» Articles » PMID: 33923055

Evaluation of , , and Mosquitoes Competence to Infection

Overview
Journal Viruses
Publisher MDPI
Specialty Microbiology
Date 2021 Apr 30
PMID 33923055
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

The emergence of new human viral pathogens and re-emergence of several diseases are of particular concern in the last decades. (OROV) is an arbovirus endemic to South and Central America tropical regions, responsible to several epidemic events in the last decades. There is little information regarding the ability of OROV to be transmitted by urban/peri-urban mosquitoes, which has limited the predictability of the emergence of permanent urban transmission cycles. Here, we evaluated the ability of OROV to infect, replicate, and be transmitted by three anthropophilic and urban species of mosquitoes, , , and . We show that OROV is able to infect and efficiently replicate when systemically injected in all three species tested, but not when orally ingested. Moreover, we find that, once OROV replication has occurred in the mosquito body, all three species were able to transmit the virus to immunocompromised mice during blood feeding. These data provide evidence that OROV is restricted by the midgut barrier of three major urban mosquito species, but, if this restriction is overcome, could be efficiently transmitted to vertebrate hosts. This poses a great risk for the emergence of permanent urban cycles and geographic expansion of OROV to other continents.

Citing Articles

Introduction of Vector-Borne Infections in Europe: Emerging and Re-Emerging Viral Pathogens with Potential Impact on One Health.

Logiudice J, Alberti M, Ciccarone A, Rossi B, Tiecco G, De Francesco M Pathogens. 2025; 14(1).

PMID: 39861024 PMC: 11768692. DOI: 10.3390/pathogens14010063.


Lack of Competence of US Mosquito Species for Circulating Oropouche Virus.

Payne A, Stout J, Dumoulin P, Locksmith T, Heberlein L, Mitchell M Emerg Infect Dis. 2025; 31(3):619-621.

PMID: 39837096 PMC: 11878313. DOI: 10.3201/eid3103.241886.


Dynamics and ecology of a multi-stage expansion of Oropouche virus in Brazil.

Tegally H, Dellicour S, Poongavanan J, Mavian C, Dor G, Fonseca V medRxiv. 2024; .

PMID: 39574858 PMC: 11581102. DOI: 10.1101/2024.10.29.24316328.


Oropouche virus: A re-emerging arbovirus of clinical significance.

Desai A, Otter A, Koopmans M, Granata G, Grobusch M, Tunali V IJID Reg. 2024; 13:100456.

PMID: 39507390 PMC: 11539570. DOI: 10.1016/j.ijregi.2024.100456.


Multiple bloodmeals enhance dissemination of arboviruses in three medically relevant mosquito genera.

Ferdous Z, Dieme C, Sproch H, Kramer L, Ciota A, Brackney D Parasit Vectors. 2024; 17(1):432.

PMID: 39427222 PMC: 11490111. DOI: 10.1186/s13071-024-06531-y.


References
1.
Hanley K, P Monath T, Weaver S, Rossi S, Richman R, Vasilakis N . Fever versus fever: the role of host and vector susceptibility and interspecific competition in shaping the current and future distributions of the sylvatic cycles of dengue virus and yellow fever virus. Infect Genet Evol. 2013; 19:292-311. PMC: 3749261. DOI: 10.1016/j.meegid.2013.03.008. View

2.
Weaver S, Chen R, Diallo M . Chikungunya Virus: Role of Vectors in Emergence from Enzootic Cycles. Annu Rev Entomol. 2019; 65:313-332. DOI: 10.1146/annurev-ento-011019-025207. View

3.
Burt F, Chen W, Miner J, Lenschow D, Merits A, Schnettler E . Chikungunya virus: an update on the biology and pathogenesis of this emerging pathogen. Lancet Infect Dis. 2017; 17(4):e107-e117. DOI: 10.1016/S1473-3099(16)30385-1. View

4.
Tilston-Lunel N, Hughes J, Acrani G, Da Silva D, Azevedo R, Rodrigues S . Genetic analysis of members of the species Oropouche virus and identification of a novel M segment sequence. J Gen Virol. 2015; 96(Pt 7):1636-50. PMC: 4635451. DOI: 10.1099/vir.0.000108. View

5.
Gorman M, Caine E, Zaitsev K, Begley M, Weger-Lucarelli J, Uccellini M . An Immunocompetent Mouse Model of Zika Virus Infection. Cell Host Microbe. 2018; 23(5):672-685.e6. PMC: 5953559. DOI: 10.1016/j.chom.2018.04.003. View