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Baculovirus actin-rearrangement-inducing factor ARIF-1 induces the formation of dynamic invadosome clusters
The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV), a pathogen of lepidopteran insects, has a striking dependence on the host cell actin cytoskeleton. During the delayed-early stage of infection, AcMNPV was shown to induce the accumulation of actin at the cortex of infecte...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351737/ https://www.ncbi.nlm.nih.gov/pubmed/34133213 http://dx.doi.org/10.1091/mbc.E20-11-0705 |
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author | Lauko, Domokos I. Ohkawa, Taro Mares, Sergio E. Welch, Matthew D. |
author_facet | Lauko, Domokos I. Ohkawa, Taro Mares, Sergio E. Welch, Matthew D. |
author_sort | Lauko, Domokos I. |
collection | PubMed |
description | The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV), a pathogen of lepidopteran insects, has a striking dependence on the host cell actin cytoskeleton. During the delayed-early stage of infection, AcMNPV was shown to induce the accumulation of actin at the cortex of infected cells. However, the dynamics and molecular mechanism of cortical actin assembly remained unknown. Here, we show that AcMNPV induces dynamic cortical clusters of dot-like actin structures that mediate degradation of the underlying extracellular matrix and therefore function similarly to clusters of invadosomes in mammalian cells. Furthermore, we find that the AcMNPV protein actin-rearrangement-inducing factor-1 (ARIF-1), which was previously shown to be necessary and sufficient for cortical actin assembly and efficient viral infection in insect hosts, is both necessary and sufficient for invadosome formation. We mapped the sequences within the C-terminal cytoplasmic region of ARIF-1 that are required for invadosome formation and identified individual tyrosine and proline residues that are required for organizing these structures. Additionally, we found that ARIF-1 and the invadosome-associated proteins cortactin and the Arp2/3 complex localize to invadosomes and Arp2/3 complex is required for their formation. These ARIF-1–induced invadosomes may be important for the function of ARIF-1 in systemic virus spread. |
format | Online Article Text |
id | pubmed-8351737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-83517372021-10-16 Baculovirus actin-rearrangement-inducing factor ARIF-1 induces the formation of dynamic invadosome clusters Lauko, Domokos I. Ohkawa, Taro Mares, Sergio E. Welch, Matthew D. Mol Biol Cell Articles The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV), a pathogen of lepidopteran insects, has a striking dependence on the host cell actin cytoskeleton. During the delayed-early stage of infection, AcMNPV was shown to induce the accumulation of actin at the cortex of infected cells. However, the dynamics and molecular mechanism of cortical actin assembly remained unknown. Here, we show that AcMNPV induces dynamic cortical clusters of dot-like actin structures that mediate degradation of the underlying extracellular matrix and therefore function similarly to clusters of invadosomes in mammalian cells. Furthermore, we find that the AcMNPV protein actin-rearrangement-inducing factor-1 (ARIF-1), which was previously shown to be necessary and sufficient for cortical actin assembly and efficient viral infection in insect hosts, is both necessary and sufficient for invadosome formation. We mapped the sequences within the C-terminal cytoplasmic region of ARIF-1 that are required for invadosome formation and identified individual tyrosine and proline residues that are required for organizing these structures. Additionally, we found that ARIF-1 and the invadosome-associated proteins cortactin and the Arp2/3 complex localize to invadosomes and Arp2/3 complex is required for their formation. These ARIF-1–induced invadosomes may be important for the function of ARIF-1 in systemic virus spread. The American Society for Cell Biology 2021-08-01 /pmc/articles/PMC8351737/ /pubmed/34133213 http://dx.doi.org/10.1091/mbc.E20-11-0705 Text en © 2021 Lauko et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles Lauko, Domokos I. Ohkawa, Taro Mares, Sergio E. Welch, Matthew D. Baculovirus actin-rearrangement-inducing factor ARIF-1 induces the formation of dynamic invadosome clusters |
title | Baculovirus actin-rearrangement-inducing factor ARIF-1 induces the formation of dynamic invadosome clusters |
title_full | Baculovirus actin-rearrangement-inducing factor ARIF-1 induces the formation of dynamic invadosome clusters |
title_fullStr | Baculovirus actin-rearrangement-inducing factor ARIF-1 induces the formation of dynamic invadosome clusters |
title_full_unstemmed | Baculovirus actin-rearrangement-inducing factor ARIF-1 induces the formation of dynamic invadosome clusters |
title_short | Baculovirus actin-rearrangement-inducing factor ARIF-1 induces the formation of dynamic invadosome clusters |
title_sort | baculovirus actin-rearrangement-inducing factor arif-1 induces the formation of dynamic invadosome clusters |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351737/ https://www.ncbi.nlm.nih.gov/pubmed/34133213 http://dx.doi.org/10.1091/mbc.E20-11-0705 |
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