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West Nile Fever (WNF)
AGENT
RNA virus, genus Flavivirus (group B), family Togaviridae
RECOGNITION
Syndrome: Human:
1. Ranges in severity from subclinical to a febrile course of
short duration to encephalitis
2. more serious illness in elderly persons than in children
3. Most common signs include sudden onset of fever, headache,
enlarged lymph nodes,
4. Maculopapular rash on the trunk, though ocular, muscular,
and joint pain may also occur.
5. Duration typically is about 3-5 days, generally followed by
rapid and complete recovery.
6. Convalescence is sometimes prolonged and accompanied by
profound weakness.
7. Myocarditis, meningitis, and encephalitis are occasional
complications.
Animal:
1. Most infections are subclinical.
2. Horses may occasionally develop meningoencephalitis.
3. No other domestic mammal clinically affected.
4. Peridomestic birds, such as pigeons, turtledoves, and crows
may be affected, as may some wild birds.
Incubation period: Human, 3-6 days.

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Case fatality rate: Negligible in humans; up to 25% in horses, and
high in experimentally infected crows.
Confirmatory tests:
Virus isolation during acute phase, or serologic testing (SN) of
paired sera.
Occurrence:
1. Occurs in summer, is both endemic and epidemic.
2. Widely distributed throughout Africa, Asia, and Europe
where the virus has been isolated from humans, other
mammals, birds, and arthropods.
3. Endemic in the Nile Delta,
4. epidemics occur in Israel, and occurs sporadically in South
Africa.
5. Human prevalence of infection in Egypt may exceed 60%.
Transmission:
1. Mosquitoborne.
2. Birds are the reservoir, developing a persistent, high-titer
viremia that allows infection of Culex mosquitoes.
3. Humans, sheep, and cattle, are accidental hosts that do not
develop viremia sufficient to infect vectors.
CONTROL AND PREVENTION
Individual/herd:
1. Prevent mosquito bites with protective clothing and use of
repellents.
2. No vaccine is available.
Local/community:

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1. Vector control is difficult because the species of mosquito
that transmits the infection to humans is not well established
in all areas affected.
2. Cula mosquitoes transmit infection bird-to-bird, but may not
infect humans.
3. Another vector that connects the wild cycle with human
outbreaks is likely, and control of this latter vector is
important.
Yellow Fever (YF)
AGENT
RNA virus, genus Flavivirus (group B), family Togaviridae
RECOGNITION
Syndrome: Human:
1. Subclinical to severe, life-threatening disease of short
duration.
2. Mild cases may be indeterminate.
3. Typically, begins with sudden onset of high fever, headache,
chills, backache, muscle pain, prostration, nausea, and
vomiting.
4. Fever may subside after 3-4 days, then return in the second
phase of illness,
5. during which hepatic and renal involvement and hemorrhage
may occur.
6. Nasal and oral bleeding, hematemesis ("black vomit"), and
melena occur.

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7. The name derives from the jaundice that often results from
liver impairment.
8. Most deaths occur between days 3 and 7, with prognosis
improving if survive at least 10 days.
Animal:
1. Nonhuman primates may be affected, with varying degrees of
severity among species.
2. Monkeys in the Americas are more severely affected and
have a higher mortality rate than those in Africa, a possible
factor being YF has long been endemic in Africa whereas it
is more recent in Neotropical regions.
3. The clinical course in primates is similar to that in humans.
Incubation period: In humans, 3-6 days.
Case fatality rate:
1. In endemic regions, often less than 5%,
2. but in nonindigenous groups and in epidemics fatalities may
exceed 50%.
Confirmatory tests:
1. Virus isolation during the first few days of illness is most
reliable.
2. Viral antigen can be detected in serum by ELISA testing.
3. Serologic tests include HI, SN, CF, and IFA.
4. Cross reactions, however, can occur with other flaviviruses,
and
antibodies
developed
after
vaccination
are
indistinguishable from those produced as a result of infection.

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Occurrence:
1. Restricted to Africa and the Americas.
2. In Africa, both urban and sylvatic cycles of infection occur.
3. The urban cycle occurs mainly in savannah areas, particularly
those bordering rain forests, such as in Burkina Faso and
Nigeria.
4. Sylvatic YF occurs from the Sahara east to Ethiopia and
Somalia and south as far as Angola and Zaire.
5. In the Americas, urban YF no longer exists, because of
successful urban mosquito eradication programs, but the
sylvatic cycle continues in forests of northern South America.
6. Most human cases occur in the Amazon Basin, the plains of
southeastern Colombia, and eastern Bolivia and Peru.
Transmission:
Mosquitoborne.
In Africa, other species of Aedes can transfer the virus from
monkeys to humans.
CONTROL AND PREVENTION
Individual/herd:
1. Vaccinate travelers to endemic areas.
2. Vaccinate family members and other contacts of YF patients.
Local/community:
1. For urban YF, mass vaccination campaigns, mosquito
control.

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2. For sylvan YF, vaccinate people living near or entering
affected forests and avoid those areas for one week post-
vaccination.
National/international:
1. If YF in a human is discovered in a nonendemic area, the
WHO and adjacent countries must be notified immediately,
as specified in the International Health Regulations.
2. YF among nonhuman vertebrates in newly discovered or
reactivated foci must also be reported.
3. Monkeys and other nonhuman primates arriving in YF-free
areas from areas where YF occurs must be quarantined for 7
days.
4. Proof of vaccination against YF is required by many
countries for travelers who have come from or through areas
where YF occurs.
Nairobi Sheep Disease (NSD)
AGENT
RNA virus, genus Nairovirus (ungrouped), family Bunyaviridae
RECOGNITION
Syndrome: Human:
1. Usually subclinical.
2. Some experience a transient influenza-like syndrome with a
diphasic fever.

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Animal:
1. A hemorrhagic gastroenteritis occurs in sheep and goats.
2. Usually subclinical among indigenous animals,
3. whereas newly introduced susceptible animals become
anoretic, have a mucopurulent nasal discharge and a fetid
diarrhea which eventually becomes bloody.
4. Pregnant animals frequently abort.
5. Death may occur in 24 hours.
Case fatality rate: For humans, 0%. For sheep, 30%-90%; for
goats,
Incubation period: 4-15 days.
Confirmatory tests:
Identify virus microscopically (FA) in mice or tissue culture
infected from blood, spleen, or mesenteric node of patient. Detect
antibody by IFA.
Occurrence:
1. Endemic in East Africa
2. serologic evidence of infection from Ethiopia to South
Africa.
3. Serologic evidence that human infection is common in
endemic areas.
4. Outbreaks in small ruminants occur when susceptible animals
are moved into endemic areas.

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Transmission:
1. Tickborne,
2. Viremia occurs during the febrile period.
3. Rhipicephalus appendiculatus is the primary vector, but
Amblyomma spp. have also been incriminated.
4. The virus can survive in ticks for two years, and transovarial
and transstadial transmission occur. The virus is maintained
in a sheep-tick-sheep cycle.
5. Transmission by blood transfusion from currently viremic
persons can occur.
6. Infection results in complete immunity. 0%-30%.
CONTROL AND PREVENTION
1. Individual/herd:
2. Prevent tick attachment by wearing protective clothing and
using repellents in endemic areas.
3. Remove attached ticks every few hours.
4. Control ticks on animals by weekly dipping or spraying.
5. An attenuated live virus vaccine is available for sheep and
goats, but it is not very satisfactory.
6. An experimental inactivated vaccine has provided excellent
protection against laboratory challenge.
7. Because of the mild disease, vaccination of humans is not
indicated.
Local/community:
1. Perform serologic screening of blood donors.
2. Prevent spread of infected ticks from endemic areas by
restricting animal movement.

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Influenza
AGENT
RNA viruses, genus Influenzavirus (types A and B), family
Orthomyxoviridae; type C is in a separate, unnamed genus.
RECOGNITION
Syndrome: Human:
1. An acute respiratory disease.
2. Signs of types A and B typically include fever, chills,
headache and muscular aches, malaise, pharyngitis, and
cough. Gastrointestinal signs, such as nausea, vomiting, and
diarrhea, occur more in children than in adults.
3. Type C is a milder illness, in which lacrimation, sneezing,
and runny nose are more pronounced than in A and B;
4. subclinical infection is frequent in type C.
5. Generally most severe among the elderly and those with
chronic, debilitating conditions, and other immunosuppressed
persons, and it is among these groups that most deaths occur.
6. May be complicated by pneumonia, both viral and bacterial.
7. Reye syndrome, which affects the CNS and liver, may occur
as a sequel in children who have taken aspirin during the
illness.
8. Recovery is usually complete in about a week.
Animal:
1. Type A occurs most notably in swine, horses, and birds.
2. In pigs, there is abrupt onset with inappetence, coughing,
coryza, dyspnea, and fever. Recovery in uncomplicated cases

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is rapid, and subclinical infections occur. Type C also occurs
in swine.
3. In horses, signs include high fever, abundant nasal discharge,
coughing, dyspnea, and depression lasting some 2-10 days,
followed by 1-3 weeks of convalescence.
4. Often more serious in colts than in mature horses.
5. Avian influenza ("fowl plague") is most known for its effects
on commercial poultry, and ranges from a subclinical or mild
infection to severe disease with high mortality.
6. Signs include anorexia, decreased egg production, coughing,
sneezing, facial edema, coryza, and diarrhea.
7. Other species from which influenza viruses have been
isolated or antibodies detected include whales, fur seals,
harbor seals, and dogs.
Incubation period: Human, 1-5 days; animal, 2-3 days.
Case fatality rate:
1. Low in humans, swine, and adult horses
2. although in some human pandemics mortality has increased
significantly.
3. High in colts and seals, and may approach 10-13% in severe
poultry outbreaks.
Confirmatory tests:
Virus isolation from throat or nasal washings early in the illness.
Serologic tests (HI, CF, SN) of paired sera.

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Occurrence:
1. Worldwide
2. Usually in epidemics or pandemics, with high morbidity and
generally low mortality, and sporadic cases.
3. Type A causes most pandemics and annual epidemics,
4. whereas type B outbreaks are less widespread and occur at
less-frequent intervals.
5. Sporadic cases and small clusters of infection are often
attributable to type C.
6. The attack rate during epidemics ranges 10%-30% in the
general population,
7. but in institutions, such as schools, nursing homes, etc., up to
70% of susceptible individuals may be affected.
8. Generally occurs during the autumn and winter in temperate
regions
9. in the tropics most cases occur during the rainy season, but
sporadic outbreaks may occur in any month.
Transmission:
1. Mainly by inhalation of aerosols
2. direct contact with droplets.
3. Among birds, also by the fecal-oral route.
CONTROL AND PREVENTION
Individual/herd:
1. Inactivated type A vaccines are highly effective.
2. Because of the frequent changes in antigenic structure of type
A viruses, vaccination is generally effective for only one
season.

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3. Amantadine or rimantadine administered early in the illness
can help alleviate symptoms and reduce the amount of virus
in secretions.
4. Inactivated vaccines are also available for horses and swine.
Local/community:
Vaccination campaigns can help reduce the magnitude of
epidemics.
Newcastle Disease (ND)
AGENT
RNA virus, genus Paramyxovirus, family Paramyxoviridae
RECOGNITION
Syndrome: Human:
1. Manifests primarily as conjunctivitis, usually unilateral,
2. with congestion, lacrimation, pain, swelling of sub-
conjunctival tissues, and pre-auricular lymphadenitis.
3. Generally no systemic involvement,
4. but persons exposed to aerosols develop an influenza-like
illness of 3-4 days’ duration.
5. Recovery is complete in about a week.
6. Subclinical infections also occur.
Animal:
Among numerous bird species affected, chickens and turkeys are
especially susceptible.
Most common signs are respiratory, nervous, or both.

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Incubation period:
1. In humans usually 1-2 days
2. 2-15 days in birds with respiratory or CNS disease, 2-4 days
for viscerotropic.
Case fatality rate:
1. None in humans.
2. In poultry can range from none (with lentogenic strains) to
100% (in some outbreaks of velogenic visce ro tropic
disease).
Confirmatory tests:
1. In humans, virus isolation is the only definitive test because a
serologic response may not occur
2. In poultry, virus isolation early in an outbreak. Serologic tests
include HI, SN, and ELISA.
Occurrence:
1. Worldwide in wild birds, semidomestic, and domestic fowl
2. Human ND is rare, and usually occurs among laboratory
personnel, poultry abattoir workers, and poultry vaccinators
using live vaccines.
Transmission:
1. Chickens are the main reservoir.
2. NDV is spread from bird to bird mainly by aerosols, although
NDV is also present in feces; the density of birds in
commercial poultry farms facilitates transmission.
3. Humans become infected when NDV contacts the eyes, as
from aerosolized vaccines.

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CONTROL AND PREVENTION
Individual/herd:
Avian ND can be controlled by:
1. maintaining good hygiene on poultry farms,
2. separating poultry houses
3. vaccination.
Human ND can be prevented by:
1. the use of goggles and masks when vaccinating poultry,
2. using care to avoid aerosols when working with NDV in the
laboratory.
National/international:
1. Imported live birds of any species should be quarantined
2. Imports from countries where ND occurs should be
prohibited.
Psittacosis (ornithosis) avian chlamydiosis (AC)
Chlamydophila psittaci (formerly known as Chlamydia psittaci)
Disease in humans
1. May be subclinical, leading to under-diagnosis.
2. incubation period of 1–2 weeks
3. symptoms similar to influenza or a respiratory infection.
Disease in animals
1. C. psittaci is widespread in both wild and domestic birds.

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2. Parrots are the most frequently encountered hosts in a
companion animal setting,
3. Other potential hosts as zoonotic reservoirs include turkeys,
ducks, geese, pigeons, starlings, pheasants and birds kept for
competitive showing.
4. The organism is resistant to drying, and can be found in dust
in hen houses, pigeon lofts and other roosting sites.
Transmission
1. Transmission to humans follows inhalation of dried bird
faeces or nasal discharge from infected birds, direct contact
with birds or their feathers and by bird bite
2. human-to-human transmission may occur by the aerosol
route.
Treatment
1. Tetracycline is given at a dose of 250–500 mg three to four
times daily for at least 7 days
2. Doxycycline, azithromycin, erythromycin
Prevention
1. Education of individuals in high-risk groups.
2. Early detection of cases in birds is an important part of any
prevention strategy.
3. Reduction in stress and overcrowding is recommended to
control infective spread.
4. Placing birds suspected of having psittacosis in isolation until
they can be tested, and subsequently treated or slaughtered
5. Treatment of imported companion birds with prophylactic
antibiotics

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Q fever
Query fever, Balkan influenza, abattoir fever
It is caused by a rickettsia, Coxiella burnetii, an obligate
intracellular bacterium.
Disease in humans
1. Most exposed individuals display no signs of clinical disease
2. incubation period of between 2 and 4 weeks
3. followed by an acute onset with high fever, associated chills,
profuse sweating and severe headache
4. fever may last anything from 9–14 days and can recur at
intervals, with a total duration of up to 3 months
5. A dry cough may be present, with pain in the chest cavity
6. A chronic form also exists that causes a prolonged
endocarditis leading to valvular damage
Transmission
1. follows exposure to infected material
2. direct contact with contaminated materials, especially the
afterbirth or material contaminated with amniotic fluid
3. Drinking milk or consuming contaminated milk
4. transmission via ticks, lice or fleas has been demonstrated
Diagnosis
serological testing: indirect immunofluorescence, complement
fixation, enzyme-linked immunosorbent assay (ELISA) and
microagglutination.
Treatment
1. C. burnetii can be difficult to treat

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2. tetracyclines at usual clinical doses
Prevention :
1. Good personal and environmental hygiene
2. Bedding contaminated by postpartum material and the
material itself should be carefully handled, with collection
and subsequent burying or incineration
3. Disinfection of housing and other areas
4. Protective clothing, including respirators, overalls and gloves
5. Carrier animals have been subject to eradication by slaughter
policy
6. All milk and milk products should be pasteurised