Chikungunya Virus 3′ Untranslated Region: Adaptation to Mosquitoes and a Population Bottleneck as Major Evolutionary Forces
The 3′ untranslated genome region (UTR) of arthropod-borne viruses is characterized by enriched direct repeats (DRs) and stem-loop structures. Despite many years of theoretical and experimental study, on-going positive selection on the 3′UTR had never been observed in ‘real-time,’ and the role of the arbovirus 3′UTR remains poorly understood. We observed a lineage-specific 3′UTR sequence pattern in all available Asian lineage of the mosquito-borne alphavirus, chikungunya virus (CHIKV) (1958–2009), including complicated mutation and duplication patterns of the long DRs. Given that a longer genome is usually associated with less efficient replication, we hypothesized that the fixation of these genetic changes in the Asian lineage 3′UTR was due to their beneficial effects on adaptation to vectors or hosts. Using reverse genetic methods, we examined the functional importance of each direct repeat. Our results suggest that adaptation to mosquitoes, rather than to mammalian hosts, is a major evolutionary force on the CHIKV 3′UTR. Surprisingly, the Asian 3′UTR appeared to be inferior to its predicted ancestral sequence for replication in both mammals and mosquitoes, suggesting that its fixation in Asia was not a result of directional selection. Rather, it may have resulted from a population bottleneck during its introduction from Africa to Asia. We propose that this introduction of a 3′UTR with deletions led to genetic drift and compensatory mutations associated with the loss of structural/functional constraints, followed by two independent beneficial duplications and fixation due to positive selection. Our results provide further evidence that the limited epidemic potential of the Asian CHIKV strains resulted from founder effects that reduced its fitness for efficient transmission by mosquitoes there.
Vyšlo v časopise:
Chikungunya Virus 3′ Untranslated Region: Adaptation to Mosquitoes and a Population Bottleneck as Major Evolutionary Forces. PLoS Pathog 9(8): e32767. doi:10.1371/journal.ppat.1003591
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.ppat.1003591
Souhrn
The 3′ untranslated genome region (UTR) of arthropod-borne viruses is characterized by enriched direct repeats (DRs) and stem-loop structures. Despite many years of theoretical and experimental study, on-going positive selection on the 3′UTR had never been observed in ‘real-time,’ and the role of the arbovirus 3′UTR remains poorly understood. We observed a lineage-specific 3′UTR sequence pattern in all available Asian lineage of the mosquito-borne alphavirus, chikungunya virus (CHIKV) (1958–2009), including complicated mutation and duplication patterns of the long DRs. Given that a longer genome is usually associated with less efficient replication, we hypothesized that the fixation of these genetic changes in the Asian lineage 3′UTR was due to their beneficial effects on adaptation to vectors or hosts. Using reverse genetic methods, we examined the functional importance of each direct repeat. Our results suggest that adaptation to mosquitoes, rather than to mammalian hosts, is a major evolutionary force on the CHIKV 3′UTR. Surprisingly, the Asian 3′UTR appeared to be inferior to its predicted ancestral sequence for replication in both mammals and mosquitoes, suggesting that its fixation in Asia was not a result of directional selection. Rather, it may have resulted from a population bottleneck during its introduction from Africa to Asia. We propose that this introduction of a 3′UTR with deletions led to genetic drift and compensatory mutations associated with the loss of structural/functional constraints, followed by two independent beneficial duplications and fixation due to positive selection. Our results provide further evidence that the limited epidemic potential of the Asian CHIKV strains resulted from founder effects that reduced its fitness for efficient transmission by mosquitoes there.
Zdroje
1. TsetsarkinKA, VanlandinghamDL, McGeeCE, HiggsS (2007) A single mutation in chikungunya virus affects vector specificity and epidemic potential. PLoS Pathog 3: e201.
2. BraultAC, HuangCY, LangevinSA, KinneyRM, BowenRA, et al. (2007) A single positively selected West Nile viral mutation confers increased virogenesis in American crows. Nat Genet 39: 1162–1166.
3. KuhnRJ, HongZ, StraussJH (1990) Mutagenesis of the 3′ nontranslated region of Sindbis virus. RNA J Virol 64: 1465–1476.
4. KuhnRJ, GriffinDE, ZhangH, NiestersHJ, StraussJH (1992) Attenuation of Sindbis virus neurovirulence by using defined mutations in nontranslated regions of the genome. RNA J Virol 66: 7121–7127.
5. MenR, BrayM, ClarkD, ChanockRM, LaiCJ (1996) Dengue type 4 virus mutants containing deletions in the 30 noncoding region of the RNA genome: Analysis of growth restriction in cell culture and altered viremia pattern and immunogenicity in rhesus monkeys. J Virol 70: 3930–3937.
6. MandlCW, HolzmannH, MeixnerT, RauscherS, et al. (1998) Spontaneous and engineered deletions in the 3′ noncoding region of tick-borne encephalitis virus: construction of highly attenuated mutants of a flavivirus. J Virol 72: 2132–2140.
7. LoMK, TilgnerM, BernardKA, ShiPY (2003) Functional analysis of mosquito-borne flavivirus conserved sequence elements within 3′ untranslated region of West Nile virus by use of a reporting replicon that differentiates between viral translation and RNA replication. J Virol 77: 10004–10014.
8. GeorgeJ, RajuR (2000) Alphavirus RNA genome repair and evolution: molecular characterization of infectious sindbis virus isolates lacking a known conserved motif at the 3′ end of the genome. J Virol 74: 9776–9785.
9. OuJH, TrentDW, StraussJH (1982) The 3′-non-coding regions of alphavirus RNAs contain repeating sequences. J Mol Biol 156: 719–730.
10. PfefferM, KinneyRM, KaadenOR (1998) The alphavirus 3′-nontranslated region: size heterogeneity and arrangement of repeated sequence elements. Virology 240: 100–108.
11. GritsunTS, GouldEA (2006) Direct repeats in the 3′ untranslated regions of mosquito-borne flaviviruses: possible implications for virus transmission. J Gen Virol 87: 3297–3305.
12. GritsunTS, GouldEA (2007) Origin and evolution of 3′UTR of flaviviruses: long direct repeats as a basis for the formation of secondary structures and their significance for virus transmission. Adv Virus Res 69: 203–248.
13. GritsunTS, GouldEA (2006) The 3′ untranslated region of tick-borne flaviviruses originated by the duplication of long repeat sequences within the open reading frame. Virology 350: 269–275.
14. ProutskiV, GouldEA, HolmesEC (1997) Secondary structure of the 3′ untranslated region of flaviviruses: similarities and differences. Nucleic Acids Res 25: 1194–1202.
15. PardigonN, LenchesE, StraussJH (1993) Multiple binding sites for cellular proteins in the 3′ end of Sindbis alphavirus minus-sense RNA. J Virol 67: 5003–5011.
16. GarneauNL, SokoloskiKJ, OpyrchalM, NeffCP, WiluszCJ, et al. (2008) The 3′ untranslated region of sindbis virus represses deadenylation of viral transcripts in mosquito and Mammalian cells. J Virol 82: 880–892.
17. SokoloskiKJ, DicksonAM, ChaskeyEL, GarneauNL, WiluszCJ, et al. (2010) Sindbis virus usurps the cellular HuR protein to stabilize its transcripts and promote productive infections in mammalian and mosquito cells. Cell Host Microbe 8: 196–207.
18. DicksonAM, AndersonJR, BarnhartMD, SokoloskiKJ, OkoL, et al. (2012) Dephosphorylating of HuR protein during alphavirus infection is associated with HuR relocalization to the cytoplasm. J Biol Chem 287: 36229–36238.
19. LeiY, HuangY, ZhangH, YuL, ZhangM, DaytonA (2011) Functional interaction between cellular p100 and the dengue virus 3′ UTR. J Gen Virol 92: 796–806.
20. HussainM, TorresS, SchnettlerE, FunkA, GrundhoffA, et al. (2012) West Nile virus encodes a microRNA-like small RNA in the 3′ untranslated region which up-regulates GATA4 mRNA and facilitates virus replication in mosquito cells. Nucleic Acids Res 40: 2210–2023.
21. PijlmanGP, FunkA, KondratievaN, LeungJ, TorresS, et al. (2008) A highly structured, nuclease-resistant, noncoding RNA produced by flaviviruses is required for pathogenicity. Cell Host Microbe 4: 579–591.
22. SilvaPA, PereiraCF, DaleboutTJ, SpaanWJ, BredenbeekPJ (2010) An RNA pseudoknot is required for production of yellow fever virus subgenomic RNA by the host nuclease XRN1. J Virol 84: 11395–11406.
23. FunkA, TruongK, NagasakiT, TorresS, FlodenN, et al. (2010) RNA structures required for production of subgenomic flavivirus RNA. J Virol 84: 11407–11417.
24. FanYH, NadarM, ChenCC, WengCC, LinYT, et al. (2011) Small noncoding RNA modulates Japanese encephalitis virus replication and translation in trans. Virol J 8: 492.
25. MoonSL, AndersonJR, KumagaiY, WiluszCJ, AkiraS, et al. (2012) A noncoding RNA produced by arthropod-borne flaviviruses inhibits the cellular exoribonuclease XRN1 and alters host mRNA stability. RNA 18: 2029–2040.
26. SchuesslerA, FunkA, LazearHM, CooperDA, TorresS, et al. (2012) West Nile virus noncoding subgenomic RNA contributes to viral evasion of the type I interferon-mediated antiviral response. J Virol 86: 5708–5718.
27. SchnettlerE, SterkenMG, LeungJY, MetzSW, GeertsemaC, et al. (2012) Noncoding flavivirus RNA displays RNA interference suppressor activity in insect and Mammalian cells. J Virol 86: 13486–13500.
28. VolkSM, ChenR, TsetsarkinKA, AdamsAP, GarciaTI, et al. (2010) Genome-scale phylogenetic analyses of chikungunya virus reveal independent emergences of recent epidemics and various evolutionary rates. J Virol 84: 6497–6504.
29. BurtFJ, RolphMS, RulliNE, MahalingamS, HeiseMT (2012) Chikungunya: a re-emerging virus. Lancet 379: 662–671.
30. WolfeND, KilbournAM, KareshWB, RahmanHA, BosiEJ, et al. (2001) Sylvatic transmission of arboviruses among Bornean orangutans. Am J Trop Med Hyg 64: 310–316.
31. HardyRW, RiceCM (2005) Requirements at the 3′ end of the sindbis virus genome for efficient synthesis of minus-strand RNA. J Virol 79: 4630–4639.
32. ZukerM (2003) Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res 31: 3406–3415.
33. van BatenburgFHD, GultyaevAP, PleijCWA (1995) An APL-programmed Genetic Algorithm for the Prediction of RNA Secondary Structure. J Theor Biol 174: 269–280.
34. HofackerIL, FeketeM, StadlerPF (2002) Secondary Structure Prediction for Aligned RNA Sequences. J Mol Biol 319: 1059–1066.
35. BernhartSH, HofackerIL, WillS, GruberAR, StadlerPF (2008) RNAalifold: Improved consensus structure prediction for RNA alignments. BMC Bioinformatics 9: 474.
36. HapuarachchiHC, BandaraKB, SumanadasaSD, HapugodaMD, LaiYL, et al. (2010) Re-emergence of Chikungunya virus in South-east Asia: virological evidence from Sri Lanka and Singapore. J Gen Virol 91: 1067–1076.
37. ZieglerSA, LuL, da RosaAP, XiaoSY, TeshRB (2008) An animal model for studying the pathogenesis of chikungunya virus infection. Am J Trop Med Hyg 79: 133–139.
38. ProutskiV, GauntMW, GouldEA, HolmesEC (1997) Secondary structure of the 3′-untranslated region of yellow fever virus: implications for virulence, attenuation and vaccine development. J Gen Virol 78: 1543–1549.
39. BryantJE, VasconcelosPF, RijnbrandRC, MutebiJP, HiggsS, et al. (2005) Size heterogeneity in the 3′ noncoding region of South American isolates of yellow fever virus. J Virol 79: 3807–3821.
40. TroyerJM, HanleyKA, WhiteheadSS, StrickmanD, KarronRA, et al. (2001) A live attenuated recombinant dengue-4 virus vaccine candidate with restricted capacity for dissemination in mosquitoes and lack of transmission from vaccinees to mosquitoes. Am J Trop Med Hyg 65: 414–419.
41. NajeraJA (1989) Malaria and the work of WHO. Bull World Health Organ 67: 229–243.
42. BrownA (2002) Personal experiences in the malaria eradication campaign 1955–1962. J R Soc Med 95: 154–156.
43. SeveroOP (1956) Aedes agypti eradication in the Americas. WHO Chron 10: 347–354.
44. CamargoS (1967) History of Aedes aegypti eradication in the Americas. Bull Wld Hlth Org 36: 602–603.
45. EckertKA, HileSE (2009) Every microsatellite is different: Intrinsic DNA features dictate mutagenesis of common microsatellites present in the human genome. Mol Carcinog 48: 379–388.
46. GritsunTS, GouldEA (2007) Origin and evolution of flavivirus 5′UTRs and panhandles: trans-terminal duplications? Virology 366: 8–15.
47. KhromykhAA, MekaH, GuyattKJ, WestawayEG (2001) Essential role of cyclization sequences in flavivirus RNA replication. J Virol 75: 6719–28.
48. BredenbeekPJ, KooiEA, LindenbachB, HuijkmanN, RiceCM, et al. (2003) A stable full-length yellow fever virus cDNA clone and the role of conserved RNA elements in flavivirus replication. J Gen Virol 84: 1261–1268.
49. GritsunTS, GouldEA (2006) The 3′ untranslated regions of Kamiti River virus and Cell fusing agent virus originated by self-duplication. J Gen Virol 87: 2615–2619.
50. NasarF, PalaciosG, GorchakovRV, GuzmanH, Da RosaAP, et al. (2012) Eilat virus, a unique alphavirus with host range restricted to insects by RNA replication. Proc Natl Acad Sci U S A 109: 14622–14627.
51. WestonJ, VilloingS, BrémontM, CastricJ, PfefferM, et al. (2002) Comparison of two aquatic alphaviruses, salmon pancreas disease virus and sleeping disease virus, by using genome sequence analysis, monoclonal reactivity, and cross-infection. J Virol 76: 6155–6163.
52. KarlsenM, VilloingS, RimstadE, NylundA (2009) Characterization of untranslated regions of the salmonid alphavirus 3 (SAV3) genome and construction of a SAV3 based replicon. Virol J 6: 173.
53. ProutskiV, GritsunTS, GouldEA, HolmesEC (1999) Biological consequences of deletions within the 3′-untranslated region of flaviviruses may be due to rearrangements of RNA secondary structure. Virus Res 64: 107–123.
54. SullivanCS, GrundhoffA (2007) Identification of viral miRNAs. Meth Enzymol 427: 3–23.
55. BlairCD (2011) Mosquito RNAi is the major innate immune pathway controlling arbovirus infection and transmission. Future Microbiol 6: 265–277.
56. TsetsarkinKA, ChenR, LealG, ForresterN, HiggsS, et al. (2011) Chikungunya virus emergence is constrained in Asia by lineage-specific adaptive landscapes. Proc Natl Acad Sci U S A 108: 7872–7877.
57. Swofford DL. (2003) PAUP*. Phylogenetic analysis using parsimony (*and other methods). Version 4. Sunderland (MA): Sinauer Associates.
58. PosadaD, CrandallKA (1998) Modeltest: testing the model of DNA substitution. Bioinformatics 14: 817–818.
59. KatohK, AsimenosG, TohH (2009) Multiple Alignment of DNA Sequences with MAFFT. Methods Mol Biol 537: 39–64.
60. ByunY, HanK (2009) PseudoViewer3: generating planar drawings of large-scale RNA structures with pseudoknots,. Bioinformatics 25: 1435–1437.
61. TsetsarkinK, HiggsS, McGeeCE, De LamballerieX, CharrelRN, et al. (2006) Infectious clones of Chikungunya virus (La Réunion isolate) for vector competence studies. Vector Borne Zoonotic Dis 6: 325–337.
Štítky
Hygiena a epidemiológia Infekčné lekárstvo LaboratóriumČlánok vyšiel v časopise
PLOS Pathogens
2013 Číslo 8
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Parazitičtí červi v terapii Crohnovy choroby a dalších zánětlivých autoimunitních onemocnění
- Koronavirus hýbe světem: Víte jak se chránit a jak postupovat v případě podezření?
Najčítanejšie v tomto čísle
- Host Immune Response to Intestinal Amebiasis
- Bed Bugs and Infectious Disease: A Case for the Arboviruses
- Discovery of Anthelmintic Drug Targets and Drugs Using Chokepoints in Nematode Metabolic Pathways
- Relevance of Trehalose in Pathogenicity: Some General Rules, Yet Many Exceptions