Whole genome screening defines a key role of autophagy in resistance of bovine cells to BVDV infection

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The study developed a bovine whole-genome knockout library to perform genome-wide screening for host resistance factors against bovine viral diarrhea virus (BVDV). Using this approach, the authors identified knockout guides that were strongly selected in infected cells, including inactivation of ADAM17 and TMEM41B, both previously implicated as important for BVDV infection, and enrichment of guides targeting VMP1, a factor reported for flavivirus infection. They also observed differential selection across multiple proteins involved in triggering autophagy, supporting a key role for autophagy in cellular resistance to BVDV. The paper’s main limitation is that the work is centered on bovine cell models and infection resistance to BVDV rather than validating effects across other systems or in vivo contexts. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract Bovine viral diarrhea virus (BVDV, genus Pestivirus, family Flaviviridae) is a notifiable pathogen of cattle which significantly impacts animal health, welfare, and the economy. Several cellular factors important for BVDV infection, such as Jiv, CD46 and ADAM17, have already been identified providing new targets development of effective defense strategies. However, our knowledge about BVDV host factor requirements remains limited, as no genome-wide studies of BVDV host resistance factors were performed to date, in part due to lack of accessible whole genome libraries. To close this gap, we have designed a novel bovine whole genome knockout library and successfully used it to identify a set of BVDV host resistance factors. The validity of our approach is highlighted by the strong selection of cells with inactivated ADAM17 and TMEM41B, which have both been described to be of pivotal importance for BVDV infection. In addition, guides targeting VMP1, recently identified as an important factor for flavivirus infection, were also significantly enriched in our screen. Furthermore, we found differential selection of several proteins essential for triggering autophagy, providing additional strong evidence of this process underlying key cellular functions involved in resistance to BVDV. Competing Interest Statement The authors have declared no competing interest. Footnotes -Author's name (Maren von Son to Maren van Son) -add the subtype of the NADL BVDV virus used (type 1a) -various typos

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last seen: 2026-05-20T01:45:00.602351+00:00