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DC 欄位 | 值 | 語言 |
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dc.contributor.advisor | 薛馬坦(Matan Shelomi) | |
dc.contributor.author | Hsueh-Lien Lai | en |
dc.contributor.author | 賴學濂 | zh_TW |
dc.date.accessioned | 2021-05-20T00:54:37Z | - |
dc.date.available | 2020-07-23 | |
dc.date.available | 2021-05-20T00:54:37Z | - |
dc.date.copyright | 2020-07-23 | |
dc.date.issued | 2020 | |
dc.date.submitted | 2020-07-16 | |
dc.identifier.citation | 1. Allan SA, Kline DL. 1998. Larval rearing water and preexisting eggs influence oviposition by Aedes aegypti and Ae. albopictus (Diptera: Culicidae). Journal of Medical Entomology 35(6): 943-947.
2. Barbosa RMR, Regis L, Vasconcelos R, Leal WS. 2010. Culex mosquitoes (Diptera: Culicidae) egg laying in traps loaded with Bacillus thuringiensis variety israelensis and baited with skatole. Journal of Medical Entomology 47(3): 345-348. 3. Beegle CC, Yamamoto T. 1992. Invitation paper (C.P. Alexander fund): history of Bacillus thuringiensis Berliner research and development. The Canadian Entomologist 124(4): 587-616. 4. Bell MR, McLaughlin RE. 1970. Influence of the protozoan Mattesia grandis McLaughlin on the toxicity to the boll weevil of four insecticides. Journal of Economic Entomology 63(1): 266-269. 5. Benzon GL, Apperson CS. 1988. Reexamination of chemically mediated oviposition behavior in Aedes aegypti (L.) (Diptera: Culicidae). Journal of Medical Entomology 25(3): 158-164. 6. Blanford S. Chan BHK, Jenkins N, Sim D, Turner RJ, Read AF, Thomas MB. 2005. Fungal pathogen reduces potential for malaria transmission. Science 308(5728): 1638-1641. 7. Blaustein L, Kotler BP. 1993. Oviposition habitat selection by the mosquito, Culiseta longiareolata: effects of conspecifics, food and green toad tadpoles. Ecological Entomology 18(2): 104-108. 8. Cabrera JG, Molla O, Monton H, Urbaneja A. 2011. Efficacy of Bacillus thuringiensis (Berliner) in controling the tomato borer, Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae). BioControl 56: 71-80. 9. Canyon DV, Hii JLK, Muller R. 1999. Adaptation of Aedes aegypti (Diptera: Culicidae) oviposition behavior in response of humidity and diet. Journal of Insect Physiology 45(10): 959-964. 10. Carrieri M, Masetti A, Albieri A, Maccaganai B, Bellini R. 2009. Larvicidal activity and influence of Bacillus thuringiensis var. israelensis on Aedes albopictus oviposition in ovitraps during a two-week check interval protocol. Journal of the American Mosquito Control Association 25(2): 149-155. 11. Chen WJ, Hsieh FC, Hsu FC, Tasy YF, Liu JR, Shih MC. 2014. Characterization of an insecticidal toxin and Pathogenicity of Pseudomonas taiwanensis against insects. PLoS Pathogens 10(8): e1004288. 12. Chung YK, Phua SGL, Chua YT, Yatiman R. 2001. Evaluation of biological and chemical insecticides mixture against Aedes aegypti larvae and adults by thermal fogging in Singapore. Medical and Veterinary Entomology 15(3): 321-327. 13. Coon KL, Vogel KJ, Brown MR, Strand AR. 2014. Mosquitoes rely on their gut microbiota for development. Molecular Ecology. 23(11): 2727-2739. 14. Davidson EW, Urbina M, Payne J, Mulla MS, Darwazeh H, Dulmage HT, Correa JA. 1984. Fate of Bacillus sphaericus 1593 and 2362 spores used as larvicides in the aquatic environment. Applied and Environmental Microbiology 47: 125-129. 15. Dom NC, Ahmad AH, Ismail R. 2013. Habitat characterization of Aedes sp. breeding in urban hotspot area. Procedia-social and Behavioral Sciences 85: 100-109. 16. Edman JD, Scott TW, Costero A, Morrison AC, Harrington LC, Clark GG. 1998. Aedes aegypti (Diptera: Culicidae) movement influenced by availability of oviposition sites. Journal of Medical Entomology 35(4): 578-583. 17. Ejiofor AO, Okafor N. 1989. Production of mosquito larvicidal Bacillus thuringiensis serotype H-14 on raw material media from Nigeria. Journal of Applied Microbiology 67: 5-9. 18. Elçin YM. 1995. Bacillus sphaericus 2362-calcium alginate microcapsules for mosquito control. Enzyme and Microbial Technology 17: 587-591. 19. Federici BA. 1995. The future of microbial insecticides as vector control agents. Journal of the American Mosquito Control Association 11(2): 260-268. 20. Fillinger U, Lindsay SW. 2006. Suppression of exposure to malaria vectors by an order of magnitude using microbial larvicides in rural Kenya. Tropical Medicine International Health 11: 1629-1642. 21. Floore TG. 2006. Mosquito larval control practices: past and present. Journal of the American Mosquito Control Association 22: 527-533. 22. Geetha I, Paily KP, Padmanaban V, Balaraman K. 2003. Oviposition response of the mosquito, Culex quinquefasciatus to the secondary metabolite(s) of the fungus, Trichoderma viride. 23. Goldberg LJ, Margalit J. 1977. A bacterial spore demonstrating rapid larvicidal activity against Anopheles sergentii, Uranotaenia unguiculata, Culex univitattus, Aedes aegypti and Culex pipiens. Mosquito News 37(3): 355-358. 24. Goldman IF, Arnold J, Carlton BC. 1986. Selection of resistance to Bacillus thuringiensis subspecies israelensis in field and laboratory populations of the mosquito Aedes aegypti. Journal of Invertebrate Pathology 47, 317-324. 25. Haddow AJ, Gillett JD. 1957. Observations on the oviposition-cycle of Aedes (Stegomyia) aegypti (Linnaeus). Annals of Tropical Medicine Parasitology 51(2): 159-169. 26. Hairi F, Ong CHS, Suhaimi A, Tsung TS, Ahmad MABA, Sundaraj C, Soe MM. 2003. A knowledge, attitude and practices (KAP) study on dengue among selected rural communities in the Kuala Kangsar District. Asia Pacific Journal of Public Health 15(1): 37-43. 27. Harrington LC, Ponlawat A, Edman JD, Scott TW, Veymeylen F. 2008. Influence of container size, location, and time of day on oviposition patterns of the dengue vector, Aedes aegypti, in Thailand. Vector-Borne and Zoonotic Diseases 8(3): 415-424. 28. Kim CH, Lampman RL, Muturi EJ. 2015. Bacterial Communities and Midgut Microbiota Associated with Mosquito Populations from Waste Tires in East-Central Illinois. Journal of Medical Entomology 52(1): 63-75. 29. Kovendan K, Murugan K, Vincent S, Kamalakannan S. 2011. Larvicidal efficacy of Jatropha curcas and bacterial insecticides, Bacillus thuringiensis, against lymphatic filarial vector, Culex quinquefasciatus Say. Parasitology Research 109: 1251-1257. 30. Kovendan K, Murugan K, Vincent S, Barnard DR. 2012. Studies on larvicidal and pupicidal activity of Leucas aspera Willd. (Lamiaceae) and bacterial insecticide, Bacillus sphaericus, against malaria vector, Anopheles stephensi Liston. (Diptera: Culicidae). Parasitology Research 110: 195-203. 31. Kulkarni GB, Sanjeevkumar S, Kirankumar B, Santoshkumar M, Karegoudar TB. 2013. Indole-3-acetic acid biosynthesis in Fusarium delphinoides strain GPK, a causal agent of wilt in chickpea. Applied Biochemistry and Biotechnology 169: 1292-1305. 32. Lacey LA, Lacey CM. 1990. The medical importance of riceland mosquitoes and their control using alternatives to chemical insecticides. Journal of American Mosquito Control Association 2: 1-93. 33. Leroux CN, Pasquier F, Charles JC, SinÈGre G, Gaven B, Pasteur N. 1997. Resistance to Bacillus sphaericus involves different mechanisms in Culex pipiens (Diptera: Culicidae) larvae. Journal of Medical Entomology 34(3): 321-327. 34. Li Y, Xu J, Zhong D, Zhang H, Yang W, Zhou G, Su X, Wu Y, Wu K, Cai S, Yan G, Chen XG. 2018. Evidence for multiple-insecticide resistance in urban Aedes albopictus populations in southern China. Parasites Vectors 11: 4. 35. Lopez DC, Salzman KZ, Ramos MJE, Sword GA. 2014. The entomopathogenic fungal endophytes Purpureocillium lilacinum (formerly Paecilomyces lilacinus) and Beauveria bassiania negatively affect cotton aphid reproduction under both greenhouse and field conditions. PLoS One 9(8): e103891. 36. Lopez DC, Sword GA. 2015. The endophytic fungal entomopathogens Beauveria bassiana and Purpureocillium lilacinum enhance the growth of cultivated cotton (Gossypium hirsutum) and negatively affect survival of the cotton bollworm (Helicoverpa zea). Biological Control 89: 53-60. 37. Majambere S, Lindsay SW, Green C, Kandeh B, Fillinger U. 2007. Microbial larvicides for malaria control in The Gambia. Malaria Journal 6: 76. McGaughey WH. 1985. Insect resistance to the biological insecticide Bacillus thuringiensis. Science 229(4709): 193-195. 38. Merritt RW, Dadd RH, Walker ED. 1992. Feedind behavior, natural food, and nutritional relationships of larval mosquitoes. Annual Reviews of Entomology 37:349-376. 39. Mulla MS, Thavara U, Tawatsin A. 2003. Emergence of resistance and resistance management in field populations of tropical Culex quinquefasciatus to the microbial control agent Bacillus sphaericus. Journal of the American Mosquito Control Association 19: 39-46. 40. Navarro DMAF, Oliveira PESD, Potting RPJ, Fital SJF. 2003. The potential attractant or repellent effects of different water types on oviposition in Aedes aegypti L. (Dipt., Culicidae). Journal of Applied Entomology 127: 46-50. 41. Nilsson LKJ, Sharma A, Bhatnagar RK, Bertillson S, Terenius O. 2018. Presence of Aedes and Anopheles mosquito larvae is correlated to bacteria found in domestic water-storage containers. FEMS Microbiology Ecology 94(6), fiy058. 42. Nishimatsu T, Jackson JJ. 1998. Interaction of insecticides, entomopathogenic nematodes, and larvae of the western corn rootworm (Coleoptera: Chrysomelidae). Journal of Economic Entomology 91(2): 410-418. 43. Nguyen AT, Newkirk AJW, Kitron UD, Chaves LF. 2014. Seasonal weater, nutrients, and conspecific presence impacts on the southern house mosquito oviposition dynamics in combined sewage overflows. Journal of Medical Entomology 49(6): 1328-1338. 44. Omolade OO, Adetutu SA. 2018. Oviposition and breeding water sites preferences of mosquitoes within Ojo Area, Lagos State, Nigeria. Biomedical Journal of Scientific and Technical Research, 7(5): 1-7. 45. Pailan S, Gupta D, Apte S, Krishnamurthi S, Saha P. 2015. Degradation of organophosphate insecticide by a novel Bacillus aryabhattai strain SanPS1, isolated from soil of argricultural field in Burdwan, West Bengal, India. International Biodeterioration Biodegradation 103: 191-195. 46. Patil CD, Patil SV, Salunke BK, Salunkhe RB. Prodigiosin produced by Serratia marcescens NMCC46 as a mosquito larvicidal agent against Aedes aegypti and Anopheles stephensi. Parasitology Research 109: 1179-1187. 47. Paula AR, Carolino AT, Paula CO, Samuels RI. 2011. The combination of the entomopathogenic fungus Metarhizium anisopliae with the insecticide Imidacloprid increases virulence against the dengue vector Aedes aegypti (Diptera: Culicidae). Parasites Vectors 4: 8. 48. Perich MJ, Kardec A, Braga IA, Portal IF, Burge R, Zeichner BC, Brogdon WA, Wirtz RA. 2003. Field evaluation of a lethal ovitrap against dengue vectors in Brazil. Medical and Veterinary Entomology 17(2): 205-210. 49. Ponnusamy L, Böröczky K, Wesson DM, Schal C, Apperson CS. 2011. Bacteria stimulate hatching of yellow fever mosquito eggs. PLoS One 6(9): e24409. 50. Ponnusamy L, Wesson DM, Arellano C, Schal C, Apperson CS. 2010. Species composition of bacterial communities influences attraction of mosquitoes to experimental plant infusions. Microbial Ecology 59: 158-173. 51. Ponnusamy L, Xu N, Böröczky K, Wesson DM, Ayyash LA, Schal C, Apperson CS. 2010. Oviposition responses of the mosquitoes Aedes aegypti and Aedes albopictus to experimental plant infusions in laboratory bioessays. Journal of Chemical Ecology 36: 709-719. 52. Ponnusamy L, Xu N, Nojima S, Wesson DM, Schal C, Apperson CS. 2008. Identification of bacteria and bacteria-associated chemical cues that mediate oviposition site preferences by Aedes aegypti. Proceedings of the National Academy of Sciences 105(27): 9262-9267. 53. Ponnusamy L, Xu N, Stav G, Wesson DM, Schal C, Apperson AS. 2008. Diversity of bacterial communities in container habitats of mosquitoes. Microbial Ecology 56: 593-603. 54. Raghavendra K, Barik TK, Reddy BPN, Sharma P, Dash AP. 2011. Malaria vector control: from past to future. Parasitology Research 108: 757-779. 55. Rao DR, Mani TR, Radendran R, Joseph AS, Gajanana A, Reuben R. 1995. Development of a high level of resistance to Bacillus sphaericus in a field population of Culex quinquefasciatus from Kochi, India. Journal of the American Mosquito Control Association 11(1): 1-5. 56. Rosner B. 2011. Fundamentals of Biostatistics. 7th ed. Boston, MA: Brooks/Cole 57. Santos SRA, Santos MAVM, Regis L, Albuquerque CMR. 2003. Field evaluation of ovitraps consociated with grass infusion and Bacillus thuringiensis var. israelensis to determine oviposition rates of Aedes aegypti. Dengue Bulletin 27: 156-162. 58. Seyoum A, Abate D. 1997. Larvicidal efficacy of Bacillus thuringiensis var. israelensis and Bacillus sphaericus on Anopheles arabiensis in Ethiopia. World Journal of Microbiology Biotechnology 13: 21-24. 59. Shelomi M. 2019. Bacterial and eukaryote microbiomes of mosquito habitats in dengue-endemic southern Taiwan. Journal of Asia-Pacific Entomology 22(2): 471-480. 60. Sota T, Mogi M, Hayamizu E. 1994. Habitat stability and the larval mosquito community in treeholes and other containers on a temperate island. Researches on Population Ecology 36: 94-104. 61. Sumba LA, Guda TO, Deng AL, Hassanali A. 2004. Mediation of oviposition site selection in the African malaria mosquito Anopheles gambiae (Diptera: Culicidae) by semiochemicals of mibrobial origin. International Journal of Tropical Insect Science 24(3): 260-265. 62. Sumba LA, Ogbunugafor CB, Deng AL, Hassanali A. 2008. Regulation of oviposition in Anopheles gambiae s.s.: role of inter- and intra-specific signals. Journal of Chemical Ecology 34: 1430-1436. 63. Tabashnik BE, Cushing NL, Finson N, Johnson MW. 1990. Field development of resistance to Bacillus thuringiensis in diamondback moth (Lepidoptera: Plutellidae). Journal of Economic Entomology 83(5): 1671-1676. 64. Thomas MB, Read AF. 2007. Can fungal biopesticides control malaria? Nature Reviews Microbiology 5: 377-383. 65. Thorne L, Garduno F, Thompson T, Decker D, Zounes M, Wild M, Walfield AM, Pollock TJ. 1986. Structural similarity between the Lepidoptera- and Diptera-specific insecticidal endotoxin genes of Bacillus thuringiensis subsp. 'kurstaki' and 'israelensis'. Journal of Bacteriology 166(3): 801-811. 66. Wang XL, Yao YJ. 2011. Host insect species of Ophiocordyseps sinensis: a review. Zookeys 127: 43-59. 67. Wong J, Stoddard ST, Astete H, Morrison AC, Scott TW. 2011. Oviposition site selection by the dengue vector Aedes aegypti and its implications for dengue control. PLoS Negl Trop Dis. 5(4):e1015. 68. World Health Organization. 2005. Guidelines for laboratory and field testing of mosquito larvicides. Geneva, World Health Organization: 39 69. Xu Y, Orozco R, Wijeratne EMK, Artiles PE, Gunatilaka AAL, Stock SP, Molnar I. 2009. Biosynthesis of the cyclooligomer depsipeptide bassianolide, an insecticidal virulence factor of Beauveria bassiana. Fungal Genetics and Biology 46(5): 353-364. 70. Yee DA, Kesavaraju B, Juliano SA. 2007. Direct and indirect effects of animal detritus on growth, survival, and mass of invasive container mosquito Aedes albopictus (Diptera: Culicidae). Journal of Medical Entomology 44(4): 580-588. 71. Yee DA, Kneitel JM, Juliano SA. 2010. Environmental correlates of abundances of mosquito species and stages in discarded vehicle tires. Journal of Medical Entomology 47(1): 53-62. 72. Yee DA, Allgood D, Kneitel JM, Kuehn KA. 2012. Constitutive differences between natural and artificial container mosquito habitats: vector communities, resources, microorganisms, and habitat parameters. Journal of Medical Entomology 49: 482-491. 73. Yuan Z, Zhang Y, Cai Q, Liu EY. 2000. High-level field resistance to Bacillus sphaericus C3-41 in Culex quinquefasciatus from southern China. Biocontrol Science and Technology 10(1): 41-49. 74. Zahiri NS, Su T, Mulla MS. 2002. Strategies for the management of resistance in mosquitoes to the mosquito control agent Bacillus sphaericus. Journal of Medical Entomology 39: 513-520. 75. Zahiri NS, Mulla MS. 2006. Ovipositional and ovicidal effects of the microbial agent Bacillus thuringiensis israelensis on Culex quinquefasciatus Say (Diptera: Culicidae). Journal of Vector Ecology 31(1): 29-34. 76.Zimmermann G. 1993. The entomopathogenic fungus Metarhizium anisopliae and its potential as a biocontrol agent. Pest Management Science 37(4): 375-379. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/8445 | - |
dc.description.abstract | 埃及斑蚊(Aedes aegypti (L.))等蚊類是茲卡、登革熱等蚊媒傳染病的病媒。在蚊子所產卵的水中有些微生物,這些微生物可以影響蚊子,例如影響蚊子產卵選擇或是可殺幼蟲,但大多數的環境微生物都還沒被測試過。本研究主要針對本實驗室在2017年於南台灣幾處可能適合蚊子產卵的水域採集的微生物,並以埃及斑蚊三齡幼蟲為實驗對象。以那些沒有蚊子存在的採集處之微生物,將高濃度的微生物放進幼蟲生長的水中並以蘇力菌作為正向控制,於24小時後觀察幼蟲的存活率。另外,將高濃度的微生物放進成蟲產卵容器中,觀察微生物是否影響成蟲的產卵行為。結果顯示,本研究測試的微生物皆無法造成幼蟲死亡或是影響成蟲產卵。這些微生物被採集時沒有幼蟲出現,可能是微生物與成蟲仍有未知的關係。原因可能在無法培養的菌或是與微生物無關,未來仍需探討此可能性。 | zh_TW |
dc.description.abstract | Mosquitoes such as Aedes aegypti (L.) are vectors of lots of severe diseases, like Zika and dengue fever. Microbes in the water where mosquitoes lay eggs can affect mosquitoes, such as by affecting adult oviposition choice or working as a larvicide. The effects of most environmental microbes on mosquitoes have not been tested. My research focuses on microbes collected from potential mosquito oviposition sites in Southern Taiwan in 2017. I used late third instar Ae. aegypti larvae as model insects. For every microbe, focusing on those cultured from mosquito-free containers, I put a high concentration into containers of water with larvae, then checked what happened after 24 hours, using Bacillus thuringiensis as a positive control. I also put the same microbes into containers of water to see if the microbes would affect mosquito oviposition behavior. The microbes I tested could not kill the larvae or attract/repel mosquito from laying eggs. The lack of mosquitoes from the containers where these microbes were collected might be due to some unknown relationship between microbes and adult mosquitoes, such as nonculturable microbes, or due to non-microbial aspects of the containers. | en |
dc.description.provenance | Made available in DSpace on 2021-05-20T00:54:37Z (GMT). No. of bitstreams: 1 U0001-1607202014583800.pdf: 2657349 bytes, checksum: ddd7cdffd6b9d58cd73598ee6f6dc50c (MD5) Previous issue date: 2020 | en |
dc.description.tableofcontents | Acknowledgement ii Chinese Abstract iii English Abstract iv Table of Contents v List of Figures vi List of Tables vii Introduction 1 I. Vector Control 1 II. Microbial Larvicide 7 1. Bacteria 7 2. Fungi 8 III. Adult Oviposition 10 Material and Methods 13 I. Mosquito Rearing 13 II. Microbe Larvicidal Test 14 III. Mosquito Oviposition Test 15 Results 18 I. Microbe Larvicidal Test 18 II. Mosquito Oviposition Test 18 Discussion 23 Conclusion 25 References 27 | |
dc.language.iso | en | |
dc.title | 環境微生物對埃及斑蚊(雙翅目:蚊科)幼蟲存活率與成蟲產卵行為之影響 | zh_TW |
dc.title | Effects of Environmental Microbes on Aedes aegypti (Diptera: Culicidae) Larval Survival and Oviposition | en |
dc.type | Thesis | |
dc.date.schoolyear | 108-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 郭奇芊(Chi-Chien Kuo),莊定武(Ting-Wu Chuang),黃旌集(Chin-Gi Huang) | |
dc.subject.keyword | 埃及斑蚊,殺幼蟲劑,產卵行為,細菌,微生物生態學, | zh_TW |
dc.subject.keyword | Aedes aegypti,larvicide,oviposition,bacteria,microbial ecology, | en |
dc.relation.page | 40 | |
dc.identifier.doi | 10.6342/NTU202001573 | |
dc.rights.note | 同意授權(全球公開) | |
dc.date.accepted | 2020-07-16 | |
dc.contributor.author-college | 生物資源暨農學院 | zh_TW |
dc.contributor.author-dept | 昆蟲學研究所 | zh_TW |
顯示於系所單位: | 昆蟲學系 |
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