Virus culex

Keywords: virus culex, southern house mosquito culex quinquefasciatus diptera culicidae
Description: Culex quinquefasciatus is a sub-tropical species usually found within the latitudes 36° N and 36° S. However, in the U.S. between 36° N and 39° N there is a broad hybrid zone where

Culex quinquefasciatus is a sub-tropical species usually found within the latitudes 36° N and 36° S. However, in the U.S. between 36° N and 39° N there is a broad hybrid zone where Culex quinquefasciatus freely mates with Culex pipiens Linnaeus, which is usually not found south of 39° N. Mating between these two members of the Culex pipiens complex produce viable offspring within the hybrid zone. The extent of the hybridization is extensive and, as a result, the members are sometimes considered to be subspecies, Culex pipiens quinquefasciatus and Culex p. pipiens respectively. Culex quinquefasciatus is found in North America, South America, Australia, Asia, Africa, the Middle East, and New Zealand.

In the U.S. this species ranges from Virginia across the southern plains to southern California, and from as far north as southern Iowa, south to Texas and Florida. There are reports of Culex quinquefasciatus as far north as Indiana in the U.S. The species has also been collected in Hawaii (Barr 1957). In Florida, Culex quinquefasciatus is found in all 67 counties.

Figure 1. World distribution of the southern house mosquito, Culex quinquefasciatus Say. Illustration by Stephanie Hill, University of Florida.

Adults: Adult Culex quinquefasciatus vary from 3.96 to 4.25 mm in length (Lima et al. 2003). The mosquito is brown with the proboscis, thorax, wings, and tarsi darker than the rest of the body. The head is light brown with the lightest portion in the center. The antennae and the proboscis are about the same length, but in some cases the antennae are slightly shorter than the proboscis. The flagellum has thirteen segments that have few to no scales (Sirivanakarn et al. 1987). The scales of the thorax are narrow and curved. The abdomen has pale, narrow, rounded bands on the basal side of each tergite. The bands barely touch the basolateral spots taking on a half-moon shape (Darsie and Ward 2005).

Figure 2. Adult female southern house mosquito, Culex quinquefasciatus Say, feeding. Photograph by James Newman, University of Florida.

Eggs: Common to the Culex genus, the eggs of Culex quinquefasciatus are laid in oval rafts loosely cemented together with 100 or more eggs in a raft which will normally hatch 24 to 30 hours after being oviposited (Bates 1949).

Figure 3. Eggs of the southern house mosquito, Culex quinquefasciatus Say. Photograph by Stephanie Hill, University of Florida.

Larvae: The larval head is short and stout becoming darker toward the base. The mouth brushes have long yellow filaments that are used for filtering organic materials. The abdomen consists of eight segments, the siphon, and the saddle. Each segment has a unique setae pattern (Sirivanakarn and White 1978). The siphon is on the dorsal side of the abdomen, and in Culex quinquefasciatus the siphon is four times longer than it is wide with multiple setae tufts (Darsie and Morris 2000). The saddle is barrel shaped and located on the ventral side of the abdomen with four long anal papillae protruding from the posterior end (Sirivanakarn and White 1978). For more detailed morphological images, see the UF/IFAS Identification Guide to Common Mosquitoes of Florida Web site.

Figure 4. Larva of the southern house mosquito, Culex quinquefasciatus Say. Head in upper right. Photograph by Stephanie Hill, University of Florida.

Pupae: Similar to other mosquito species, Culex quinquefasciatus pupae are comma shaped and consist of a fused head and thorax (cephalothorax and an abdomen). The cephalothorax color varies with habitat and darkens on the posterior side. The trumpet, which is used for breathing, is a tube that widens and becomes lighter in color as it extends away from the body. The abdomen has eight segments. The first four segments are the darkest, and the color lightens towards the posterior. The paddle, at the apex of the abdomen, is translucent and robust with two small setae on the posterior end (Sirivanakarn and White 1978).

Figure 5. Pupa of the southern house mosquito, Culex quinquefasciatus Say. Photograph by Stephanie Hill, University of Florida.

Gravid Culex quinquefasciatus females fly during the night to nutrient-rich standing water where they will lay their eggs. They will oviposit in waters ranging from waste water areas to bird baths, old tires, or any container that holds water. If the water evaporates before the eggs hatch or the larvae complete their life cycle, they die (Mosquito Information Website 2007).

The larvae feed on biotic material in the water and require between five to eight days to complete their development at 30°C (Gerberg et al. 1994). The larvae progress through four larval instars, and towards the end of the fourth instar they stop eating and molt to the pupal stage. Following 36 hours at 27°C the adults emerge from the pupal stage (Gerberg et al. 1994). The time of development under natural conditions for all stages is variable and dependant on temperature.

Both males and females take sugar meals from plants. Following mating, the female seeks a blood meal. Culex quinquefasciatus are opportunistic feeders, feeding on mammals and/or birds throughout the night. Males survive only on sugar meals, while the female will take multiple blood meals. After a female mosquito digests the blood meal and the eggs develop, she finds a suitable place to lay her eggs, and the cycle begins again. A single female can lay up to five rafts of eggs in a lifetime (Gerberg et al. 1994). The number of eggs per raft varies with climatic conditions.

Figure 6. Female southern house mosquito, Culex quinquefasciatus Say, ovipositing an egg raft. Photograph by Sean McCann.

Culex quinquefasciatus is a vector of many pathogens of humans, and both domestic and wild animals. Viruses transmitted by this species include WNv, SLEv and Western equine encephalitis virus (WEEv). Culex quinquefasciatus is the principal vector of SLEv in the southern U.S. The virus increases its numbers in birds and then infects mosquitoes feeding on birds during the bird nesting season in the spring. The mosquito may then transmit the virus to humans. St. Louis encephalitis is age-dependent, affecting older humans more than the young. Symptoms of the disease are flu-like and can range from fever and headaches to stiffness and confusion. After a period of several days the brain may begin to swell, accompanied by depression, extreme excitement, sleepiness, or sleeplessness (CDC June 2007). Humans do not develop high levels of the virus in the blood and therefore are considered dead-end hosts unable to infect mosquitoes (Foster and Walker 2002). In Florida, major St. Louis encephalitis epidemics occurred in 1959, 1961, 1962, 1977, and 1990 (Day and Stark 2000, Shroyer 2004). Other epidemics in the U.S. include Colorado 1985, Arkansas 1991, New York 1999, and Louisiana 2001 (CDC October 2007). For more information on St. Louis encephalitis in Florida, see the UF/IFAS publication Saint Louis Encephalitis: A Florida Problem.

Although Culex quinquefasciatus is not considered the likely primary vector of WNv in Florida, it likely plays an important role in maintaining the virus within bird populations, and is capable to transmitting it to humans. For more information on West Nile virus in Florida, see the UF/IFAS publication West Nile Virus.

Outside the U.S. Culex quinquefasciatus is responsible for transmitting the filarial nematode, Wuchereria bancrofti (Tropical Africa and Southeast Asia), and Rift Valley fever virus (RVF) (Africa) (Foster and Walker 2002). Wuchereria bancrofti is a filarial nematode that can cause lymphatic filariasis. Currently, worldwide there are approximately 120 million cases of lymphatic filariasis (WHO 2000). The mosquito picks up the microfilaria from an infected vertebrate. The nematode develops inside the mosquito, and is passed on to another vertebrate (Foster and Walker 2002). Rift Valley fever has been responsible for major epidemics in Africa and Asia. In 1997, 300 human cases of RVF were reported in Kenya and southern Somalia (DHPE 2005).

Cultural control. Personal protection, reduction of larval habitats, and chemical control are the best ways to reduce mosquito bites and therefore the transmission of mosquito-borne pathogens. Because Culex quinquefasciatus feeds at night, long sleeve shirts and insect repellent are recommended for outside nighttime activity. Reducing the amount of outside activity also lowers the risk of Culex quinquefasciatus bites (Mosquito Information Website 2007).

Culex quinquefasciatus is dependent upon humans for the creation of its nutrient-rich aquatic habitats. It is essential to reduce or eliminate this type of aquatic environment. Around the home this can be done by not over watering plants, changing water in pet water dishes frequently, changing water in bird baths at least once a week, removing unnecessary water-holding containers, and and keeping ponds stocked with mosquito fish (Kern 2007). Water-holding containers that cannot be removed can be covered or turned upside down, old tires need to be removed, and drainage ditches need to be kept clear of debris that will obstruct flow (Mosquito Information Website 2007).

Large man-made aquatic habitats such as storm-water catch basins and waste water containers should be eliminated or reduced (O'Meara 1993).

Chemical control. Insecticides can be used to control larvae and adults. Larvicides are applied to bodies of water near where the larvae are concentrated. This method reduces the greatest number of immature mosquitoes with the least amount of pesticide. Adulticides are used to quickly reduce the population of adult mosquitoes in an area. In general, mosquito resistance to specific insecticides may reduce the effectiveness of chemical control. Some chemicals require a licensed pesticide applicator to perform the application. Before proceeding with a chemical control, contact your local Cooperative Extension Service (CES) or Mosquito Control District (AMCA 2005). In Florida, you can find your local CES office through the UF/IFAS listing of those offices.

  • AMCA. (2005). Mosquito Information: Control. American Mosquito Control Association. (29 November 2012).
  • Barr AR. 1957. The distribution of Culex p. pipiens and C. p. quinquefasciatus in North America. Journal of Tropical Medicine and Hygiene 6: 153-165.
  • Bates M. 1949. The Natural History of Mosquitoes. Macmillian Company. New York, NY. 379 pp.
  • Belkin JN. 1977. Quinquefasciatus or Fatigans for the tropical (southern) house mosquito (Diptera: Culicidae). Proceedings of the Entomological Society of Washington 79: 45-52.
  • CDC. (June 2007). CDC answers your questions about St. Louis encephalitis. Center for Disease Control. (29 November 2012).
  • CDC. (October 2007). Saint Louis Encephalitis. Center for Disease Control. (29 November 2012).
  • Connelly CR. 2006. Common Mosquitoes of Florida. UF/IFAS. Card Set. SP 370
  • Cutwa-Francis MM, O'Meara GF. (2008). Culex quinquefasciatus . Identification Guide to Common Mosquitoes of Florida . (29 November 2012).
  • Darsie Jr RF, Morris CD. 2000. Keys to the adult females and fourth-instar larvae of the mosquitoes of Florida (Diptera: Culicidae). Technical Bulletin of the Florida Mosquito Control Association 1: 148-155.
  • Darsie Jr RF, Ward RA. 2005. Identification and Geographical Distribution of the Mosquitoes of North America, North of Mexico. University of Florida Press. Gainesville, FL. 300 pp.
  • Day JF, Stark LM. 2000. Frequency of Saint Louis encephalitis virus in humans from Florida, USA: 1990-1999. Journal of Medical Entomology 37: 626-633.
  • DHPE. (2005). Rift Valley Fever. Directors of Health Promotion and Education. (no longer online- 29 November 2012).
  • Fonseca DM, Keyghobadi N, Malcolm CA, Mehmet C, Schaffner F, Mogi M, Fleischer RC, Wilkerson RC. 2004. Emerging Vectors in the Culex pipiens Complex. Science 303: 1535-1538.
  • Foster WA, Walker ED. 2002. Mosquitoes (Culicidae), pp. 245-249. In Mullen G, Durden L. (editors). Medical and Veterinary Entomology. Academic Press. New York, NY.
  • Gerberg EJ, Barnard DR, Ward RA. 1994. Manual for Mosquito Rearing and Experimental Techniques. American Mosquito Control Association Bulletin No. 5: 61-62.
  • ITIS. 2009. Culex quinquefasciatus Say, 1823. Integrated Taxonomic Information System. (29 November 2012).
  • Kern WH. (September 2007). Some small native freshwater fish recommended for mosquito and midge control in ornamental ponds. EDIS. (29 November 2012).
  • King WV, Bradley GH, Smith CN, McDuffie WC. 1960. A Handbook of the Mosquitoes of the Southern United States. Agriculture Handbook No. 173. United States Department of Agriculture. Washington D.C. pp. 118-119.
  • Lima CA, Almeida WR, Hurd H, Albuquerque CM. 2003. Reproductive aspects of the mosquito Culex quinquefasciatus (Diptera: Culicidae) infected with Wuchereria bancrofti (Spirurida: Onchocercidae). Memórias do Instituto Oswaldo Cruz. 98: 217-222.
  • Mosquito Information Website. (2009). University of Florida, Florida Medical Entomology Laboratory. (29 November 2012).
  • O'Meara GF. (2003). Mosquito associated with stormwater detention/retention areas. EDIS. (29 November 2012).
  • Savage HM, Anderson M, Gordon E, McMillen L, Colton L, Charnetzky D, Delorey M, Aspen S, Burkhalter K, Biggerstaff BJ, Godsey M. 2006. Oviposition activity patterns and West Nile virus infection rates for members of the Culex pipiens complex, at different habitat types within the hybrid zone, Shelby County, TN, 2002 (Diptera: Culicidae). Journal of Medical Entomology 43: 1227-1238.
  • Sirivanakarn S, White GB. 1978. Neotype designation of Culex quinquefasciatus Say (Diptera: Culicidae). Proceedings of the Entomological Society of Washington 80: 360-372.
  • Shroyer DA. (June 2004). Saint Louis encephalitis: a Florida problem. EDIS .(29 November 2012).
  • WRBU. (undated). Adult Culex quinquefasciatus . The Walter Reed Biosystematics Unit .(29 November 2012).
  • WHO. (September 2000). Lymphatic filariasis. World Health Organization. (29 November 2012).

Photogallery Virus culex:

The costs of infection and resistance as determinants of West Nile ...

Estimation du risque d'introduction du virus de la fivre de la ...

First record of a mosquito iridescent virus in Culex pipiens L ...

La presentacin "Phylum Arthropoda Morfologa externa. Tipos de ...

West Nile virus showing up in mosquitoes across Dallas County ...

Viruses | Free Full-Text | Arboviral Bottlenecks and Challenges to ...

Eurosurveillance - West Nile virus circulation in Emilia-Romagna ...

Viruses | Free Full-Text | Flavivirus-Mosquito Interactions | HTML

Viruses | Free Full-Text | Vector-Virus Interactions and ...

La presentacin "La Fiebre del Oeste del Nilo y los Parque Urbanos ...

West Nile Virus Mosquitoes Fact Sheet

Characterization of Dak Nong virus, an insect nidovirus isolated ...

Japanese Encephalitis: A Neglected Viral Disease and Its Impact on ...

Mosquitos | Public Health and Medical Entomology | Purdue ...

La presentacin "FIEBRE DEL NILO OCCIDENTAL Jorge Chucn Villaizn."

La presentacin "Subfilo Unirrameos. Clase Chilopoda Largos ...

Eurosurveillance - Japanese encephalitis virus RNA detected in ...

Westnile virus book2

Figure - Culex torrentium Mosquito Role as Major Enzootic Vector ...