Exposure of in vitro-produced bovine embryos to foot-and-mouth disease virus

• Published in: Theriogenology 1998-07, Vol.50 (1), p.109-116
• Main Authors: Marquant-Le Guienne, B, Rémond, M, Cosquer, R, Humblot, P, Kaiser, C, Lebreton, F, Crucière, C, Guerin, B, Laporte, J, Thibier, M
• Format: Article
• Language: English
• Subjects: Animals; APHTHOVIRUS; BOVIN; bovine embryo; CATTLE; Cattle - embryology; Cattle - virology; CELL CULTURE; CULTIVO DE CELULAS; CULTIVO DE EMBRIONES; CULTURE D'EMBRYON; CULTURE DE CELLULE; Cytopathogenic Effect, Viral; DISEASE TRANSMISSION; EMBRYO CULTURE; EXPERIMENTACION IN VITRO; EXPERIMENTATION IN VITRO; Fertilization in Vitro - veterinary; foot and mouth disease virus; GANADO BOVINO; IN VITRO EXPERIMENTATION; LAVADO; LAVAGE; OVA; OVULE; OVULO; PCR; POLYMERASE CHAIN REACTION; TRANSMISION DE ENFERMEDADES; TRANSMISSION DES MALADIES; VIRUS FIEBRE AFTOSA; VIRUS FIEVRE APHTEUSE; WASHING; ZONA PELLUCIDA
• ISSN: 0093-691X; 1879-3231
• DOI: 10.1016/S0093-691X(98)00118-6

The aim of this study was to investigate whether foot and mouth disease virus (FMDV) interacts with in vitro produced (IVP) bovine embryos. One milliliter of a suspension of FMDV (2x10 7 TCID 50/mL) was added to several batches of these embryos 7 d after in vitro fertilization, by which time they had either developed to the morula / blastocyst stage (n = 256) or degenerated (n = 260). Six experiments were performed in which developed or degenerated batches of embryos were incubated with FMDV for periods of 1 h (3), 2 h (2) or 4h (1). After this, the embryos were washed 10 times according to the International Embryo Transfer Society (IETS), then pooled and ground up to form a suspension, and assayed on cell cultures for FMDV. The cell cultures were observed daily for cytopathic effects for 3 d post exposure. In addition to the cell culture method, the polymerase chain reaction (PCR) technique was used to assay for the presence of the virus in the washing fluids. Assays for FMDV were also conducted on the first and second wash and on the pooled sample constituting the eigth, ninth and tenth wash. With the exception of the second wash from a batch of embryos exposed to FMDV for 2 h, all samples of the first and second wash produced FMDV cytopathic effects, but none occurred with the pooled samples of the 8th, 9th and 10th wash. FMDV was also isolated from all but 1 of the batches of embryos after 1 h of incubation, from 1 of 4 batches after 2 h of incubation and from all batches after 4 h incubation. By contrast, the presence of virus could not be demonstrated by PCR based on the technique used here. These results show that 7 d old IVP bovine embryos can retain FMDV after washing, unlike in vivo-derived embryos, which do not appear to carry risks of FMDV transmission when washed according to IETS recommendations. Stricter controls are, therefore, necessary when using IVP embryos from cattle in a non-FMD-free zone in domestic or international trade.