Discriminable roles of Aedes aegypti and Aedes albopictus in establishment of dengue outbreaks in Taiwan

Acta Tropica

Volumn 130, Issue 1, 2014, Pages 17-23

  Yang, Chao Fu ^a   Hou, Jion Nun ^a   Chen, Tien Huang ^a,c   Chen, Wei June ^a,b  

^a CHANG GUNG UNIVERSITY   (Taiwan)

^b CHANG GUNG UNIVERSITY COLLEGE OF MEDICINE   (Taiwan)

^c Centers for Disease Control   (Taiwan)

Author keywords

Aedes; Dengue outbreaks; Mosquito vectors; Taiwan

Indexed keywords

DENGUE FEVER; DISEASE CONTROL; DISEASE PREVALENCE; IMMUNITY; MOSQUITO;

AEDES AEGYPTI; AEDES ALBOPICTUS; BREEDING; DENGUE; DENGUE VIRUS; DISEASE CARRIER; DISEASE PREDISPOSITION; DISEASE TRANSMISSION; EPIDEMIC; GEOGRAPHIC DISTRIBUTION; HUMAN; MOSQUITO BITE; NONHUMAN; REVIEW; RISK FACTOR; SPECIES DIFFERENTIATION; SPECIES DISTRIBUTION; TAIWAN; TRAVEL; AEDES; ANIMAL; TRANSMISSION;

TAIWAN;

AEDES AEGYPTI; AEDES ALBOPICTUS;

AEDES; ANIMALS; DENGUE; DENGUE VIRUS; DISEASE OUTBREAKS; HUMANS; INSECT VECTORS; TAIWAN;

EID: 84887286152     PISSN: 0001706X     EISSN: 18736254     Source Type: Journal    
DOI: 10.1016/j.actatropica.2013.10.013     Document Type: Review

References (77)

1. Armstrong C. Dengue fever. Pub. Health Rep. 1923, 38:1750-1784.
2. Barrera R., Delgado N., Jiménez M., Valero S. Eco-epidemiological factors associated with hyperendemic dengue haemorrhagic fever in Maracay City, Venezuela. Dengue Bull. 2002, 26:84-95.
3. Brady O.J., Gething P.W., Bhatt S., Messina J.P., Brownstein J.S., Hoen A.G., et al. Refining the global spatial limits of dengue virus transmission by evidence-based consensus. PLoS Negl. Trop. Dis. 2012, 6:e1760.
4. Calderón-Arguedas O., Troyo A., Solano M.E., Avendaño A., Beier J.C. Urban mosquito species (Diptera: Culicidae) of dengue endemic communities in the Greater Puntarenas area, Costa Rica. Rev. Biol. Trop. 2009, 57:1223-1234.
5. Calisher C.H., Karabatsos N., Dalrymple J.M., Shope R.E., Porterfield J.S., Westaway E.G., et al. Antigenic relationships between flaviviruses as determined by cross-neutralization tests with polyclonal antisera. J. Gen. Virol. 1989, 70:37-43.
6. Caminade C., Medlock J.M., Ducheyne E., McIntyre K.M., Leach E., Baylis M., et al. Suitability of European climate for the Asian tiger mosquito Aedes albopictus: recent trends and future scenarios. J. R. Soc. Interface 2012, 9:2708-2717.
7. Canyon D.V., Hii J.L.K., Muller R. The frequency of host biting and its effect on oviposition and survival in Aedes aegypti (Diptera: Culicida). Bull. Entomol. Res. 1999, 89:35-39.
8. Center for Disease Control, Taiwan Response to the Dengue Fever Epidemic in Taipei 2008, Available online: http://www.doh.gov.tw/CHT2006/DM/DM2_p01.aspx?class_no=25&now_fod_list_no=9009&level_no=2&doc_no=68797.
9. Chang L.H., Hsu E.L., Teng H.J., Ho C.M. Aedes albopictus (Diptera: Culicidae) larvae exposed to low temperatures in Taiwan. J. Med. Entomol. 2007, 44:205-210.
10. Chaudhry S., Swaminathan S., Khanna N. Viral genetics as a basis of dengue pathogenesis. Dengue Bull. 2006, 30:121-132.
11. Chen C.F., Shu P.Y., Teng H.J., Su C.L., Wu J.W., Wang J.H., et al. Screening of dengue virus in field-caught Aedes aegypti and Aedes albopictus (Diptera: Culicidae) by one-step SYBR green-based reverse transcriptase-polymerase chain reaction assay during 2004-2007 in southern Taiwan. Vector Borne Zoonotic Dis. 2010, 10:1017-1025.
12. Chen W.J., Chen S.L., Chien L.J., Chen C.C., King C.C., Harn M.R., et al. Silent transmission of the dengue virus in southern Taiwan. Am. J. Trop. Med. Hyg. 1996, 55:12-16.
13. Chen W.J., Wu H.R., Chiou S.S. E/NS1 modifications of dengue 2 virus after serial passages in mammalian and/or mosquito cells. Intervirology 2003, 46:289-295.
14. Chen W.J., Hwang K.P., Fang A.H. Detection of IgM antibodies from cerebrospinal fluid and sera of dengue fever patients. Southeast Asian J. Trop. Med. Pub. Health 1991, 22:659-663.
15. Chen W.J., Wei H.L., Hsu E.L., Chen E.R. Vector competence of Aedes albopictus and Ae. aegypti (Diptera: Culicidae) to dengue 1 virus in Taiwan: development of the virus in the orally and parenterally infected mosquitoes. J. Med. Entomol. 1993, 30:524-530.
16. Chow V.T.K., Chan Y.C., Yong R., Lee K.M., Lim L.K., Chung Y.K., et al. Monitoring of dengue viruses in field-caught Aedes aegypti and Aedes albopictus mosquitoes by a type-specific polymerase chain reaction and cycle sequencing. Am. J. Trop. Med. Hyg. 1998, 58:578-586.
17. Chung Y.K., Pang F.Y. Dengue virus infection rate in field populations of female Aedes aegypti and Aedes albopictus in Singapore. Trop. Med. Int. Health 2002, 7:322-330.
18. Cummings D.A.T., Iamsirithaworn S., Lessler J.T., McDermott A., Prasanthong R., Nisalak A., et al. The impact of the demographic transition on dengue in Thailand: insights from a statistical analysis and mathematical modeling. PLoS Med. 2009, 6:e1000139.
19. Day J.F. Host-seeking strategies of mosquito disease vectors. J. Am. Mosq. Control Assoc. 2005, 21(Suppl. 4):17-22.
20. Delatte H., Desvars A., Bouétard A., Bord S., Gimonneau G., Vourc'h G., et al. Blood-feeding behavior of Aedes albopictus, a vector of Chikungunya on La Réunion. Vector Borne Zoonotic Dis. 2010, 10:249-258.
21. Eigen M. On the nature of virus quasispecies. Trends Microbiol. 1996, 4:216-217.
22. Endy T.P., Anderson K.B., Nisalak A., Yoon I.K., Green S., Rothman A.L., et al. Determinants of inapparent and symptomatic dengue infection in a prospective study of primary school children in Kamphaeng Phet, Thailand. PLoS Negl. Trop. Dis. 2011, 5:e975.
23. European Centre for Disease Prevention and Control Development of Aedes albopictus Risk Maps. Stockholm 2009, Available online: http://ecdc.europa.eu/.
24. Goh K.T., Ng S.K., Chan Y.C., Lim S.J., Chua E.C. Epidemiological aspects of an outbreak of dengue fever/dengue haemorrhagic fever in Singapore. Southeast Asian J. Trop. Med. Pub. Health 1987, 18:291-294.
25. Gubler D.J. Epidemic dengue/dengue hemorrhagic fever as a public health, social and economic problem in the 21st century. Trends Microbiol. 2002, 10:100-103.
26. Gubler D.J. The global emergence/resurgence of arboviral diseases as public health problems. Arch. Med. Res. 2002, 33:330-342.
27. Gubler D.J. Aedes albopictus in Africa. Lancet Infect. Dis. 2003, 3:751-752.
28. Guerdan B.R. Dengue fever/dengue hemorrhagic fever. Am. J. Clin. Med. 2010, 7:51-53.
29. Gratz N.G. Critical review of the vector status of Aedes albopictus. Med. Vet. Entomol. 2004, 18:215-227.
30. Halstead S.B. Pathogenesis of dengue: challenges to molecular biology. Science 1988, 239:476-481.
31. Hawley A.H. The biology of Aedes albopictus. J. Am. Mosq. Control Assoc. 1988, 4:2e39.
32. Herrera-Martinez A.D., Rodríguez-Morales A.J. Potential influence of climate variability on dengue incidence registered in a western pediatric hospital of Venezuela. Trop. Biomed. 2010, 27:280-286.
33. Holland J.J. Visualizing virus fitness gains. Nat. Biotechnol. 1996, 14:431-432.
34. Holmes E.C. The phylogeography of human viruses. Mol. Ecol. 2004, 13:745-756.
35. Hwang J.S., Hsu E.L., Chen Y.R. Investigations on the density and breeding habitats of Aedes mosquitoes in dengue epidemic areas in Taiwan. Chin. J. Pub. Health (Taiwan) 1995, 14:228-236.
36. Jelinek T. Dengue fever in international travelers. Clin. Infect. Dis. 2000, 31:144-147.
37. Kalra N.L., Kaul S.M., Rastogi R.M. Prevalence of Aedes aegypti and Aedes albopictus - vectors of dengue and dengue haemorrhagic fever in north, north-east and central India. Dengue Bull. 1997, 21:84-92.
38. Ko Y.C. Epidemiology of dengue fever in Taiwan. Kaohsiung J. Med. Sci. 1989, 5:1-11.
39. Kong Y.Y., Thay C.H., Tin T.C., Devi S. Rapid detection, serotyping and quantitation of dengue viruses by TaqMan real-time one-step RT-PCR. J. Virol. Methods 2006, 138:123-130.
40. Lambrechts L., Scott T.W., Gubler D.J. Consequences of the expanding global distribution of Aedes albopictus for dengue virus transmission. PLoS Negl. Trop. Dis. 2010, 4:e646.
41. Lin T.H. Surveillance and control of Aedes aegypti in epidemic areas of Taiwan. Kaohsiung J. Med. Sci. 1994, 10:88-93.
42. Lu P., Bian G., Pan X., Xi Z. Wolbachia induces density-dependent inhibition to dengue virus in mosquito cells. PLoS Negl. Trop. Dis. 2012, 6:e1754.
43. Moreira L.A., Iturbe-Ormaetxe I., Jeffery J.A., Lu G., Pyke A.T., Hedges L.M., et al. A Wolbachia symbiont in Aedes aegypti limits infection with dengue, Chikungunya, and Plasmodium. Cell 2009, 139:1268-1278.
44. Mousson L., Zouache K., Arias-Goeta C., Raquin V., Mavingui P., Failloux A.B. The native Wolbachia symbionts limit transmission of dengue virus in Aedes albopictus. PLoS Negl. Trop. Dis. 2012, 6:e1989.
45. Muñoz J., Ruiz S., Soriguer R., Alcaide M., Viana D.S., Roiz D., et al. Feeding patterns of potential West Nile virus vectors in south-west Spain. PLoS ONE 2012, 7:e39549.
46. Nelson M.J. Aedes aegypti: Biology and Ecology 1986, Pan American Health Organization, Washington, DC.
47. Nishiura H. Duration of short-lived cross-protective immunity against a clinical attack of dengue: a preliminary estimate. Dengue Bull. 2008, 32:55-66.
48. Noisakran S., Perng G.C. Alternate hypothesis on the pathogenesis of dengue hemorrhagic fever (DHF)/dengue shock syndrome (DSS) in dengue virus infection. Exp. Biol. Med. (Maywood) 2008, 233:401-408.
49. Ocazionez R.E., Cortes F.M., Villar L.A., Gomez S.Y. Temporal distribution of dengue virus serotypes in Colombian endemic area and dengue incidence: re-introduction of dengue-3 associated to mild febrile illness and primary infection. Mem. Inst. Oswaldo Cruz 2006, 101:725-731.
50. Padmanabha H., Durham D., Correa F., Diuk-Wasser M., Galvani A. The interactive roles of Aedes aegypti super-production and human density in dengue transmission. PLoS Negl. Trop. Dis. 2012, 6:e1799.
51. Paupy C., Ollomo B., Kamgang B., Moutailler S., Rousset D., Demanou M., et al. Comparative role of Aedes albopictus and Aedes aegypti in the emergence of dengue and Chikungunya in Central Africa. Vector Borne Zoonotic Dis. 2010, 10:259-266.
52. Peng H.J., Lai H.B., Zhang Q.L., Xu B.Y., Zhang H., Liu W.H., et al. A local outbreak of dengue caused by an imported case in Dongguan China. BMC Pub. Health 2012, 12:83.
53. Ponlawat A., Harrington L.C. Blood feeding patterns of Aedes aegypti and Aedes albopictus in Thailand. J. Med. Entomol. 2005, 42:844-849.
54. Powers C. Dengue, or break-bone fever. Boston Med. Surg. J. 1860, 62:368-371.
55. Richards S.L., Ponnusamy L., Unnasch T.R., Hassan H.K., Appperson C.S. Host-feeding patterns of Aedes albopictus (Diptera: Culicidae) in relation to availability of human and domestic animals in suburban landscapes. J. Med. Entomol. 2006, 43:542-551.
56. Rigau-Pérez J.G., Clark G.G., Gubler D.J., Reiter P., Sanders E.J., Vorndam A.V. Dengue and dengue haemorrhagic fever. Lancet 1998, 352:971-977.
57. Rosen L. The Pathogenesis of dengue haemorrhagic fever: a critical appraisal of current hypotheses. South Afr. Med. J. 1986, 70:40-42.
58. Rudnick A., Marchette N.J., Garcia R. Possible jungle dengue - recent studies and hypotheses. Jpn. J. Med. Sci. Biol. 1967, 20:69-74.
59. Salazar M.I., Richardson J.H., Sánchez-Vargas I., Olson K.E., Beaty B.J. Dengue virus type 2: replication and tropisms in orally infected Aedes aegypti mosquitoes. BMC Microbiol. 2007, 7:9.
60. Sam S.S., Omar S.F., Teoh B.T., Abd-Jamil J., AbuBakar S. Review of dengue hemorrhagic fever fatal cases seen among adults: a retrospective study. PLoS Negl. Trop. Dis. 2013, 7:e2194.
61. Schmidt W.P., Suzuki M., Thiem V.D., White R.G., Tsuzuki A., Yoshida L.M., et al. Population density, waters, and the risk of dengue fever in Vietnam: cohort study and spatial analysis. PLoS Med. 2011, 8:e1001082.
62. Scott T.W., Clark G.G., Lorenz L.H., Amerasinghe P.H., Reiter P., Edman J.D. Detection of multiple blood feeding in Aedes aegypti (Diptera: Culicidae) during a single gonotrophic cycle using a histologic technique. J. Med. Entomol. 1993, 30:94-99.
63. Scott T.W., Chow E., Strockman D., Kittayapong P., Wirtz R.A., Lorenz L.H., et al. Blood-feeding patterns of Aedes aegypti (Diptera: Culicidae) collected in a rural Thai village. J. Med. Entomol. 1993, 30:922-927.
64. Simmons C.P., Farrar J.J., Chau N.v.V.Wills B. Current concept: dengue. N. Engl. J. Med. 2012, 366:1423-1432.
65. Solomon T., Dung N.M., Vaughn D.W., Kneen R., Thao L.T., Raengsakulrach B., et al. Neurological manifestations of dengue infection. Lancet 2000, 355:1053-1059.
66. Tabachnick W.J. Evolutionary genetics and arthropod-borne disease: the yellow fever mosquito. Am. Entomol. 1991, 37:14-26.
67. Teng H.J., Wu Y.L., Lin T.H. Mosquito fauna in water-holding containers with emphasis on dengue vectors (Diptera: Culicidae) in Chungho, Taipei County, Taiwan. J. Med. Entomol. 1999, 36:468-472.
68. Teoh B.T., Sam S.S., Abd-Jamil J., AbuBakar S. Isolation of ancestral sylvatic dengue virus type 1, Malaysia. Emerg. Infect. Dis. 2010, 16:1783-1785.
69. Thavara U., Tawatsin A., Chansang C. Larval occurrence, oviposition behavior and biting activity of potential mosquito vectors of dengue on Samui Island, Thailand. J. Vector Ecol. 2001, 26:172-180.
70. Tsai K.H., Huang C.G., Lien J.C., Wu W.J., Chen W.J. Molecular (sub-)grouping of the endosymbiont Wolbachia infection among mosquitoes of Taiwan. J. Med. Entomol. 2004, 41:677-683.
71. Varatharaj A. Encephalitis in the clinical spectrum of dengue infection. Neurol. India 2010, 58:585-591.
72. Vazeille M., Rosen L., Mousson L., Failloux A.B. Low oral receptivity for dengue type 2 viruses of Aedes albopictus from Southeast Asia compared with that of Aedes aegypti. Am. J. Trop. Med. Hyg. 2003, 68:203-208.
73. Vezzani D., Carbajo A.E. Aedes aegypti, Aedes albopictus, and dengue in Argentina: current knowledge and future directions. Mem. Inst. Oswaldo Cruz 2008, 103:66-74.
74. WHO Dengue Guidelines for Diagnosis, Treatment, Prevention and Control-new Edition 2009, 147. World Health Organization, Geneva.
75. Wu H.H., Wang C.Y., Teng H.J., Lin C., Lu L.C., Jian S.W., et al. A dengue vector surveillance by human population-stratified ovitrap survey for Aedes (Diptera: Culicidae) adult and egg collections in high dengue-risk areas of Taiwan. J. Med. Entomol. 2013, 50:261-269.
76. Xue R.D., Edman J.D., Scott T.W. Age and body size effects on blood meal size and multiple blood feeding by Aedes aegypti (Diptera: Culicidae). J. Med. Entomol. 1995, 32:471-474.
77. Xue R.D., Barnard D.R., Ali A. Influence of multiple blood meals on gonotrophic dissociation and fecundity in Aedes Albopictus. J. Am. Mosq. Control Assoc. 2009, 25:504-507.