Contamination of Cell Cultures with Bovine Viral Diarrhea Virus (BVDV)
The incidence of contamination of cell strains used in biological and virological studies and of fetal calf sera (FCS) manufactured by Russian and foreign companies used for cell culturing with noncytocidal bovine viral diarrhea virus (BVDV; Pestivirus , Flaviviridae ) was analyzed. The virus was de...
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| Published in: | Bulletin of experimental biology and medicine Vol. 153; no. 1; pp. 77 - 81 |
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| Main Authors: | , , , , , , , , , |
| Format: | Journal Article |
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| Abstract | The incidence of contamination of cell strains used in biological and virological studies and of fetal calf sera (FCS) manufactured by Russian and foreign companies used for cell culturing with noncytocidal bovine viral diarrhea virus (BVDV;
Pestivirus
,
Flaviviridae
) was analyzed. The virus was detected by reverse transcription PCR and indirect immunofluorescence with monoclonal antibodies to BVDV virion envelope glycoprotein in 25% of 117 cell strains and 45% of 35 tested FCS lots. The virus multiplied and persisted in a wide spectrum of human cell strains and in monkey, swine, sheep, rabbit, dog, cat, and other animal cells. The levels of BVDV genome RNA in contaminated cell cultures reached 10
2
-10
3
g-eq/cell and in serum samples 10
3
-10
7
g-eq/ml. These facts necessitate testing of cells and FCS for BVDV reproduced in cells without signs of infection detectable by light microscopy. The molecular mechanisms of long-term virus persistence in cells without manifestation of cell destruction are unknown. |
|---|---|
| AbstractList | The incidence of contamination of cell strains used in biological and virological studies and of fetal calf sera (FCS) manufactured by Russian and foreign companies used for cell culturing with noncytocidal bovine viral diarrhea virus (BVDV; Pestivirus, Flaviviridae) was analyzed. The virus was detected by reverse transcription PCR and indirect immunofluorescence with monoclonal antibodies to BVDV virion envelope glycoprotein in 25% of 117 cell strains and 45% of 35 tested FCS lots. The virus multiplied and persisted in a wide spectrum of human cell strains and in monkey, swine, sheep, rabbit, dog, cat, and other animal cells. The levels of BVDV genome RNA in contaminated cell cultures reached 10 super(2)-10 super(3) g-eq/cell and in serum samples 10 super(3)-10 super(7) g-eq/ml. These facts necessitate testing of cells and FCS for BVDV reproduced in cells without signs of infection detectable by light microscopy. The molecular mechanisms of long-term virus persistence in cells without manifestation of cell destruction are unknown. The incidence of contamination of cell strains used in biological and virological studies and of fetal calf sera (FCS) manufactured by Russian and foreign companies used for cell culturing with noncytocidal bovine viral diarrhea virus (BVDV; Pestivirus, Flaviviridae) was analyzed. The virus was detected by reverse transcription PCR and indirect immunofluorescence with monoclonal antibodies to BVDV virion envelope glycoprotein in 25% of 117 cell strains and 45% of 35 tested FCS lots. The virus multiplied and persisted in a wide spectrum of human cell strains and in monkey, swine, sheep, rabbit, dog, cat, and other animal cells. The levels of BVDV genome RNA in contaminated cell cultures reached [10.sup.2]-[10.sup.3] g-eq/cell and in serum samples [10.sup.3]-[10.sup.7] g-eq/ml. These facts necessitate testing of cells and FCS for BVDV reproduced in cells without signs of infection detectable by light microscopy. The molecular mechanisms of long-term virus persistence in cells without manifestation of cell destruction are unknown. Key Words: cell strains; fetal calf serum; virus contamination; bovine viral diarrhea virus; reverse transcription-polymerase chain reaction (RT-PCR) and indirect immunofluorescence Issue Title: This issue is a translation of Byulleten' Eksperimental'noi Biologii i Meditsiny (Bulletin of Experimental Biology and Medicine) and Kletochnye Tekhnologii v Biologii i Meditsine (Cell Technologies in Biology and Medicine) The incidence of contamination of cell strains used in biological and virological studies and of fetal calf sera (FCS) manufactured by Russian and foreign companies used for cell culturing with noncytocidal bovine viral diarrhea virus (BVDV; Pestivirus, Flaviviridae) was analyzed. The virus was detected by reverse transcription PCR and indirect immunofluorescence with monoclonal antibodies to BVDV virion envelope glycoprotein in 25% of 117 cell strains and 45% of 35 tested FCS lots. The virus multiplied and persisted in a wide spectrum of human cell strains and in monkey, swine, sheep, rabbit, dog, cat, and other animal cells. The levels of BVDV genome RNA in contaminated cell cultures reached 10^sup 2^-10^sup 3^ g-eq/cell and in serum samples 10^sup 3^-10^sup 7^ g-eq/ml. These facts necessitate testing of cells and FCS for BVDV reproduced in cells without signs of infection detectable by light microscopy. The molecular mechanisms of long-term virus persistence in cells without manifestation of cell destruction are unknown.[PUBLICATION ABSTRACT] The incidence of contamination of cell strains used in biological and virological studies and of fetal calf sera (FCS) manufactured by Russian and foreign companies used for cell culturing with noncytocidal bovine viral diarrhea virus (BVDV; Pestivirus, Flaviviridae) was analyzed. The virus was detected by reverse transcription PCR and indirect immunofluorescence with monoclonal antibodies to BVDV virion envelope glycoprotein in 25% of 117 cell strains and 45% of 35 tested FCS lots. The virus multiplied and persisted in a wide spectrum of human cell strains and in monkey, swine, sheep, rabbit, dog, cat, and other animal cells. The levels of BVDV genome RNA in contaminated cell cultures reached [10.sup.2]-[10.sup.3] g-eq/cell and in serum samples [10.sup.3]-[10.sup.7] g-eq/ml. These facts necessitate testing of cells and FCS for BVDV reproduced in cells without signs of infection detectable by light microscopy. The molecular mechanisms of long-term virus persistence in cells without manifestation of cell destruction are unknown. The incidence of contamination of cell strains used in biological and virological studies and of fetal calf sera (FCS) manufactured by Russian and foreign companies used for cell culturing with noncytocidal bovine viral diarrhea virus (BVDV; Pestivirus, Flaviviridae) was analyzed. The virus was detected by reverse transcription PCR and indirect immunofluorescence with monoclonal antibodies to BVDV virion envelope glycoprotein in 25% of 117 cell strains and 45% of 35 tested FCS lots. The virus multiplied and persisted in a wide spectrum of human cell strains and in monkey, swine, sheep, rabbit, dog, cat, and other animal cells. The levels of BVDV genome RNA in contaminated cell cultures reached 10(2)-10(3) g-eq/cell and in serum samples 10(3)-10(7) g-eq/ml. These facts necessitate testing of cells and FCS for BVDV reproduced in cells without signs of infection detectable by light microscopy. The molecular mechanisms of long-term virus persistence in cells without manifestation of cell destruction are unknown. The incidence of contamination of cell strains used in biological and virological studies and of fetal calf sera (FCS) manufactured by Russian and foreign companies used for cell culturing with noncytocidal bovine viral diarrhea virus (BVDV; Pestivirus , Flaviviridae ) was analyzed. The virus was detected by reverse transcription PCR and indirect immunofluorescence with monoclonal antibodies to BVDV virion envelope glycoprotein in 25% of 117 cell strains and 45% of 35 tested FCS lots. The virus multiplied and persisted in a wide spectrum of human cell strains and in monkey, swine, sheep, rabbit, dog, cat, and other animal cells. The levels of BVDV genome RNA in contaminated cell cultures reached 10 2 -10 3 g-eq/cell and in serum samples 10 3 -10 7 g-eq/ml. These facts necessitate testing of cells and FCS for BVDV reproduced in cells without signs of infection detectable by light microscopy. The molecular mechanisms of long-term virus persistence in cells without manifestation of cell destruction are unknown. |
| Audience | Academic |
| Author | Ionova, K. S. Uryvaev, L. V. Dedova, A. V. Gushina, E. A. Podchernjaeva, R. J. Parasjuk, N. A. Selivanova, T. K. Grebennikova, T. V. Bunkova, N. I. Dedova, L. V. |
| Author_xml | – sequence: 1 givenname: L. V. surname: Uryvaev fullname: Uryvaev, L. V. email: uryvaev_lv@mail.ru organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 2 givenname: A. V. surname: Dedova fullname: Dedova, A. V. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 3 givenname: L. V. surname: Dedova fullname: Dedova, L. V. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 4 givenname: K. S. surname: Ionova fullname: Ionova, K. S. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 5 givenname: N. A. surname: Parasjuk fullname: Parasjuk, N. A. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 6 givenname: T. K. surname: Selivanova fullname: Selivanova, T. K. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 7 givenname: N. I. surname: Bunkova fullname: Bunkova, N. I. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 8 givenname: E. A. surname: Gushina fullname: Gushina, E. A. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 9 givenname: T. V. surname: Grebennikova fullname: Grebennikova, T. V. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation – sequence: 10 givenname: R. J. surname: Podchernjaeva fullname: Podchernjaeva, R. J. organization: D. I. Ivanovsky Institute of Virology, Ministry of Health and Social Development of the Russian Federation |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22808499$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1016/0166-0934(94)90120-1 10.1080/01652176.2003.9695140 10.1053/tvjl.2000.0500 10.1006/biol.2002.0343 |
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| Keywords | cell strains reverse transcription–polymerase chain reaction (RT-PCR) and indirect immunofl uorescence fetal calf serum virus contamination bovine viral diarrhea virus |
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| SubjectTerms | Animals Antibodies, Monoclonal - immunology Biomedical and Life Sciences Biomedicine Bovine viral diarrhea virus Cats Cattle Cell Biology Cell Line Cells Contamination Diarrhea Diarrhea Viruses, Bovine Viral - genetics Diarrhea Viruses, Bovine Viral - growth & development Diarrhea Viruses, Bovine Viral - isolation & purification Dogs Flaviviridae Fluorescent Antibody Technique, Indirect Genomics Haplorhini Humans Internal Medicine Laboratory Medicine Monoclonal antibodies Pathology Pestivirus Rabbits Reverse Transcriptase Polymerase Chain Reaction RNA RNA, Viral - genetics Sheep Swine Viral Envelope Proteins - immunology Virology Virus diseases |
| Title | Contamination of Cell Cultures with Bovine Viral Diarrhea Virus (BVDV) |
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