Laboratory and field evaluation of polymerase chain reaction-based forensic DNA profiling for use in identification of human blood meal sources of Aedes aegypti (Diptera : Culicidae)
E. Chow-shaffer et al., Laboratory and field evaluation of polymerase chain reaction-based forensic DNA profiling for use in identification of human blood meal sources of Aedes aegypti (Diptera : Culicidae), J MED ENT, 37(4), 2000, pp. 492-502
We modified polymerase chain reaction (PCR)-based forensic DNA profiling fo
r field studies on the feeding behavior of Aedes aegypti, the principal mos
quito vector of dengue virus. Human DNA was extracted from oral swabs of hu
man subjects and from blood-engorged mosquitoes, DNA was quantified by slot
blot, and alleles at variable number tandem repeats and three short tandem
repeats loci were amplified by PCR. Alleles were separated electrophoretic
ally and then visualized by silver staining. A custom software program was
written to match DNA fingerprints of potential human hosts to allelic profi
les detected in engorged mosquitoes, and to calculate error rates for ident
ification of human hosts of single and multiple-host blood meals. At 29 deg
rees C in the laboratory, human DNA recovered from mosquito blood meals dec
lined an average of 67% 8 h after feeding and 90% after 21 h. We obtained c
omplete allelic profiles from seven of 10 mosquitoes collected after 24 h.
In a field trial, complete DNA profiles were obtained successfully for 43 p
eople living in a rural village in south central Thailand and for 20 of 100
Ae. aegypti that contained blood and were collected in those peoples' home
s. Blood imbibed from more than one person was detected in 45% (9 of 20) of
the meals. Sixty-five percent of the meals contained blood from nonresiden
ts of the house in which the mosquito was collected or from people who were
not profiled; data consistent with the hypothesis that human movement is i
mportant for the spread of dengue virus within and among communities. When
using alleles at four loci, all of the Thais and nine members spanning thre
e generations of a Chinese-American family had unique allelic profiles. Err
or rates from classifying possible multiple-host meals as single-host meals
were low (1-8%), with the highest error associated with closely related pe
ople. Results front our laboratory and field studies indicated that DNA pro
filing can be used to study the details and epidemiological implications of
Ae. aegypti blood-feeding behavior.