References
- Weaver SC. Host range, amplification and arboviral disease emergence. Arch Virol Suppl 2005; 19(19):33-44; PMID:16358422; https://doi.org/https://doi.org/10.1007/3-211-29981-5_4
- Taylor Katherine G, Paessler S. Pathogenesis of venezuelan equine encephalitis. Vet Microbiol 2013; 167(1–2):145-50; PMID:23968890; https://doi.org/https://doi.org/10.1016/j.vetmic.2013.07.012
- Weaver SC, Salas R, Rico-Hesse R, Ludwig GV, Oberste MS, Boshell J, Tesh RB. Re-emergence of epidemic venezuelan equine encephalomyelitis in south america. The Lancet 1996; 348(9025):436-40; https://doi.org/https://doi.org/10.1016/S0140-6736(96)02275-1
- Weaver Scott C, Ferro C, Barrera R, Boshell J, Navarro J-C. Venezuelan equine encephalitis. Annu Rev Entomol 2004; 49:141-74; PMID:14651460; https://doi.org/https://doi.org/10.1146/annurev.ento.49.061802.123422
- Paessler S, Weaver SC. Vaccines for venezuelan equine encephalitis. Vaccine 2009; 27(4):D80-85; PMID:19837294; https://doi.org/https://doi.org/10.1016/j.vaccine.2009.07.095
- Amaya M, Voss K, Sampey G, Senina S, de la Fuente C, Mueller C, Calvert V, Kehn-Hall K, Carpenter C, Kashanchi F, et al. The role of IKKβ in venezuelan equine encephalitis virus infection. PloS One 2014; 9(2):e86745; PMID:24586253; https://doi.org/https://doi.org/10.1371/journal.pone.0086745
- Voss K, Amaya M, Mueller C, Roberts B, Kehn-Hall K, Bailey C, Petricoin E, 3rd, Narayanan A. Inhibition of host extracellular signal-regulated kinase (ERK) activation decreases new world alphavirus multiplication in infected cells. Virology 2014; 468–470:490-503; PMID:25261871; https://doi.org/https://doi.org/10.1016/j.virol.2014.09.005
- Amaya M, Keck F, Lindquist M, Voss K, Scavone L, Kehn-Hall K, Roberts B, Bailey C, Schmaljohn C, Narayanan A. The ubiquitin proteasome system plays a role in venezuelan equine encephalitis virus infection. PloS One 2015; 10(4):e0124792; PMID:25927990; https://doi.org/https://doi.org/10.1371/journal.pone.0124792
- Amaya M, Brooks-Faulconer T, Lark T, Keck F, Bailey C, Raman V, Narayanan A. Venezuelan equine encephalitis virus non-structural protein 3 (nsP3) interacts with RNA helicases DDX1 and DDX3 in infected cells. Antiviral Res 2016; 131:49-60; PMID:27105836; https://doi.org/https://doi.org/10.1016/j.antiviral.2016.04.008
- Atasheva S, Krendelchtchikova V, Liopo A, Frolova E, Frolov I. Interplay of acute and persistent infections caused by venezuelan equine encephalitis virus encoding mutated capsid protein. J Virol 2010; 84(19):10004-15; PMID:20668087; https://doi.org/https://doi.org/10.1128/JVI.01151-10
- Ernster L, Schatz G. Mitochondria: a historical review. J Cell Biol 1981; 91(3):227s-255s; PMID:7033239
- Chan DC. Mitochondria: dynamic organelles in disease, aging, and development. Cell 2006; 125(7):1241-52; PMID:16814712; https://doi.org/https://doi.org/10.1016/j.cell.2006.06.010
- McBride HM, Neuspiel M, Wasiak S. Mitochondria: more than just a powerhouse. Curr Biol 2006; 16(14):R551-60; PMID:16860735; https://doi.org/https://doi.org/10.1016/j.cub.2006.06.054
- Khan M, Syed GH, Kim S-J, Siddiqui A. Mitochondrial dynamics and viral infections: a close nexus. Biochim Biophys Acta BBA - Mol Cell Res 2015; 1853(10, Part B):2822-33; https://doi.org/https://doi.org/10.1016/j.bbamcr.2014.12.040
- Detmer Scott A, Chan David C. Functions and dysfunctions of mitochondrial dynamics. Nat Rev Mol Cell Biol 2007; 8(11):870-9; PMID:17928812; https://doi.org/https://doi.org/10.1038/nrm2275
- Su B, Wang X, Zheng L, Perry G, Smith MA, Zhu X. Abnormal mitochondrial dynamics and neurodegenerative diseases. Biochim Biophys Acta 2010; 1802(1):135-42; PMID:19799998; https://doi.org/https://doi.org/10.1016/j.bbadis.2009.09.013
- Rahmani Z, Huh K-W, Lasher R, Siddiqui A. Hepatitis B virus X protein colocalizes to mitochondria with a human voltage-dependent anion channel, HVDAC3, and alters its transmembrane potential. J Virol 2000; 74(6):2840-6; PMID:10684300
- Bouchard MJ, Wang L-H, Schneider RJ. Calcium signaling by HBx protein in hepatitis B virus DNA replication. Science 2001; 294(5550):2376-8; PMID:11743208; https://doi.org/https://doi.org/10.1126/science.294.5550.2376
- Waris G, Huh K-W, Siddiqui A. Mitochondrially Associated hepatitis B virus X protein constitutively activates transcription factors STAT-3 and NF-κB via oxidative stress. Mol Cell Biol 2001; 21(22):7721-30; PMID:11604508; https://doi.org/https://doi.org/10.1128/MCB.21.22.7721-7730.2001
- Bouchard Michael J, Navas-Martin S. Hepatitis B and C virus hepatocarcinogenesis: lessons learned and future challenges. Cancer Lett 2011; 305(2):123-43; PMID:21168955; https://doi.org/https://doi.org/10.1016/j.canlet.2010.11.014
- Kim S-J, Syed GH, Siddiqui A. Hepatitis C virus induces the mitochondrial translocation of parkin and subsequent mitophagy. PLoS Pathog 2013; 9(3):e1003285; PMID:23555273; https://doi.org/https://doi.org/10.1371/journal.ppat.1003285
- Kim S-J, Syed GH, Khan M, Chiu W-W, Sohail MA, Gish RG, Siddiqui A. Hepatitis C virus triggers mitochondrial fission and attenuates apoptosis to promote viral persistence. Proc Natl Acad Sci U S A 2014; 111(17):6413-8; PMID:24733894; https://doi.org/https://doi.org/10.1073/pnas.1321114111
- Boyapalle S, Wong T, Garay J, Teng M, San Juan-Vergara H, Mohapatra S, Mohapatra S. Respiratory syncytial virus NS1 protein colocalizes with mitochondrial antiviral signaling protein MAVS following infection. PLoS One 2012; 7(2):e29386; PMID:22383950; https://doi.org/https://doi.org/10.1371/journal.pone.0029386
- Narayanan A, Amaya M, Voss K, Chung M, Benedict A, Sampey G, Kehn-Hall K, Luchini A, Liotta L, Bailey C, et al. Reactive oxygen species activate NFκB (p65) and p53 and induce apoptosis in RVFV infected liver cells. Virology 2014; 449:270-86; PMID:24418562; https://doi.org/https://doi.org/10.1016/j.virol.2013.11.023
- Terasaki K, Won S, Makino S. The c-terminal region of rift valley fever virus NSm protein targets the protein to the mitochondrial outer membrane and exerts antiapoptotic function. J Virol 2013; 87(1):676-82; PMID:23097454; https://doi.org/https://doi.org/10.1128/JVI.02192-12
- Garmashova N, Gorchakov R, Volkova E, Paessler S, Frolova E, Frolov I. The old world and new world alphaviruses use different virus-specific proteins for induction of transcriptional shutoff. J Virol 2007; 81(5):2472-84; PMID:17108023; https://doi.org/https://doi.org/10.1128/JVI.02073-06
- Atasheva S, Kim Dal Y, Frolova Elena I, Frolov I. Venezuelan equine encephalitis virus variants lacking transcription inhibitory functions demonstrate highly attenuated phenotype. J Virol 2015; 89(1):71-82; PMID:25320296; https://doi.org/https://doi.org/10.1128/JVI.02252-14
- Narayanan A, Popova T, Turell M, Kidd J, Chertow J, Popov SG, Bailey C, Kashanchi F, Kehn-Hall K. Alteration in superoxide dismutase 1 causes oxidative stress and p38 MAPK activation following RVFV infection. PloS One 2011; 6(5):e20354; PMID:21655261; https://doi.org/https://doi.org/10.1371/journal.pone.0020354
- Kehn-Hall K, Narayanan A, Lundberg L, Sampey G, Pinkham C, Guendel I, Van Duyne R, Senina S, Schultz KL, Stavale E, et al. Modulation of GSK-3β activity in venezuelan equine encephalitis virus infection. PLoS One 2012; 7(4):e34761; PMID:22496857; https://doi.org/https://doi.org/10.1371/journal.pone.0034761
- Lundberg L, Pinkham C, Baer A, Amaya M, Narayanan A, Wagstaff KM, Jans DA, Kehn-Hall K. Nuclear import and export inhibitors alter capsid protein distribution in mammalian cells and reduce venezuelan equine encephalitis virus replication. Antiviral Res 2013; 100(3):662-72; PMID:24161512; https://doi.org/https://doi.org/10.1016/j.antiviral.2013.10.004
- Chen TH, Lo YP, Yang CF, Chen WJ. Additive protection by antioxidant and apoptosis-inhibiting effects on mosquito cells with dengue 2 virus infection. PLoS Negl Trop Dis 2012; 6(4):e1613; PMID:22530071; https://doi.org/https://doi.org/10.1371/journal.pntd.0001613
- Chen T-H, Tang P, Yang C-F, Kao LH, Lo Y-P, Chuang C-K, Shih YT, Chen WJ. Antioxidant defense is one of the mechanisms by which mosquito cells survive dengue 2 viral infection. Virology 2011; 410(2):410-7; PMID:21216424; https://doi.org/https://doi.org/10.1016/j.virol.2010.12.013
- Yang T-C, Lai C-C, Shiu S-L, Chuang P-H, Tzou B-C, Lin YY, Tsai FJ, Lin CW. Japanese encephalitis virus down-regulates thioredoxin and induces ROS-mediated ASK1-ERK/p38 MAPK activation in human promonocyte cells. Microbes Infect 2010; 12(8–9):643-51; PMID:20430109; https://doi.org/https://doi.org/10.1016/j.micinf.2010.04.007
- Murata T, Goshima F, Daikoku T, Inagaki-Ohara K, Takakuwa H, Kato K, Nishiyama Y. Mitochondrial distribution and function in herpes simplex virus-infected cells. J Gen Virol 2000; 81(2):401-6; PMID:10644838; https://doi.org/https://doi.org/10.1099/0022-1317-81-2-401
- Wang X, Su B, Fujioka H, Zhu X. Dynamin-like protein 1 reduction underlies mitochondrial morphology and distribution abnormalities in fibroblasts from sporadic alzheimer's disease patients. Am J Pathol 2008; 173(2):470-82; PMID:18599615; https://doi.org/https://doi.org/10.2353/ajpath.2008.071208
- Gegg Matthew E, Cooper JM, Chau K-Y, Rojo M, Schapira Anthony HV, Taanman J-W. Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy. Hum Mol Genet 2010; 19(24):4861-70; PMID:20871098; https://doi.org/https://doi.org/10.1093/hmg/ddq419
- Narendra Derek P, Youle Richard J. Targeting mitochondrial dysfunction: role for PINK1 and parkin in mitochondrial quality control. Antioxid Redox Signal 2011; 14(10):1929-38; PMID:21194381; https://doi.org/https://doi.org/10.1089/ars.2010.3799
- Okatsu K, Oka T, Iguchi M, Imamura K, Kosako H, Tani N, Kimura M, Go E, Koyano F, Funayama M, et al. PINK1 autophosphorylation upon membrane potential dissipation is essential for parkin recruitment to damaged mitochondria. Nat Commun 2012; 3:1016; PMID:22910362; https://doi.org/https://doi.org/10.1038/ncomms2016
- Barry G, Fragkoudis R, Ferguson MC, Lulla A, Merits A, Kohl A, Fazakerley JK. Semliki forest virus-induced endoplasmic reticulum stress accelerates apoptotic death of mammalian cells. J Virol 2010; 84:7369-77; PMID:20427528; https://doi.org/https://doi.org/10.1128/JVI.02310-09
- Sharma A, Bhattacharya B, Puri RK, Maheshwari RK. Venezuelan equine encephalitis virus infection causes modulation of inflammatory and immune response genes in mouse brain. BMC Genomics 2008; 9:289; PMID:18558011; https://doi.org/https://doi.org/10.1186/1471-2164-9-289
- Jackson AC, Rossiter JP. Apoptotic cell death is an important cause of neuronal injury in experimental venezuelan equine encephalitis virus infection of mice. Acta Neuropathol (Berl) 1997; 93:349-53; https://doi.org/https://doi.org/10.1007/s004010050626
- Baer A, Lundberg L, Swales D, Waybright N, Pinkham C, Dinman JD, Jacobs JL, Kehn-Hall K. Venezuelan equine encephalitis virus induces apoptosis through the unfolded protein response activation of EGR1. J Virol 2016; 90(7):3558-72; PMID:26792742; https://doi.org/https://doi.org/10.1128/JVI.02827-15
- Atkins GJ. The pathogenesis of alphaviruses. Int Sch Res Not 2012; 2013:e861912; https://doi.org/https://doi.org/10.5402/2013/861912
- Coleman Mathew L, Sahai Erik A, Yeo M, Bosch M, Dewar A, Olson Michael F. Membrane blebbing during apoptosis results from caspase-mediated activation of ROCK I. Nat Cell Biol 2001; 3(4):339-45; PMID:11283606; https://doi.org/https://doi.org/10.1038/35070009
- Lazarou M, Sliter Danielle A, Kane Lesley A, Sarraf Shireen A, Wang C, Burman JL, Sideris DP, Fogel AI, Youle RJ. The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy. Nature 2015; 524(7565):309-14; PMID:26266977; https://doi.org/https://doi.org/10.1038/nature14893
- Williams R, Yao H, Peng F, Yang Y, Bethel-Brown C, Buch S. Co-operative induction of CXCL10 involves NADPH oxidase: implications for HIV dementia. Glia 2010; 58(5):611-21; PMID:19941336; https://doi.org/https://doi.org/10.1002/glia.20949
- Santana S, Sastre I, Recuero M, Bullido Maria J, Aldudo J. Oxidative stress enhances neurodegeneration markers induced by herpes simplex virus type 1 infection in human neuroblastoma cells. PLoS One 2013; 8(10):e75842; PMID:24124518; https://doi.org/https://doi.org/10.1371/journal.pone.0075842
- Chen Eunice C, Yagi S, Kelly Kristi R, Mendoza Sally P, Maninger N, Rosenthal A, Spinner A, Bales KL, Schnurr DP, Lerche NW, et al. Cross-species transmission of a novel adenovirus associated with a fulminant pneumonia outbreak in a new world monkey colony. PLoS Pathog 2011; 7(7):e1002155; PMID:21779173; https://doi.org/https://doi.org/10.1371/journal.ppat.1002155
- Kramer T, Enquist Lynn W. Alphaherpesvirus infection disrupts mitochondrial transport in neurons. Cell Host Microbe 2012; 11(5):504-14; PMID:22607803; https://doi.org/https://doi.org/10.1016/j.chom.2012.03.005
- Liu S, Sawada T, Lee S, Yu W, Silverio G, Alapatt P, Millan I, Shen A, Saxton W, Kanao T, et al. Parkinson's disease-associated kinase PINK1 regulates miro protein level and axonal transport of mitochondria. PLoS Genet 2012; 8(3):e1002537; PMID:22396657; https://doi.org/https://doi.org/10.1371/journal.pgen.1002537
- Willows S, Ilkow Carolina S, Hobman Tom C. Phosphorylation and membrane association of the rubella virus capsid protein is important for its anti-apoptotic function. Cell Microbiol 2014; 16(8):1201-10; PMID:24456140; https://doi.org/https://doi.org/10.1111/cmi.12272
- Shiba-Fukushima K, Inoshita T, Hattori N, Imai Y. PINK1-mediated phosphorylation of parkin boosts parkin activity in drosophila. PLOS Genet 2014; 10(6):e1004391; PMID:24901221; https://doi.org/https://doi.org/10.1371/journal.pgen.1004391
- Wang X, Winter D, Ashrafi G, Schlehe J, Wong Yao L, Selkoe D, Rice S, Steen J, LaVoie MJ, Schwarz TL. PINK1 and parkin target miro for phosphorylation and degradation to arrest mitochondrial motility. Cell 2011; 147(4):893-906; PMID:22078885; https://doi.org/https://doi.org/10.1016/j.cell.2011.10.018
- Ordureau A, Heo J-M, Duda David M, Paulo Joao A, Olszewski Jennifer L, Yanishevski D, Rinehart J, Schulman BA, Harper JW. Defining roles of parkin and ubiquitin phosphorylation by PINK1 in mitochondrial quality control using a ubiquitin replacement strategy. Proc Natl Acad Sci U S A 2015; 112(21):6637-42; PMID:25969509; https://doi.org/https://doi.org/10.1073/pnas.1506593112
- Beatch Martin D, Hobman Tom C. Rubella virus capsid associates with host cell protein p32 and localizes to mitochondria. J Virol 2000; 74(12):5569-76; PMID:10823864
- Gottlieb Robert A, Bernstein D. Mitochondrial remodeling: rearranging, recycling, and reprogramming. Cell Calcium 2016; 60(2):88-101; PMID:27130902; https://doi.org/https://doi.org/10.1016/j.ceca.2016.04.006
- Morciano G, Pedriali G, Sbano L, Iannitti T, Giorgi C, Pinton P. Intersection of mitochondrial fission and fusion machinery with apoptotic pathways: role of Mcl-1. Biol Cell 2016; 108:279-293; PMID:27234233; https://doi.org/https://doi.org/10.1111/boc.201600019
- Nykky J, Vuento M, Gilbert L. Role of mitochondria in parvovirus pathology. PLoS One 2014; 9(1):e86124; PMID:24465910; https://doi.org/https://doi.org/10.1371/journal.pone.0086124
- Chu Victor C, Bhattacharya S, Nomoto A, Lin J, Zaidi Syed K, Oberley TD, Weinman SA, Azhar S, Huang TT. Persistent expression of hepatitis C virus non-structural proteins leads to increased autophagy and mitochondrial injury in human hepatoma cells. PLoS One 2011; 6(12):e28551; PMID:22164304; https://doi.org/https://doi.org/10.1371/journal.pone.0028551
- Sasaki M, Miyazaki K, Koga Y, Kimura G, Nomoto K, Yoshida H. Calcineurin-dependent mitochondrial disturbances in calcium-induced apoptosis of human immunodeficiency virus gp160-expressing CD4+ cells. J Virol 2002; 76(1):416-20; PMID:11739707; https://doi.org/https://doi.org/10.1128/JVI.76.1.416-420.2002
- Gullberg RC, Jordan SJ, Moon SL, Soltani E, Geiss Brian J. Oxidative stress influences positive strand RNA virus genome synthesis and capping. Virology 2015; 475:219-29; PMID:25514423; https://doi.org/https://doi.org/10.1016/j.virol.2014.10.037
- Lopez Sanchez MI, Crowston JG, Mackey DA, Trounce IA. Emerging mitochondrial therapeutic targets in optic neuropathies. Pharmacol Ther 2016; 165:132-152; PMID:27288727; https://doi.org/https://doi.org/10.1016/j.pharmthera.2016.06.004
- Hall Andrew M, Schuh Claus D. Mitochondria as therapeutic targets in acute kidney injury. Curr Opin Nephrol Hypertens 2016; 25(4):355-62; PMID:27166518; https://doi.org/https://doi.org/10.1097/MNH.0000000000000228
- Kinney RM, Chang GJ, Tsuchiya KR, Sneider JM, Roehrig JT, Woodward TM, Trent DW. Attenuation of venezuelan equine encephalitis virus strain TC-83 is encoded by the 5′-noncoding region and the E2 envelope glycoprotein. J Virol 1993; 67(3):1269-77; PMID:7679745
- Vialat P, Muller R, Vu Thuy H, Prehaud C, Bouloy M. Mapping of the mutations present in the genome of the rift valley fever virus attenuated MP12 strain and their putative role in attenuation. Virus Res 1997; 52(1):43-50; PMID:9453143; https://doi.org/https://doi.org/10.1016/S0168-1702(97)00097-X
- Caplen H, Peters CJ, Bishop David HL. Mutagen-directed attenuation of rift valley fever virus as a method for vaccine development. J Gen Virol 1985; 66(10):2271-7; PMID:4045430; https://doi.org/https://doi.org/10.1099/0022-1317-66-10-2271
- Kim S-J, Khan M, Quan J, Till A, Subramani S, Siddiqui A. Hepatitis B virus disrupts mitochondrial dynamics: induces fission and mitophagy to attenuate apoptosis. PLoS Pathog 2013; 9(12):e1003722; PMID:24339771; https://doi.org/https://doi.org/10.1371/journal.ppat.1003722