conditions, real‐time
PCR
showed that
C
y
HV
‐3 was present with low viral
DNA
loads, suggesting that
C
y
HV
‐3 may establish latent infection in
CCF
‐
K
104 cells. Amplification of the left and right terminal repeat sequences of the
C
y
HV
‐3 genome arranged in a head‐to‐tail manner was detected by nested
PCR
following an upshift in temperature from 25 °C to 35 °C. The
PCR
results suggested that the circular genome may represent a latent form of
C
y
HV
‐3.</abstract><doi>10.1111/jfd.12252</doi><tpages>8</tpages></addata></record> |
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language | eng |
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title | Establishment of a new cell line susceptible to Cyprinid herpesvirus 3 ( C y HV ‐3) and possible latency of C y HV ‐3 by temperature shift in the cells |
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