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:

Mosquito cell lines have been used extensively in research to isolate and propagate arthropod-borne viruses and understand virus-vector interactions. Despite their utility as an in vitro tool, these cell lines are poorly defined and may harbor insect-specific viruses. Accordingly, we screened four commonly-used mosquito cell lines, C6/36 and U4.4 cells from Aedes albopictus, Aag2 cells from Aedes aegypti, and Hsu cells from Culex quinquefasciatus, for the presence of adventitious (i.e. exogenous) viruses. All four cell lines stained positive for double-stranded RNA, indicative of RNA virus replication. We subsequently identified viruses infecting Aag2, U4.4 and Hsu cell lines using untargeted next-generation sequencing, but not C6/36 cells. PCR confirmation revealed that these sequences stem from active viral replication and/or integration into the cellular genome. Our results show that these commonly-used mosquito cell lines are persistently-infected with several viruses. This finding may be critical to interpreting data generated in these systems.

Surveillance for diurnal container-inhabiting mosquitoes such as Aedes albopictus (Skuse), Aedes japonicus japonicus (Theobald), and Aedes triseriatus (Say) have routinely relied on the deployment of multiple trap types, including CO2-baited light traps, gravid traps, oviposition traps, and BG-Sentinel. These trap configurations have met with varying degrees of effectiveness and in many instances likely under-sample these key mosquito vectors. Most recently, the BG-Sentinel trap used in conjunction with the human-scent lure has been largely accepted as the gold-standard for monitoring Ae. albopictus. However, its ability to attract other container-inhabiting Aedes species has not been fully evaluated. During 2018, we tested new scent lures, TrapTech Lure-A and Lure-H (Bedoukian Research, Inc.), using BG-Sentinel traps with CO2 in two regions of Connecticut, Stamford and Hamden, against the BG-Lure. Pooled mosquitoes were additionally screened for arbovirus infection. A total of 47,734 mosquitoes representing 8 genera and 32 species were captured during the study, with the Stamford site deriving on average three times as many mosquitoes per trap, adjusting for sampling effort. Lure-A and Lure-H outperformed the BG-Lure in terms of total numbers, diversity evenness, and the proportion of both Ae. j. japonicus and Ae. triseriatus. There were no significant differences among lures in capturing Ae. albopictus, and in terms of species richness. Fifty-seven isolates of virus (West Nile, Jamestown Canyon, and La Crosse viruses) were obtained during the study, with no significant difference between trap-lure. We highlight both novel lures as effective attractants for use in mosquito surveillance=, which either outperform, or equal, BG-Lure.

Seasonal abundance of mosquitoes, their viruses, and blood-feeding habits were determined at an open-faced quarry in North Branford, CT, in 2010 and 2011. This unique habitat had not previously been sampled for mosquitoes and mosquito-borne viruses. Thirty species of mosquitoes were identified from 41,719 specimens collected. Coquillettidia perturbans, Aedes trivittatus, and Ae. vexans were the most abundant species and represented 34.5%, 17.7%, and 14.8% of the totals, respectively. Jamestown Canyon virus was isolated from 6 species of mosquitoes collected from mid-June through July: Cq. perturbans (3 pools), Ae. cantator (3), Ae. trivittatus (2), Ae. aurifer (1), Ae. excrucians (1), and Culex pipiens (1). West Nile virus was cultured from 8 pools of Cx. pipiens and from 1 pool of Culiseta melanura collected from mid-August through late September. Cache Valley virus was isolated from 4 species of mosquitoes in 3 genera from about mid-August through late September 2011: Cq. perturbans (5 pools), Ae. trivittatus (2), Anopheles punctipennis (1), and An. quadrimaculatus (1). Nine different mammalian hosts were identified as sources of blood for 13 species of mosquitoes. White-tailed deer, Odocoileus virginianus, were the most common mammalian hosts (90.8%), followed by raccoon, Procyon lotor (3.1%), coyote, Canis latrans (2.4%), and human, Homo sapiens (1.2%). Exclusive mammalian blood-feeding mosquitoes included: Ae. canadensis, Ae. cantator, Ae. excrucians, Ae. japonicus, Ae. vexans, An. punctipennis, and Cx. salinarius. Fourteen species of birds, mostly Passeriformes, were identified as sources of blood from 6 mosquito species. Five species that fed on mammals (Ae. thibaulti, Ae. trivittatus, Ae. cinereus, Cq. perturbans, and Cx. pipiens) also fed on birds.

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