Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-25T04:18:12.311Z Has data issue: false hasContentIssue false

Extent of digestion affects the success of amplifying human DNA from blood meals of Anopheles gambiae (Diptera: Culicidae)

Published online by Cambridge University Press:  09 March 2007

W.R. Mukabana*
Affiliation:
International Centre of Insect Physiology and Ecology (ICIPE), PO Box 30772, Nairobi, Kenya Laboratory of Entomology, Wageningen University and Research Center, PO Box 8031, 6700 EH Wageningen, The Netherlands Department of Zoology, University of Nairobi, PO Box 30197, Nairobi, Kenya
W. Takken
Affiliation:
Laboratory of Entomology, Wageningen University and Research Center, PO Box 8031, 6700 EH Wageningen, The Netherlands
P. Seda
Affiliation:
International Centre of Insect Physiology and Ecology (ICIPE), PO Box 30772, Nairobi, Kenya
G.F. Killeen
Affiliation:
International Centre of Insect Physiology and Ecology (ICIPE), PO Box 30772, Nairobi, Kenya Department of Tropical Medicine, Tulane University Health Sciences Center, New Orleans, LA 70112, USA
W.A. Hawley
Affiliation:
Division of Parasitic Diseases, Centers for Disease Control and Prevention (CDC), MF22, GA 30333, USA
B.G.J. Knols
Affiliation:
International Centre of Insect Physiology and Ecology (ICIPE), PO Box 30772, Nairobi, Kenya
*
*Fax: +254 385 22190 E-mail: [email protected]

Abstract

The success of distinguishing blood meal sources of Anopheles gambiae Giles through deoxyribonucleic acid (DNA) profiling was investigated by polymerase chain reaction (PCR) amplification at the TC-11 and VWA human short tandem repeats (STR) loci. Blood meal size and locus had no significant effect on the success of amplifying human DNA from blood meals digested for 0, 8, 16, 24 and 32 h (P = 0.85 and 0.26 respectively). However, logistic regression found a significant negative relationship between time since ingestion and the success probability of obtaining positive PCR products among meals digested for between 8 and 32 h (P = 0.001). Approximately 80% of fresh blood meals were successfully profiled. After 8 h, the proportion of blood meals that could be successfully profiled decreased slowly with time after ingestion, dropping to below 50% after approximately 15 h. There was no significant difference in the success of amplifying human DNA from blood meals of mosquitoes killed at time 0 and 8 h after ingestion (P = 0.272).

Type
Research Article
Copyright
Copyright © Cambridge University Press 2002

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Allen, R.C., Graves, G. & Budowle, B. (1989) Polymerase chain reaction amplification products separated on rehydratable polyacrylamide gels and stained with silver. BioTechniques 7, 736744.Google ScholarPubMed
Billingsley, P.F. & Hecker, H. (1991) Blood digestion in the mosquito Anopheles stephensi Liston (Diptera: Culicidae): activity and distribution of trypsin, aminopeptidase and & alpha;-glucosidase in the midgut. Journal of Medical Entomology 28, 865871.CrossRefGoogle ScholarPubMed
Boreham, P.F.L. & Lenahan, J.K. (1976) Methods for detecting multiple blood meals in mosquitoes (Diptera: Culicidae). Bulletin of Entomological Research 66, 671679.CrossRefGoogle Scholar
Briegel, H. & Lea, A.O. (1975) Relationship between protein and proteolytic activity in the midgut of mosquitoes. Journal of Insect Physiology 21, 15971604.CrossRefGoogle ScholarPubMed
Bryan, J.H. & Smalley, M.E. (1978) The use of ABO blood groups as markers for mosquito biting studies. Transactions of the Royal Society of Tropical Medicine and Hygiene 72, 357360.CrossRefGoogle ScholarPubMed
Budowle, B., Comey, C.T. & Baechtel, F.S. (1993) Forensic analysis. pp 617640. in Keller, G.H. & Manak, M.M. (ed.) DNA probes: background, applications and procedures. New York, Stockton Press.Google Scholar
Cairns, M.J. & Murray, V. (1994) Rapid silver staining and recovery of PCR products separated on polyacrylamide gels. Biotechniques 17, 915919.Google Scholar
Chow-Shaffer, E.C., Sina, B., Hawley, W.A., Benedicts, J.D. & Scott, T.W. (2000) Laboratory and field evaluation of polymerase chain reaction-based DNA profiling for use in identification of human blood meal sources of Aedes aegypti (Diptera: Culicidae). Journal of Medical Entomology 37, 492502.CrossRefGoogle ScholarPubMed
Clements, A.N. (1992) Adult food and feeding mechanisms. pp 220250 in The biology of mosquitoes, Vol 1. London: Chapman & Hall.Google Scholar
Coulson, R.M.R., Curtis, C.F., Ready, P.D., Hill, N. & Smith, D. (1990) Amplification and analysis of human DNA present in mosquito blood meals. Medical and Veterinary Entomology 4, 357366.CrossRefGoogle Scholar
Edwards, A., Civitello, A., Hammond, H.A. & Caskey, C.T. (1991) DNA typing and genetic mapping with trimeric and tetrameric tandem repeats. American Journal of Human Genetics 49, 746756.Google ScholarPubMed
Gokool, S., Smith, D.F. & Curtis, C.F. (1992) The use of PCR to help quantify the protection provided by impregnated bednets. Parasitology Today 8, 347350.CrossRefGoogle ScholarPubMed
Gokool, S., Curtis, C.F. & Smith, D.F. (1993) Analysis of mosquito blood meals by DNA profiling. Medical and Veterinary Entomology 7, 208215.CrossRefGoogle Scholar
Jeffreys, A.J., Wilson, V. & Thein, S.L. (1985) Hypervariable ‘minisatellite’ regions in human DNA. Nature 314, 6773.CrossRefGoogle ScholarPubMed
Jeffreys, A.J., Wilson, V., Neumann, R. & Keyte, J. (1988) Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells. Nucleic Acids Research 16, 1095310971.CrossRefGoogle ScholarPubMed
Koella, J.C., Sørensen, F.L. & Anderson, R.A. (1998) The malaria parasite, Plasmodium falciparum, increases the frequency of multiple feeding of its mosquito vector, Anopheles gambiae. Proceedings of the Royal Society of London B 265, 763768.CrossRefGoogle ScholarPubMed
Kimpton, C.P., Walton, A. & Gill, P. (1992) A further tetranucleotide repeat polymorphism in the VWF gene. Human Molecular Genetics. 1, 287.CrossRefGoogle ScholarPubMed
Kreiker, S. & Kampfer, S. (1999) Isolation and characterization of human DNA from mosquitoes (Culicidae). International Journal of Legal Medicine 112, 380382.CrossRefGoogle Scholar
Nijhout, H.F. & Carrow, G.M. (1978) Diuresis after a blood meal in female Anopheles freeborni. Journal of Insect Physiology 24, 293298.CrossRefGoogle Scholar
Noriega, F.G. & Wells, M.A. (1999) A molecular view of trypsin synthesis in the midgut of Aedes aegypti. Journal of Insect Physiology 45, 613620.CrossRefGoogle ScholarPubMed
Pant, C.P., Houba, V. & Engers, H.D. (1987) Blood meal identification in vectors. Parasitology Today 3, 324326.Google Scholar
Polymeropoulos, M.H., Xiao, H., Rath, D.S. & Merril, C.R. (1991) Tetranucleotide repeat polymorphism at the human tyrosine hydrolase gene (TH). Nucleic Acids Research. 19, 3753.Google Scholar
Redington, B.C. & Hockmeyer, W.T. (1976) A method for estimating blood meal volume in Aedes aegypti using a radioisotope. Journal of Insect Physiology 22, 961966.CrossRefGoogle ScholarPubMed
Rees, H. & Jones, R.N. (1972) The origin of the wide species variation in nuclear DNA content. International Review of Cytology 32, 5392.CrossRefGoogle ScholarPubMed
Replogle, J., Lord, W.D., Budowle, B., Meinking, T.L. & Taplin, D. (1994) Identification of host DNA by amplified fragment length polymorphism analysis: preliminary analysis of human crab louse (Anoplura: Pediculidae) excreta. Journal of Medical Entomology 31, 686690.CrossRefGoogle ScholarPubMed
Saiki, R.K., Gelfand, D.H., Stoffel, S., Scharf, S.J., Higuchi, R., Horn, G.T., Mullis, K.B. & Erlich, H.A. (1988) Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239, 487491.CrossRefGoogle ScholarPubMed
Sato, C., Furuya, Y., Harada, M. & Suguri, S. (1992) Identification of human blood in mosquitoes (Diptera: Culicidae) using nonradioactive DNA dot blot hybridization. Journal of Medical Entomology 29, 10451048.CrossRefGoogle ScholarPubMed
Service, M.W. (1977) A critical review of procedures for sampling populations of adult mosquitoes. Bulletin of Entomological Research 67, 343382.CrossRefGoogle Scholar
Tempelis, C.H. (1975) Host-feeding patterns of mosquitoes, with a review of advances in analysis of blood meals by serology. Journal of Medical Entomology 11, 635653.CrossRefGoogle ScholarPubMed
Torr, S.J., Wilson, P.J., Schofield, S., Mangwiro, T.N.C., Akber, S. & White, B.N. (2001) Application of DNA markers to identify the individual-specific hosts of tsetse feeding on cattle. Medical and Veterinary Entomology 15, 7886.CrossRefGoogle ScholarPubMed
Urquhart, A., Oldroyd, N.J., Kimpton, C.P. & Gill, P. (1995) Highly discriminating heptaplex short tandem repeat PCR system for forensic identification. BioTechniques 18, 116121.Google ScholarPubMed
Vaughan, J.A., Noden, B.H. & Beier, J.C. (1991) Concentration of human erythrocytes by anopheline mosquitoes (Diptera: Culicidae) during feeding. Journal of Medical Entomology 28, 780786.CrossRefGoogle ScholarPubMed
Washino, R.K. & Tempelis, C.H. (1983) Mosquito host blood meal identification. Annual Review of Entomology 28, 179201.CrossRefGoogle Scholar
Wetton, J.H., Carter, R.E., Parkin, D.T. & Walters, D. (1987) Demographic study of a wild house sparrow population by DNA fingerprinting. Nature 327, 147149.CrossRefGoogle ScholarPubMed