Culex salinarius is a bridge vector to humans, while Cx. pipiens and Cx. restuans are more efficient enzootic vectors.

Dengue is the most common mosquito-borne viral disease in humans. The spread of both mosquito vectors and viruses has led to the resurgence of epidemic dengue fever (a self-limited flu-like syndrome) and the emergence of dengue hemorrhagic fever (severe dengue with bleeding abnormalities) in urban centers of the tropics. There are no animal or laboratory models of dengue disease; indirect evidence suggests that dengue viruses differ in virulence, including their pathogenicities for humans and epidemic potential. We developed two assay systems (using human dendritic cells and Aedes aegypti mosquitoes) for measuring differences in virus replication that correlate with the potential to cause hemorrhagic dengue and increased virus transmission. Infection and growth experiments showed that dengue serotype 2 viruses causing dengue hemorrhagic fever epidemics (Southeast Asian genotype) can outcompete viruses that cause dengue fever only (American genotype). This fact implies that Southeast Asian genotype viruses will continue to displace other viruses, causing more hemorrhagic dengue epidemics.

The vertebrate hosts of 672 blood-engorged Culex quinquefasciatus Say, collected in Harris County, Texas, during 2005, were identified by nucleotide sequencing PCR products of the cytochrome b gene. Analysis revealed that 39.1% had acquired blood from birds, 52.5% from mammals, and 8.3% were mixed avian and mammalian blood meals. Most frequent vertebrate hosts were dog (41.0%), mourning dove (18.3%), domestic cat (8.8%), white-winged dove (4.3%), house sparrow (3.2%), house finch (3.0%), gray catbird (3.0%), and American robin (2.5%). Results are interpreted in conjunction with concurrent avian and mosquito West Nile virus (WNV) surveillance activities in Harris County. We conclude that Cx. quinquefasciatus is an opportunistic feeder and principal mosquito vector of WNV in this metropolitan area; however, transmission by other mosquito species or by other modes of infection, such as ingestion, must account for the high WNV infection rates among local blue jays and American crows.

We evaluated the blood-feeding patterns in several mosquito species that may serve as vectors of disease agents in the northeastern United States. Blood-fed mosquitoes were collected from 91 different sites throughout Connecticut over a 6-yr period (June-October 2002-2007), and the host-feeding patterns of 23 mosquito species representing six genera were examined by using a polymerase chain reaction-based assay and sequencing portions of the cytochrome b gene of mitochondrial DNA. This study was part of a statewide surveillance program and for some of the mosquito species a limited number of specimens were examined [e.g., Aedes communis (De Geer) (1), Anopheles barberi Coquillett (1), Uranotaenia sapphirina (Osten Sacken) (5)]. With the exception of Culex territans Walker that acquired bloodmeals from all four classes of vertebrates--birds, reptiles, amphibians, and mammals--all species of Aedes, Anopheles, Coquillettidia, Psorophora, and to a lesser degree, Uranotaenia, were found to feed predominately upon mammalian hosts. Fourteen mammalian species were identified as sources of blood, but the majority of feedings were taken from the white-tailed deer, Odocoileus virginianus. Human-derived bloodmeals were identified from 13 of the 23 mosquito species. Limited avian-derived bloodmeals were detected in Aedes canadensis (Theobald), Aedes cantator (Coquillett), Aedes cinereus Meigen, Aedes triseriatus (Coquillett), Aedes trivittatus (Coquillett), Coquillettidia perturbans (Walker) Cx. territans, Psorophoraferox (von Humboldt), and Ur. sapphirina. American robin, Turdus migratorius, was the most common source of avian blood, followed by a few other mostly Passeriformes birds. We conclude that the white-tailed deer serve as the main vertebrate host for these mammalophilic mosquitoes in this region of the United States. This feeding pattern supports enzootic amplification of arboviruses, including Jamestown Canyon, Cache Valley, and Potosi viruses that perpetuate in cervid hosts. Occasional feeding on avian hosts suggests that some of these mosquito species, such as Cq. perturbans, also could facilitate transmission of West Nile and eastern equine encephalitis viruses from viremic birds to mammalian hosts.

The recent Zika virus (ZIKV) and chikungunya virus (CHIKV) epidemics highlight the explosive nature of arthropod-borne (arbo)viruses transmitted by Aedes spp. mosquitoes 1,2. Vector competence and the extrinsic incubation period (EIP) are two key entomological parameters used to assess the public health risk posed by arboviruses 3. These are typically measured empirically by offering mosquitoes an infectious bloodmeal and temporally sampling mosquitoes to determine infection and transmission status. This approach has been used for the better part of a century; however, it does not accurately capture the biology and behavior of many mosquito vectors which refeed frequently (every 2-3 days) 4. Here we demonstrate that acquisition of a second noninfectious bloodmeal significantly shortens the EIP of ZIKV-infected Ae. aegypti by enhancing Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: