Abstract
Arboviruses do not represent a based-related phylogenetic group, but they are all transmitted by arthropods. Fifty arboviruses pathogenic for animals (including humans) have been reported, belonging to the families Asfarviridae, Bunyaviridae, Flaviviridae, Orthomyxoviridae, Rhabdoviridae, Reoviridae, and Togaviridae. A wide variety of hematophagous arthropods transmits the arboviruses: biting midges, cimicid bugs, mosquitoes, sand flies, and ticks. The vector acquires the infection by blood feeding from a viremic host and transmits the virus to a new host by the oral route (inoculating infected saliva). However, vertical transmission routes already exist (transovarial, venereal). Arbovirus can be amplified by a diverse range of vertebrate hosts including birds, rodents, equines, humans, and monkeys. Through biological evolution and cultural development, human beings were able to modify the environments according to their needs. Thus, deforestation has produced new areas for agriculture, livestock, farming activities, and urbanization. These anthropogenic activities have produced great changes to host and vector communities and population abundance, sometimes driving emergence and reemergence of arboviruses. In this chapter, we give a general view for most important aspects of arboviruses, their classification, transmission and maintenance mechanisms, ecology, and emergence process.
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Allan B, Langerhans R, Ryberg W et al (2009) Ecological correlates of risk and incidence of West Nile virus in the United States. Oecologia 158:699–708
Antonis AF, Kortekaas J, Kant J et al (2013) Vertical transmission of Rift Valley fever virus without detectable maternal viremia. Vector Borne Zoonotic Dis 13:601–606
Barrett AD, Monath TP (2003) Epidemiology and ecology of yellow fever virus. Adv Virus Res 61:291–315
Brown CR, Strickler SA, Moore AT et al (2010) Winter ecology of Buggy Creek virus (Togaviridae, Alphavirus) in the Central Great Plains. Vector Borne Zoonotic Dis 10:355–363
Chancey C, Grinev A, Volkova E et al (2015) The global ecology and epidemiology of West Nile virus. Biomed Res Int 2015:376230
Coffey LL, Forrester N, Tsetsarkin K et al (2013) Factors shaping the adaptive landscape for arboviruses: implications for the emergence of disease. Future Microbiol 8:155–176
Daubney R, Hudson J, Garnham P (1931) Enzootic hepatitis or Rift Valley fever: an undescribed virus disease of sheep, cattle and man from East Africa. J Pathol Bacteriol 34:545–579
Díaz LA, Albrieu Llinás G, Vázquez A et al (2012) Silent circulation of St. Louis encephalitis virus prior to an encephalitis outbreak in Cordoba, Argentina (2005). PLoS Negl Trop Dis 6, e1489
Diaz LA, Flores FS, Quaglia A et al (2013) Intertwined arbovirus transmission activity: reassessing the transmission cycle paradigm. Front Physiol 3:493
Diaz LA, Nemeth NM, Bowen RA et al (2011) Comparison of Argentinean Saint Louis encephalitis virus non-epidemic and epidemic strain infections in an avian model. PLoS Negl Trop Dis 5, e1177
EFSA (2011) Panel on Animal Health and Welfare (AHAW); Scientific Opinion on bluetongue serotype 8. EFSA J 9(5):2189 [51 pp]. doi:10.2903/j.efsa.2011.2189, Available online: www.efsa.europa.eu/efsajournal.htm
Ezenwa V, Godsey M, King R et al (2006) Avian diversity and West Nile virus: testing associations between biodiversity and infectious disease risk. Proc Biol Sci 273:109–117
Ezenwa V, Milheim L, Coffey M et al (2007) Land cover variation and West Nile virus prevalence: patterns, processes, and implications for disease control. Vector Borne Zoonotic Dis 7:173–180
Hassan HK, Cupp EW, Hill GE et al (2003) Avian host preference by vectors of eastern equine encephalomyelitis virus. Am J Trop Med Hyg 69:641–647Higgs S and Beaty BJ (2005) Natural cycles of Vector-borne pathogens. In “Biology of Diseases Vectors”. Marquardt WC (ed). Elsevier, San Diego, CA, p. 167-185
Hubálek Z, Rudolf I, Nowotny N (2014) Arboviruses pathogenic for domestic and wild animals. Adv Virus Res 89:201–275
Hughes MT, Gonzalez JA, Reagan KL et al (2006) Comparative potential of Aedes triseriatus, Aedes albopictus, and Aedes aegypti (Diptera: Culicidae) to transovarially transmit La Crosse virus. J Med Entomol 43:757–761
Iranaia AM, Cruz-Oliveira C, DaPoian AT (2013) Molecular mechanisms involved in the pathogenesis of alphavirus-induced arthritis. Biomed Res Int 2013:973516
Karabatsos N (1985) International catalogue of arboviruses including certain other viruses of vertebrates. American Society Tropical Medicine and Hygiene, San Antonio, TX
Kenney JL, Brault AC (2014) The role of environmental, virological and vector interactions in dictating biological transmission of arthropod-borne viruses by mosquitoes. Adv Virus 89:39–83
Kilpatrick A (2011) Globalization, land use and invasion of West Nile virus. Science 334:323–327
Komar N, Dohm DJ, Turell MJ et al (1999) Eastern equine encephalitis virus in birds: relative competence of European starlings (Sturnus vulgaris). Am J Trop Med Hyg 60:387–391
Komar N, Langevin S, Hinten S et al (2003) Experimental infection of North American birds with the New York 1999 strain of West Nile virus. Emerg Infect Dis 9:311–322
Kramer LD, Ebel GD (2003) Dynamics of flavivirus infection in mosquitoes. Adv Virus Res 60:187–232
Kuno G (1995) Review of the factors modulating dengue transmission. Epidemiol Rev 17:321–335
Kuno G, Chang G (2005) Biological transmission of arboviruses: reexamination of and new insights into components, mechanisms, and unique traits as well as their evolutionary trends. Clin Microbiol Rev 18:608–637
Labuda M, Nuttall PA (2004) Tick-borne viruses. Parasitology 129(Suppl):S221–S245
Lazear HM, Diamond MS (2014) New insights into innate immune restriction of West Nile virus infection. Curr Opin Virol 11:1–6
Le Flohic G, Porphyre V, Barbazan P et al (2013) Review of climate, landscape, and viral genetics as drivers of the Japanese encephalitis virus ecology. PLoS Negl Trop Dis 7, e2208
Lequime S, Lambrechts L (2014) Vertical transmission of arboviruses in mosquitoes: a historical perspective. Infect Genet Evol 28:681–690
Loss S, Hamer G, Walker E et al (2009) Avian host community structure and prevalence of West Nile virus in Chicago, Illinois. Oecologia 159:415–424
Maclachlan NJ (2011) Bluetongue: history, global epidemiology, and pathogenesis. Prev Vet Med 102:107–111
McKenzie V, Goulet N (2010) Bird community composition linked to human West Nile virus cases along the Colorado front range. Ecohealth 7:439–447
McLean RG, Bowen GS (1980) Vertebrate hosts. In: Monath TP (ed) St Louis encephalitis. American Publich Health Association, Washington, DC, pp 381–450
McLean RG, Ubico SR, Docherty DE et al (2001) West Nile virus transmission and ecology in birds. Ann N Y Acad Sci 951:54–57
Morris CD (1988) Eastern equine encephalomyelitis. In: Monath TP (ed) The arboviruses: epidemiology and ecology, vol 3. CRC Press, Boca Raton, FL, pp 1–20
Muñoz M, Navarro JC (2012) Mayaro: a re-emerging Arbovirus in Venezuela and Latin America. Biomedica 32:286–302
Oncü S (2013) Crimean-Congo hemorrhagic fever: an overview. Virol Sin 28:193–201
Reeves WC (2001) Partners: serendipity in arbovirus research. J Vector Ecol 26:1–6
Reinert JF (2009) List of abbreviations for currently valid generic-level taxa in family Culicidae (Diptera). Eur Mosq Bull 27:68–76
Reisen WK, Barker CM, Carney R et al (2006) Role of corvids in epidemiology of west Nile virus in southern California. J Med Entomol 43:356–367
Reisen WK, Chiles RE, Martinez VM et al (2003) Experimental infection of California birds with western equine encephalomyelitis and St. Louis encephalitis viruses. J Med Entomol 40:968–982
Reisen WK, Monath TP (1989) Western equine encephalomyelitis. In: Monath TP (ed) The arboviruses: epidemiology and ecology, vol 3. CRC Press, Boca Raton, FL, pp 89–137
Schmid MA, Diamond MS, Harris E (2014) Dendritic cells in dengue virus infection: targets of virus replication and mediators of immunity. Front Immunol 5:647
Scott TW (1988) Vertebrate host ecology. In: Monath TP (ed) The arboviruses: epidemiology and ecology, vol 3. CRC Press, Boca Raton FL, pp 257–280
Solomon T, Mallewa M (2001) Dengue and other emerging flaviviruses. J Infect 42:104–115
Suen WW, Prow NA, Hall RA et al (2014) Mechanism of West Nile virus neuroinvasion: a critical appraisal. Viruses 6:2796–2825
Swaddle JP, Calos SE (2008) Increased avian diversity is associated with lower incidence of human West Nile infection: observation of the dilution effect. PLoS One 3, e2488. doi:10.1371/journal.pone.0002488
Tatem AJ, Hay SI, Rogers DJ (2006) Global traffic and disease vector dispersal. Proc Natl Acad Sci U S A 103:6242–6247
Tsetsarkin KA, Vanlandingham DL, McGee CE, Higgs S (2007) A single mutation in chikungunya virus affects vector specificity and epidemic potential. PLoS Pathog 3(12), e201
Turtle L, Griffiths MJ, Solomon T (2012) Encephalitis caused by flaviviruses. QJM 105:219–223
Vasconcelos P, Travassos da Rosa A, Rodrigues S et al (2001) Inadequate management of natural ecosystem in the Brazilian Amazon region results in the emergence and reemergence of arboviruses. Cad Saude Publica 17:155–164
Weaver SC, Anishchenko M, Bowen R et al (2004a) Genetic determinants of Venezuelan equine encephalitis emergence. Arch Virol Suppl 18:43–64
Weaver SC, Barrett AD (2004) Transmission cycles, host range, evolution and emergence of arboviral disease. Nat Rev Microbiol 2:789–801
Weaver SC, Ferro C, Barrera R et al (2004b) Venezuelan equine encephalitis. Ann Rev Entomol 49:141–174
Weaver SC, Forrester NL (2015) Chikungunya: evolutionary history and recent epidemic spread. Antiviral Res 120:32–39
Weaver SC, Reisen WK (2010) Present and future arboviral threats. Antiviral Res 85:328–345
Wernike K, Conraths F, Zanella G et al (2014) Schmallenberg virus-two years of experiences. Prev Vet Med 116:423–434
White DM, Wilson WC, Blair CD et al (2005) Studies on overwintering of bluetongue viruses in insects. J Gen Virol 86(Pt 2):453–462
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Contigiani, M.S., Diaz, L.A., Spinsanti, L.I. (2017). General Aspects on Arboviruses. In: Marcondes, C. (eds) Arthropod Borne Diseases. Springer, Cham. https://doi.org/10.1007/978-3-319-13884-8_5
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