Professional Documents
Culture Documents
Sr. Scientist1, Pr. Scientist and Head2, Ph.D Scholar3, M.V.Sc. Scholar4 Division of Vety. Public Health, I.V.R.I., Izatnagar
Zoonotic Diseases
Why important ? (64% (14/ 22) infectious agents identified between 1973 & 1994 are Zoonoses ( 75% of Human infections are shared by animals (Zoonoses) ( Over 300 in Nos.
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(Chomel,1998)
Impact
(Affect the efficient production of food - animal protein ( Serious occupational hazards : Close association of farmers/animal handlers with livestock. ( Obstacles in international trade in animals and animal products ( High number of deaths ( Loss of work efficiency
Aim of Control
Protecting yourself and your family from animal diseases and infections 5
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Tuberculosis
Indian scenario
30% of the total global TB cases in India Leading cause of death in Indian women with a total of 4,21,000 deaths annually 1000 Indians die from TB per day i.e. one per min 95% of new TB cases every year
(WHO,1999) (Krishnaswami, 2000)
Social trauma Rejection of 100,000 women patients by their families More than 3 lac children rejected by schools because their parents had TB 15% rural & 11% urban patients unaccepted and ill treated by family members
12 (Rajeshwari et al., 1999, Geetharamani et al., 2001)
Zoonotic Tuberculosis
(TB in Animals(M. Bovis) spreading to Humans) 1. More severe than the Human TB,which spreads mainly from Man-to-Man
Growth on T2CH
2. Can spread in all directions (Animal-Man, Man-man,Man-Animal and Animal-to-animal) 3. Isolation and identification of M. Bovis is very difficult as well as needs more time and special media to grow 4. Zoonotic TB is grossly under reported and undiagnosed
M. TB M. TB M. Bovis
Niacin Reaction
13 M. Bovis
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Brucellosis
Occupational zoonosis for farmers, veterinarians & workers in meat industry. One of the leading cause of infectious abortions (OIE, 2002) Prevalence rate on organized dairy farms: 17% Brucellosis in India is common in areas with high rainfall and humidity
Indian scenario
Species Cattle Buffalo Sheep Goat Human Prevalence rate 1.9% 1.8% 3.6 % 0.6 % 0.45 41.25% Reference OIE, 2002 OIE, 2002 Singh et al., 1994 Singh et al., 1994 Barbuddhe, 1993
Animal to human transmission
In India, brucellosis as a whole shown to cost Rs. 350 million in the form of food (Schwabe, 1984) animals and mandays of labour Losses due to abortion in the affected animal population. Loss of progeny & reduced milk production Human brucellosis causing physical incapacity 16 (Patel et al., 1986). Loss of 3 million mandays of labour annually
Never drink or eat raw milk/ milk products Cook thoroughly and Handle properly Avoid cross-contamination
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Anthrax
Economically important agricultural disease People at Risk: Agri. workers, butchers, tanners & woolsorters Endemic in Tamil Nadu, Karnataka & Andhra.Pradesh 205 documented human cases majority of cutaneous anthrax
(Rao et al., 2005)
Cutaneous anthrax accounts for more than 95% of human cases (Ghaffar,2003) Disease forms 1. Cutaneous (low mortality) 2. Grastrointestinal (50% mortality) 3. Pulmonary (High mortality) Indian Scenario
State & Year Orissa (2005) Andhra P. (1990) Karnataka (1991) Kerala (1994-95) Human Cases 23 6 3 23 Remarks CFR: 25-60% Epidemic Emerging zoonoses Reference Peoples daily online, 2005 Bachhil & Malik, 2005
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Bacillus anthracis
Disease known for thousands of years. Organism first described in mid-1800s Used as proof of Henles postulates by Koch. First vaccines developed by Greenfield and Toussaint; public demonstration by Pasteur in 1881. Livestock and human vaccines.
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HYPOACUTE
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Cutaneous anthrax
This is a pathognomic skin lesion with a raised vesiculated edge, inflamed, and with a black base to the ulcer, e.g., charbon, Siberian ulcer.
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Cutaneous anthrax
This postman had borrowed his sons woolen scarf; the son worked in a bone meal plant. Without prompt treatment, it carries a 10% case fatality rate.
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Cutaneous anthrax
Cutaneous lesions follow occupational exposure. Usually seen in men after butchering an affected cow; or from handling hides, especially sun-dried hides; or from carrying contaminated building insulation. Also following insect bites.
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HYPOACUTE
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(5)
GASTROENTERIC
Onset usually 2-5 days after eating contaminated food Nausea, fever, malaise, abdominal pain, bloody vomiting & diarrhea Often fatal even with treatment
HYPOACUTE
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Gastroenteric anthrax
Seen only in poor, developing countries with food shortages or inadequate veterinary inspection recent cases in SubSahelian Africa, Central Asia, Russia, India & Thailand. Usually have concurrent cutaneous cases from butchering the affected animal or handling the infected meat. Probable frequency: one outbreak per 64 infected animals eaten.
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Not reported
ANTHRAX
Epidemiology 101
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Concerns
Anthrax is an emerging zoonosis in southern India. Anthrax strains are showing increasing resistance to penicillin & other Antibiotics
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Leptospirosis
Disease contracted from infected rats urine/ contaminated watercourses Population at high risk - Rural farm workers, rice field workers, sugarcane cutters, cattle farmers, fishermen, slaughterhouse & sewer workers (CDC, 2002) incidence: TN, Kerala, Andaman over the last 2 decades due to farming & inadequate rodent control. Economic impact
Cost for medical treatment Decreased productivity Impact on trade animals, Semen losses by reproductive failures & Reduced milk yield
Indian scenario
State Andaman Chennai Incidence/ 105 50.0 10.5 Mortality 21.0 Ref. Hartskeerl, 2004
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Kerala
5.6
10.1
Q fever
( Notable zoonoses (occupational/foodborne)
(Marrie, 1990)
( High Mortality (1-11%) in chronic cases ( Endemic in many countries including India (> 51)
(Raoult, 1990)
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Q fever
Host Range
Domestic animals
Cat Dog Cattle Sheep Goat Horse Poultry
Wild animals
Arthropods Birds Rodents Primates Carnivores Poikilotherms
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Encephalitis
Common carriers Pigs Birds Horses Rodents
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Encephalitis
Transmission
Mosquito bites Tick bites
Clinical presentation
Lethargy Fever Headache Disorientation
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Rabies
( More than 99 % of all human rabies deaths occur in developing world ( Human mortality from endemic area estimated to be 30,000- 55, 000 deaths/ year ( Half of the global human population lives in canine rabies endemic areas
(WHO, 2005)
Economic impact
96% of cases due to bite of dogs (18 billion) 3 - 3.5 million take post-exposure vaccines Economic cost due to rabies in Asia US $ 563 million Livestock losses: rabies incidence rate / lac cattle = 5 Costs / head of cattle US $ 500; Costs / dog killed US $ 5 Annual no. of cattle deaths = 21,150
Human mortality Total population (millions) Population at risk (millions) No. of bites from suspected rabid dogs (1000) No. of rabies deaths No. of deaths/ 1 lac people Urban 284.7 284.7 409.4 1058 0.37 Rural 732.2 710.4 893.4 18201 2.49
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Rabies
Transmission
Animal Bite Contact with infected tissue, fluids or feces
Clinical presentation
Fever Furious/paralytic look Headache Agitation Confusion Seizures Excessive salivation 44
Rabies
Common Carriers
Cats Dogs Raccoons Skunks Bats Foxes
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Japanese Encephalitis
A disease of rural areas & people of lower socio-economic group. Leading cause of viral encephalitis & approx. 30,000 to 50,000 cases & 15000 deaths annually, India: 24 states/ UTs JE reported (PN Rao, 2000) 378 Million population is living at the risk
Incidence of JE in India Year 2000 2001 2002 2003 2004 Cases 2593 2061 1765 2241 67 Deaths 556 479 460 670 0
Socio-economic impact
Pigs: High mortality in piglets; Great economic impact in swine market Equines: Morbidity: 2% during outbreak Mortality : upto 5% Humans: Mortality: 5-35% Severe neurological sequelae: 33-50% Economic costs: Approx. US $ 1 million/Yr
(CDC fact sheet)
Transmission
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Swine
Expulsion- litters( stillborn or mummified fetuses) Piglets die - after birth Tremor and convulsions before expiring. Boars- sperm count & motility of sperm. Transmitted to gilts by way of infected semen. Fetuses are mummified and dark Post mortem lesions - . Hydrocephalus, cerebellar hypoplasia and spinal hypomyelinogeneisis may be seen.
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Human beings
flu-like illness - headache, fever,nuchal rigidity and often G.I symptoms majority a symptomatic or nonspecific Children and the elderly -common Encephalitis- 1 : 300 patients (Tsai T,
1993)
I.P 6-16 days 25-30% recovered patientparalysis, ataxia and speech difficulties.
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Vector Control
In India, JEV isolated from 16 species of mosquitoes; the majority from Cx. vishnui complex in rice ecosystem. (Philip Samuel P, 2000) JE mosquito vectors are zoophilic; consequently, cows &other animals may human risk by diverting vector mosquitoes (zoo prophylaxis).
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Immunization against JE
JE vaccines in worldwide use
1990): (Theodore F, et. al.
1.Inactivated Mouse Brain-Derived, 2.Inactivated Primary Hamster Kidney Cell-Derived. 3.Live Attenuated.
Indian JE vaccine : Formalin inactivated brain of suckling mice inoculated with the Nakayama JE strain, (CRI, Kasauli,H.P). (Rao PN, 2001)
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Immunization against JE
Table . Japanese encephalitis vaccine
Doses Subcutaneous route 12 years of age Primary series1,2, and3 Booster 0.5 mL 3 or more years of age 1.0 mL Days0,7, and 30 1 dose at 24 months or later Comments
0.5 mL
1.0 mL
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An emerging zoonosis
Increased demands of human and animal population. Altered the ecosystem where virus previously circulated between wild animal and their vectors. Initially virus activity in few sq. miles of Sagar Sorab taluks within few months it spread in >2000 sq. miles. Earlier Serological surveys showed antibodies to KFD virus or a related virus in Kutch and Saurashtra, other parts of country. (Banergee, 1996) Recently in Andaman & Nicobar Islands, showed highest (22.4% ) positivity in human population (Padbidri et al., 2004)
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1982 1983 1984 1985 1986 1987 1999 2001 2002 2003 2004-05
Source of infection
Primates are the primary host. Maximum mortality among two spp. Of monkeysThe grey langur Presbytis entellus, and The bonnet macaque Macaca radiata.
Virus isolated in large numbers from these two species. (WHO, 1985) Monkeys are amplifiers of the virus
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Reservoirs
Small forest mammals, rodents become infected but do not die Virus isolated from several species of rodents and presence of neutralizing antibodies confirmed. Main reservoirs: Indian crested porcupine Hystrix indica
(Bhat, 1976)
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Transmission
Human infection by bite of infected tick. Fifteen species of Ixodid spp. found to be infected naturally. - ten spp. belong to genus Haemaphysalis Important species H. spinigera, H. kyasanurensis, H. turturis, H. wellingtoni, Ixodes petauristae.
(Boshell et al., 1968; Bhat et al., 1975)
Mode of transmission: trans stadial. Trans ovarian transmission: only in Ixodes petauristae.
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Disease in monkeys: Epidemics are usually preceded by epizootics in monkeys a warning sign. Diseases in humans: Incubation period 3 to 8 days. Sudden onset of high fever(40 C), headache, myalgia, haemorrhagic manifestations epistaxis and hematuria. febrile period 6 to 11 days. Haemorrhages
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Treatment
Analgesics and antipyretics to reduce the temperature. Paracetamol preferred than aspirin due to bleeding tendency. (Gupta and Yashpal, 1975) Supportive treatment intravenous fluids to combat dehydration, if needed blood transfusion. Prevention and control Protective measures individual human protection from ticks. Insecticidal sprays Lindane highly effective in killing 66 ticks.
Vaccination
Formalin inactivated chicken embryo cell culture KFD virus vaccine developed by Haffkine institute, Bombay.
(Manasharamani et al., 1967)
Good immune response in monkeys but during field trial 59.32% seroconversion in humans. Two doses of vaccine, 1 ml each at an interval of four weeks. Vaccine efficacy six months to one year. Children half the dose given to adults (Dandawate et al.,1980) Mouse brain vaccine of RSSE virus also used but not effective
(Aniker et al., Shah et al., Pavri et al., 1962)
Attenuated Langet virus vaccine 70% to100% protection against KFD virus in mice, experimentally used in human volunteers without any adverse reaction
(Thind et al., 1981)
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Cat-Scratch Disease
Common carriers
Cats Dogs
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Cat-Scratch Disease
Transmission
Scratches and puncture wounds from infected animals
Clinical presentation
Fever Skin papule Swollen lymph nodes
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Salmonellosis
Foods : Raw poultry, eggs Illness: Illness Fever, cramps, diarrhea sometimes vomiting Onset: Onset 7 hrs to 3 days after eating
Salmonellosis
Common carriers
Cattle Cats Dogs Horses Poultry
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Salmonellosis
Transmission
Direct contact with animal or feces Contaminated food
Clinical Presentation
Chills Fever Headache Diarrhea Vomiting
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Cook eggs thoroughly Never eat runny yolks or raw eggs Always refrigerate processed meat products
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Campylobacter
Common Carriers:
Poultry (main) Cattle Sheep Pigs Dogs Rodents
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Campylobacter
Transmission Contaminated food or animals Clinical presentation Stomach ache Nausea Headache Diarrhea
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Campylobacteriosis
Foods Associated : Raw chicken eggs, poultry, raw beef,
Diarrhea, often associated with fever, Abdominal pain, nausea, headache and muscle pain. Illness can appear very similar to Salmonellosis
Onset: 2-5 days after eating contaminated food. Duration: Illness may last 7-10 days.
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Handle foods properly & Cook thoroughly Avoid cross-contamination Use sodium hypochlorite (Domex)solution in water(1:100) for disinfection of utensils & hands
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LISTERIOSIS
Foods: Raw poultry meat, luncheon meats, hot dogs, refrigerated ready-to-eat foods soft cheese, ice-cream, salad-type products Illness: In healthy Flu-like illness Diarrhea, vomiting and nausea
In immuno-compromised- e.g. pregnant women Septicemia, meningitis, encephalitis Spontaneous abortion or stillbirth Onset: Duration: 12 hrs to a few weeks after consumption 24 to 48 hrs
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The Disease
Emerging foodborne bacterial zoonosis Nagging Public health hazard (25-30% CFR)
Deaths caused(28%) ranks next to salmonellosis (36%)
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Avoid consumption of contaminated food stuff particularly soft cheese. Special care for pregnant women and alike
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Colibacillosis
Foods : Raw poultry meat, undercooked hamburgers Illness: Bloody diarrhea Hemolytic uremic syndrome (HUS) kidney failure thrombotic throbocytopenic purpura (TTP) Onset: 12 - 72 hrs after consumption
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Clostridial Infections
Clostridium perfringens
Foods: Foods Meat and/or gravy contaminated with soil,
dishes (Meat, poultry, and other foods) held warm, but not hot, for serving
Illness: Illness Abdominal cramp and diarrhea, headache, chills,, Onset: 8 to 22 hrs after consumption
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Psittacosis
Transmission
Inhalation from infected birds Carcasses Secretions Contaminated facilities
Clinical presentation
Fever Headache Pneumonia
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Avoid air and touch contact with sick birds with ruffled
feathers, yellowish-green diarrhoea
Clean & disinfect the cages and droppings by wet mopping Observe hygienic practices & take antibiotics if sick
In Birds
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Lesions in Chickens
o Lesions may be absent in cases of sudden death o Nasal and oral cavity discharge o Severe congestion of the musculature o Subcutaneous oedema of the head and neck area o Severe congestion of conjunctivae, sometimes with petechiae o Excessive mucous exudate in the lumen of the trachea, or severe haemorrhagic tracheitis o Petechiae hemorrhages on the inside of the sternum, on the serosa and abdominal fat, serosal surfaces and in the body cavity o Severe kidney congestion, sometimes with urate deposits 94 in the tubules
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HPAI - Congestion and petechiae in the skin on the hocks and shanks
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Effect on Proventriculus
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Control Measures
Effective disease surveillance for early detection & reporting of outbreak. Enhanced biosecurity of poultry farms. Control of movements of birds & products that may contain virus. Rapid humane destruction of poultry at high risk of infection. Disposal of carcasses & potentially infective material in a biosecure manner. Proper use of vaccination.
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Vaccination (Poultry)
Nonviable oil-emulsion vaccine To be effective, the vaccine must be produced using the autogenous virus. Recombinant vaccine fowl pox virus or infectious laryngotracheitis as virus vector A baculovirus-expression system has been used to produce recombinant H5 and H7 antigens for incorporation into vaccines. DNA encoding H5 haemagglutinin Evaluated as a potential vaccine in poultry DIVA (Differentiation of Infected from Vaccinated Animals) DIVA strategy to differentiatee infected from 100 vaccinated
Antiviral Prophylaxis
In Humans Ion-channel blockers
eg., amantadine resistance develops quickly (eg H5N1)
Neuraminidase inhibitors
- Oseltamivir : TAMIFLU 75 mg p.o.q.d prophylaxis. 75 mg p.o bid for 5 days as treatment. - Zanamivir : RELENZA 5 mg inhalation for 5 days as treatment
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In Humans:
INACTIVATED INFLUENZA VACCINE First developed in US by Armed Services 1940s Made of split viruses or viral subunits containing hemaglutinin and neuraminidase Contain 2 type A viruses and 1 type B virus Try to match what will most likely be in circulation each season
Age group 6-35m 3-8yrs. >9yrs. Dose 0.25ml 0.5ml 0.5ml No. of doses 1 or 2 1 or 2 1 Route IM
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IM IM
LIVE ATTENUATED INFLUENZA VACCINE FluMistR (Med Immune Inc),FluzoneR (Aventis pasteur Inc) & FluvirinR (Chiron) Produced by recombinant gene technology Viruses express contemporary influenza vaccine antigens Used only intra-nasally Dose is 0.5ml ; O.25ml to each nostril Sprayed when the recipient is in an upright position
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Ringworm
Common Carriers Cattle Cats
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Ringworm
Transmission
Direct contact with infected animal
Clinical presentation
Skin lesions
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Ringworm
Transmission
Direct contact with infected animal
Clinical presentation
Skin lesions
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Toxoplasmosis
Common carriers
Cats Sheep
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Toxoplasmosis
Transmission
Ingestion of infected meats Fecal contaminated soil
Clinical Presentation
Fever Swollen nodes Abortion Still-birth Mental retardation
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Clinical symptoms
In Humans :
Asymtomatic/flu-like symptoms CONGENITAL Abortion, foetal death, retinochoroiditis, hydrocephalus, convulsions, cerebral calcification, mental retardation Trimester Congenital infection 1st 2nd 3rd 13% 29% 50% Severity 80% 30% 70 to 90%
POSTNATAL
I. P. : 1-2 week Lymphadenitis, fever, malaise, fatigue, muscle pain, sore throat & headache Encephalitis in AIDS patients
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Clinical symptoms
Animals: Usually Sub clinical or Acute: Diarrhoea, lymphadenopathy, Hepatic lesions, encephalitis & ocular lesions Transplacental infection Early embryonic death Foetal death & mummification Abortion Still birth Birth of weak youngone
Scabies
Common Carriers Dogs Raccoons
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Scabies
Transmission
Direct contact with infected animals
Clinical presentation
Itching skin lesions
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Milkers Nodules
Common carrier
Cow teats Ulcers from calves mouth
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Milkers Nodules
Transmission
Milking or touching the teat of infected cow Contact with a mouth ulcer in a calve
Clinical presentation
5-14 day incubation period 2-5 small, red spots on hands
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PERSONAL HYGIENE
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PERSONAL CLEANLINESS
Personal effects Hand washing Use of antiseptic on hands
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E. coli O157:H7 Salmonella spp. Staphylococcus aureus Listeria monocytogenes Campylobacter jejuni Yersinia enterocolitica BSE (Mad cow disease)
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Trichinella spiralis Toxoplasma gondii Escherichia coli Salmonella Staphylococcus aureus Listeria monocytogenes.
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Salmonella spp. Campylobacter jejuni Listeria monocytogenes Escherichia coli O157:H7 Staphylococcus spp. Streptococcus spp.
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Cooking guidelines
Cook eggs until firm Avoid foods with partially cooked eggs Cook meats until juices are clear
Poultry internal temp of 180 degrees Beef internal temp of 160 degrees
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Storing leftovers
Store food in appropriate containers Set refrigerator temp to 40C and freezer to 00C Refrigerate leftovers immediately Never leave food out for more than 2 hours
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Packaging
Packaging materials Protection of food Prevent recontamination
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Pest control
Entrance sites External and Internal inspection Assess the facilitys capacity for excluding pests.
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Wear appropriate clothing and gloves Spray dead animals before moving them Dispose of animals according to law Wash hands afterwards
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Aim
The contribution to complete physical, mental and social well being through an understanding and application of veterinary 145 medical sciences
: Sr.Sci. & I/C, Comp. Patho. Biomed. Lab. : Sr.Sci. & I/C, Salmonella Centre (B&M) : Sr.Sci. & I/C, Brucella Lab.
Dr. K.N. Bhilegaonkar : Sr.Sci. & I/C, Foodborne Infection Lab. Dr. R.S. Rathore Dr. S.C Das : Sr.Sci. & I/C, Bacterial Zoonoses Lab. & Animal Shed : Sr.Sci. , Calcutta Centre, IVRI
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Distinctions conferred
FAO/WHO Collaborating Center
for Research and Training in Veterinary Public Health (Till 2000, fresh proposal submitted on new guidelines by WHO)
WHO Expert Team from SEARO & Indian HQ Director, Rajbhasha, ICAR
OBJECTIVES
Research on diagnosis, prevention & control of
Zoonoses Foodborne infections & intoxications Environmental pollution PG Education and Research
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+ ve 3 9 12
- ve 29 11 40
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