Transmission potential of Mayaro virus by Aedes albopictus, and Anopheles quadrimaculatus from the USA

Mayaro virus (MAYV; Alphavirus, Togaviridae) is an emerging pathogen endemic in South American countries. The increase in intercontinental travel and tourism-based forest excursions has resulted in an increase in MAYV spread, with imported cases observed in Europe and North America. Intriguingly, no local transmission of MAYV has been reported outside South America, despite the presence of potential vectors. We assessed the vector competence of Aedes albopictus from New York and Anopheles quadrimaculatus for MAYV. The results show that Ae. albopictus from New York and An. quadrimaculatus are competent vectors for MAYV. However, Ae. albopictus was more susceptible to infection. Transmission rates increased with time for both species, with rates of 37.16 and 64.44% for Ae. albopictus, and of 25.15 and 48.44% for An. quadrimaculatus, respectively, at 7 and 14 days post-infection. Our results suggest there is a risk of further MAYV spread throughout the Americas and autochthonous transmission in the USA. Preventive measures, such as mosquito surveillance of MAYV, will be essential for early detection.


Background
Mayaro virus (MAYV; Togaviridae, Alphavirus) is an emerging virus first isolated in Trinidad in 1954 from the serum of febrile patients. Mayaro virus strains are grouped into three distinct genotypes: L (limited), N (new), and D (widely dispersed) [1][2][3][4]. Similar to other medically important alphaviruses, MAYV is a mosquitoborne arbovirus that causes fever, headache, myalgia, rash, and arthralgia of large joints and, occasionally, arthritis in humans [5]. New World primates of the families Cebidae and Callithricidae are considered to be potential natural reservoirs for the virus [6,7]. The virus has also been found in a migrating bird, equids, anteaters, armadillos, opossums, and rodents [8,9].
Endemic in South America countries, the frequency of Mayaro virus disease in humans has increased in number in recent years, and imported cases have been detected in previously unaffected areas, such as Europe and the USA [3]. Further expansion of MAYV range could be facilitated by global climate change, rapid urbanization and higher mobility of the population, lack of effective vector control, and spreading of vector populations to new geographic regions [5,10,11]. Different mosquito species have been found to be infected with the virus, including Mansonia venezuelensis, Haemagogus janthinomys, Sabethes spp., and Culex spp. [7,10]. Moreover, Aedes albopictus, Aedes aegypti, Anopheles gambiae,

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Parasites & Vectors

Mosquito vector competence for Mayaro virus
Mayaro virus strain TRVL-4675 (isolated from the serum of an infected human in Trinidad in 1954 and belonging to the D genotype) was freshly propagated in Vero (African Green Monkey kidney) cell cultures maintained at 37 °C, 5% CO 2 . At 48 h following infection (multiplicity of infection ≈ 1.0), the supernatant was harvested and diluted 1:1 with defibrinated sheep blood plus a final concentration of 2.5% sucrose. For each species, three biological replicates at different times were performed, and for each experiment 90-100 female mosquitoes were allowed to feed. Female An. quadrimaculatus mosquitoes (3-5 days old) deprived of sugar for 1-2 h and female Ae. albopictus (5-7 days old) deprived of sugar for 24 h were allowed to feed on MAYV-blood suspension for 45 min via a Hemotek membrane feeding system (Discovery Workshops, Acrington, UK) with a porcine sausage casing membrane, at 37 °C [15]. Following feeding, females were anesthetized with CO 2 , and fully engorged mosquitoes were transferred to 0.6-L cardboard containers and maintained with 10% sucrose at 27 °C until harvested for testing. Aliquots (1 mL) of each blood meal pre-feeding were frozen at − 80 °C to determine MAYV titer by plaque assay on Vero cells.

Detection of Mayaro virus
Infection, dissemination, and transmission were determined on days 7 and 14 post-infectious blood meal (dpi: days post-infection), as previously described [15]. Blood meals, mosquito bodies, legs, and salivary secretions were assayed for infection by plaque assay on Vero cells [16]. Briefly, Vero cells were seeded in six-well plates at a density of 6.0 × 10 5 cells per well and incubated for 3-4 days at 37 °C, 5% CO 2, to produce a confluent monolayer. The cell monolayers were inoculated with 0.1 mL of 10-fold 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% fetal bovine serum, and 0.6% Oxoid agar supplemented with 0.2× penicillin-streptomycin/mL, 0.5 μg of fungizone (amphotericin B)/mL, and 20 μg of gentamicin/mL was added at the conclusion of adsorption. The infected monolayers were incubated at 37 °C, 5% CO 2 . 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 overnight at 37 °C, 5% CO 2 . For the blood meal, the plaques were counted, and the viral titer was calculated and expressed as plaque-forming units per milliliter. For mosquito samples, presence or absence of plaques was checked.
Dissemination rate was defined the proportion of mosquitoes with infected legs among the mosquitoes with infected bodies and transmission rate as the proportion of mosquitoes with infectious saliva collected by capillary transmission method [15] among mosquitoes with disseminated infection. Dissemination efficiencies and transmission efficiencies refer to the proportion of mosquitoes with infectious virus in the legs or in the saliva, respectively, among all mosquitoes that fed.

Statistical analysis
A Fisher's exact test was used to compare combined infection rates, dissemination rates, dissemination efficiencies, transmission rates, and transmission efficiencies   Within mosquito species similar mean dissemination rates were observed for Ae. albopictus and An. quadrimaculatus for both time points (95.56% at 7 dpi vs. 100% at 14 dpi and 61.0% at 7 dpi vs. 59.9% at 14 dpi, respectively; Table 1). Dissemination efficiencies at 7 and 14 dpi were significantly different between mosquito species (P < 0.0001, OR 21.5, 95% CI 7.27-63.58 and P < 0.0001, OR 213.9, 95% CI 12.88-3554, at 7 dpi and 14 dpi, respectively; Table 1). Detection of infectious viral particules in mosquitoes collected at 7 and 14 dpi indicated that Ae. albopictus and An. quadrimaculatus are highly susceptible to MAYV through oral challenge and subsequently support viral replication.

Discussion
To our knowledge, this is the first study to examine the vector competence of a temperate population of Ae. albopictus from the Northeast USA, and the second study on An. quadrimaculatus, a native and abundant anopheline mosquito in the Northeast USA, including New York, for MAYV. As mosquitoes and their viruses continue to expand their geographic range and emerge in unpredictable ways, the USA could face an increased threat from MAYV in the future. Our data demonstrate that New York Ae. albopictus and An. quadrimaculatus are highly competent vectors of MAYV.
When multiple mosquito species are involved in the transmission of an arbovirus, the effort needed to prevent human exposure increases. Determining the role of each species is important [17]. We found that dissemination and transmission rates were lower for An. quadrimaculatus than for Ae. albopictus. In locations where Ae. albopictus is prevalent, this difference might play a role in the epidemiology of MAYV considering its high vector competence, were it to be introduced.
Aedes albopictus is a highly invasive species that has been introduced into the USA where it has become permanently established in at least 27 states, including New York [18,19]. It is predicted that this mosquito species will continue to spread globally over the coming decades, increasing the risk to human health [20]. In the USA, Ae. albopictus may be infected with a number of arboviruses, including Eastern Equine Encephalitis virus, Dengue virus, St. Louis encephalitis virus, La Crosse orthobunyavirus, and West Nile virus [19]. In addition, its role as a vector is recognized for Chikungunya virus and Zika virus, both introduced recently into the USA [19,20]. Using a temperate population of Ae. albopictus from New York, we confirmed earlier studies that demonstrated the potential of Ae. albopictus to transmit MAYV [13,14,21].
The high infection rates (85-100%) obtained in our results are similar to the reports of others [13,14]. Moreover, the high dissemination and transmission rates observed in our study corroborate the findings of Diop et al [13]. However, Wiggins et al [14], using the same MAYV strain that we used, found lower transmission rates compared to our study and Pereira et al. [21]. These differences could be due to the genetic background (geographical origin) of the vector and/or the difference in mosquito incubation temperature, as has been shown for Chikungunya virus [22,23].
Anopheles mosquitoes are persistently exposed in nature to diverse arboviruses, but in general an assessment of their potential to transmit arboviral pathogens has been neglected. In addition to MAYV, vector competence of Anopheles mosquitoes for O'nyong nyong (ONNV) virus, Rift Valley fever phlebovirus, Eastern equine encephalitis virus, and Cache Valley orthobunyavirus has been reported [12,[24][25][26]. However, only ONNV is known to rely on Anopheles spp. as primary vectors [27,28]. Anopheles quadrimaculatus are primarily mammalophagic mosquitoes. In the Northeast USA, whitetailed deer are the predominately identified vertebrate host [29]. However, this may be an artefact of human accessibility rather than an indication of preference. Anopheles quadrimaculatus mosquitoes are historically important vectors of human malaria parasites (Plasmodium vivax) [30], suggesting that they have a high level of anthropophily. Furthermore, white-tailed deer overabundance and availability throughout the region may explain mosquitoes feeding behavior [17,31]. It is suggested that An. quadrimaculatus and An. punctipennis may contribute to the transmission of Eastern equine encephalitis, Jamestown Canyon, and Cache Valley viruses in the Northeast USA [29]. Recently, the capacity of An. quadrimaculatus to transmit MAYV at 7 dpi but not at 14 dpi was demonstrated [12]. In our study, An. quadrimaculatus mosquitoes were able to transmit the virus at both time points, suggesting this species may be an overlooked vector for MAYV emergence and invasion in the USA.

Conclusion
Information on the competence of mosquito vectors is essential for controlling and preventing viruses transmitted by arthropods. While it is not possible to accurately predict the emergence of a disease, in light of our results, MAYV presents a health threat to the USA, and local authorities should reinforce epidemiological and entomological surveillance to detect the introduction of this viral pathogen.