Introduction

Baculoviruses are a large group of rod-shaped, enveloped, circular, double-stranded DNA viruses, which are specifically pathogenic to arthropod [1]. The sizes of baculovirus genomes vary from approximately 80 to 180 kb, which encode 89 to 183 genes [2]. Baculoviruses ubiquitously exist in the environment and have been isolated from more than 600 host insect species, which predominantly belong to the orders Lepidoptera, Hymenoptera, and Diptera [3]. Autographa californica multiple nucleopolyhedrovirus (AcMNPV), the prototype of the Baculoviridae family, is the first baculovirus to be sequenced [4]. So far, more than 80 baculoviruses have been sequenced. They are divided into four genera, Alphabaculovirus, Betabaculovirus, Gammabaculovirus, and Deltabaculovirus [5]. On the basis of molecular phylogenetic analysis of the polyhedrin (polh) gene, the members of the Alphabaculovirus genus can be further subdivided into group I and II NPVs [6].

The unique life cycle of baculoviruses is that baculoviruses produce two types of virions during the infection, one is the occlusion-derived virus (ODV), and the other is the budded virus (BV). ODV and BV have similar nucleocapsid structure, but the origin and composition of their envelopes are different. The main envelope protein of BV is GP64. GP64 can mediate budding, attachment, and entry of BVs, which resulted in the system infection. The ODV envelope contains many associated and integral viral proteins. ODV is responsible for spreading infection among insects [3,7].

Actin is one of the most abundant proteins in eukaryotes and exists in the whole cell. Actin is widely involved in the construction of cytoskeleton, maintenance of cell morphology, muscle cell contraction and cell motility, phagocytosis, regulation of cell division, secretion, intracellular material transport and signal transduction. Actin exists in two forms: monomeric globular actin (G-actin) and filamentous actin (F-actin). F-actin and G-actin can be converted into each other under certain conditions, so as to maintain the dynamic balance of intracellular actin, which is the basis for the movement and replication of many pathogenic microorganisms in host cells, including baculoviruses. This review will focus on the recent advances and summarize the function of actin in the baculovirus infection and the regulation of baculovirus on intracellular actin rearrangement.

Infection cycle of baculovirus

The infection cycle of baculovirus can be divided into two stages: primary infection and systemic infection (Figure 1). Upon oral ingestion, the occlusion bodies (OBs) are dissolved in the insect midgut, releasing ODVs embedded in OBs. ODVs penetrate the peritrophic matrix of insect midgut, and then ODV envelopes fuse with microvillar membranes, releasing virus nucleocapsids into the midgut epithelial cells, initiating primary infection. In the early infection stage, newly assembled nucleocapsids egress from the nucleus, migrate across the cytoplasm, and bud from the plasma membrane to form BVs. Then, BVs spread throughout the organism, resulting in systemic infection [3]. In the later stage of virus infection, the nucleocapsids remain in the infected nucleus, and obtain envelopes which may be derived from nuclear membranes to form ODVs [1]. The ODVs are further packaged into OBs. Upon the death and disintegration of the insect, OBs are released into the natural environment, thus starting the next infection cycle.

The relation of baculovirus infection and actin network rearrangement

It has been found that baculovirus infection can cause multiple sequential rearrangements of actin network in host cells [8,9]. After the viruses enter into cells, early cables are formed within the cytoplasm of infected cells, and a single nucleocapsid is at an end of most cables, suggesting that nucleocapsids or nucleocapsid-associated proteins of viruses induce the polymerization or bundling of actin [8,9]. With the expression of early viral gene, the second rearrangement of actin occurs in cells, and the F-actin cables gather near the plasma membrane [9]. Actin rearrangement-inducing factor 1 was found to be able to induce actin rearrangement and colocalize with F-actin at the plasma membrane. The various deletion mutants showed a loss of actin concentration at the plasma membrane [10,11]. At the late stage of virus infection, actin accumulates in the nucleus to form F-actin, which distributes in the ring zone surrounding the virogenic stroma (VS) [8,9]. Although G-actin and F-actin also exist in the nuclei of uninfected cells [12] and participate in many nuclear activities [13], baculovirus can cause a large number of G-actin aggregation in the nucleus and form F-actin [9]. The F-actin in the nucleus is very important for the morphogenesis of nucleocapsid. In the presence of either Cytochalasin D or Latrunculin A, two actin-binding agents that interfere with F-actin-dependent processes, the proper intranuclear assembly of viral nucleocapsids and the production of infectious progeny are prevented, showing that intranuclear F-actin is essential for baculovirus to produce progeny [14-17]. It has been reported that AcMNPV ie-1, pe38, ac4, he65, ac102, and ac152, known as the nuclear localization of actin (NLA) genes, may be required for mediating nuclear localization of G-actin [18,19]. Further studies showed that among the six NLA genes, only ac102 is required in the nuclear localization of G-actin, and the other five NLA genes are not necessary for this process [20].

The role of actin in the transport of nucleocapsid in cells

After the nucleocapsid is released into the cytoplasm, it is transported into the nucleus via the nuclear pore complex to start the cascade expression of baculovirus genes. In general, the transport of viruses in cells requires the assistance of microtubule [21], while the transport of bacteria relies on microfilament [22]. Some viruses, such as vaccinia virus, use both microtubules and actin filaments for intracellular movement and egress [23]. Studies have found that baculovirus uses microfilament to mediate the activity of nucleocapsid in cells, and the microtubule depolymerization has no effect on the movement of nucleocapsid in cells [24,25]. In addition, nucleocapsids of AcMNPV have been found to interact with actin as soon as they enter the cytoplasm, suggesting that the nucleocapsids may use microfilament to move in cells [8,26]. Inhibition of actin entry into nucleus can delay the start of viral gene expression, suggesting that actin movement facilitates the entry of viruses into the nucleus [27]. The visualization of AcMNPV movements in cells showed that nucleocapsids of AcMNPV undergo intracellular motility driven by actin polymerization [24].

Electron tomography showed that baculovirus is propelled by a fishbone-like array of actin filaments constructed from subsets linked by branch junctions, with an average of four filaments pushing the virus by their fast polymerizing ends at any one time [28]. Using a stochastic mathematical model, the simulations of actin comet tail organization as well as the tracks adopted by baculovirus inside cells showed that the actin filaments are continuously tethered to the virus surface as they grow, branch, and push [28,29]. Therefore, F-actin is necessary for the directional transport of baculovirus nucleocapsid in cells [27,30].

The baculovirus protein that interacted with actin

At the late stage of baculovirus infection, six viral actininteracting proteins are synthesized, which are P78/83, BV/ODV-C42, VP39, VP80, Ac102 and Ac34 [31-35]. VP80 is associated with the nucleocapsid of both BVs and ODVs, typically at one end of the nucleocapsids. VP80 has sequence motifs with homology to invertebrate paramyosin proteins, and VP80 is entirely localized in nuclei, adjacent to the virus-triggered F-actin scaffold [32]. Although deletion of the AcMNPV vp80 does not affect assembly of nucleocapsids, these nucleocapsids cannot migrate from the VS to the nuclear periphery to form viral progeny, showing VP80 is involved in the process of nucleocapsid egress from the VS toward the nuclear periphery along F-actin [36-39]. VP39 is the major capsid protein of baculovirus. VP39 can bind both G-actin and F-actin, but shows higher affinity for G-actin [40]. However, the function of VP39 binding G-actin is still unclear. Ac34 distributes in both the cytoplasm and the nuclei of infected cells but was not a viral structural protein [41]. The potential C3H zinc finger in Ac34 is required for its nuclear localization and optimal virus multiplication [42]. Ac34 can bind to the actinrelated protein complex (Arp2/3) subunits of Sf9 cells, P40, P34, and P20, which is essential for Ac34 to relocate Arp2/3 subunits to the nucleus [33]. The subcellular distribution of Arp2/3 under steady-state conditions is controlled by chromosomal maintenance 1 (CRM1)-dependent nuclear export. Upon AcMNPV infection, Ac34 inhibits CRM1 pathway and leads to Arp2/3 retention in the nucleus to assist in virus replication [34].

P78/83 is a Wiskott-Aldrich syndrome protein (WASP)- like protein, also known as nucleation promoting factors (NPFs), locates at one end of nucleocapsid, and is involved in nuclear actin assembly during the baculovirus infection [43]. The main substrate of WASP is Arp2/3 complex, which is the most direct and important activator of F-actin formation in cells [44]. The purified Arp2/3 complex has no activity, but it can be activated by NPFs to promote the polymerization of G-actin [1,43-45].

NPFs contain two domains, the C-terminal conserved output domain (VCA domain) and the N-terminal diverse regulatory domain. The C-terminal VCA domain includes a verprolin homology motif or V, an amphipathic connector region or C, and an acidic peptide or A. V domain can bind G-actin and CA domain is responsible for binding Arp2/3 complex [46,47]. The N-terminal regulatory region of WASP contains a GTPase-binding domain, which binds to the C-terminal VCA domain through intramolecular interaction, making WASP in an inactive state [48]. Under the external stimulation, GTPase Cdc42 can competitively bind to the GTPase-binding domain, and the intramolecular interaction disintegrates subsequently to release the VCA domain, then WASP is activated to direct Arp2/3 complex to initiate G-actin polymerization to form F-actin [48]. However, the N-terminal region of P78/83 does not show similarity with any identified NPFs, there is a unique multifunctional regulatory sequence (MRS) located near the N terminus of P78/83 [49]. MRS can serve as a degron to mediate P78/83 degradation in a proteasome dependent manner. In AcMNPV-infected Sf9 cells, MRS can bind to BV/ODV-C42, which modulates the P78/83-Arp2/3 interaction to orchestrate actin polymerization [49]. In addition, nucleocapsids are found to be able to nucleate actin polymerization in a concentration-dependent manner in vitro, and P78/83 is found to bind actin directly [40]. In conclusion, P78/83-Arp2/3 complex plays a key role in baculovirus nucleocapsid transport.

BV/ODV-C42, a nucleocapsid structural protein, is capable of directly interacting with the viral proteins P78/83 and ODVEC27 to form a complex [50]. BV/ODV-C42 contains a nuclear localization signal (NLS) motif at the C terminus. During AcMNPV infection, BV/ODV-C42 binds to P78/83 in the cytoplasm to form a protein complex and cotransports to the nucleus under the direction of the NLS motif of BV/ODV-C42 [51]. In addition, studies have shown that BV/ODV-C42 plays a key role in the nuclear actin polymerization process, besides its role in recruiting P78/83 to the nucleus [52]. In the absence of BV/ODV-C42, even if P78/83 was tagged with a NLS, polymerized F-actin filaments could not be found in the nuclei of virus-transfected cells, despite other actin polymerization elements (i.e., G-actin, P78/83, and Arp2/3 complex) are present [52]. Furthermore, both the kinetics of pyrene-actin polymerization and F-actin-specific staining by phalloidin indicated that anti-BV/ODV-C42 can significantly attenuate the efficiency of F-actin formation [52]. Therefore, BV/ODV-C42 is directly involved in the formation of F-actin in vivo and in vitro. One possible hypothesis is that BV/ODV-C42 not only mediates the entry of P78/83 into the nucleus, but also maintains the stability of P78/83 via its interaction with P78/83, thus indirectly participates in the formation of F-actin.

In addition, it is interesting that BV/ODV-C42 was found to contain a putative pocket protein binding site (PPBS), which may be involved in the interaction with pocket proteins of host cells, such as retinoblastoma protein (pRB), p130 and p107 [50], subsequently regulate other cell activities via pRB. Tyrosine kinase activity of nuclear c-Abl is regulated in the cell cycle through a specific interaction with pRB [53]. c-Abl can phosphorylate neural WASP (N-WASP) to regulate actin comet tail formation [54]. There are two molecular masses of 78 and 83 kDa P78/83 synthesized late in baculovirus infection, and the 83-kDa protein was a phosphorylated derivative of the 78-kDa protein [55]. Therefore, it is possible that there is a c-Abl homolog exists in insect cells to phosphorylate P78/83. Studies showed that elimination of the interaction between BV/ODV-C42 and pRB resulted in the separation of c-Abl homolog from P78/83, and the hypo phosphorylated P78/83 cannot effectively activate the Arp2/3 complex to initiate actin polymerization [52]. Hence, BV/ODV-C42 may serve as a scaffold protein that provides a molecular platform for c-Abl homolog to phosphorylate P78/83 to regulate the activity of Arp2/3 complex, and ultimately regulate the polymerization of F-actin. Recently, Ac102 was found to be a component of the P78/83-C42-EC27-Ac102 protein complex [31], and be involved in modulating BV/ODV-C42 ubiquitination and consequently ensures P78/83 activity as an NPF to initiate actin polymerization [35].

In conclusion, the possible roles of actin in the transportation of nucleocapsids in host cells are as follows (Figure 2). Shortly after the baculovirus nucleocapsid is released from the endocytosis into the host cytoplasm, cytoplasmic G-actin is induced by P78/83 to polymerize to form F-actin cable, propelling the nucleocapsid to migrate to the nuclear membrane. At the nuclear membrane, P78/83 is degraded, P78/83-induced actin polymerization is ended, and the nucleocapsid is detached from the F-actin tail, then the nucleocapsid enters the nucleus via the nuclear pore complex, releasing the viral genome to the VS, subsequently initiating the replication and transcription of viral genes. With production of early viral proteins, G-actin in cytoplasm is recruited into nucleus. At the late stage of infection, P78/83, BV/ODV-C42, Ac102, VP80 and Ac34 are produced, P78/83 and Arp2/3 complex are transported into the nucleus, initiating the nucleus G-actin polymerization to form F-actin. Then nucleocapsid is assembled and egresses from the nucleus along F-actin under the interaction of VP80 and myosin. Progeny virus is produced, one replication cycle is complete. A recent study showed that the host microtubule transport system is also involved in the nucleocapsid transport from nucleus to plasma membrane to produce BV [56].

Conclusion and future direction

Viruses are non-cellular organisms that must parasitize and propagate in host cells. Viruses have no metabolic mechanism and enzyme system, they use the material and energy in the host cells to complete their replication cycle. Cytoskeleton has been used by almost all viruses to complete the key process of infection in cells, including virus localization, virus replication and gene transcription. The Baculoviridae family is widely used in both biotechnology and biological control, and potentially hides a treasure trove of genes and molecules that could lead to innovative biotechnology [57]. Baculovirus infection can induce G-actin to accumulate in the nucleus to form F-actin, which is unique among all pathogens. The studies on the interaction between baculovirus and actin are helpful to further uncover the transport mechanism of viral nucleocapsid and the role of actin played in the nucleus of virus infection cell. At present, more and more attention has been paid to the role of nuclear actin in cell life activities, and baculovirus infection can be used as a useful tool to reveal the function of nuclear actin and study the role of different motor proteins played in cells, which will be beneficial to promote the progress of the whole life science.

On the other hand, the specific mechanism of actin in the process of baculovirus infection is still unclear. The entry, polymerization, and depolymerization of actin are regulated by a variety of cellular signals. To date, these signal pathways, and the virus or host proteins involved in them are little known. One important reason is that, unlike mammalian systems, there are relatively little studies on the actin polymerization and depolymerization in insect systems, and many important genes involved in actin regulation have not been cloned and studied. With the elucidation of the specific mechanism of interaction between baculovirus proteins and actin in the future, the mechanism of actin rearrangement in baculovirus infected cells will be clearer understood, which will promote the understand on the baculovirus molecular biology and the interaction between baculovirus and actin network.

Acknowledgements

We are grateful to Dr. Shimao Zhu of Shenzhen Weiguang Biological Products Co., Ltd, China, for his valuable suggestions. This work was supported by the Provincial Regular University Key Research Platform and Project Foundation of Guangdong (2018KTSCX248).

Conflicts of Interest

The authors declare no conflict of interest.

Figue 1: The infection cycle of baculovirus. (A) Occlusion bodies (OBs) ingested by an insect dissolve in the alkaline midgut lumen and release ODVs. Then, ODVs infect midgut epithelial cells, initiating primary infection. (B) The virions bud out from the basement membrane of the cells, initiating a systemic infection. Early in the systemic infection, more newly assembled nucleocapsids bud from the plasma membrane to form budded viruses (BVs), which spread the infection throughout the organism. (C) Late in the virus infection, the nucleocapsids remained in the infected nucleus obtain envelopes to form ODVs, which are further packaged into OBs. (D) Upon the death of the cells, OBs are released. (E) OBs enter into the natural environment, thus starting the next infection cycle. VS, virogenic stroma.

Figure 2: The possible roles of actin in the transportation of nucleocapsids in host cells. (I) Shortly after the baculovirus nucleocapsids enter into the host cytoplasm, cytoplasmic G-actin is induced to polymerize to form F-actin cable, propelling the nucleocapsids to migrate to the nuclear membrane. (II) At the nuclear membrane, induced actin polymerization is ended, the nucleocapsid is detached from the F-actin tail, then the nucleocapsid enters the nucleus via the nuclear pore complex. (III) The viral genome is released to the virogenic stroma (VS). (IV) The viral genes are replicated and transcripted. (V) With production of early viral proteins, G-actin in cytoplasm is recruited into nucleus. (VI) At the late stage of infection, P78/83, BV/ODV-C42, Ac102, VP80 and Ac34 are produced. (VII) P78/83 and Arp2/3 complex are transported into the nucleus, initiating the nucleus G-actin polymerization to form F-actin. (VIII) Nucleocapsids are assembled and egresses from the nucleus along F-actin.

References

1. Rohrmann GF (2019) Baculovirus Molecular Biology, 4th ed., National Library of Medicine, National Center for Biotechnology Information, Bethesda.
2. Ferrelli ML, Marcelo FB, Mariano NB, Ghiringhelli PD, et al. (2012) The Baculoviral Genome.
3. Slack J, Arif BM (2007) The baculoviruses occlusion-derived virus: virion structure and function. "Adv Virus Res 69: 99-165.
4. Ayres MD, Howard SC, Kuzio J, Lopez-Ferber M, et al. (1994) The complete DNA sequence of Autographa californica nuclear polyhedrosis virus. Virology 202: 586-605.
5. Jehle JA, Blissard GW, Bonning BC, Cory JS, et al. (2006) "On the classification and nomenclature of baculoviruses: a proposal for revision." Archives of virology 151: 1257-1266.
6. de A. Zanotto PM, Kessing BD, Maruniak JE (1993) "Phylogenetic interrelationships among baculoviruses: evolutionary rates and host associations." Journal of invertebrate pathology 62: 147-164.
7. Braunagel SC, Summers MD (1994) "Autographa californica nuclear polyhedrosis virus, PDV, and ECV viral envelopes and nucleocapsids: structural proteins, antigens, lipid and fatty acid profiles." Virology 202: 315-328.
8. Charlton CA, Volkman LE (1993) "Penetration of Autographa californica nuclear polyhedrosis virus nucleocapsids into IPLB Sf21 cells induces actin cable formation." Virology 197: 245-254.
9. Charlton CA, Volkman LE (1991) "Sequential rearrangement and nuclear polymerization of actin in baculovirus-infected Spodoptera frugiperda cells." Journal of virology 65: 1219-1227.
10. Dreschers S, Roncarati R, Knebel-Morsdorf D (2001) "Actin rearrangement-inducing factor of baculoviruses is tyrosine phosphorylated and colocalizes to F-actin at the plasma membrane." Journal of virology 75: 3771-3778.
11. Roncarati R, Knebel-Morsdorf D (1997) "Identification of the early actin-rearrangement-inducing factor gene, arif-1, from Autographa californica multicapsid nuclear polyhedrosis virus." Journal of virology 71: 7933-7941.
12. McDonald D, Carrero G, Andrin C, de Vries G, et al. (2006) "Nucleoplasmic beta-actin exists in a dynamic equilibrium between low-mobility polymeric species and rapidly diffusing populations." The Journal of cell biology 172: 541-552.
13. Pederson T, Aebi U (2005) "Nuclear actin extends, with no contraction in sight." Molecular biology of the cell 16: 5055-5060.
14. Hess RT, Goldsmith PA, Volkman LE (1989) "Effect of cytochalasin D on cell morphology and AcMNPV replication in a Spodoptera frugiperda cell line." Journal of invertebrate pathology 53: 169-182.
15. Kasman LM, Volkman LE (2000) Filamentous actin is required for lepidopteran nucleopolyhedrovirus progeny production. The Journal of general virology 81: 1881-1888.
16. Ohkawa T, Volkman LE (1999) "Nuclear F-actin is required for AcMNPV nucleocapsid morphogenesis." Virology 264: 1-4.
17. Volkman LE (1988) "Autographa californica MNPV nucleocapsid assembly: inhibition by cytochalasin D." Virology 163: 547-553.
18. Ohkawa T, Rowe AR, Volkman LE (2002) "Identification of six Autographa californica multicapsid nucleopolyhedrovirus early genes that mediate nuclear localization of G-actin." Journal of virology 76: 12281-12289.
19. Wang Q, Chen JZ, Wang Y, Wang XJ, et al. (2012) "Localization of AcMNPV NLA genes in Sf9 cells." Bing du xue bao Chinese journal of virology 28: 172-177.
20. Gandhi KM, Ohkawa T, Welch MD, Volkman LE (2012) "Nuclear localization of actin requires AC102 in Autographa californica multiple nucleopolyhedrovirus-infected cells." The Journal of general virology 93: 1795-1803.
21. Greber UF, Way M (2006) "A superhighway to virus infection." Cell 124: 741-754.
22. Gouin E, Welch MD, Cossart P (2005) "Actin-based motility of intracellular pathogens." Current opinion in microbiology 8: 35-45.
23. Hollinshead M, Rodger G, Van Eijl H, Law M, et al. (2001) "Vaccinia virus utilizes microtubules for movement to the cell surface." The Journal of cell biology 154: 389-402.
24. Ohkawa T, Volkman LE, Welch MD (2010) "Actin-based motility drives baculovirus transit to the nucleus and cell surface." The Journal of cell biology 190: 187-195.
25. Volkman LE, Zaal KJ (1990) "Autographa californica M nuclear polyhedrosis virus: microtubules and replication." Virology 175: 292-302.
26. Qin F, Xu C, Lei C, Hu J, et al. (2018) "Autographa californica multiple nucleopolyhedrovirus enters host cells via clathrin-mediated endocytosis and direct fusion with the plasma membrane." Viruses 10.
27. Newsome TP, Marzook NB (2015) "Viruses that ride on the coat-tails of actin nucleation." Seminars in cell & developmental biology 46: 155-163.
28. Mueller J, Pfanzelter J, Winkler C, Narita A, et al. (2014) "Electron tomography and simulation of baculovirus actin comet tails support a tethered filament model of pathogen propulsion." PLoS biology 12: e1001765.
29. Small JV (2015) "Pushing with actin: from cells to pathogens." Biochemical Society transactions 43: 84-91.
30. Wang IH, Burckhardt CJ, Yakimovich A, Greber UF (2018) Imaging, Tracking and Computational Analyses of Virus Entry and Egress with the Cytoskeleton. Viruses 10.
31. Hepp SE, Borgo GM, Ticau S, Ohkawa T, et al. (2018) "Baculovirus AC102 is a nucleocapsid protein that is crucial for nuclear actin polymerization and nucleocapsid morphogenesis." Journal of virology.
32. Marek M, Merten OW, Galibert L, Vlak JM, et al. (2011) "Baculovirus VP80 protein and the F-actin cytoskeleton interact and connect the viral replication factory with the nuclear periphery." Journal of virology 85: 5350-5362.
33. Mu J, Zhang Y, Hu Y, Hu X, et al. (2016) "The role of viral protein Ac34 in nuclear relocation of subunits of the actin-related protein 2/3 complex." Virologica Sinica 31: 480-489.
34. Mu J, Zhang Y, Hu Y, Hu X, et al. (2016) "Autographa californica multiple nucleopolyhedrovirus Ac34 protein retains cellular actin-related protein 2/3 complex in the nucleus by subversion of CRM1-dependent nuclear export." PLoS pathogens 12: e1005994.
35. Zhang Y, Hu X, Mu J, Hu Y, et al. (2018) "Ac102 Participates in Nuclear Actin Polymerization by Modulating BV/ODV-C42 Ubiquitination during Autographa californica Multiple Nucleopolyhedrovirus Infection." Journal of virology.
36. Marek M, Merten OW, Francis-Devaraj F, Oers MM (2012) "Essential C-terminal region of the baculovirus minor capsid protein VP80 binds DNA." Journal of virology 86: 1728-1738.
37. Marek M, van Oers MM, Devaraj FF, Vlak JM, et al. (2011) "Engineering of baculovirus vectors for the manufacture of virion-free biopharmaceuticals." Biotechnology and bioengineering 108: 1056-1067.
38. Tang XD, Xu YP, Yu LL, Lang GJ, et al. (2008) "Characterization of a Bombyx mori nucleopolyhedrovirus with Bmvp80 disruption." Virus research 138: 81-88.
39. Blissard GW, Theilmann DA (2018) "Baculovirus entry and egress from insect cells." Annual review of virology 5: 113-139.
40. Lanier LM, Volkman LE (1998) "Actin binding and nucleation by Autographa california M nucleopolyhedrovirus." Virology 243: 167-177.
41. Cai Y, Long Z, Qiu J, Yuan M, et al. (2012) "An ac34 deletion mutant of Autographa californica nucleopolyhedrovirus exhibits delayed late gene expression and a lack of virulence in vivo." Journal of virology 86: 10432-10443.
42. Qiu J, Tang Z, Yuan M, Wu W, et al. (2017) "The 91-205 amino acid region of AcMNPV ORF34 (Ac34), which comprises a potential C3H zinc finger, is required for its nuclear localization and optimal virus multiplication." Virus research 228: 79-89.
43. Goley ED, Ohkawa T, Mancuso J, Woodruff JB, et al. (2006) "Dynamic nuclear actin assembly by Arp2/3 complex and a baculovirus WASP-like protein." Science 314: 464-467.
44. Mullins RD, Pollard TD (1999) "Structure and function of the Arp2/3 complex." Current opinion in structural biology 9: 244-249.
45. Mullins RD, Heuser JA, Pollard TD (1998) "The interaction of Arp2/3 complex with actin: nucleation, high affinity pointed end capping, and formation of branching networks of filaments." Proceedings of the National Academy of Sciences of the United States of America 95: 6181-6186.
46. Chereau D, Kerff F, Graceffa P, Grabarek Z, et al. (2005) "Actin-bound structures of Wiskott-Aldrich syndrome protein (WASP)-homology domain 2 and the implications for filament assembly." Proceedings of the National Academy of Sciences of the United States of America 102: 16644-16649.
47. Welch MD, Mullins RD (2002) "Cellular control of actin nucleation." Annual review of cell and developmental biology 18: 247-288.
48. Kim AS, Kakalis LT, Abdul-Manan N, Liu GA, et al. (2000) "Autoinhibition and activation mechanisms of the Wiskott-Aldrich syndrome protein." Nature 404: 151-158.
49. Wang Y, Zhang Y, Han S, Hu X, et al. (2015) "Identification of a novel regulatory sequence of actin nucleation promoting factor encoded by Autographa californica multiple nucleopolyhedrovirus." The Journal of biological chemistry 290: 9533-9541.
50. Braunagel SC, Guidry PA, Rosas-Acosta G, Engelking L, et al. (2001) "Identification of BV/ODV-C42, an Autographa californica nucleopolyhedrovirus orf101-encoded structural protein detected in infected-cell complexes with ODV-EC27 and p78/83." Journal of virology 75: 12331-12338.
51. Wang Y, Wang Q, Liang C, Song J, et al. (2008) "Autographa californica multiple nucleopolyhedrovirus nucleocapsid protein BV/ODV-C42 mediates the nuclear entry of P78/83." Journal of virology 82: 4554-4561.
52. Li K, Wang Y, Bai H, Wang Q, et al. (2010) "The putative pocket protein binding site of Autographa californica nucleopolyhedrovirus BV/ODV-C42 is required for virus-induced nuclear actin polymerization." Journal of virology 84: 7857-7868.
53. Welch PJ, Wang JY (1993) "A C-terminal protein-binding domain in the retinoblastoma protein regulates nuclear c-Abl tyrosine kinase in the cell cycle." Cell 75: 779-790.
54. Burton EA, Oliver TN, Pendergast AM (2005) "Abl kinases regulate actin comet tail elongation via an N-WASP-dependent pathway." Molecular and cellular biology 25: 8834-8843.
55. Vialard JE, Richardson CD (1993) "The 1,629-nucleotide open reading frame located downstream of the Autographa californica nuclear polyhedrosis virus polyhedrin gene encodes a nucleocapsid-associated phosphoprotein." Journal of virology 67: 5859-5866.
56. Biswas S, Blissard GW, Theilmann DA (2016) "Trichoplusia ni kinesin-1 associates with Autographa californica multiple nucleopolyhedrovirus nucleocapsid proteins and is required for production of budded virus." Journal of virology 90: 3480-3495.
57. Theze J, Lopez-Vaamonde C, Cory JS, Herniou EA (2018) "Biodiversity, evolution and ecological specialization of baculoviruses: A treasure trove for future applied research." Viruses 10.

Citation: Li S, Jiang H, Gan T, Lv Y, Huang L, et al. (2021) Overview of the Role of Actin in the Intracellular Transport of Baculovirus. Adv Biochem Biotechnol 6: 10105. DOI: https://doi.org/10.29011/2574-7258.010105