The La Crosse virus M segment determines virus isolate cell-to-cell spread and virulence
- 1Stony Brook University
Abstract
La Crosse virus (LACV) is an orthobunyavirus spread by mosquitoes in North America and can cause severe neurological disease. Despite this burden, there is a lack of LACV antiviral treatments as our fundamental understanding of how LACV spreads and causes disease remains incomplete. To investigate LACV biology, we took advantage of two genetically similar LACV lineage I isolates (LACV1960 and LACV1978) where we found that LACV1960 infects and replicates at a higher rate than LACV1978, while LACV1978 exhibits enhanced cell-cell spread and in vivo virulence and dissemination. To investigate the genomic determinants behind these phenotypes, we generated reassortants between each isolate. We found that each genomic segment contributed to LACV pathogenesis with the M segment as a dominant determinant for LACV pathogenesis in vivo and plaque size and replication in vitro. To address which M segment protein contributes to plaque size and infectivity, we generated M segment chimeric viruses using a LACV1978 background and swapping in regions of the LACV1960 M segment. We found that the Gc head domain determined plaque size and infectivity, with the LACV1960 Gc head chimera producing small plaques but having increased infectivity over the wild-type LACV1978. Finally, using natural LACV lineage isolates, we showed that plaque size is variable across and within lineages suggesting changes in the M segment may impact LACV in nature. In future studies, we will continue to investigate the mechanisms behind how cell-to-cell spread influences dissemination to better understand how LACV genome segments affect spread, infectivity, virulence, and viral fitness.
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BibTeX
@misc{durawa2026crosse,
title = {{The La Crosse virus M segment determines virus isolate cell-to-cell spread and virulence}},
author = {M. V. Durawa and N. C. Rondeau and S. N. Spector and S. A. Thannickal and A. E. Weight and A. Dedvukaj and M. C. Lutchko and H. M. Lazear and K. A. Stapleford},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.17.752448},
url = {https://www.biorxiv.org/content/10.64898/2026.09.17.752448v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - The La Crosse virus M segment determines virus isolate cell-to-cell spread and virulence
AU - M. V. Durawa
AU - N. C. Rondeau
AU - S. N. Spector
AU - S. A. Thannickal
AU - A. E. Weight
AU - A. Dedvukaj
AU - M. C. Lutchko
AU - H. M. Lazear
AU - K. A. Stapleford
PY - 2026
DA - 2026/09/17
PB - bioRxiv
DO - 10.64898/2026.09.17.752448
UR - https://www.biorxiv.org/content/10.64898/2026.09.17.752448v1
AB - La Crosse virus (LACV) is an orthobunyavirus spread by mosquitoes in North America and can cause severe neurological disease. Despite this burden, there is a lack of LACV antiviral treatments as our fundamental understanding of how LACV spreads and causes disease remains incomplete. To investigate LACV biology, we took advantage of two genetically similar LACV lineage I isolates (LACV1960 and LACV1978) where we found that LACV1960 infects and replicates at a higher rate than LACV1978, while LACV1978 exhibits enhanced cell-cell spread and in vivo virulence and dissemination. To investigate the genomic determinants behind these phenotypes, we generated reassortants between each isolate. We found that each genomic segment contributed to LACV pathogenesis with the M segment as a dominant determinant for LACV pathogenesis in vivo and plaque size and replication in vitro. To address which M segment protein contributes to plaque size and infectivity, we generated M segment chimeric viruses using a LACV1978 background and swapping in regions of the LACV1960 M segment. We found that the Gc head domain determined plaque size and infectivity, with the LACV1960 Gc head chimera producing small plaques but having increased infectivity over the wild-type LACV1978. Finally, using natural LACV lineage isolates, we showed that plaque size is variable across and within lineages suggesting changes in the M segment may impact LACV in nature. In future studies, we will continue to investigate the mechanisms behind how cell-to-cell spread influences dissemination to better understand how LACV genome segments affect spread, infectivity, virulence, and viral fitness.
ER -