Cultured early goat embryos and cells are susceptible to infection with caprine encephalitis virus

Zona-pellucida-free embryos at 8–16 cell stage were co-cultured for 6 days in an insert over a mixed cell monolayer infected with CAEV-pBSCA. Embryos were washed and transferred to an insert on CAEV indicator goat synovial membrane cells for 6 h, then they were washed and cultivated in B2 Ménézo for...

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Published inVirology (New York, N.Y.) Vol. 353; no. 2; pp. 307 - 315
Main Authors Ali Al Ahmad, M.Z., Fieni, F., Guiguen, F., Larrat, M., Pellerin, J.L., Roux, C., Chebloune, Y.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 30.09.2006
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Abstract Zona-pellucida-free embryos at 8–16 cell stage were co-cultured for 6 days in an insert over a mixed cell monolayer infected with CAEV-pBSCA. Embryos were washed and transferred to an insert on CAEV indicator goat synovial membrane cells for 6 h, then they were washed and cultivated in B2 Ménézo for 24 h, finally, embryo cells were dissociated and cultivated on a feeder monolayer for 8 days. After 5 weeks, multinucleated giant cells typical of CAEV infection were observed in indicator GSM cell monolayers. In the acellular medium, the early embryonic cells produced at least 10 3.25 TCID 50/ml over 24 h. The monolayer of cultivated embryonic cells developed cytopathic lesions within 8 days, and CAEV RNA, CAEV proviral DNA and protein p28 of the capsid were detected. All of these results clearly demonstrate that caprine early embryonic cells are susceptible to infection with CAEV and that infection with this virus is productive.
AbstractList Zona-pellucida-free embryos at 8-16 cell stage were co-cultured for 6 days in an insert over a mixed cell monolayer infected with CAEV-pBSCA. Embryos were washed and transferred to an insert on CAEV indicator goat synovial membrane cells for 6 h, then they were washed and cultivated in B2 Ménézo for 24 h, finally, embryo cells were dissociated and cultivated on a feeder monolayer for 8 days. After 5 weeks, multinucleated giant cells typical of CAEV infection were observed in indicator GSM cell monolayers. In the acellular medium, the early embryonic cells produced at least 10(3.25) TCID50/ml over 24 h. The monolayer of cultivated embryonic cells developed cytopathic lesions within 8 days, and CAEV RNA, CAEV proviral DNA and protein p28 of the capsid were detected. All of these results clearly demonstrate that caprine early embryonic cells are susceptible to infection with CAEV and that infection with this virus is productive.
Zona-pellucida-free embryos at 8-16 cell stage were co-cultured for 6 days in an insert over a mixed cell monolayer infected with CAEV-pBSCA. Embryos were washed and transferred to an insert on CAEV indicator goat synovial membrane cells for 6 h, then they were washed and cultivated in B2 Menezo for 24 h, finally, embryo cells were dissociated and cultivated on a feeder monolayer for 8 days. After 5 weeks, multinucleated giant cells typical of CAEV infection were observed in indicator GSM cell monolayers. In the acellular medium, the early embryonic cells produced at least 10 super(3) super(.) super(2) super(5) TCID sub(5) sub(0)/ml over 24 h. The monolayer of cultivated embryonic cells developed cytopathic lesions within 8 days, and CAEV RNA, CAEV proviral DNA and protein p28 of the capsid were detected. All of these results clearly demonstrate that caprine early embryonic cells are susceptible to infection with CAEV and that infection with this virus is productive.
Zona-pellucida-free embryos at 8–16 cell stage were co-cultured for 6 days in an insert over a mixed cell monolayer infected with CAEV-pBSCA. Embryos were washed and transferred to an insert on CAEV indicator goat synovial membrane cells for 6 h, then they were washed and cultivated in B2 Ménézo for 24 h, finally, embryo cells were dissociated and cultivated on a feeder monolayer for 8 days. After 5 weeks, multinucleated giant cells typical of CAEV infection were observed in indicator GSM cell monolayers. In the acellular medium, the early embryonic cells produced at least 10 3.25 TCID 50/ml over 24 h. The monolayer of cultivated embryonic cells developed cytopathic lesions within 8 days, and CAEV RNA, CAEV proviral DNA and protein p28 of the capsid were detected. All of these results clearly demonstrate that caprine early embryonic cells are susceptible to infection with CAEV and that infection with this virus is productive.
Author Guiguen, F.
Chebloune, Y.
Fieni, F.
Pellerin, J.L.
Roux, C.
Ali Al Ahmad, M.Z.
Larrat, M.
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Keywords CAEV
Tropism
Replication
Cytopathic effect
Embryo cells
EMBRYO CELLS
TROPISM
REPLICATION
CYTOPATHIC EFFECT
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Snippet Zona-pellucida-free embryos at 8–16 cell stage were co-cultured for 6 days in an insert over a mixed cell monolayer infected with CAEV-pBSCA. Embryos were...
Zona-pellucida-free embryos at 8-16 cell stage were co-cultured for 6 days in an insert over a mixed cell monolayer infected with CAEV-pBSCA. Embryos were...
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SubjectTerms Animals
Arthritis-Encephalitis Virus, Caprine - chemistry
Arthritis-Encephalitis Virus, Caprine - genetics
Arthritis-Encephalitis Virus, Caprine - growth & development
CAEV
Capsid Proteins - metabolism
Cells, Cultured
Coculture Techniques
Cytopathic effect
DNA, Viral - genetics
Embryo cells
Embryo, Mammalian - virology
Genome, Viral - genetics
Goats
Immunohistochemistry
Lentivirus Infections - virology
Life Sciences
Polymerase Chain Reaction
Proviruses - genetics
Proviruses - isolation & purification
Replication
Sensitivity and Specificity
Tropism
Virus Replication
Title Cultured early goat embryos and cells are susceptible to infection with caprine encephalitis virus
URI https://dx.doi.org/10.1016/j.virol.2006.06.007
https://www.ncbi.nlm.nih.gov/pubmed/16859728
https://search.proquest.com/docview/19386939
https://search.proquest.com/docview/68886528
https://hal.inrae.fr/hal-02665234
Volume 353
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