Publication:
Resolving the intersection of HIV and F-actin in the context of cell-cell viral spread

dc.contributor.advisor Turville, Stuart en_US
dc.contributor.advisor Anupriya, Aggarwal en_US
dc.contributor.author Ospina Stella, Alberto en_US
dc.date.accessioned 2022-03-15T08:29:55Z
dc.date.available 2022-03-15T08:29:55Z
dc.date.issued 2020 en_US
dc.description.abstract HIV has evolved elaborate mechanisms to manipulate the host cell’s actin cytoskeleton. This supports specific steps of the viral life cycle but also leads to cell-type specific changes in leukocyte shape and behaviour that promote overall spread of the infection. In particular, actin manipulation is important for direct cell-cell transfer of HIV (CCTH), which is now recognized as a highly efficient mode of viral spread. This study aimed to further resolve the molecular players and mechanisms involved in this process. Through the use of CRISPR–Cas9-mediated gene editing, herein we systematically interrogated the loss-of-function phenotype of over 50 cytoskeletal regulators, in both HIV-donor and target cells during CCTH. This was then combined with a portfolio of complementary assays ranging from live cell microscopy through to the ultrastructural resolution of focused ion beam scanning electron microscopy. This approach identified several core actin regulators to be required on both sides of viral transfer, including the Rho-GTPases Cdc42/Rac1 (signalling), upstream of the Arp2/3 complex (actin nucleator), and Profilin (which indirectly supports F-actin elongation, e.g. via Formins). In infected myeloid cells, Cdc42-Arp2/3 and Formins collaborated to form distinct “HIV-Filopodia”, which were shown to be important for CCTH. The overall findings of this work support that, while HIV uses diverse strategies to influence numerous cytoskeletal targets, there is a high tolerance for the individual loss of many manipulated regulators in the context of CCTH. However, core regulators that secure the cellular ability to mediate F-actin polymerization remain essential to this process, in particular via their contribution to cortical F-actin membrane protrusions that facilitate intercellular contacts and later maturation of the virological synapse. To conclude, we have mapped a landscape of complex interactions between HIV and the actin cytoskeleton. This not only builds on our understanding of F-actin regulation in cells of our immune system but will also facilitate the continued development of host-directed therapeutics for lentiviral and/or other pathogenic infections. en_US
dc.identifier.uri http://hdl.handle.net/1959.4/65595
dc.language English
dc.language.iso EN en_US
dc.publisher UNSW, Sydney en_US
dc.rights CC BY-NC-ND 3.0 en_US
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/3.0/au/ en_US
dc.subject.other Cytoskeleton en_US
dc.subject.other HIV en_US
dc.subject.other Actin en_US
dc.title Resolving the intersection of HIV and F-actin in the context of cell-cell viral spread en_US
dc.type Thesis en_US
dcterms.accessRights open access
dcterms.rightsHolder Ospina Stella, Alberto
dspace.entity.type Publication en_US
unsw.accessRights.uri https://purl.org/coar/access_right/c_abf2
unsw.date.embargo 2022-04-01 en_US
unsw.description.embargoNote Embargoed until 2022-04-01
unsw.identifier.doi https://doi.org/10.26190/unsworks/2103
unsw.relation.faculty Medicine & Health
unsw.relation.originalPublicationAffiliation Ospina Stella, Alberto, Kirby Institute, Faculty of Medicine, UNSW en_US
unsw.relation.originalPublicationAffiliation Turville, Stuart, Kirby Institute, Faculty of Medicine, UNSW en_US
unsw.relation.originalPublicationAffiliation Anupriya, Aggarwal, Kirby Institute, Faculty of Medicine, UNSW en_US
unsw.relation.school The Kirby Institute *
unsw.thesis.degreetype PhD Doctorate en_US
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