Skip to main content

First report of Culex flavivirus infection from Culex coronator (Diptera: Culicidae), Colombia



Flaviviruses are important pathogens for humans and animals (Dengue viruses, Yellow fever virus, Zika virus and West Nile virus). Culex flavivirus (CxFV) is an insect-specific virus of the genus Flavivirus, detected in a wide variety of mosquito species.


To detect Flavivirus in mosquitoes of a tropical region of the Colombian Caribbean.


In 2014, an entomological surveillance of arboviruses was conducted in the department of Cordoba area of the Caribbean, Colombia. A total of 8270 mosquitoes were captured as follow: Mansonia (n = 3271/39.5%), Culex (n = 2668/32.26%), Anopheles (n = 840/10.15%), Aedeomyia (n = 411/4.9%), Psorophora (n = 397/4.8%), Coquilletidia (n = 369/4.46%), Uranotaenia (n = 261/3.15%) and Aedes (n = 53/0.6%). All mosquito species were collected in dry tropical forest of the Caribbean area. Universal primers for NS5 gene (958 pb), RT-PCR for flavivirus and sequencing were used for molecular identification of viruses detected.


Two pools belonging to Culex coronator were positive for flavivirus RNA sequence by RT-PCR. The sequences of the PCR amplicons, matched that of the Culex flaviviruses, CxFv COL PM_149 (GenBank: KR014201) and CxFv COL PM_212 (GenBank: KT307717). Phylogenetic analysis of the NS5 protein sequences of the Culex flaviviruses sequences with those of reference sequences available in GenBank indicated viruses of Genotype II, closely related to the Brazilian strain, BR_SJRP_01_ (GenBank: KT726939), from Culex sp. The alignment of Culex flavivirus sequences CxFv COL_ PM 212 and CxFv COL_ PM 149 with sequences of strains detected in different geographical regions grouped the strains in a Latin American clade reported in Brazil, Argentina and Mexico.


The present work illustrated that CxFV was circulating among vectors of human pathogenic arboviruses in Colombia, but the impact of CxFV on other flaviviruses which are endemic in the study area still remains to be explored.

Culex flavivirus (CxFV) is an insect-specific virus of the genus Flavivirus detected in mosquitoes. The present report shows the first detection of CxFV in mosquitoes Culex coronator in Colombia. The strains detected are phylogenetically related to Africa/Caribbean/Latin America genotype 2.


Arboviruses are a serious public health problem in tropical countries, the genus flavivirus included a group of these viruses which some of them are highly pathogenic, and can cause encephalitis or hemorrhagic fevers in humans [1]. In each region, there are different mosquito species vectors and different animals which serves as virus reservoirs.

Culex flavivirus (CxFV) is an insect-specific virus of the genus Flavivirus. CxFV strains have been detected from mosquitoes Culex pipiens, Culex quinquefasciatus, and other Culex sp. around the world [2, 3]. CxFV belongs to Flaviviridae, the viruses within this family are transmitted horizontally between vertebrate hosts and hematophagous arthropods. However, certain members of the genus Flavivirus are known to be vertebrate-specific whilst others are insect-specific flaviviruses (ISFV). Transmission of ISFVs in natural mosquito populations is maintained by vertical transmission and in minor role the venereal transmission [4,5,6].

In Europe, species of ISFV have been identified in field mosquitoes from Italy, Portugal, Spain, the United Kingdom, the Czech Republic and Greece [7,8,9]. Sequences related to those viruses have been detected worldwide. In Algeria, Spain and Portugal ISFV RNA has also been detected in sand flies of the family Psychodidae [8]. Despite the large number of ISFV, they have been not completely characterized phylogenetically [8].

ISFV do not cause disease in humans or animals, but they are important because they co-infect mosquito vectors and compete with the viruses that are pathogenic to humans and animals [10].

The circulation of ISFVs in nature is of increasing interest due to their influence onarboviruses transmission [9]. In vitro co-infection studies with mosquito-borne flaviviruses and ISFV have shown that they alter vector competence for the mosquito-borne flaviviruses in both enzootic and epizootic transmission cycles [10]. Several investigations have addressed co-infection exclusion effects between CxFV and arboviruses such as West Nile virus (WNV) and Rift Valley fever virus, however, studies are not conclusive [10]. Ongoing questions about the role of ISFV in the control of pathogenic arboviruses like dengue, Yellow Fever (YF), Zika and Ckinkungunya suggest the possibility of their use in the biological control of arbovirus vectors.

Colombia, due to its geographical location, has a great biodiversity of reservoirs and arthropods, which have supported the emergence of viruses such as Chikungunya and Zika. These viruses have adapted to the vectors circulating in the tropics, which facilitated their spread, and caused the two most recent major epidemics of arboviruses in the Americas. The Colombian Caribbean also maintains circulation of pathogenic Saint Louis encephalitis virus (SLEV) and West Nile Virus (WNV), transmitted by mosquitoes of Culex erraticus, Cx. quinquefasciatus and Mansonia titillans, confirming that these ecological conditions are favorable to high viral biodiversity [11,12,13].

The objective of this work was to detect Flaviviruses in mosquitoes of a tropical region of the Colombian Caribbean.


Type of study, geographic area and sampling sites

From August 2012 to December 2014, an observational, descriptive and prospective study was conducted to identify circulating flaviviruses in different mosquito species of the department of Córdoba, Colombia. The department is located in the Caribbean region between 09° 26′16" and 07° 22′05 “N, and 74° 47’ 43” and 76° 30’01 ‘W. The department of Córdoba has areas with wetlands and tropical dry forest, the area is characterized by rainfall that does not exceed 2000 mm per year, of which, 80% is during the rainy season (May-October). The tropical climate has an average annual temperature of 28°C, with heights between 0 and 40 masl. The department is divided geographically into sub-regions according to the territorial development plan: High, Medium and Low Sinú, and the samplings were carried out in these areas. One of the geographical zones corresponded to the municipality of Montería (8 ° 43’15.80 “N -075 ° 59′27.27” W (Medium Sinú), where the circulation of WNV and SLEV have been reported [14, 15]. The two remaining areas were the municipalities of Tierralta (8° 09′19.20 “N -076° 00′ 55.40” W-High Sinu) and Purisima (9° 14’ 57.60 “N -075° 42′ 34.62” W -Low Sinú)

Mosquitoes collections

In each of the selected sites, a total of five samplings were set-up. Four Light-CDC traps were used to capture mosquitoes, and 2 BG Centinell ™ traps fed with CO2 were used to capture gravid females of different genera. The sampling sites were close to small lagoons and areas of tropical dry forest. During each sampling, the traps were placed between 17:00 and 6:00 h. Manual aspirators were also used. The collected mosquitoes were kept at 6 °C, until being transported to the laboratory of the Biological Research Institute of the Tropic (IIBT), in less than 12 h post-capture. Once in the laboratory the mosquitoes were stored at − 80 °C for molecular analysis.

Taxonomic identification of mosquitoes

Male mosquitoes were identified first. It was necessary to clarify Terminalia [16], due to the difficulty to identify some species of the Culex genus. They were classified according to their morphology based on specialized taxonomic keys [16,17,18]. To morphological confirmation and mounting of genitalia, it was verified the characters used to taxonomical identification such as: 1. Subapical lobe of the gonocoxite as a quadrate at the outer third, bearing a row of eight rods that are progressively smaller distally; gonostyle bearing a small terminal claw and two minute setae situated on inner face before tip, ventral arm of the phallosome long and curved, and lateral arm with several large teeth with angular rounded corners, using description provided by Howard (1915). Recently discussion about this species by Laurito et al. (2017), allow consider other description about genitalia of male, such as: subapical lobe of the gonocoxite more or less divided with four similar stout rod-like, setae on the proximal part of the lobe (toward the base of the gonocoxite) and several subequal filiform setae on the distal part of the lobe (toward the apex of the gonocoxite); gonocoxite with an apical cluster of fine setae that extend to mid-length of the gonostylus [19]. For females we used Forattini characters described as: 1. Feminine maxillary palps are entirely dark. 2. There are no post-spiracular scales in the pleura. 3. The wing and devoid of sets of clear scales. 4. The tarsi are clearly marked and the tarsomer 5 presents a clear basal area [20]. The identification was carried out at 14 °C. Pools of 2 to 50 individuals of engorged or non-engorged female mosquitoes of the same species, location area, date and type of trap were grouped.

Flavivirus detection

RNA extraction was performed using the QIAamp Viral RNA Mini kit (QIAGEN, Inc.) following the manufacturer’s instructions. The RNA was extracted from 140 μl of the homogenized mosquitoes sample. For detection of flavivirus reverse transcription RT-PCR with universal primers previously described by Bronzoni et al. [21] were used; the primers amplify a fragment of 958 base pairs (bp) of the NS5 protein: Forward FG1-TCAAGGAACTCCACACATGAGATGTACT and Reverse FG2-GTGTCCCATCCTGCTGTGTCATCAGCATACA. The positive control used was Dengue virus 2.

Sequencing and phylogenetic analysis

The amplified fragments were sequenced in both directions in an ABI 3730 XL Automated sequencer. Thirty-six representative sequences belonging to different geographic regions were downloaded from Genbank and aligned using MUSCLE in MEGA v7 [22]. Alignments in FASTA format were also evaluated in jModelTest v2.1.4 [23], using the Akaike criterion informative to model appropriate nucleotide substitutions (Additional file 1). The XML file for bayesian analysis was built in BEAUti v1.5.4, to model sequence evolution, invariants, gamma distribution, size of the chain run (20 million generations), coalescent constant population and uncorrelated molecular clock were chosen for this inference [24].


Nine thousand eight hundred ninety eight mosquitoes were captured, and 8270 of them were identified and grouped in 334 pools. 41 species were identified and distributed in 8 genera: Mansonia (N = 3271/39.5%), Culex (n = 2668/32.2%), Anopheles (n = 840/10.1%), Aedeomyia (n = 411/4.9%), Psorophora (n = 397/4.8%), Coquilletidia (n = 369 / 4.4%), Uranotaenia (n = 261/3.1%) and Aedes (n = 53/0.6%). The genus of mosquitoes of greater medical importance, distributed monthly is shown in the Fig. 1.

Fig. 1
figure 1

Distribution monthly of mosquitoes of great medical importance captured in the study

Detection of viral RNA in mosquitoes and sequencing analysis

Of the 334 analyzed pools, 2 pools of Culex coronator were positive for flavivirus. These mosquitoes were collected in the municipality of Montería (PM 149 and PM 212). The 958-bp amplicons from the NS5 gene were sequenced, and the sequences were edited and assembled to obtain a fragment of 758 bp for analyses. Sequences were aligned and a 99% similarity was obtained with Culex flavivirus virus sequences from position 8142 to position 8899 of the complete genome of the isolate (Strain: BR_SJRP_01_2012, Genbank accession number: KT726939). Sequences were deposited in the GenBank: CxFv COL_ PM 212 (Genbank accession number: KT307717) and CxFv COL_ PM 149 (Genbank accession number: KR014201).

Phylogenetic analysis

Alignments of the NS5 sequences from the Culex flaviviruses, CxFv COL_ PM 212 and CxFv COL_ PM 149, with NS5 sequences from strains detected in different geographical regions allowed their grouping in a clade that includes virus strains reported in Brazil, Argentina and Mexico and belonging to the genotype II group of strains of Africa/Caribbean/Latin America (Fig. 2).

Fig. 2
figure 2

Phylogenetic tree estimated by Bayesian analysis of 80 sequence strains (NS5) of Culex Flavivirus virus data under the GTR + G + I model of nucleotide substitution. The number accession of Genbank is followed by abbreviated name of strain. The branches in red belong to our characterized sequences


In the present study, the most abundant mosquito genera were Mansonia (39.5%) and Culex (32%), these results differ somewhat from those reported by Hoyos et al. [12] in a nearby area where the genus Culex (50%) was the most abundant. The difference between these results is possibly due to the geographic, climatic and environmental characteristics of the selected areas.

The limited number of positive samples (pools) in the present study 0.6% (2/334 pools) is similar to reported by Bryant et al 2005 in Vietnam, where only 2.3% of analyzed pools were positives (26/1122) [25]. Ochieng et al., during 2007 and 2012 in Kenia, captured 450.680 mosquitoes and analyzed 15.890 groups, 53 were positives 0.3% [26]. Loftin et al., in Virginia, USA, reported 0.8% of positives pools of 14.949 analyzed [27]. Finally, Burgueño in Uruguay analyzed 244 pools and found only 2% (5 pools) of positives pools with Culex Flavivirus virus. However, Morais-Bronzoni et al., suggest that nested PCR assays for detection of flaviviruses strategy could be more sensitive in samples with low viral load [21].

According to the taxonomic definition of flaviviruses, based on the identity of the conserved region of NS5 gene (> 84%) [28], the detected strains CxFv COL_PM 212 and CxFv COL_PM 149 are specific ISFV of the species CxFV. The sequences detected in the present study have an identity of 99% (756/758 bp) with isolated CxFV BR_SJRP_01_2012, (KT726939) from Brazil [29]. These results confirm for the first time the presence of CxFV in Cx. coronator species in Colombia. CxFV was previously reported in Colombia, in the department of Córdoba in Cx. quinquefasciatus (KM031075) and Cx. erraticus (KM031073) species [12]. Interestingly, the nucleotide identity between the CxFV strains reported by Hoyos et al., was 94% (338/358 bp) with respect to ours results, which implied a possible wide range of strains with significant genetic diversity.

CxFV have a great diversity of reservoirs and their phylogeny could be influenced by these. The phylogenetic tree shows two clades (Fig. 2): the first clade is associated with Asian strains and strains from the USA, where Cx. pipiens is the main reservoir. However, other mosquito species, such as Cx. tritaeniorhynchus and Anopheles sinensis [30], have been reported with CxFV in the first clade. These isolates were classified in genotype I (Asian/USA).

The second phylogenetic group of CxFV have been reported mostly in the Americas and Africa, with Cx. quinquefasciatus as the main reservoir [3, 29, 30], the strains detected in this study are more phylogenetically related to this group, described as genotype II, (Africa/Caribbean/Latin America; Fig. 1). However, it is important to clarify that the genotypes are based on the phylogenetic analysis of the viral envelope protein (E) and our phylogenetic was performed with the NS5 gene.

The present study reports the first description of CxFV in Cx. coronator in the department of Córdoba, the presence of these viruses in mosquitoes could play an important role from the public health point of view, because it has been shown that previous CxFV infection can increase or block the infection of the mosquito by other pathogenic flaviviruses. CxFV-positive mosquitoes also differ in flight activity, which could decrease contact with arbovirus amplification hosts [10, 31,32,33,34]. Future studies should be carried out, in order to detect CxFV in other areas of Colombia to define the distribution of the virus, its genetic characteristics and relationship with other mosquito species.



base pairs






Culex flavivirus


insect-specific Flavivirus


non-structural protein


Reverse transcription polymerase chain reaction


Saint Louis encephalitis virus


West Nile Virus


Yellow Fever


  1. Mattar S, Tique V, Miranda J, Montes E, Garzon D. Undifferentiated tropical febrile illness in Cordoba, Colombia: not everything is dengue. J Infect Public Health. 2017;10(5):507–12.

    Article  Google Scholar 

  2. Hoshino K, Isawa H, Tsuda Y, Yano K, Sasaki T, Yuda M, et al. Genetic characterization of a new insect flavivirus isolated from Culex pipiens mosquito in Japan. Virology. 2007;359(2):405–14.

    Article  CAS  Google Scholar 

  3. Goenaga S, Fabbri CM, Garcia JB, Rondan JC, Gardenal N, Calderon GE, et al. New strains of Culex flavivirus isolated in Argentina. J Med Entomol. 2014;51(4):900–6.

    Article  Google Scholar 

  4. Newman CM, Krebs BL, Anderson TK, Hamer GL, Ruiz MO, Brawn JD, et al. Culex Flavivirus during West Nile virus epidemic and Interepidemic years in Chicago, United States. Vector Borne Zoonotic Dis. 2017;17(8):567–75.

    Article  Google Scholar 

  5. Blitvich BJ, Firth AE. Insect-specific flaviviruses: a systematic review of their discovery, host range, mode of transmission, superinfection exclusion potential and genomic organization. Viruses. 2015;7(4):1927–59.

    Article  CAS  Google Scholar 

  6. Bolling BG, Olea-Popelka FJ, Eisen L, Moore CG, Blair CD. Transmission dynamics of an insect-specific flavivirus in a naturally infected Culex pipiens laboratory colony and effects of co-infection on vector competence for West Nile virus. Virology. 2012;427(2):90–7.

    Article  CAS  Google Scholar 

  7. Calzolari M, Ze-Ze L, Ruzek D, Vazquez A, Jeffries C, Defilippo F, et al. Detection of mosquito-only flaviviruses in Europe. J Gen Virol. 2012;93(Pt 6):1215–25.

    Article  CAS  Google Scholar 

  8. Calzolari M, Ze-Ze L, Vazquez A, Sanchez Seco MP, Amaro F, Dottori M. Insect-specific flaviviruses, a worldwide widespread group of viruses only detected in insects. Infect Genet Evol. 2016;40:381–8.

    Article  Google Scholar 

  9. Talavera S, Birnberg L, Nunez AI, Munoz-Munoz F, Vazquez A, Busquets N. Culex flavivirus infection in a Culex pipiens mosquito colony and its effects on vector competence for Rift Valley fever phlebovirus. Parasit Vectors. 2018;11(1):310.

    Article  Google Scholar 

  10. Kent RJ, Crabtree MB, Miller BR. Transmission of West Nile virus by Culex quinquefasciatus say infected with Culex Flavivirus Izabal. PLoS Negl Trop Dis. 2010;4(5):e671.

    Article  Google Scholar 

  11. Hoyos-Lopez R, Soto SU, Rua-Uribe G, Gallego-Gomez JC. Molecular identification of Saint Louis encephalitis virus genotype IV in Colombia. Mem Inst Oswaldo Cruz. 2015;110(6):719–25.

    Article  CAS  Google Scholar 

  12. Hoyos-Lopez R, Suaza-Vasco J, Rua-Uribe G, Uribe S, Gallego-Gomez JC. Molecular detection of flaviviruses and alphaviruses in mosquitoes (Diptera: Culicidae) from coastal ecosystems in the Colombian Caribbean. Mem Inst Oswaldo Cruz. 2016;111(10):625–34.

    Article  Google Scholar 

  13. Lopez RH, Soto SU, Gallego-Gomez JC. Evolutionary relationships of West Nile virus detected in mosquitoes from a migratory bird zone of Colombian Caribbean. Virol J. 2015;12:80.

    Article  Google Scholar 

  14. Mattar S, Edwards E, Laguado J, Gonzalez M, Alvarez J, Komar N. West Nile virus antibodies in Colombian horses. Emerg Infect Dis. 2005;11(9):1497–8.

    Article  Google Scholar 

  15. Álvarez J, González M, Máttar S. Actividad del virus del oeste del Nilo y otros flavivirus en cinco departamentos del Caribe colombiano. Revista MVZ Córdoba. 2010;15(1):2021–2.

    Article  Google Scholar 

  16. Lane J. Neotropical Culicidae. Dixinae CaC, tribes Anophelini, Toxorhglnchit& i and Culicini (Genus Culex only). Sao Paulo: University of Sao Paulo; 1953.

    Google Scholar 

  17. Cova PSZ, Rausseo JA. Mosquitos (Culicinos) de Venezuela. Venezuela: Ministerio de sanidad y asistencia social; 1966.

    Google Scholar 

  18. Clark-Gil S, Darsie R. The mosquitoes of Guatemala their identification, distribution and bionomics with keys to adult females and larvae. Mosquito Systematics Journal. 1983;15(3):151–282.

    Google Scholar 

  19. Laurito M, Briscoe AG, AlmirÓn WR, Harbach RE. Systematics of the Culex coronator complex (Diptera: Culicidae): morphological and molecular assessment. Zool J Linnean Soc. 2018;182(4):735–57.

    Article  Google Scholar 

  20. Forattini O. 2002. Culicidologia médica. Volume 2. Identificação, biologia, epidemiologia. São Paulo: Editora da Universidade de São Paulo.

  21. de Morais Bronzoni RV, Baleotti FG, Ribeiro Nogueira RM, Nunes M, Moraes Figueiredo LT. Duplex reverse transcription-PCR followed by nested PCR assays for detection and identification of Brazilian alphaviruses and flaviviruses. J Clin Microbiol. 2005;43(2):696–702.

    Article  Google Scholar 

  22. Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016;33(7):1870–4.

    Article  CAS  Google Scholar 

  23. Darriba D, Taboada GL, Doallo R, Posada D. jModelTest 2: more models, new heuristics and parallel computing. Nat Methods. 2012;9(8):772.

    Article  CAS  Google Scholar 

  24. Drummond AJ, Suchard MA. Bayesian random local clocks, or one rate to rule them all. BMC Biol. 2010;8:114.

    Article  Google Scholar 

  25. Bryant JE, Crabtree MB, Nam VS, Yen NT, Duc HM, Miller BR. Isolation of arboviruses from mosquitoes collected in northern Vietnam. Am J Trop Med Hyg. 2005;73(2):470–3.

    Article  Google Scholar 

  26. Ochieng C, Lutomiah J, Makio A, Koka H, Chepkorir E, Yalwala S, et al. Mosquito-borne arbovirus surveillance at selected sites in diverse ecological zones of Kenya; 2007 - 2012. Virol J. 2013;10:140.

    Article  Google Scholar 

  27. Loftin KC, Diallo AA, Herbert MW, Phaltankar PG, Yuan C, Grefe N, et al. Five-year surveillance of West Nile and eastern equine encephalitis viruses in southeastern Virginia. J Environ Health. 2006;68(9):33–40.

    PubMed  Google Scholar 

  28. Kuno G, Chang GJ, Tsuchiya KR, Karabatsos N, Cropp CB. Phylogeny of the genus Flavivirus. J Virol. 1998;72(1):73–83.

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Bittar C, Machado DC, Vedovello D, Ullmann LS, Rahal P, Araujo Junior JP, et al. Genome sequencing and genetic characterization of Culex Flavirirus (CxFV) provides new information about its genotypes. Virol J. 2016;13(1):158.

    Article  Google Scholar 

  30. Liang W, He X, Liu G, Zhang S, Fu S, Wang M, et al. Distribution and phylogenetic analysis of Culex flavivirus in mosquitoes in China. Arch Virol. 2015;160(9):2259–68.

    Article  CAS  Google Scholar 

  31. Farfan-Ale JA, Lorono-Pino MA, Garcia-Rejon JE, Hovav E, Powers AM, Lin M, et al. Detection of RNA from a novel West Nile-like virus and high prevalence of an insect-specific flavivirus in mosquitoes in the Yucatan peninsula of Mexico. Am J Trop Med Hyg. 2009;80(1):85–95.

    Article  CAS  Google Scholar 

  32. Burivong P, Pattanakitsakul SN, Thongrungkiat S, Malasit P, Flegel TW. Markedly reduced severity of dengue virus infection in mosquito cell cultures persistently infected with Aedes albopictus densovirus (AalDNV). Virology. 2004;329(2):261–9.

    Article  CAS  Google Scholar 

  33. Pacca CC, Severino AA, Mondini A, Rahal P, D'Avila SG, Cordeiro JA, et al. RNA interference inhibits yellow fever virus replication in vitro and in vivo. Virus Genes. 2009;38(2):224–31.

    Article  CAS  Google Scholar 

  34. Newman CM, Anderson TK, Goldberg TL. Decreased flight activity in Culex pipiens (Diptera: Culicidae) naturally infected with Culex flavivirus. J Med Entomol. 2016;53(1):233–6.

    Article  CAS  Google Scholar 

Download references


To Joel Rovnak from Colorado State University, for the critics and style grammar corrections.


This study was supported by the University of Cordoba, Research Project number FMV-01-17.

Availability of data and materials

The sequences of CxFV have been deposited into GenBank database under the accession number KT307717 for CxFv COL_ PM 212 and KR014201 for CxFv COL_ PM 149.

Author information

Authors and Affiliations



SM, AA, MG and JA conceived and designed the experiments; JM, AA and JA performed the experiments; JM, SM and RHL analyzed the data, wrote and revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Salim Mattar.

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.

Publisher’s Note

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

Additional file

Additional file 1:

Culex flavivirus aligment Bayesian inference phylogeny of representatives CxFv sequences belonging to different geographic regions strains obtained from the GenBank database. (FAS 29 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Miranda, J., Mattar, S., Gonzalez, M. et al. First report of Culex flavivirus infection from Culex coronator (Diptera: Culicidae), Colombia. Virol J 16, 1 (2019).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: