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Modified:
Jul 13, 2005
West Nile Virus

Responses

What is the health risk to people from the West Nile Virus?

handout: [pdf - 44KB]

  • SYMPTOMS of SERIOUS ILLNESS: fever, disorientation, muscle weakness, neck stiffness, headache, nausea
  • RISK of SERIOUS ILLNESS: greater for older people and the immuno-compromised
  • CHILDREN ARE NOT PARTICULARLY VULNERABLE (few if any cases of serious illness have involved children)
  • INCUBATION PERIOD: 3-14 days after being bitten by an infected mosquito
  • CALL a DOCTOR if you or someone you care about shows symptoms of serious illness, whether or not caused by WNV
  • TREAT the SYMPTOMS -- there is no vaccine or medication specific to WNV
  • AUGUST & SEPTEMBER are when WNV has been most likely to bridge into the human population in the Northeast US. Human illness has occurred earlier in the Southeast and Gulf Coast states of the US in 2002
  • "FLU-LIKE" SYMPTOMS have been reported by about 30% of infected people, but most of those infected do not get sick
  • In US outbreaks, about 1 infected person in 150 has become seriously ill with central nervous system infection (encephalitis &/or meningitis)
  • About 12% of hospitalized cases have been fatal (7 of 62 hospitalized in 1999, 2 of 20 in 2000, 9 of 64 in 2001, )
  • Most mosquitoes bites will not lead to a WNV infection
  • BIRDS are far more likely than people to become infected & sickened by West Nile Virus

In some areas where West Nile Virus is showing up for the third and fourth year, there is some complacency about taking precautionary and preventative measures. Although fortunately WNV has not caused widespread human mortality--as was initially feared by some--it can cause unpleasant (flu-like) and sometimes long-lasting symptoms in people. It also presents a serious risk to unvaccinated horses and has had a not-yet-fully-understood impact on susceptible wildlife (e.g., crows).
See Petersen and Marfin. 2002. West Nile Virus: A Primer for the Clinician for more information about how to prevent, treat and evaluate WNV as a health risk for people.


How can I reduce my personal risk and my community's risk from the West Nile virus?

"Mosquito hygiene" includes source reduction of mosquito breeding sites and avoidance of biting mosquitoes--Both are key to reducing risk from WNV. Precautions should continue for the duration of the mosquito season. In the North this is into the Fall until after there have been two hard frosts. [See "Mosquito Hygiene throughout Life Cycle of Culex Mosquitoes" available as a full color 11 x 17 poster and in simplified black and white copy for handouts and presentations (4-page pdf)].

Mosquitoes breed in wet areas, and Culex are found particularly where there is decaying organic matter (e.g., leaves, grass clippings, animal wastes). There does not have to be much water and the water does not have to be left standing for very long - Some species can reproduce within a week! Check for standing water especially after each rainstorm, drizzle, watering of the garden or washing the car). Reduce mosquito breeding opportunites by:

  • Eliminate or empty the "artificial water-collecting containers" that are prime breeding spots for the mosquito species implicated in transmission of West Nile Virus
  • Clean out rain gutters
  • Aerate swimming pools and ponds (and perhaps stock with mosquito-eating fish)
  • Empty unused buckets, water troughs, etc.
  • Keep unused tires under cover so they do not collect water
  • Drill drainage holes in tires and other containers used in construction sites, farms, gardens and play areas
  • Clean bird baths and animal water bowls at least once a week

Avoid mosquito bites by wearing long clothes and/or by using insect repellent when out after dusk or in shaded areas (such as woods) during the daytime. This is when and where most vector species are more likely to bite. People should be especially careful when in "mass gatherings" where the CO2 given off by the crowd attracts more mosquitoes from a greater distance.

The New York State Department of Health is urging people to take common sense precautions to reduce their exposure to mosquito bites and to continue to eliminate stagnant water where mosquitoes breed. The NYS DOH WNV materials do not advocate widespread application of mosquito adulticide pesticides. However, in NYS, decisions about mosquito control methods are made by local jurisdictions.


What should I know about mosquitoes?

Mosquitoes are insects. They go through 4 life stages (complete metamorphosis) and look completely different at each stage: egg, larva, pupa and adult. The first 3 life stages are spent in water or wet places. Adults emerge from the pupal stage and are full size and able to fly. Adult females bite to get a blood meal that provides the nutrients they need to form each brood of eggs. (For great pictures and descriptions of each life stage, see ERAP's "Mosquito Hygiene" poster.)

Culex pipiens (Northern House Mosquitoes) are the type (species) of mosquitoes that have been most closely associated with transmitting West Nile Virus in the Northeast US. C. pipiens breed in standing water, especially in water containing decaying organic matter (plant debris, animal wastes). These mosquitoes "prefer" to bite birds, but it has been thought that if breeding sites are available near people's homes and domestic animal enclosures, Culex pipiens may bite people and domestic animals. Culex pipiens are most active dawn and dusk. Culex quinquefasciatus (Southern House Mosquitoes) fill this niche in the Southern United States but are more likely to bite people.

Although Culex mosquitoes of several species (Cx. pipiens, Cx. restuans, Cx. salinarius, Cx. quinquefasciatus and Cx. tarsalis) accounted for 55% of the WNV-positive mosquito pools collected in 2002, 36 different mosquito species have been reported WNV-positive since 1999. As the range of WNV has spread across the US, into the habitats of different types of mosquitoes, additional species are added to the roster of WNV vectors. In 2002, 7 species were reported for the first time: Aedes aegypti, Anopheles walkeri, Cx. erraticus, Cx. tarsalis, Cx. territans, Culiseta inornata and Psorophora ciliata. Of greatest concern in terms of risk to human health (and horses) are vector species that feed readily on large mammals e.g., Culex salinarius, Cx. tarsalis, and Aedes vexans. However, CDC's Dec 20 MMWR states that although other species may contribute to human WNV transmission, control of Culex mosquitoes continues to be the most important strategy to reduce risk for WNV transmission to humans.

WNV-infected mosquitoes are difficult to catch and are therefore not a good sentinel of WNV activity. WNV-positive mosquitoes were the first indicator of WNV activity in only 3% of US counties reporting cases in 2002!

For more information about mosquitoes, see ERAP's "Mosquito Hygiene" poster; ERAP's West Nile Virus Resources for the General Public, Section III, and Bibliography of Scientific Literature--use the search term "mosquito" or the name of a specific group of mosquito.


Should I (or someone in my family) be tested for West Nile Virus if bitten by a mosquito?

No. Testing for West Nile Virus is a complex process. It takes a long time to get test results and only a very small percentage of the mosquitoes that might bite you are infected. While test results are important to scientists and medical doctors studying the disease, they would not be very useful to you as an individual. There has not been* a particular cure for West Nile Virus--so a sick person does not become better off by being tested for WNV infection. If you become seriously ill, you should see your doctor, no matter what the cause or name of the illness. If you show signs of WNV, you would be treated for relief of your symptoms. (* In late Aug 2002, the US Food and Drug Administration approved clinical trials to see how useful the drug interferon might be in treating WNV patients, but this drug is not widely available for this purpose and its efficacy in treating WNV is unknown [More].

If you are bitten by mosquitoes, you should not assume that you are at high risk for WNV. See West Nile Virus as a Health Risk for People for more information about likelihood of infection and illness for different groups of people and other animals.

In previous years of the WNV outbreak in North America, for the most part, only people participating in a scientific study or those who had become very ill were tested to see if they had been infected by WNV. This year some people with a wider range of symptoms have also been tested. The purpose of the scientific studies involving testing for WNV infection are to answer questions like: "How many people in a certain area were infected?" "Of the number infected, how many had mild symptoms?" "What percentage of those infected get seriously ill?" (For more information about such epidemiological studies, see ERAP's West Nile Virus Bibliography of Scientific Literature


Can I be vaccinated against West Nile Virus? Is there a vaccine for horses? For birds? For other animals?

People: Two independent research teams have taken similar promising pathways to develop a WNV vaccine for people. Both efforts involve creating a hybrid "modified live virus" that include genes from the West Nile virus spliced into the "backbone" genome of a distantly related virus. When a vaccine is made from a modified life virus it has to replicate within the vaccinated person or animal. A government research group is splicing two genes for West Nile coat proteins into a dengue virus backbone that has been stripped of its own corresponding genes. The other research group, from the Acambis Company, are swapping the same two WNV genes into the backbone genome of an attenuated yellow fever virus. Acambis has already demonstrated that its hybrid vaccine protects horses and primates from WNV infection. They hope to start human clinical trials by summer 2002 [More] [ Still More].

Top US health officials from several agencies (CDC, NIH, FDA) reported at a Sept 24, 2002, Senate Committee Hearing that a nucleic acid blood test may be ready by summer 2003 and a vaccine based on the yellow fever vaccine may be ready in three years [Senate Hearing] [Summary of Senate Hearing].

While the vaccines may be developed rapidly, it will likely take 3-4 years for them to be approved for human use. The use of a vaccine that itself poses risk is controversial, especially given the typically very low risk to people of serious illness from WNV.

Horses: On August 1, 2001, USDA issued a one-year conditional license for development, manufacture and distribution of a killed-virus vaccine intended to prevent WNV in horses. Such vaccines are regulated under the Virus-Serum-Toxin Act, which permits conditional licenses to be issued to meet special circumstances--such as presented by West Nile Virus--if the product is pure and safe, and has reasonable expectation of efficacy. The conditional license was issued to Fort Dodge Laboratories, Inc., previously a division of American Home Products, Inc. and now a division of Wyeth (NYSE:WYE), for the 1-year period Aug 1, 2001-Aug 1 2002. At the end of the conditional period (which has now been extended), data obtained in support of the product efficacy, potency, and performance are to be evaluated to determine if the conditional license should be renewed or if a regular product license may be issued. During the first year of distribution CDC reported that more than 3 million doses were distributed nationwide (Aug 21, 2002 CDC News release). The vaccine is apparently recommended for use on other equine species as well as horses. This is the only one of several equine vaccines under development that has received government approvals. Very little information about the other vaccines is publicly available.

Use of the vaccine is restricted to veterinarians in those states where the product has been approved by the appropriate state regulatory authorities. The vaccine is administered to healthy horses in 2 (1 ml) intramuscular (IM) doses 3 to 6 weeks apart, followed by a yearly booster. Since the vaccine is not effective for 5 weeks after it is administered, the first dose should be given at least 6 weeks prior to expected mosquito activity in the area. Horses bitten by an infected mosquito before receiving the second dose of vaccine may become infected and ill. Texas Animal Health Commission recommends that 'booster' shots are given yearly or every 6 months in warmer areas with large mosquito populations in order to maintain maximum immunity.

Preliminary observations of efficacy look promising: e.g., of the 20,000 equines vaccinated in Florida in 2001, only one developed WNV infection. Efficacy and other information about the vaccine are discussed in WestNileVirus-L listserve postings on April 1, 2002, and in a series of postings the week of Sept 9 2002. It is possible that the much lower rate of WNV equine infections in East Coast states in 2003 as compared with Midwest states is reflective of the efficacy of the equine virus (assuming that more East Coast horses were vaccinated than in states where WNV was not expected).

Other Animals: The Ft Dodge horse vaccine has been experimentally used (off-label) on other zoo animals. It does not seem to cause harm, but its efficacy for many species is uncertain. Tests of the vaccine on some species of birds (e.g., crows) have shown that it is ineffective.

Birds: Impetus for developing vaccines protective of birds has come from zoos, captive breeding facilities, and conservationists concerned about threatened and endangered species in the wild and exotics in captive collections. In Israel concern about WNV impact on commercial flocks of geese provided impetus. According to a Sept 20 2002 American Bird Conservancy (ABC) press release, birds vaccinated with a new recombinant DNA vaccine prior to inoculation with WNV showed a 60% increase in survival over unvaccinated birds in trials by the CDC. CDC is also collaborating with other institutions to develop an oral vaccine for wild bird populations. Meanwhile a number of zoos were reported to be inoculating birds and other animals in their collections with the experimental horse vaccine (e.g., the National Zoo in Washington, D.C., July 2002 [More]). The efficacy of the equine vaccine on birds is not resolved and probably differs by species, according to rates of infectivity and seroconversion. Recent research by Dr. Nick Komar, an arbovirus specialist with CDC found that the vaccine did not protect American crows challenged with the West Nile 99 strain of virus (i.e., vaccinated crows became ill and died). Another unpublished study, however, showed significant antibody response in four species of birds, which could confer protection.

Geese: In August 2001, the State Laboratory for Vaccine Control in Israel began field testing of a killed-virus vaccine for geese. About 300,000 geese in commercial flocks were vaccinated twice, at 2 and 4 weeks of age, using virus replicated in suckling-mice. Field observations, as well as laboratory challenge trials carried out in sampled vaccinated geese, confirmed the efficiency of the vaccine in field conditions. Source: Veterinary Services and Animal Health, Israel, Jan 2002 [More].


Was West Nile Virus brought to the United States by bioterrorists?

In the Sept 13, 2002 New York Times, Senator Patrick Leahy is quoted* as asking for investigation into the possibility that the current WNV outbreak is a result of biological terrorism. This question was asked before, at the time of the initial WNV outbreak in NYC in 1999.

Evidence (and logic) indicated that the answer is "no," although we do not know if the rejection of this hypothesis has been expressed formally and/or officially. In press briefings in that first year, CDC listed bioterrorism as one of the possible means by which WNV might have entered this country, but spokespersons did not seem to support the hypothesis nor to bring it up more recently.**

An article in the New Yorker -- West Nile Mystery: How did it get here? The C.I.A. would like to know. Richard Preston. Oct 18 & 25, 1999 -- focused attention on this hypothesis, but presented a body of evidence that essentially rejected it. For example:

"An Army expert on bioweapons told me [Richard Preston] that the military has known for some time that Soviet biologists working for the USSR's biowarfare program had evaluated the West Nile virus for use as a biological weapon. 'The Russians did this kind of crap back in the seventies...They abandoned it because it didn't work very well...'"

"I [Richard Preston] spoke with a person at the CDC who said 'We're taking it seriously. We'll see where the data takes us. It could be done. You'd have to bring in a lot of mosquitoes....' He went on, 'But West Nile is not a great biological weapon because it doesn't hurt most people very much.' "

Before this call for investigation goes too far, in terms of allocating resources or feeding panic, some key characteristics of WNV should be recalled:

  • WNV is primarily a disease of birds that cycles between infected birds and mosquitoes;
  • historically only sporadic outbreaks have affected people (and < 1% of people infected become seriously ill);
  • with the possibility of only rare exceptions, people are "dead end hosts" to the virus and can't pass it on to other people or to mosquitoes that bite them (i.e., it is not highly infectious);
  • with the exception of horses, WNV does not seem to affect domestic animals nor animals of commercial value (livestock, poultry), so is unlikely to disrupt the domestic food supply or to affect food security;
  • the elderly population at greatest risk from serious WNV illness would generally not be considered a key target of one's enemies.

*NYTimes Sept 13, 2002
Vermont Senator Wants Study of Terror Link to West Nile Virus
By CHRISTOPHER MARQUIS

WASHINGTON, Sept. 12 - Senator Patrick J. Leahy, Democrat of Vermont, said today that the authorities should examine whether the spread of the West Nile virus in this country is a result of biological terrorism. "I think we have to ask ourselves: Is it a coincidence that we are seeing such an increase in West Nile virus, or is that something that is being tested as a biological weapon against us?" Mr. Leahy, who is chairman of the Senate Judiciary Committee, said in a radio interview in Waterbury, Vt. "There are some people, credibly, who feel that it is a test of our defenses and is a biological weapon or somebody doing this for commercial purposes."

** Other candidates for carrying the WNV into the US that were mentioned by CDC at that time included: infected mosquitoes, people, legally or illegally imported birds, or birds migrating across the Atlantic Ocean. Ornithologists have said that the last mentioned of these would be extremely unlikely, and would have caused a very excited stir in the bird-watching community had it been seen. More recently, in a March 5, 2001 National Public Radio interview, a CDC scientist reported on results of a simulated probability model that pointed to infected frogs from Western Asia as the most likely means of WNV entry into the US. Little has been heard about this hypothesis since. Most persons talking about this subject in recent years have repeated that the answer is simply not known--e.g., CDC's Petersen and Marfin introduce their recent publication West Nile Virus: A Primer for the Clinician (2002) by saying "It remains unknown how the West Nile virus came to North America."


What are the issues and the risks of human-to-human West Nile Virus transmission (e.g, via organ transplant, blood transfusions, or from mother to baby)?

(revised Dec 23, 2002)
Health officials have become convinced that WNV can be transmitted via organ transplant and blood transfusion, as well as from mother to fetus and possibly to babies in breast milk.

As of Labor Day Weekend 2002 there was a growing body of evidence that WN virus can be transmitted via organ transplant from an infected person (and an associated risk that it might also be transmitted by blood transfusion). By end of the first week in September, during a Sept 5 telebriefing, and then in the Sept 6 MMWR, CDC confirmed with a high level of certainty that organs from an infected donor had transmitted the infection to 4 organ recipients.

Research to determine if WNV can also be transmitted via blood transfusion was prompted by trying to understand how the organ donor had become infected, since blood tests before she received blood transfusions did not show she was WNV-positive, while later tests did. Interest was spurred when it was learned that at least 4 other people had been diagnosed with WNV infection after receiving blood transfusions. Since all patients resided in areas with high levels of WNV activity, CDC and others needed to investigate further to find evidence that WNV was in fact transmitted through blood transfusion.

During the period Aug 28 to Oct 26, CDC received reports of 47 persons with possible transfusion-related WNV infection (17 reports received since Oct 16), 14 of whom were later found not to have WNV infection or did not acquire WNV infection through transfusion. Of the remaining 33 (reported from 17 states), 6 cases now provide evidence that WNV can be transmitted through blood transfusion. Investigations are ongoing for the other 27 cases. These 33 cases are people who had confirmed or probable WNV infection who had received blood components in the month before illness onset (Oct 28 2002 CDC dispatch).

Of the 30 cases tallied in the Oct 16 2002 MMWR (9 fatalities with WNV the likely cause of death), 25 patients had meningoencephalitis, 4 had other WNV-associated illnesses, and demographic and clinical information was not yet published for 1 patient. As of Oct 16, 4 investigations provided evidence of transmission via blood transfussion: 2 of the 4 developed WNV-encephalitis after receiving different blood components derived from a single blood donation. In follow-up testing, the donor seroconverted and developed WNV IgM antibody. In the 3rd case (Investigation 3, detailed by CDC in the Sept 13 and Sept 20 MMWR) WNV was isolated from a withdrawn unit of frozen plasma from the suspected donation, indicating that the virus can survive in some blood components, likely for several days. The donor of this plasma subsequently developed an acute febrile illness and seroconverted following the suspect collection.

Three of the cases providing evidence of WNV transmission via transfusion are people who received transfusions while under treatment for malignancies (cases 4-6, detailed in the Oct 28 CDC dispatch). Case 4, an adolescent hospitalized for 65 days, developed WNV-meningoencephalitis after receiving a component derived from a donation that contained WNV RNA. Follow-up found that the donor had developed a febrile WNV-illness within days of the suspect donation. In another of the 7 initial investigations conducted by CDC, it was shown that not all recipients of WNV-contaminated units will become infected with WNV (Investigation 7: a 55-year-old woman received contaminated blood after an orthopedic procedure in July but has not tested WNV-positive). Note that as recently as the Sept 20, 2002 MMWR, evidence for transfusion-associated transmission was "highly suspicious" but not conclusive. A similar case is under investigation in Ontario, Canada re: a 47-year-old woman who received many blood transfusions during treatment for cancer and was found to be WNV-positive around the time of her death in Toronto, Nov 21, 2002. It is considered highly unlikely that she contracted WNV through a mosquito bite (source: The Edmunton Sun, Nov 29 2002).

While evidence that WNV can be transmitted through blood transfusions adds a wrinkle to the set of assumptions about disease transmission, the general population is at no greater risk of contracting WNV than previously thought. The news does make us aware that a sub-population of people about to undergo high risk organ transplants and/or receive blood transfusions (about 4.5 million persons in the US receive blood or blood products annually) may be at still greater health risk due to the increased risk of contracting WNV. However, CDC health officials point out that the additional risk of contracting WNV is quite small in comparison with the much larger risks from these medical procedures. The process of donating blood poses no risk to the blood donor for contracting WNV.

Related to these investigations, research is also underway to develop more rapid tests for determining if asymptomatic people are infected with WNV. Such a test could enable screening for WNV in donated blood. However, in a Sept 19, 2002 press briefing it was noted (a) that screening would be quite difficult because there would be relatively small amounts of the virus in blood of an asymptomatic infected person; and (b) it would be necessary to detect the virus itself, not antibodies the body produces in response to infection [More].

On Oct 25, the Food and Drug Administration issued a guidance to the blood industry regarding procedures for screening and quarantine of suspect blood donations [More]. CDC requests that cases of WNV infection in patients who have received blood transfusions within the 4 weeks preceding illness onset be reported to CDC through state and local public health authorities. Serum or tissue samples should be retained for later studies. In addition, cases of WNV infection in persons with illness onset within 2 weeks after blood donation should be reported. Prompt reporting of these cases will facilitate withdrawal of potentially infectious blood components.

On Sept 2 a 40 year old woman gave birth to an infant, then required a blood transfusion for anemia. The woman began breast-feeding her child on the day of delivery. On Oct 3 CDC announced that a sample of the breast milk tested positive for the WNV-specific IgM and IgG antibodies, indicating that NV genetic material was transiently present in the breast milk. The infant remained healthy, but tests when the infant was 25 days old revealed presence of the WNV-specific IgM antibody, which could not have been passed from mother to child. The infant had little contact with mosquitoes and thus is believed to have contracted the infection via virus in breastmilk. Because the health benefits of breast-feeding are well established and the risk for WNV transmission through breast-feeding is unknown, the CDC does not suggest a change in breast-feeding recommendations.

Intrauterine, Transplacental (Vertical) Transmission (Dec 20 2002): An infant born in November to a woman who contracted WNV while pregnant was hospitalized in Syracuse, New York, (Onondaga County Health Dept, PR Dec 18, 2002). "WNV has not previously been associated with intrauterine infection or adverse birth outcomes" in the formal record, although at least one other human case of transplacental transmission has been described anecdotally. Details are described in the CDC MMWR Dec 20, 2002 and were also covered in the Dec 19 CDC press conference. CDC recommends that "pregnant women should take precautions to reduce their risk for WNV or other arboviral infection and should undergo diagnostic testing when clinically appropriate." [For additional information and background, see WestNileVirus-l listserv postings from Oct 13, 15, and 17 and Dec 20].

More on these topics: CDC's MMWR for Sept 6, Sept 13, Sept 20, Oct 16, and Oct 28 (Dispatch, Vol 51, "Investigations of West Nile Virus Infections in Recipients of Blood Transfusions," 2002; a Sept 27 CDC Advisory; transcripts from CDC's Sept 3 and Sept 19 2002 telebriefings; ERAP postings to the WESTNILEVIRUS-L listserv Sept 3, Sept 4, Sept 6, Sept 19, Oct 28 and Oct 29, 2002.

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ERAP's West Nile Virus education program has been supported by Smith-Lever funds from the USDA Cooperative State Research, Education and Extension Service (CSREES), through a grant from Cornell Cooperative Extension, and by a grant from the National Oceanic & Atmospheric Administration's Office of Global Programs (NOAA-OGP) for the project "Climate Effects, West Nile Virus Vector Development, and Transmission Risk" (Sept 1, 2004-Aug 31, 2007).