Skip to main content

Vector competence of Anopheles quadrimaculatus and Aedes albopictus for genetically distinct Jamestown Canyon virus strains circulating in the Northeast United States



Jamestown Canyon virus (JCV; Peribunyaviridae, Orthobunyavirus) is a mosquito-borne pathogen belonging to the California serogroup. The virus is endemic in North America and increasingly recognized as a public health concern. In this study, we determined the vector competence of Anopheles (An.) quadrimaculatus and Aedes (Ae.) albopictus for five JCV strains belonging to the two lineages circulating in the Northeast.


An. quadrimaculatus and Ae. albopictus were fed blood meals containing two lineage A strains and three lineage B strains. Vector competence of both mosquito species was evaluated at 7- and 14-days post-feeding (dpf) by testing for virus presence in bodies, legs, and saliva.


Our results demonstrated that Ae. albopictus mosquitoes are a competent vector for both lineages, with similar transmission levels for all strains tested. Variable levels of infection (46–83%) and dissemination (17–38%) were measured in An. quadrimaculatus, yet no transmission was detected for the five JCV strains evaluated.


Our results demonstrate that establishment of Ae. albopictus in the Northeast could increase the risk of JCV but suggest An. quadrimaculatus are not a competent vector for JCV.

Graphical Abstract


Jamestown Canyon virus (JCV; Peribunyaviridae, Orthobunyavirus) belongs to the California serogroup with La Crosse virus (LACV) and snowshoe hare virus (SSHV) [1]. JCV is broadly distributed throughout the USA and Canada [2]. The genome of JCV is comprised of three single-stranded segments of negative-sense RNA designated as the small (S), medium (M), and large (L), encoding the nucleocapsid, surface glycoprotein precursor, and RNA polymerase, respectively [3,4,5]. JCV isolates fall into two lineages, designated A and B [3, 4]. Both lineages have been detected in Connecticut and Massachusetts [2, 4, 5]; however, only circulation of lineage A has been reported in New York State (NYS) [6].

The number of JCV cases in the US has increased in recent years [2, 7]. The virus affects mostly adults and can cause acute febrile illness, severe meningitis, and encephalitis [2, 8, 9]. Despite the high incidence of neuroinvasive disease cases (54–79%), mortality is rare, with only five total deaths reported in the US [7, 10, 11]. In NYS, JCV has been documented since 1971 with at least four confirmed human cases [11, 12]. Moreover, sera from patients with and without central nervous system (CNS) disease revealed that JCV is the most prevalent arbovirus in NYS patients with antibody to California serogroup viruses, followed by LACV [13]. A previous study in Connecticut demonstrated seroprevalence rates for JCV ranging from 3.9–10.1%, yet recent increases in diagnosed cases would suggest seroprevalence likely exceeds historic rates [14, 15].

JCV infects a variety of free-ranging ungulates (deer, bison, moose, elk), but white-tailed deer are recognized as a principal amplification host [3, 8]. The seroprevalence rates of white-tailed deer for JCV were estimated to be 21% and 54.7% in Connecticut and NYS, respectively [16, 17]. In NYS, the virus was found associated with 12 mosquito species including An. punctipennis and An. quadrimaculatus, which regularly feed on white-tailed deer [6, 18]. In total, JCV has been isolated from 26 mosquito species in several genera including Aedes (Ae.), Anopheles (An.), Culex, Coquillettidia, and Culiseta [17, 19]. While it has been suggested that Aedes mosquitoes act as principal vectors [17], the primary vector of JCV in the Northeast, including in NYS, is unknown. Isolation of JCV from Ae. albopictus and An. quadrimaculatus is suggestive of their potential involvement in the transmission cycle of the virus [17]. Furthermore, Anopheles spp. have been shown to play a primary role in vectoring the orthobunyavirus Cache Valley virus (CVV) in NYS [20, 21].

The objective of this study was to determine the vector competence of An. quadrimaculatus and Ae. albopictus for JCV strains belonging to the two lineages circulating in the Northeast.



A colony of unknown generations of An. quadrimaculatus (Orlando strain) was obtained from BEI (MRA-139) and were maintained at 27 °C under standard rearing [22, 23]. Aedes albopictus colony (Spring Valley, New York, kindly provided by Laura Harrington, Cornell University) was established in 2019 from field-collected eggs. Aedes albopictus were hatched in distilled water, reared and maintained similarly to Anopheles as described [23].

Experimental infections of mosquitoes with Jamestown Canyon virus

Five JCV strains originally isolated from mosquito pools in Connecticut (kindly provided by Philip Armstrong, CAES), and previously found to be genetically distinct, were freshly propagated in Vero (African Green Monkey kidney) cell cultures in separated plates maintained at 37 °C, 5% CO2. These included 3836–05 (lineage A, 2005; S, M, L accession nos. EF681835, EF687050, EF687103), 11,497–03 (lineage A, 2003; S, M, L accession nos. EF81845, EF87121, EF687059), 1441–01 (lineage B, 2001; S, M, L accession nos. EF681814, EF687110, EF687027), 1425–02 (lineage B, 2002; S, M, L accession nos. EF681813, EF687091, EF687039) and 4148–03 (lineage B, 2003; S, M, L accession nos. EF681827, EF687114, EF687051). At 48 h following infection (multiplicity of infection ≈ 1.0), the supernatant of each strain was harvested and diluted 1:1 with defibrinated sheep blood plus a final concentration of 2.5% sucrose. Female An. quadrimaculatus mosquitoes (3–5 days old) from unknown generations were deprived of sugar for 1–2 h, and F7 female Ae. albopictus (5–7 days old) deprived of sugar for 24 h were offered a JCV-blood suspension for 45 min via a Hemotek membrane feeding system (Discovery Workshops, Acrington, UK) with porcine sausage casing membrane at 37 °C [22]. Following feeding, females were anesthetized with CO2, and fully engorged mosquitoes were transferred to 0.6-l cardboard containers and maintained with 10% sucrose at 27 °C until harvested for testing [24]. A 1-ml aliquot of each pre-feeding blood meal was frozen at − 80 °C to determine JCV blood meal titers.

Evaluation of mosquito vector competence for Jamestown Canyon virus

Infection, dissemination, and transmission were determined on days 7 and 14 post-infectious blood (dpi) meal as previously described [22, 23]. Blood meals, mosquito bodies, legs and salivary secretions were assayed for infection by plaque assay on Vero cells [23, 24]. Briefly, Vero cells were seeded in six-well plates at a density of 6.0 × 105 cells per well and were incubated for 3–4 days at 37 °C in 5% CO2, to produce a confluent monolayer. The cell monolayers were inoculated with 0.1-ml of tenfold serial dilutions of the blood meals (diluted in BA-1) in duplicate or with undiluted mosquito bodies, legs and salivary secretions from each homogenized mosquito sample. Viral adsorption was allowed to proceed for 1 h at 37 °C with rocking of the plates every 15 min. A 3-ml overlay of MEM, 5% FBS and 0.6% Oxoid agar supplemented with 0.2 × penicillin/streptomycin per ml, 0.5 μg fungizone (Amphotericin B) per ml and 20 ug gentamicin per ml was added at the conclusion of adsorption. The infected monolayers were incubated at 37 °C in 5% CO2. After 2 days of infection, a second overlay, similar to the first but with the addition of 1.5% neutral red (Sigma-Aldrich Co., St. Louis, MO), was added to the wells, and the plates were incubated at 37 °C in 5% CO2 overnight. For the blood meal, the plaques were counted, and the viral titer was calculated and expressed as plaque-forming units (PFU) per ml. For mosquito samples, presence or absence of plaques was checked.

Dissemination rate is the proportion of mosquitoes with infected legs among the mosquitoes with infected bodies. Transmission rate is the proportion of mosquitoes with infectious saliva collected by capillary transmission method among mosquitoes with disseminated infection [22, 23].

Statistical analysis

A Fisher’s exact test was used to compare infection, dissemination and transmission rates within mosquito species and between both time points and virus strains [21, 23]. All statistical analyses were carried out at a significance level of p < 0.05. OpenEpi, version 3, open-source calculator-TwobyTwo ( was used for all statistical analysis.


Anopheles quadrimaculatus mosquitoes were orally exposed to five genetically distinct JCV strains (two lineage A [3836–05, 11,497–03] and three lineage B [1441–04, 1425–02, 4148–03]). Pairwise percent identity for these strains ranges from 99.6 to 88.6 across segments, with distinct mutations identified in each segment for all strains. Viral load of blood meals ranged from 6.2 to 6.6 log10 PFU/ml. Mosquitoes were processed at days 7 and 14 dpi to determine infection, dissemination and transmission rates. Infection rates of An. quadramaculatis at 7 dpi ranged from 70.00 to 83.33% and were statistically similar among strains. Interestingly, an overall trend of decreasing infection was measured between time points for all strains, with the exception of 4148–03. This decrease of infection rate was only significant for the 1425–02 strain (83.33% vs. 46.67%, Fisher’s exact test, P < 0.003, OR: 5.714, 95% CI 1.526, 23.7; Table 1). In addition, a significant difference in infection rates was measured at 14 dpi between strains 1425–02 and 4148–03 (46.67% vs. 76.67%, respectively; Fisher’s exact test, P = 0.016, OR: 3.755, 95% CI 1.097–13.43; Table 1). Except for the 1441–04 strain, which was not disseminated at 7 dpi, similar dissemination rates were observed within strains and between time points. No transmission was detected for any JCV strain at 7 or 14 dpi for An. quadramaculatis (Table 1).

Table 1 Vector competence of Anopheles quadrimaculatus for genetically distinct Jamestown Canyon virus strains

Following Ae. albopictus exposure to similar JCV blood meal titers (6.5–7.1 log10 PFU/ml), high rates of infection (90.00–100% at 7 dpi, 96.67–100% at 14 dpi) and dissemination (96.30–100% at 7dpi, 93.10–100% at 14 dpi) were measured, with no statistical differences between strains and time points (Table 2). Overall, a significant effect of species was measured independent of strain, with higher infection, dissemination and transmission rates at both time points in Ae. albopictus relative to An. quadramaculatis (two-way ANOVA, P < 0.05). All JCV strains were transmitted at 7 dpi by Ae. albopictus. A decrease in transmission rates with time was measured for all strains, with no detectable virus in saliva of two strains (3836–05 and 1441–04) at 14 dpi. Significantly lower infection rates were measured following exposure to blood meals with lower input titers (4.7 to 5.2 log10 PFU/ml; Fisher’s exact test, P < 0.0001, OR: 10.8, 95% CI 2.168–68.39). Interestingly, following both high and low dose exposure, infected Ae. albopictus showed high dissemination rates (96.30–100% vs. 85.71–100% at 7 dpi and 100% at 14 dpi for both doses). Similar transmission rates were also measured at 7 and 14 dpi for both lineages, with one strain of each lineage not transmitted at 14 dpi. Our results indicate that Ae. albopictus mosquitoes are a highly competent vector for both JCV lineages (Table 2).

Table 2 Vector competence of Aedes albopictus for genetically distinct Jamestown Canyon virus strains


With the increase of JCV cases in the US, it is important to identify mosquito species that are implicated in virus transmission to better understand the epidemiological risk in the Northeast and adapt vector control strategies. Thus, we assessed the vector competence of the most abundant Anopheles species (An. quadrimaculatus) and the most abundant invasive species (Ae. albopictus) in NYS for both JCV lineages circulating in the Northeast [20, 21]. Our results suggest that Ae. albopictus is highly competent for JCV but An. quadrimaculatus is not.

Recent studies demonstrated that An. quadrimaculatus mosquitoes are able to transmit viruses such as Mayaro virus and CVV [20, 23, 25, 26]. In the US, JCV has been consistently isolated from at least four Anopheles species including An. punctipennis, An. quadrimaculatus, An. crucians and An. walkeri [17]. In the Northeast, JCV is regularly detected from An. punctipennis and An. walkeri in Connecticut [17, 19], from An. punctipennis, An. quadrimaculatus and An. walkeri in Massachusetts [27] and from An. punctipennis and An. quadrimaculatus in NYS [6]. Consistent isolation of JCV from An. quadrimaculatus could either suggest that this species is involved in virus transmission or simply be a reflection of frequent feeding on competent hosts such as white-tailed deer [18]. Heard et al. showed An. punctipennis mosquitoes are a competent vector for JCV while the virus failed to infect An. quadrimaculatus [28]. In contrast, our results showed relatively high infectivity, yet also low dissemination and no transmission for representative JCV strains from both lineages. Together, these results suggest that despite the association with JCV in nature, An. quadrimaculatus mosquitoes appear to play little role in horizontal transmission of the virus. These results stand in contrast to the orthobunyavirus CVV, for which An. quadrimaculatus are highly competent and likely to play a primary role in transmission, particularly for the emergent lineage 2 CVV [22]. However, it has been demonstrated that forced salivation methods tend to underestimate virus transmission, so low-level transmission in natural systems remains plausible [29]. Moreover, transmission of arboviruses is influenced by interactions among viral genotype, vector genotype and environment [30, 31]. Since we used a colony of unknown generations of An. quadrimaculatus under controlled environmental conditions, further variability in competence for JCV could exist with field populations subjected to distinct or fluctuating environments.

Aedes albopictus is one of the most successful invasive species globally and continues to expand its geographic distribution both in the US and other countries [32, 33]. In NYS, Ae. albopictus populations are well established in Long Island, the Hudson Valley and New York City counties; however, the species is still undergoing population invasion and establishment [20, 34]. Furthermore, endemic viruses such as CVV, eastern equine encephalitis virus, JCV, West Nile virus, Potosi virus and LACV have been isolated from this species in the US [35, 36]. However, the role of Ae. albopictus as a vector of local arboviruses is not yet fully elucidated [36, 37]. Grimstad et al. reported JCV transmission at 14 dpi by Ae. albopictus [38]. Additional studies assessing vector competence of local Aedes mosquitoes for JCV broadly demonstrate transmissibility [28, 39, 40]. Importantly, we now demonstrate transmission of both JCV lineages by Ae. albopictus and high competence at a large range of doses. These data have important implications for infectiousness during viremic phases of primary hosts, but additionally suggest the potential for less competent hosts to contribute to transmission cycles. Surprisingly, we also found that JCV is consistently better transmitted at 7 dpi relative to 14 dpi. Since there is no evidence that JCV or other arboviral infections are regularly cleared from mosquitoes, these data suggest that virulence of JCV in vectors could impact longevity and transmissibility.

Although JCV cases are more frequently diagnosed in the upper Midwest, prevalence in the Eastern US has been increasing [7]. In addition, in North Carolina the only documented case of JCV occurred in a liver transplant patient [41]. Furthermore, JCV has consistently been detected from diverse mosquito species in the Northeast, with Aedes species most strongly associated with the virus [10, 17, 19]. Three exotic invasive mosquito species (Ae. albopictus, Ae. aegypti and Ae japonicus) have been shown to be competent vectors for local endemic orthobunyaviruses including JCV, LACV and CVV [21, 42,43,44,45]. Together, these data suggest that the transmission risk of these native mosquito-borne diseases may be increased by the introduction and establishment of invasive mosquito species.


To the best of our knowledge, our study provides the first evidence of infection of JCV in An. quadrimaculatus and vector competence of Ae. albopictus for both lineages. Establishment of Ae. albopictus in the Northeast could increase the threat of JCV transmission in the region.

Availability of data and materials

Data generated in this study are available from the corresponding authors upon reasonable request.



Days post-infection






Jamestown Canyon virus


La Crosse virus


Cache Valley virus




Infection rate


Dissemination rate


Transmission rates


United States


New York State


  1. Webster D, Dimitrova K, Holloway K, Makowski K, Safronetz D, Drebot MA. California serogroup virus infection associated with encephalitis and cognitive decline, Canada, 2015. Emerg Infect Dis. 2017;23:1423–4.

    Article  Google Scholar 

  2. Kinsella CM, Paras ML, Smole S, Mehta S, Ganesh V, Chen LH, et al. Jamestown Canyon virus in Massachusetts: clinical case series and vector screening. Emerg Microbes Infect. 2020;9:903–12.

    Article  CAS  Google Scholar 

  3. Bennett RS, Nelson JT, Gresko AK, Murphy BR, Whitehead SS, Andreadis TG, et al. The full genome sequence of three strains of Jamestown Canyon virus and their pathogenesis in mice or monkeys. Virol J. 2011.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Armstrong PM, Andreadis TG. Genetic relationships of Jamestown Canyon virus strains infecting mosquitoes collected in Connecticut. Am J Trop Med Hyg. 2007;77:1157–62.

    Article  CAS  Google Scholar 

  5. Solomon IH, Ganesh VS, Yu G, Deng XD, Wilson MR, Miller S, et al. Fatal case of chronic Jamestown Canyon virus encephalitis diagnosed by metagenomic sequencing in patient receiving rituximab. Emerg Infect Dis. 2021;27:238–42.

    Article  CAS  Google Scholar 

  6. Dieme C, Maffei J, Ngo K, Zink SD, Koetzner C, Kuo L, et al. Cache Valley virus and Jamestown Canyon virus surveillance, diversity, and vector competence. Poster Sess Northeast Reg Cent Excell Vector-Borne Dis. 2021 ; 2021

  7. Statistics and Maps, Jamestown Canyon virus, CDC n.d. Accessed 2 Nov 2021.

  8. Sahu SP, Landgraf J, Wineland N, Pedersen D, Alstad D, Gustafson G. Isolation of Jamestown Canyon virus (California virus group) from vesicular lesions of a horse. J Vet Diagn Investig. 2000;12:80–3.

    Article  CAS  Google Scholar 

  9. Vosoughi R, Walkty A, Drebot MA, Kadkhoda K. Jamestown Canyon virus meningoencephalitis mimicking migraine with aura in a resident of Manitoba. CMAJ. 2018;190:E262–4.

    Article  Google Scholar 

  10. VanderVeen N, Nguyen N, Hoang K, Parviz J, Khan T, Zhen A, et al. Encephalitis with coinfection by Jamestown Canyon virus (JCV) and varicella zoster virus (VZV). IDCases. 2020;22:e00966.

    Article  Google Scholar 

  11. Pastula DM, Johnson DKH, White JL, Ii APD, Fischer M, Staples JE. Jamestown Canyon virus disease in the United States—2000–2013. Am J Trop Med Hyg. 2015;93:384–9.

    Article  Google Scholar 

  12. Artsob H, Spence L, Brodeur BR, Th’ng C. Monoclonal antibody characterization of Jamestown Canyon (California serogroup) virus topotypes isolated in Canada. Viral Immunol. 1992;5:233–42.

    Article  CAS  Google Scholar 

  13. Srihongse S, Grayson MA, Deibel R. California serogroup viruses in New York State: the role of subtypes in human infections. Am J Trop Med Hyg. 1984;33:1218–27.

    Article  CAS  Google Scholar 

  14. McDonald E, Martin SW, Landry K, Gould CV, Lehman J. West Nile virus and other domestic nationally notifiable arboviral diseases—United States, 2018. MMWR Morb Mortal Wkly Rep. 2019;68:673.

    Article  Google Scholar 

  15. Mayo D, Karabatsos N, Scarano FJ, Brennan T, Buck D, Fiorentino T, et al. Jamestown Canyon virus: seroprevalence in Connecticut. Emerg Infect Dis. 2001;7:911–2.

    Article  CAS  Google Scholar 

  16. Dupuis AP, Prusinski MA, Russell A, Connor CO, Maffei JG, Oliver J, et al. Serologic survey of mosquito-borne viruses in hunter-harvested white-tailed deer (Odocoileus virginianus ), New York State. Am J Trop Med Hyg. 2020;104:593–603.

    Article  Google Scholar 

  17. Andreadis TG, Anderson JF, Armstrong PM, Main AJ. Isolations of Jamestown Canyon virus (Bunyaviridae: Orthobunyavirus) from field-collected mosquitoes (Diptera: Culicidae) in Connecticut, USA: a ten-year analysis, 1997–2006. Vector Borne Zoonotic Dis. 2008;8:175–88.

    Article  Google Scholar 

  18. Molaei G, Farajollah A, Armstrong PM, Oliver J, Howard JJ, Andreadis TG. Identification of bloodmeals in Anopheles quadrimaculatus and Anopheles punctipennis from eastern equine encephalitis virus foci in northeastern USA. Med Vet Entomol. 2009;23:350–6.

    Article  CAS  Google Scholar 

  19. McMillan JR, Armstrong PM, Andreadis TG. Patterns of mosquito and arbovirus community composition and ecological indexes of arboviral risk in the Northeast United States. PLoS Negl Trop Dis. 2020;14:1–21.

    Article  Google Scholar 

  20. Dieme C, Ngo KA, Tyler S, Maffei JG, Zink SD, Dupuis AP, et al. Role of Anopheles mosquitoes in Cache Valley virus lineage displacement, New York, USA. Emerg Infect Dis. 2022;28:303.

    Article  CAS  Google Scholar 

  21. Dieme C, Maffei JG, Diarra M, Koetzner CA, Kuo L, Ngo KA, et al. Aedes albopictus and Cache Valley virus: a new threat for virus transmission in New York State. Emerg Microbes Infect. 2022;11:741–8.

    Article  CAS  Google Scholar 

  22. Ciota AT, Bialosuknia SM, Zink SD, Brecher M, Ehrbar DJ, Morrissette MN, et al. Effects of Zika virus strain and Aedes mosquito species on vector competence. Emerg Infect Dis. 2017;23:1110–7.

    Article  CAS  Google Scholar 

  23. Dieme C, Ciota AT, Kramer LD. Transmission potential of Mayaro virus by Aedes albopictus, and Anopheles quadrimaculatus from the USA. Parasit Vectors. 2020;13:4–9.

    Article  Google Scholar 

  24. Ebel GD, Carricaburu J, Young D, Bernard KA, Kramer LD. Genetic and phenotypic variation of West Nile virus in New York, 2000–2003. Am J Trop Med Hyg. 2004;71:493–500.

    Article  CAS  Google Scholar 

  25. Brustolin M, Pujhari S, Henderson CA, Rasgon JL. Anopheles mosquitoes may drive invasion and transmission of Mayaro virus across geographically diverse regions. PLoS Negl Trop Dis. 2018;12:e0006895.

    Article  CAS  Google Scholar 

  26. Blackmore CCGM, Blackmore MMS, Grimstad PPR. Role of Anopheles quadrimaculatus and Coquillettidia perturbans (Diptera: Culicidae) in the transmission cycle of Cache Valley virus (Bunyaviridae: Bunyavirus) in the midwest, USA. J Med Entomol. 1998;35:660–4.

    Article  CAS  Google Scholar 

  27. Walker ED, Grayson MA, Edman JD. Isolation of Jamestown Canyon and snowshoe hare viruses (California serogroup) from Aedes mosquitoes in western Massachusetts. J Am Mosq Control Assoc. 1993;9:131–4.

    CAS  PubMed  Google Scholar 

  28. Heard PB, Zhang M, Grimstad PR. Laboratory transmission of Jamestown Canyon and snowshoe hare viruses (Bunyaviridae: California Serogroup) by several species of mosquitoes. J Am Mosq Control Assoc. 1997;7:94.

    Google Scholar 

  29. Soria AG, Brackney DE, Armstrong PM. Saliva collection via capillary method may underestimate arboviral transmission by mosquitoes. Parasit Vectors. 2022.

    Article  Google Scholar 

  30. Viglietta M, Bellone R, Blisnick AA, Failloux A-B. Vector specificity of arbovirus transmission. Front Microbiol. 2021;12:1–24.

    Article  Google Scholar 

  31. Lambrechts L. Dissecting the genetic architecture of host-pathogen specificity. PLoS Pathog. 2010;6:9–10.

    Article  Google Scholar 

  32. Armstrong PM, Andreadis TG, Shepard JJ, Thomas MC. Northern range expansion of the asian tiger mosquito (Aedes albopictus): analysis of mosquito data from Connecticut, USA. PLoS Negl Trop Dis. 2017;11:1–13.

    Article  Google Scholar 

  33. Hahn MB, Eisen RJ, Eisen L, Boegler KA, Moore CG, McAllister J, et al. Reported distribution of Aedes (Stegomyia) aegypti and Aedes (Stegomyia) albopictus in the United States, 1995–2016 (Diptera: Culicidae). J Med Entomol. 2016;53:1169–75.

    Article  Google Scholar 

  34. Kache PA, Eastwood G, Collins-Palmer K, Katz M, Falco RC, Bajwa WI, et al. Environmental determinants of Aedes albopictus abundance at a northern limit of its range in the United States. Am J Trop Med Hyg. 2020;102:436–47.

    Article  Google Scholar 

  35. Harrison BA, Mitchell CJ, Apperson CS, Smith GC, Karabatsos N, Engber BR, et al. Isolation of Potosi virus from Aedes albopictus in North Carolina. J Am Mosq Control Assoc. 1995;11:225–9.

    CAS  PubMed  Google Scholar 

  36. Little EAH, Harriott OT, Akaratovic KI, Kiser JP, Abadam CF, Shepard JJ, et al. Host interactions of Aedes albopictus, an invasive vector of arboviruses, in Virginia, USA. PLoS Negl Trop Dis. 2021;15:1–19.

    Article  Google Scholar 

  37. Gratz NG. Critical review of the vector status of Aedes albopictus. Med Vet Entomol. 2004;18:215–27.

    Article  CAS  Google Scholar 

  38. Grimstad PR, Kobayashi JF, Zhang MB, Craig GB. Recently introduced Aedes albopictus in the United States: potential vector of La Crosse virus (Bunyaviridae: California serogroup). J Am Mosq Control Assoc. 1989;5:422–7.

    CAS  PubMed  Google Scholar 

  39. Kramer LD, Bowen MD, Hardy JL, Reeves WC, Presser SB, Eldridge BF. Vector Competence of Alpine, Central Valley, and Coastal mosquitoes (Diptera: Culicidae) from California for Jamestown Canyon virus. J Med Entomol. 1993;30:398–406.

    Article  CAS  Google Scholar 

  40. Boromisa RD, Grayson MA. Oral transmission of Jamestown Canyon virus by Aedes provocans mosquitoes from northeastern New York. J Am Mosq Control Assoc. 1991;7:42–7.

    CAS  PubMed  Google Scholar 

  41. Ciccone EJ, Markmann AJ, Srinivas ML, Levinson KJ, Miller MB, Van Duin D, et al. Encephalitis caused by Jamestown Canyon virus in a liver transplant. Open Forum Infect Dis. 2022.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Ayers VB, Huang YJS, Lyons AC, Park SL, Dunlop JI, Unlu I, et al. Infection and transmission of Cache Valley virus by Aedes albopictus and Aedes aegypti mosquitoes. Parasit Vectors. 2019.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Yang F, Chan K, Marek PE, Armstrong PM, Liu P, Bova JE, et al. Cache Valley virus in Aedes japonicus japonicus mosquitoes, Appalachian Region. United States Emerg Infect Dis. 2018;24:553.

    Article  Google Scholar 

  44. Cheng LL, Rodas JD, Schultz KT, Christensen BM, Yuill TM, Israel BA. Potential for evolution of California serogroup bunyaviruses by genome reassortment in Aedes albopictus. Am J Trop Med Hyg. 1999;60:430–8.

    Article  CAS  Google Scholar 

  45. Bara JJ, Parker AT, Muturi EJ. Comparative susceptibility of Ochlerotatus japonicus, Ochlerotatus triseriatus, Aedes albopictus, and Aedes aegypti (Diptera: Culicidae) to La Crosse virus. J Med Entomol. 2016;53:1415–21.

    Article  Google Scholar 

Download references


We thank Phil Armstrong at The Connecticut Agricultural Experimental Station for providing virus strains. We thank the New York State Department of Health, Wadsworth Center Media and Tissue Core Facility for providing cells and media for these studies. We additionally thank the NYS Arbovirus Laboratory insectary staff for assistance with rearing and experimentation.


This publication was supported by Cooperative Agreement number U01CK000509, funded by the Centers for Disease Control and Prevention. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the Centers for Disease Control and Prevention or the Department of Health.

Author information

Authors and Affiliations



Designed research: CD, ATC and LDK. Performed research: CD. Analyzed data: CD, ATC and LDK. Wrote the paper: CD, ATC and LDK. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Constentin Dieme.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Dieme, C., Kramer, L.D. & Ciota, A.T. Vector competence of Anopheles quadrimaculatus and Aedes albopictus for genetically distinct Jamestown Canyon virus strains circulating in the Northeast United States. Parasites Vectors 15, 226 (2022).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: