- Short report
- Open Access
The effect of hybridization of Culex pipiens complex mosquitoes on transmission of West Nile virus
© Ciota et al.; licensee BioMed Central Ltd. 2013
- Received: 23 April 2013
- Accepted: 18 October 2013
- Published: 23 October 2013
Culex pipiens L. complex mosquitoes have a global distribution and are primary vectors of pathogens of public health significance. In the U.S., Cx. pipiens bioformes, Cx. pipiens form pipiens and Cx. pipiens form molestus, as well as Cx. quinquefasciatus, are primary vectors of West Nile virus (WNV; Flaviviridae, Flavivirus). These mosquitoes reside in distinct but overlapping ecological niches and readily hybridize in areas where they coexist. Although species and population-specific differences in vector competence of Culex mosquitoes for WNV have been identified, the extent to which hybridization within this complex alters WNV transmission potential has not been well characterized.
WNV vector competence of laboratory colonies of Cx. p. f. pipiens, Cx. p. f. molestus, and Cx. quinquefasciatus was assessed and compared to hybrid populations created from reciprocal mating of these lines. The results demonstrate that hybridization has a significant effect on WNV infection, dissemination, and, particularly, transmission in Culex pipiens L. complex mosquitoes. Specifically, enhanced transmission of WNV was measured in all hybrid populations relative to one or both parental stains.
These findings demonstrate that environmental or anthropogenic changes resulting in fluctuations in the distribution and extent of hybrid populations of Culex mosquitoes could have a significant impact on transmission patterns of WNV in nature.
- West Nile Virus
- Hybrid Population
- Vector Competence
- Culex Mosquito
- Form Molestus
The Culex pipiens L. complex includes Cx. pipiens and Cx. quinquefasciatus in North America, South America, Africa, and Asia; as well as Cx. australicus and Cx. globocoxitus in Australia . Mosquitoes in this complex are primary vectors of West Nile virus (WNV; Flaviviridae, Flavivirus) in the United States, i.e., Cx pipiens north of 36° latitude and Cx quinquefasciatus, south [2, 3], with hybrids of the two found in a zone stretching from approximately 30°N to 40oN latitude in N. America [4, 5]. Each species possesses a unique genetic signature as well as distinct physiology [6, 7]. Cx pipiens is comprised of two bioformes, Cx pipiens form pipiens and Cx pipiens form molestus. Cx. p. f. molestus populations are present throughout the Americas where they are most often found in more subterranean areas, whereas Cx. p. f. pipiens and Cx. quinquefasciatus occupy aboveground habitats. Additional biological differences further distinguish Cx. p. f. molestus, including autogeny, mating in enclosed spaces, and lack of diapause [2, 8]. An excellent review of the Cx. pipens complex has been published elsewhere . Although many Northern European populations of Cx. p. f. pipiens are pure, U.S. populations generally contain varying levels of Cx. p. f. molestus signature, a characteristic which may increase propensity for U.S. Cx. pipiens to feed on mammals and contribute to the increased number of human cases of WNV in the U.S. . Vector competence for WNV also has been shown to vary among Culex species and populations [10, 11], yet the extent to which hybridization within this complex alters WNV transmission has not been fully evaluated. Here, we sought to characterize variation in WNV transmission potential in laboratory colonies of Cx. p. f. pipiens, Cx p. f. molestus, and Cx. quinquefasciatus, as well as hybrids resulting from mating of these parental lines. Our results demonstrate that the extent of hybridization among Cx. pipiens complex mosquitoes may significantly alter patterns of WNV transmission in the U.S.
All colonized Culex mosquitoes were maintained in 30.5 cm3 cages in an environmental chamber at 27+/-2°C with a relative humidity of 45-65% and a photoperiod of 16:8 (light:dark) hours prior to the collection of experimental egg rafts. Cx. p. f. pipiens colony mosquitoes were originally collected in Pennsylvania in 2004 (courtesy of M. Hutchinson) and colonized at the Arbovirus laboratory. Cx. quinquefasciatus colony mosquitoes were derived from a laboratory colony provided by D. Fonseca (Rutgers Univ.) derived from egg rafts from Benzon Research Inc. (Carlisle, PA) originating from a highly colonized US population. Cx. p. f. molestus were colonized in 2009 following collection from the basement of the state house in New Jersey (courtesy of D. Fonseca). Two-way crosses were completed with the 3 parental strains to produce hybrid progeny. Genetic signatures were confirmed using species-specific primers on a subset (10 individuals) of F0 and F1 mosquitoes [12, 13]. Parental Cx. p. f. pipiens were confirmed to be genetically distinct from Cx. quinquefasciatus yet, as expected, did contain Cx. p. f. molestus signature. Cx. quinquefasciatus and Cx. p. f. molestus individuals tested were genetically pure at the loci evaluated and the presence of mixed signatures were confirmed among all F1 hybrid populations used for experimental feedings.
Experimental infections and vector competence
WNV strain WNV02-1956 was originally isolated from an American crow in New York State in 2005 and passaged once on mammalian cells (Vero; ATCC CC1-81) and once on Aedes albopictus mosquito cells (C6/36, ATCC CRL-1660). After an additional passage of 72 hours on C6/36 cells, supernatants and cells from infected cultures were mixed 1:1 with defibrinated bovine blood (HemaResources, Inc, Aurora, OR) plus a 2.5% final sucrose concentration. 7-day old female mosquitoes were deprived of sucrose for 12–16 hours and offered a porcine sausage casing filled with the bloodmeal mixture. Following 1 hour, mosquitoes were sedated with CO2 and fully engorged mosquitoes were transferred to 0.6 L cartons and maintained at 27°C for experimental testing. Infection, dissemination, and transmission rates were determined as previously described  on days 7 and 13/14 post-feeding. 25–50 mosquitoes/timepoint/group/experiment were sedated and legs were removed and placed in 1 ml mosquito diluent [MD; 20% heat-inactivated fetal bovine serum (FBS) in Dulbecco’s phosphate-buffered saline (PBS) plus 50 μg/ml penicillin/streptomycin, 50 μg/ml gentamicin, and 2.5 μg/ml Fungizone]. Mosquitoes were allowed to expectorate for approximately 30 minutes into capillary tubes filled with FBS plus 50% sucrose (1:1), at which time the mixture was ejected into 0.3 ml MD. Mosquito bodies were then placed in individual tubes with MD. All samples were held at -80°C until tested. Bodies, legs, and salivary secretions were processed and screened by duplicate plaque assay on Vero cells to test for infection, dissemination, and transmission, respectively. Data were analyzed using GraphPad prism 4.0 and rates were compared with Pearson’s chi-squared tests.
Results and discussion
Vector competence of Culex mosquitoes for WNV02 following feeding on infectious bloodmeals
Population (female x male)
% Infected disseminating
% Infected transmitting
Cx. p f pipiens (CxP)
89.3 M↑ Q↓
Cx. quinquefasciatus (CxQ)
Cx. p f molestus (CxM)
CxM x CxP
CxP x CxM
CxM x CxQ
CxQ x CxM
CxP x CxQ
CxQ x CxP
The authors would like to thank members of the Arbovirus laboratory insectary staff for assistance with this project. We thank the Wadsworth Center tissue and media facility for supplying cells and media for these studies. The construction of the Arbovirus laboratory insectary facilities was partially funded by National Institutes of Health (NIH) grant C06-RR-17715. This research was funded by NIH grant R01AI090159.
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