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Am. J. Trop. Med. Hyg., 77(3), 2007, pp. 485-487
Copyright © 2007 by The American Society of Tropical Medicine and Hygiene

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A New Robust Diagnostic Polymerase Chain Reaction for Determining the Mating Status of Female Anopheles gambiae Mosquitoes

Kija R. Ng’habi*, Ashley Horton, Bart G. J. Knols, AND Gregory C. Lanzaro
Ifakara Health Research and Development Centre, Tanzania; Center for Vectorborne Diseases, University of California, Davis, California; Wageningen University and Research Centre, Wageningen, The Netherlands

The principal malaria vector in Africa, Anopheles gambiae, contains two pairs of autosomes and one pair of sex chromosomes. The Y chromosome is only associated with males and other Y chromosome–specific DNA sequences, which are transferred to women during mating. A reliable tool to determine the mating status of dried wild An. gambiae females is currently lacking. DNA was extracted from dried virgin and mated females and used to test whether Y chromosome–specific polymerase chain reaction (PCR) markers can be successfully amplified and used as a predictor of mating. Here we report a new PCR-based method to determine the mating status among successfully inseminated and virgin wild An. gambiae females, using three male-specific primers. This dissection-free method has the potential to facilitate studies of both population demographics and gene flow from dried mosquito samples routinely collected in epidemiologic monitoring and aid existing and new malaria-vector control approaches.


Received January 31, 2007. Accepted for publication April 30, 2007.

Acknowledgments: We thank the Vector Genetic Laboratory (University of California) for cooperation during the entire period of this study; Claudio Meneses for invaluable technical assistance during mosquito rearing and PCR optimization; Dr. Mark Benedict for suggestions and literature that made this study possible; and Dr. Heather Ferguson for reviewing the manuscript before submission.

Financial support: We acknowledge the International Atomic Energy Agency (IAEA) for financial support through a fellowship awarded to KRN to work at UC Davis. This research forms part of a VIDI Grant 864.03.004 from the Dutch Scientific Organization (NWO) awarded to BGJK. In addition, we acknowledge support to GCL through Grant AI040308 from the National Institutes of Health.

* Address correspondence to Kija R. Ng’habi, Ifakara Health Research and Development Centre, PO Box 53, Ifakara, United Republic of Tanzania. E-mail: kija{at}ihrdc.or.tz

Authors’ addresses: Kija R Ng’habi, Ifakara Health Research and Development Centre, PO Box 53, Ifakara, United Republic of Tanzania, E-mail: kija{at}ihrdc.or.tz. Ashley Horton and Gregory Lanzaro, Department of Entomology, University of California, Davis, 396C Briggs, One Shield Avenue, Davis, CA 95616-8584, E-mails: gclanzaro{at}ucdavis.edu and ahorton{at}ucdavis.edu. Bart G. J. Knols, Laboratory of Entomology. PO Box 8031, 6700 EH, Wageningen University and Research Centre, Wageningen, The Netherlands, E-mail: Bart.Knols{at}wur.nl.







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Copyright © 2007 by the American Society of Tropical Medicine and Hygiene.