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. 2013 Feb 6;88(2):245–253. doi: 10.4269/ajtmh.2012.12-0048

Table 2.

Field-identification of arboviruses, bloodmeals, and mosquito genera using the ArboChip3.0 in Lopburi and Kamphaeng Phet, Thailand, April to March, 2011

Sample number Arthropod species (pool size) Collection method* location Microarray identification
Virus Blood- meal Mosquito genus
Th9-0011 Cx. quinquefasciatus (1) BA House CxFV Human Culex
Th9-0024 Ae. aegypti (1) BA House NA NA Aedes
Th9-0042 Armigeres subalbatus (1) BA House NA NA Armigeres
Th9-0047 Cx. quinquefasciatus (10) BA House NA Human Culex
Th9-0122 Ae. aegypti (1) BA House DENV-3 DNP Aedes
Th9-0164 Cx. tritaeniorhynchus (24) LT Farm JEV NA Culex
Th9-0167 Ae. albopictus (1) LT Farm NA NA Aedes
Th9-0175 Cx. tritaeniorhynchus (25) LT Farm JEV NA Culex
Th9-0235 Cx. tritaeniorhynchus (25) BA Cow pen NA Mammal§ Culex
Th9-0278 Mansonia uniformis (6) LT Farm NA NA Mansonia
Th9-0643 Dermacentor species (1) NA Lab NA Dog NA
*

BA = backpack aspiration; LT = Centers for Disease Control and Prevention CO2 baited light trap.

DNP = did not prime; NA = not applicable; CxFV, Culex flavivirus; DENV-3, dengue virus type 3; JEV = Japanese encephalitis virus. Mosquito pools that were not suspected of being infected with flaviviruses by polymerase chain reaction (PCR) screening or not containing any bloodfed mosquitoes were not analyzed on the microarray for flavivirus or bloodmeal identification.

Mosquito contained a bloodmeal but did not amplify with mammalian or avian primers.

§

Bloodmeal PCR amplicon was identified as Bos indictus (brahman cow) Cytb by sequencing, cow-specific probes were not present on this microarray design.