Structures of the Tilapia Lake Virus replication complex show that ANP32 is a host factor for replication across the Articulavirales order

Authors

Arragain, B., Pelosse, M., Cusack, S.

Abstract

Tilapia Lake Virus (TiLV) is a species in the Amnoonviridae family within the Articulavirales order of nuclear-replicating, segmented, negative-strand RNA viruses. This order also encompasses the well-known, but phylogenetically distant Orthomyxoviridae family that includes influenza and Thogoto viruses. Influenza virus replication, but not Thogoto virus, essentially relies on the host acidic nuclear phosphoprotein 32 (ANP32) to form a functional genome replication complex, which comprises an asymmetric viral polymerase dimer composed of a replicase bridged by ANP32 to an encapsidase. However, remains unclear whether this dependency is conserved in divergent viruses from the same order. Using in vitro reconstitution, biophysical and biochemical analyses and high-resolution structure determination by single-particle cryo-electron microscopy, we investigate the complexes formed between the TiLV RNA-dependent RNA polymerase (TiLV-Pol) and either tilapia (ti) or human (hu) ANP32A. We show that the tiANP32 leucine-rich repeat domain acts as a scaffold that stabilizes apo-TiLV-Pol in an encapsidase conformation. The tiANP32-encapsidase complex is then able to recruit and stabilise a second TiLV-Pol in a replicase conformation. The tiANP32-stabilised asymmetric TiLV-Pol dimer has an architecture that is remarkably similar to its orthomyxovirus replication complex counterpart, despite the 40% smaller size of TiLV-Pol. We also demonstrate that the ANP32 low-complexity acidic region interacts with the TiLV nucleoprotein, consistent with a conserved role in co-ordinating ribonucleoprotein assembly. Overall, our findings suggest that ANP32 is an ancient and likely broadly conserved host factor for viral genome replication and encapsidation across the Articulavirales order. Furthermore, TiLV is an emerging fish pathogen causing high mortality in aquaculture and our results provide insight into tilapia ANP32 modifications that could be used to engineer TiLV-resistant tilapia.

Preprint server: bioRxiv
The authors list and abstract were imported from bioRxiv on 18 Sep 2026.

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