SlideShare ist ein Scribd-Unternehmen logo
1 von 54
EPIDEMIOLOGY
OF
ZOONOTIC BACTERIAL
DISEASES
WITH
THEIR PREVENTION AND
CONTROL
BRUCELLOSIS
• It is one of the major bacterial zoonotic disease
and in humans is also known as undulent fever
,malta fever or mediterranean fever.
• it is caused by different species of brucella group
of organisms
• It is characterized by: enlarged spleen
arthritis
irregular febrile attacks
with profuse sweating
• The disease may last for several days,months or
years
2
• Brucellosis is a recognised public health problem
with worldwide distribution.
• It is endemic wherever cattle,pigs,goats and
sheep are raised in large numbers.
• Important endemic area for brucellosis exist in
Mediterranean zones,europe,central asia,mexico
and south America.
• Animal brucellosis is reported from practically
every state in india.
• And human brucellosis is difficult to estimate
3
EPIDEMIOLOGICAL DETERMINANTS
AGENT FACTORS
1. AGENT: the agents are small,gram negative
rod shaped,non-motile,non-sporing and
intracellular coccobacilli of the genous
Brucella.
Four species infect man:
(a) B.melitensis : most virulent and invasive
species; usually infects goats
and sheeps.
4
(b) B.abortus: less virulent and is primarly
(c) B.suis: intermediate virulent and chiefly
(d) B.canis:is a parasite of dogs.
2. RESERVOIR OF INFECTION
The reservoir for human infection are:-
cattle,goats,swine,buffaloes,horses and
dogs.
5
disease of cattle.
infects pigs.
• The infected animal excrete Brucella in
urine,milk,placenta,uterine and vaginal
discharges.
HOST FACTORS:-
• Human brucellosis is predominantly a disease
of adult male.
• People at high risk are-
farmers,butchers,shephards ,abattoir workers
and lab workers , due to occupational
exposure
6
• ENVOIRMENTAL FACTORS
Conditions favouring the spread of brucellosis are:
Absence of standards of hygiene
Overcrowding of herds
Lack of exposure to sunlight
Unhygienic practices in milk and meat
production
INCUBATION PERIOD
Highly variable,usually 1-3 weeks,but may last for
6 months or more.
7
Transmission
8
ROUTES OF TRANSMISSION
• Oral : unpasteurised milk & products, raw milk or
meat
• Respiratory: lab workers.
• Skin: accidental penetration or abrasion
– - at risk farmers & veterinarians.
• Other routes:
Conjunctival, Blood transfusion, Transplacental,
person to person.
9
10
PATTERN OF DISEASE
• It may vary from an acute febrile disease to a chronic low
grade disease.
• The acute phase is characterized by:
pyrexia(up to 40-41deg c)
rigors and sweating
arthritis/arthralgia involving larger
joints.
low back pain
headache
insomnia
spleenomegaly and hepatomegaly
leucopenia
If patient is treated with tetracycline,the symptoms may
disappear quickly ,but infection ,being intracellular,may
persist giving rise to subacute or relapsing disease. 11
12
CONTROL OF BRUCELLOSIS• IN THE ANIMALS
The most rational approach for preventing human brucellosis is control and
eradication of the infection from animal reservoirs which is based on
combination of the following measures:
(a)TEST AND SLAUGHTER: case finding done by mass survey. Skin test are
available. The complement fixation test is recommended.
Those animals infected with brucellosis are slaughtered with full compensation
paid to farmers.
This is the only satisfactory solution aimed at eradication of the disease.
(b)VACCINATION: vaccine of B.abortus strain 19 is commonly used for young
animals. a compulsory vaccination programme is given on yearly basis to
reduce rate of infection.
Systemic vaccination of period of 7-10 years may result in elimination of the
disease
(c) HYGIENIC MEASURES: these comprise provision of clean sanitary
envoirnment for animals sanitary disposal of urine and faeces and health
eduction of all those who are occupationaly involved
13
• IN THE HUMANS
(a) EARLY DIAGNOSIS AND TREATMENT:
in uncomplicated case the antibiotic of choice is tetracycline .
For adults in the acute stage ,the dose is 500g every 6 hours for
3 weeks.
In patients with skeletal or other complication , intramuscular
streptomycin 1g daily in addition to tetracycline usually
achieves a cure.
(b) PASTEURIZATION OF MILK
(c) PROTECTIVE MEASURES-prevent direct contact with infected
animals.
persons at risk should observe high standards of personal
hygiene.
They should wear protective clothing when handling
carcasses.
Exposed areas of skin should be washed and soiled clothing
renewed
14
(d)VACCINATION : human live vaccine of B.abortus strain
19-BA is available.
BRUCELLOSIS WOULD DISAPPEAR IF IT WERE ERADICATED
FROM ANIMALS.
The national and international centre for brucellosis is
located at FAO/WHO Brucella reference centre, Indian
veterinary research institute ,Izatnagar,(Uttar Pradesh).15
HUMAN
SALMONELLOSIS
• The term ‘salmonellosis’ covers a complex
group of food borne infections affecting both
man and animals. The disease causes illness
and even death in humans as well as
economic losses in the animal and food
industries. The term ‘food poisoning’ is
commonly applied to salmonellosis.
PROBLEM STATEMENT
• Salmonellosis is a global problem. Human
salmonellosis represents 60 to 80% of all
reported cases of food borne diseases.
• While the incidence of typhoid fever has
declined, the incidence of other salmonella
infections has increased in the developed
countries. The problem is aggrevated by the
widespread use of animal feeds containing
antimicrobial drugs that favour drug-resistant
salmonellae and their potential transmission to
humans.
EPIDEMIOLOGICAL DETERMINANTS
AGENT FACTORS
AGENT:- Salmonellae comprises a large and
important group of bacteria. This group is now
known to comprise more than 2,500 serotypes
capable of infecting humans.
Compared with other gram-negative rods,
salmonellae are relatively resistant to various
environmental factors. They have been shown to
be resistant to drying, salting, smoking and
freezing even for years.
Cont..
• As a result, salmonellae have been isolated
from divergent foods such as chocolates,
biscuits, coconuts and spices. The bacterium is
sensitive to heat and will survive temperatures
above 70 degree centigrade.
Cont..
• From an epidemiological point of view,
salmonellae can be classified into three main
groups:-
(i) Those which infect only man- e.g S. typhi, S.
paratyphi A and C.
(ii) Those are host- S. cholera-suis , S. Dublin.
(iii) Those infect both man and animals- S.
typhimurium, S. Enteriditis.
20
Cont..
RESERVOIR AND SOURCE OF INFECTION:-
(a) FOODS
Foods of animal origin, particularly commercially prepared
foods such as meat, poultry and egg products are
considered to be primary sources of salmonellosis.
(b) ANIMALS
Animals are the hosts and the principal vectors of zoonotic
salmonellosis. E.g cattle, swine, rodents etc.
(c) ENVIRONMENT
Salmonellae are widely distributed in the environment in
dust, water, manure, sewage, sludge, vegetables, insects,
birds, fish, rodents and other mammals.
MODE OF TRANSMISSION
• By ingestion of contaminated food and drink,
direct contact with domestic animals
especially such as dogs, pigeons, rats, mice
and insects. Once man is infected, he becomes
a source and the infection may spread to
others by the faecal-oral route.
• INCUBATION PERIOD:- 6 to 72 hours (usually).
23
CLINICAL FEATURES
• Clinically, the disease may be manifest by one of the
three syndromes:
(i) ENTERIC FEVER:- the term ‘enteric fever’ includes
both typhoid and paratyphoid fevers. The disease
may occur sporadically, epidemically or endemically.
(ii) SALMONELLA ENTEROCOLITIS (gastroenteritis) : This
is the most common manifestation of Salmonellae
infection. 6 to 48 hours of ingestion of Salmonellae
there is nausea, headache, vomiting and diarrhoea.
Low grade fever is common. Most infections are mild
with diarrhoea, in severe cases there may be
dehydration.
Cont..
(iii) SEPTICAEMIA WITH FOCAL LESION:- Non-
typhoid salmonellae may occasionally invade
the blood stream leading to generalized or
localized infection presenting itself as pyrexia
of unknown origin. Focal infection may result
in osteomyelitis, pyelonephritis, arthritis,
meningitis, cholecystitis and endocarditis.
PREVENTON AND CONTROL
• Since salmonellosis is zoonotic in origin,
preventive measures should begin at the farm
and embrace all the elements of the food chain
through live animals, animal products,
processing, final food preparation to
consumption. Approaches indicated at the farm
level are :
(i) Disease control e.g immunization of farm
animals against salmonellosis.
(ii) The use of hygienic animal feed.
(iii) Ensuring a sanitary environment for the animals
LEPTOSPIROSIS
Leptospirosis is essentially animal infection by several
serotype of liptospira & transmitted to man under
certain environmental condition.
The disease manifestations are many & varied, ranging
severity from a mild febrile illness to severe &
sometime fatal disease with liver & kidney involvement.
• Leptospirosis is considered to be most widespread of the
disease transmissible from animals to man
• It has high prevalence in warm humid tropical countries.
Out break mostly occur as a result of heavy rain fall.
• The global burden of disease in unknown approx
500,000 cases of leptospirosis are estimated to occur
worldwide every year
EPIDEMOLOGICAL DETERMINATION
Agent factor
(a) Agent: leptospira are thin & light motile
spirochetes 0.1-0.2 µm wide & 5-15µm long &
hooked ends. This organisms are visible by dark-
field illumination & silver staining.
(b) Source of infection: leptospira are excreted in
the urine of infections animal for a long time often
for an enter life time in case of rodents.
(c)Animal reservoirs: leptospirosis effects wild
& domestic animal worldwide especially rodents
such as rat ,mice etc. most domestic animal
including cattle ship , goat, water buffallo, pigs &
horse may be infected through pet animal
particularly dogs may also be infected.
Host factors
(a)Age: children acquire the infection from
dogs more frequently then do adults.
Human infection is only accidental.
(b)occupation: human infections are
usually due to occupational exposure to the
urine of infected animals e.g.-
Agriculture,livestocks farmers, workers in
rice fields ,sugarcane fields etc.
(c)Immunity: A solid serovar specific
immunity follows infection.
Environmental factors
• Leptospirosis infection is unique in that it is acquired
through contact with an environment contaminated by
urine and faeces from carrier animal or other infected
animals.
• Leptospira shed in the urine can survive for wks in soil
and water, so environmental contamination may reach
high levels in areas where carrier animals frequently
urinate.
• The association of poor housing, limited water
supply, inadequate method of water disposal,
all combine to make the disease a significant
risk for the poor population in both urban and
rural areas.
Mode of transmission
(a)Direct contact: leptospira can enter the
body through skin abrasions or through
intact mucous membrane by direct contact
with urine or tissue of infected animal.
(b)Indirect contact :through the contact of the
broken skin with soil, water or vegetation
contamination by urine of infected animals
or through ingestion of food or water
contaminated with leptospirosis.
(c) Droplet infection: infection may also occur
through inhalation as when milking infected
cows or goats by breathing air polluted with
droplets of urine.
Direct man to man infection is rare.
• Incubation period:
Usually 10 days with a range of 4 to 20
days
Diagnosis
• It is not possible to diagnose leptospirosis
with certainty on clinical grounds alone.
Because of the wide spectrum of sign &
symptoms, thee diagnosis is made by isolation
of leptospires from blood during the acute
illness and from urine after the 1 wks.
• Early in the disease the organisms may be
identified by dark fields examination of the
patient’s blood or by culture on a semisolid
medium.
• The organism may also be grown from the
urine from 10th day to 6 wks.
• Diagnosis is usually made by means of
serological tests , of which several are
available.
• Agglutination tests & become positive after 7-
8 days of illness and peaks at 3-4 wks & may
persist at high level for many yrs.
• indirect haemagglutination ,
immunoflourescent antibody and ELISA tests
also available .
Control
(a) antibiotics: penicillin is the drugs of choice
by other antibiotics(tetracycline &
doxycycline) are also effective
(b) Environmental measures: this includes
preventing exposure to potentially
contaminated water, reducing contamination
by rodent control and protection of workers
in hazardous occupation. Measures should
be taken to control rodents, proper disposal
of wastes & health education etc.
vaccination
• Immunization of farmers & pets prevent disease.
In some countries for instance Italy, USSR &
China, where certain occupations carry a high risk
of infections, vaccines are available.
• It is important that they should incorporate stains
of the serotypes that predominant in the
particular area since immunity to one type of
leptospira may not protect against infection by
another.
PLAGUE
• Plague is primarily and basically a zoonoses,
caused by Y. pestis, involving rodents and
fleas. It exists in natural foci, and is
transmitted by infected flea bites to human
living or intruding into the same ecological
environment. Plague occurs in many forms-
enzootically, epizootically, sporadically and in
epidemics of all types including anthroponotic
and primary pneumonic forms.
37
PROBLEM STATEMENT
• WORLD
Plague is often seen as problem of the past or
an ancient disease that is unlikely to reappear.
But continued outbreaks throughout the
world attest to its tenacious presence.
Although plague is predominantly a rural
disease, there have been outbreaks among
urban population in Madagascar and the
United Republic of Tanzania.
38
Cont..
• The data shows that from 2004 to 2009, a
total of 12,503 cases of human plague,
including 843 deaths, were reported by 16
countries in Africa, Asia and America. The
global case-fatality rate was 6.7%.
• In 2004, India reported a localized outbreak of
bubonic plague (8 cases and 3 deaths) in the
Dangud village, District of Uttarkashi.
39
EPIDEMIOLOGICAL DETERMINANTS
(a) AGENT : The causative agent, Y. pestis is a
Gram-negative, non-motile, cocco-bacillus
that exhibits bipolar staining with special
stains ( Wayson’s stain). The bacilli occur in
great abundance in the buboes, blood, spleen,
liver and other viscera of infected persons,
and in the sputum in cases of pneumonic
plague.
40
Cont..
(b) RESERVOIR OF INFECTIION : Wild rodents
are the natural reservoirs of plague. These are
found in mountains, deserts, cultivated areas
and forests in temperate and tropical regions.
(c) SOURCE OF INFECTION : Infected rodents
and fleas and case of pneumonic plague.
41
Cont..
HOST FACTORS
(a) AGE AND SEX : All ages and both sexes are
susceptible.
(b) HUMAN ACTIVITIES : Man may come into
contact with natural foci in the course of
hunting, grazing, cultivation.
(c) MOVEMENT OF PEOPLE : Plague is associated
with movement of people and cargo by sea or
land. Rats and fleas are transported in this way.
(d) IMMUNITY : Man has no natural immunity.
Immunity after recovery is relative.
42
ENVIRONMENTAL FACTORS
(a) SEASON : Plague season starts from September
until May. The disease tends to die out with the
onset of hot weather.
(b) TEMPERATURE AND HUMIDITY : A mean
temperature of 20 to 25 degree C and a relative
humidity of 60% and above are considered
favourable for the spread of plague.
(c) RAINFALL : Heavy rainfall, especially in the flat
fields tend to flood the rat burrows.
43
VECTORS OF PLAGUE
• The commonest and the most efficient vector
of plague is the rat flea, X. cheopis, but other
fleas may also transmit the infection, e.g X.
astia , X. brasiliensis and Pulex irritants
(human flea). Both sexes of the flea bite and
transmit the disease.
44
BLOCKED FLEA
• A flea ingest upto 0.5 cu.mm of blood which
may contain as many as 5,000 plague bacilli.
The bacilli multiply enormously in the gut of
the rat flea and may block the proventriculus
so that no food can pass through. Such a flea
is called a ‘blocked flea’.
45
FLEA INDICES
(a) TOTAL FLEA INDEX : the average number of fleas
of all species per rat.
(b) CHEOPIS INDEX : the average number of X.
cheopis per rat.
(c) SPECIFIC PERCENTAGE OF FLEAS : the
percentage of different species of fleas that are
found on rats.
(d) BURROW INDEX : the average number of free-
living fleas per species per rodent burrow.
46
HUMAN PLAGUE
MODE OF TRANSMISSION : There are atleast 5
basic types of transmission cycles in plague.
1. Commensal rat rat fleas man.
2. Wild rodentswild rodent fleas or direct
contactman.
3. Wild rodents, predomestic rodents, commensal
rodentswild rodent fleas, predomestic rodent
fleas, commensal rodent fleas man.
4. Manhuman fleasman.
5. Manman.
47
DISEASE IN MAN
(a) Bubonic plague : most common type of the disease.
The infected rat fleas usually bite on the lower
extremities and inoculate the bacilli. The bacilli are
intercepted by the regional lymphatic glands where
they prolifetare. Incubation period-2 to 7 days.
(b) Pneumonic plague : Primary pneumonic plague is
rare. Pneumonic plague is highly infectious and
spreads from man to man by droplet infection.
Incubation period – 2 to 7 days.
(c) Septicaemic plague : Primary septicaemic plague is
rare except for accidental laboratory infections.
Incubation period- 1 to 3 days.
48
LABORATORY INVESTIGATIONS
(a) Staining : it is important to prepare smears of
the clinical materials (e.g. bubo fluid, sputum)
(b) Culture : blood for culture should be collected
from all patients.
(c) Serology : acute and convalescent specimens of
blood sera should be collected for antibody
studies.
(d) Other methods : these include inoculation of
guinea pigs or mice or immunofluorescent
microscopic test.
49
PREVENTION AND CONTROL
1) Control of cases
(a) Early diagnosis- it is essential that plague-suspected
humans and rodents be examined bacteriologically to
confirm the presence of plague.
(b) Notification- If a human or rodent case is diagnosed,
health authorities must be notified promptly.
(c) Isolation- all patients with pneumonic plague should
be isolated.
(d) Treatment- must be started without waiting for
confirmation of the diagnosis.
50
Cont..
2) Control of fleas
The most effective method to break the chain
of transmission (rodentfleaman) is the
destruction of rat fleas by the proper
application of an effective insecticide.
3) Control of rodents
Continuous mass destruction of rodents is an
important plague-preventive measure.
51
Cont..
4) Vaccination
52
Cont..
5) Chemoprophylaxis
Chemoprophylaxis is a valuable preventive
measure, highly recommended. It should be
offered to all plague contacts, medical,
nursing, and public health personnel exposed
to the risk of infection. The drug of choice is
tetracycline. For adults, the dose is 500 mg 6
hourly for 5 days.
53
THANK YOU
54

Weitere ähnliche Inhalte

Was ist angesagt? (20)

Zoonosis
ZoonosisZoonosis
Zoonosis
 
Bacterial Zoonotic diseases of pets
Bacterial Zoonotic diseases of petsBacterial Zoonotic diseases of pets
Bacterial Zoonotic diseases of pets
 
Viral zoonotic disease
Viral zoonotic diseaseViral zoonotic disease
Viral zoonotic disease
 
Zoonotic infection
Zoonotic infectionZoonotic infection
Zoonotic infection
 
West nile fever
West nile feverWest nile fever
West nile fever
 
Zoonosis
ZoonosisZoonosis
Zoonosis
 
Zoonosis history and bacterial zoonotic diseases
Zoonosis history and bacterial zoonotic diseasesZoonosis history and bacterial zoonotic diseases
Zoonosis history and bacterial zoonotic diseases
 
Rabies ,microbiology
Rabies ,microbiologyRabies ,microbiology
Rabies ,microbiology
 
ZOONOSES (www.ubio.in)
ZOONOSES (www.ubio.in)ZOONOSES (www.ubio.in)
ZOONOSES (www.ubio.in)
 
Rickettsiae
RickettsiaeRickettsiae
Rickettsiae
 
Plague
PlaguePlague
Plague
 
Rabies
RabiesRabies
Rabies
 
Rabies virus
Rabies virusRabies virus
Rabies virus
 
Vector borne disease
Vector borne diseaseVector borne disease
Vector borne disease
 
Zoonotic disease
Zoonotic diseaseZoonotic disease
Zoonotic disease
 
Rotavirus
RotavirusRotavirus
Rotavirus
 
Nipah Virus infection
Nipah Virus infectionNipah Virus infection
Nipah Virus infection
 
Rhabdovirus lecture
Rhabdovirus lectureRhabdovirus lecture
Rhabdovirus lecture
 
zoonoses
zoonoseszoonoses
zoonoses
 
Human salmonellosis
Human salmonellosisHuman salmonellosis
Human salmonellosis
 

Ähnlich wie Epidemiology of bacterial zoonotic diseases with their prevention and control

Biological disaster tam 2014-12
Biological disaster tam 2014-12Biological disaster tam 2014-12
Biological disaster tam 2014-12Vijay Kumar
 
Epidemiology of kfd, brucellosis and leptospirosis
Epidemiology of kfd, brucellosis and leptospirosisEpidemiology of kfd, brucellosis and leptospirosis
Epidemiology of kfd, brucellosis and leptospirosisNamita Batra
 
Emerging and re-emerging diseses part2 (INCLUDES ANTIMICROBIAL RESISTANCE)
Emerging and re-emerging diseses part2 (INCLUDES ANTIMICROBIAL RESISTANCE)Emerging and re-emerging diseses part2 (INCLUDES ANTIMICROBIAL RESISTANCE)
Emerging and re-emerging diseses part2 (INCLUDES ANTIMICROBIAL RESISTANCE)Dr. Mamta Gehlawat
 
Crimean congo hemorrhagic fever
Crimean congo hemorrhagic feverCrimean congo hemorrhagic fever
Crimean congo hemorrhagic feverismailzai
 
Plague & leptospirosis class.pptx
Plague & leptospirosis class.pptxPlague & leptospirosis class.pptx
Plague & leptospirosis class.pptxShwetha Hariba
 
Community health nursing 1 mahir
Community health nursing  1 mahirCommunity health nursing  1 mahir
Community health nursing 1 mahirvhoramahir
 
Community health nursing 1 mahir
Community health nursing  1 mahirCommunity health nursing  1 mahir
Community health nursing 1 mahirMahir vhora
 
Salmonellosis Including Enteric Fever.pdf
Salmonellosis Including Enteric Fever.pdfSalmonellosis Including Enteric Fever.pdf
Salmonellosis Including Enteric Fever.pdfIrisPeraltaGarca
 
MSN I COMMUNICABLE DISEASES.pptx
MSN I COMMUNICABLE DISEASES.pptxMSN I COMMUNICABLE DISEASES.pptx
MSN I COMMUNICABLE DISEASES.pptx M.Josephin Dayana
 
Bovine tuberculosis
Bovine tuberculosisBovine tuberculosis
Bovine tuberculosisismailzai
 

Ähnlich wie Epidemiology of bacterial zoonotic diseases with their prevention and control (20)

Zoonosss
ZoonosssZoonosss
Zoonosss
 
Zoonotic tuberculosis
Zoonotic tuberculosisZoonotic tuberculosis
Zoonotic tuberculosis
 
PLAGUE.pptx
PLAGUE.pptxPLAGUE.pptx
PLAGUE.pptx
 
Zoonotic disease and pathogens slideshare
Zoonotic disease and pathogens slideshare Zoonotic disease and pathogens slideshare
Zoonotic disease and pathogens slideshare
 
Biological disaster tam 2014-12
Biological disaster tam 2014-12Biological disaster tam 2014-12
Biological disaster tam 2014-12
 
BACTERIAL ZOONOSES.pptx
BACTERIAL ZOONOSES.pptxBACTERIAL ZOONOSES.pptx
BACTERIAL ZOONOSES.pptx
 
Yellow fever
Yellow feverYellow fever
Yellow fever
 
Epidemiology of kfd, brucellosis and leptospirosis
Epidemiology of kfd, brucellosis and leptospirosisEpidemiology of kfd, brucellosis and leptospirosis
Epidemiology of kfd, brucellosis and leptospirosis
 
Emerging and re-emerging diseses part2 (INCLUDES ANTIMICROBIAL RESISTANCE)
Emerging and re-emerging diseses part2 (INCLUDES ANTIMICROBIAL RESISTANCE)Emerging and re-emerging diseses part2 (INCLUDES ANTIMICROBIAL RESISTANCE)
Emerging and re-emerging diseses part2 (INCLUDES ANTIMICROBIAL RESISTANCE)
 
Crimean congo hemorrhagic fever
Crimean congo hemorrhagic feverCrimean congo hemorrhagic fever
Crimean congo hemorrhagic fever
 
Plague & leptospirosis class.pptx
Plague & leptospirosis class.pptxPlague & leptospirosis class.pptx
Plague & leptospirosis class.pptx
 
brucellosis.pptx
brucellosis.pptxbrucellosis.pptx
brucellosis.pptx
 
Community health nursing 1 mahir
Community health nursing  1 mahirCommunity health nursing  1 mahir
Community health nursing 1 mahir
 
Community health nursing 1 mahir
Community health nursing  1 mahirCommunity health nursing  1 mahir
Community health nursing 1 mahir
 
Salmonellosis Including Enteric Fever.pdf
Salmonellosis Including Enteric Fever.pdfSalmonellosis Including Enteric Fever.pdf
Salmonellosis Including Enteric Fever.pdf
 
MSN I COMMUNICABLE DISEASES.pptx
MSN I COMMUNICABLE DISEASES.pptxMSN I COMMUNICABLE DISEASES.pptx
MSN I COMMUNICABLE DISEASES.pptx
 
Leptospirosis in english
Leptospirosis in englishLeptospirosis in english
Leptospirosis in english
 
Presentation
PresentationPresentation
Presentation
 
Congo virus by ishfaq ahmad
Congo virus by ishfaq ahmadCongo virus by ishfaq ahmad
Congo virus by ishfaq ahmad
 
Bovine tuberculosis
Bovine tuberculosisBovine tuberculosis
Bovine tuberculosis
 

Kürzlich hochgeladen

Glomerular Filtration and determinants of glomerular filtration .pptx
Glomerular Filtration and  determinants of glomerular filtration .pptxGlomerular Filtration and  determinants of glomerular filtration .pptx
Glomerular Filtration and determinants of glomerular filtration .pptxDr.Nusrat Tariq
 
Study on the Impact of FOCUS-PDCA Management Model on the Disinfection Qualit...
Study on the Impact of FOCUS-PDCA Management Model on the Disinfection Qualit...Study on the Impact of FOCUS-PDCA Management Model on the Disinfection Qualit...
Study on the Impact of FOCUS-PDCA Management Model on the Disinfection Qualit...MehranMouzam
 
Giftedness: Understanding Everyday Neurobiology for Self-Knowledge
Giftedness: Understanding Everyday Neurobiology for Self-KnowledgeGiftedness: Understanding Everyday Neurobiology for Self-Knowledge
Giftedness: Understanding Everyday Neurobiology for Self-Knowledgeassessoriafabianodea
 
SYNDESMOTIC INJURY- ANATOMICAL REPAIR.pptx
SYNDESMOTIC INJURY- ANATOMICAL REPAIR.pptxSYNDESMOTIC INJURY- ANATOMICAL REPAIR.pptx
SYNDESMOTIC INJURY- ANATOMICAL REPAIR.pptxdrashraf369
 
epilepsy and status epilepticus for undergraduate.pptx
epilepsy and status epilepticus  for undergraduate.pptxepilepsy and status epilepticus  for undergraduate.pptx
epilepsy and status epilepticus for undergraduate.pptxMohamed Rizk Khodair
 
Lippincott Microcards_ Microbiology Flash Cards-LWW (2015).pdf
Lippincott Microcards_ Microbiology Flash Cards-LWW (2015).pdfLippincott Microcards_ Microbiology Flash Cards-LWW (2015).pdf
Lippincott Microcards_ Microbiology Flash Cards-LWW (2015).pdfSreeja Cherukuru
 
Nutrition of OCD for my Nutritional Neuroscience Class
Nutrition of OCD for my Nutritional Neuroscience ClassNutrition of OCD for my Nutritional Neuroscience Class
Nutrition of OCD for my Nutritional Neuroscience Classmanuelazg2001
 
History and Development of Pharmacovigilence.pdf
History and Development of Pharmacovigilence.pdfHistory and Development of Pharmacovigilence.pdf
History and Development of Pharmacovigilence.pdfSasikiranMarri
 
PULMONARY EMBOLISM AND ITS MANAGEMENTS.pdf
PULMONARY EMBOLISM AND ITS MANAGEMENTS.pdfPULMONARY EMBOLISM AND ITS MANAGEMENTS.pdf
PULMONARY EMBOLISM AND ITS MANAGEMENTS.pdfDolisha Warbi
 
Big Data Analysis Suggests COVID Vaccination Increases Excess Mortality Of ...
Big Data Analysis Suggests COVID  Vaccination Increases Excess Mortality Of  ...Big Data Analysis Suggests COVID  Vaccination Increases Excess Mortality Of  ...
Big Data Analysis Suggests COVID Vaccination Increases Excess Mortality Of ...sdateam0
 
The next social challenge to public health: the information environment.pptx
The next social challenge to public health:  the information environment.pptxThe next social challenge to public health:  the information environment.pptx
The next social challenge to public health: the information environment.pptxTina Purnat
 
April 2024 ONCOLOGY CARTOON by DR KANHU CHARAN PATRO
April 2024 ONCOLOGY CARTOON by  DR KANHU CHARAN PATROApril 2024 ONCOLOGY CARTOON by  DR KANHU CHARAN PATRO
April 2024 ONCOLOGY CARTOON by DR KANHU CHARAN PATROKanhu Charan
 
Primary headache and facial pain. (2024)
Primary headache and facial pain. (2024)Primary headache and facial pain. (2024)
Primary headache and facial pain. (2024)Mohamed Rizk Khodair
 
world health day presentation ppt download
world health day presentation ppt downloadworld health day presentation ppt download
world health day presentation ppt downloadAnkitKumar311566
 
SWD (Short wave diathermy)- Physiotherapy.ppt
SWD (Short wave diathermy)- Physiotherapy.pptSWD (Short wave diathermy)- Physiotherapy.ppt
SWD (Short wave diathermy)- Physiotherapy.pptMumux Mirani
 
Presentation on General Anesthetics pdf.
Presentation on General Anesthetics pdf.Presentation on General Anesthetics pdf.
Presentation on General Anesthetics pdf.Prerana Jadhav
 
Informed Consent Empowering Healthcare Decision-Making.pptx
Informed Consent Empowering Healthcare Decision-Making.pptxInformed Consent Empowering Healthcare Decision-Making.pptx
Informed Consent Empowering Healthcare Decision-Making.pptxSasikiranMarri
 
ANTI-DIABETICS DRUGS - PTEROCARPUS AND GYMNEMA
ANTI-DIABETICS DRUGS - PTEROCARPUS AND GYMNEMAANTI-DIABETICS DRUGS - PTEROCARPUS AND GYMNEMA
ANTI-DIABETICS DRUGS - PTEROCARPUS AND GYMNEMADivya Kanojiya
 
Wessex Health Partners Wessex Integrated Care, Population Health, Research & ...
Wessex Health Partners Wessex Integrated Care, Population Health, Research & ...Wessex Health Partners Wessex Integrated Care, Population Health, Research & ...
Wessex Health Partners Wessex Integrated Care, Population Health, Research & ...Wessex Health Partners
 

Kürzlich hochgeladen (20)

Glomerular Filtration and determinants of glomerular filtration .pptx
Glomerular Filtration and  determinants of glomerular filtration .pptxGlomerular Filtration and  determinants of glomerular filtration .pptx
Glomerular Filtration and determinants of glomerular filtration .pptx
 
Study on the Impact of FOCUS-PDCA Management Model on the Disinfection Qualit...
Study on the Impact of FOCUS-PDCA Management Model on the Disinfection Qualit...Study on the Impact of FOCUS-PDCA Management Model on the Disinfection Qualit...
Study on the Impact of FOCUS-PDCA Management Model on the Disinfection Qualit...
 
Giftedness: Understanding Everyday Neurobiology for Self-Knowledge
Giftedness: Understanding Everyday Neurobiology for Self-KnowledgeGiftedness: Understanding Everyday Neurobiology for Self-Knowledge
Giftedness: Understanding Everyday Neurobiology for Self-Knowledge
 
SYNDESMOTIC INJURY- ANATOMICAL REPAIR.pptx
SYNDESMOTIC INJURY- ANATOMICAL REPAIR.pptxSYNDESMOTIC INJURY- ANATOMICAL REPAIR.pptx
SYNDESMOTIC INJURY- ANATOMICAL REPAIR.pptx
 
epilepsy and status epilepticus for undergraduate.pptx
epilepsy and status epilepticus  for undergraduate.pptxepilepsy and status epilepticus  for undergraduate.pptx
epilepsy and status epilepticus for undergraduate.pptx
 
Lippincott Microcards_ Microbiology Flash Cards-LWW (2015).pdf
Lippincott Microcards_ Microbiology Flash Cards-LWW (2015).pdfLippincott Microcards_ Microbiology Flash Cards-LWW (2015).pdf
Lippincott Microcards_ Microbiology Flash Cards-LWW (2015).pdf
 
Nutrition of OCD for my Nutritional Neuroscience Class
Nutrition of OCD for my Nutritional Neuroscience ClassNutrition of OCD for my Nutritional Neuroscience Class
Nutrition of OCD for my Nutritional Neuroscience Class
 
History and Development of Pharmacovigilence.pdf
History and Development of Pharmacovigilence.pdfHistory and Development of Pharmacovigilence.pdf
History and Development of Pharmacovigilence.pdf
 
PULMONARY EMBOLISM AND ITS MANAGEMENTS.pdf
PULMONARY EMBOLISM AND ITS MANAGEMENTS.pdfPULMONARY EMBOLISM AND ITS MANAGEMENTS.pdf
PULMONARY EMBOLISM AND ITS MANAGEMENTS.pdf
 
Big Data Analysis Suggests COVID Vaccination Increases Excess Mortality Of ...
Big Data Analysis Suggests COVID  Vaccination Increases Excess Mortality Of  ...Big Data Analysis Suggests COVID  Vaccination Increases Excess Mortality Of  ...
Big Data Analysis Suggests COVID Vaccination Increases Excess Mortality Of ...
 
The next social challenge to public health: the information environment.pptx
The next social challenge to public health:  the information environment.pptxThe next social challenge to public health:  the information environment.pptx
The next social challenge to public health: the information environment.pptx
 
April 2024 ONCOLOGY CARTOON by DR KANHU CHARAN PATRO
April 2024 ONCOLOGY CARTOON by  DR KANHU CHARAN PATROApril 2024 ONCOLOGY CARTOON by  DR KANHU CHARAN PATRO
April 2024 ONCOLOGY CARTOON by DR KANHU CHARAN PATRO
 
Primary headache and facial pain. (2024)
Primary headache and facial pain. (2024)Primary headache and facial pain. (2024)
Primary headache and facial pain. (2024)
 
world health day presentation ppt download
world health day presentation ppt downloadworld health day presentation ppt download
world health day presentation ppt download
 
Epilepsy
EpilepsyEpilepsy
Epilepsy
 
SWD (Short wave diathermy)- Physiotherapy.ppt
SWD (Short wave diathermy)- Physiotherapy.pptSWD (Short wave diathermy)- Physiotherapy.ppt
SWD (Short wave diathermy)- Physiotherapy.ppt
 
Presentation on General Anesthetics pdf.
Presentation on General Anesthetics pdf.Presentation on General Anesthetics pdf.
Presentation on General Anesthetics pdf.
 
Informed Consent Empowering Healthcare Decision-Making.pptx
Informed Consent Empowering Healthcare Decision-Making.pptxInformed Consent Empowering Healthcare Decision-Making.pptx
Informed Consent Empowering Healthcare Decision-Making.pptx
 
ANTI-DIABETICS DRUGS - PTEROCARPUS AND GYMNEMA
ANTI-DIABETICS DRUGS - PTEROCARPUS AND GYMNEMAANTI-DIABETICS DRUGS - PTEROCARPUS AND GYMNEMA
ANTI-DIABETICS DRUGS - PTEROCARPUS AND GYMNEMA
 
Wessex Health Partners Wessex Integrated Care, Population Health, Research & ...
Wessex Health Partners Wessex Integrated Care, Population Health, Research & ...Wessex Health Partners Wessex Integrated Care, Population Health, Research & ...
Wessex Health Partners Wessex Integrated Care, Population Health, Research & ...
 

Epidemiology of bacterial zoonotic diseases with their prevention and control

  • 2. BRUCELLOSIS • It is one of the major bacterial zoonotic disease and in humans is also known as undulent fever ,malta fever or mediterranean fever. • it is caused by different species of brucella group of organisms • It is characterized by: enlarged spleen arthritis irregular febrile attacks with profuse sweating • The disease may last for several days,months or years 2
  • 3. • Brucellosis is a recognised public health problem with worldwide distribution. • It is endemic wherever cattle,pigs,goats and sheep are raised in large numbers. • Important endemic area for brucellosis exist in Mediterranean zones,europe,central asia,mexico and south America. • Animal brucellosis is reported from practically every state in india. • And human brucellosis is difficult to estimate 3
  • 4. EPIDEMIOLOGICAL DETERMINANTS AGENT FACTORS 1. AGENT: the agents are small,gram negative rod shaped,non-motile,non-sporing and intracellular coccobacilli of the genous Brucella. Four species infect man: (a) B.melitensis : most virulent and invasive species; usually infects goats and sheeps. 4
  • 5. (b) B.abortus: less virulent and is primarly (c) B.suis: intermediate virulent and chiefly (d) B.canis:is a parasite of dogs. 2. RESERVOIR OF INFECTION The reservoir for human infection are:- cattle,goats,swine,buffaloes,horses and dogs. 5 disease of cattle. infects pigs.
  • 6. • The infected animal excrete Brucella in urine,milk,placenta,uterine and vaginal discharges. HOST FACTORS:- • Human brucellosis is predominantly a disease of adult male. • People at high risk are- farmers,butchers,shephards ,abattoir workers and lab workers , due to occupational exposure 6
  • 7. • ENVOIRMENTAL FACTORS Conditions favouring the spread of brucellosis are: Absence of standards of hygiene Overcrowding of herds Lack of exposure to sunlight Unhygienic practices in milk and meat production INCUBATION PERIOD Highly variable,usually 1-3 weeks,but may last for 6 months or more. 7
  • 8. Transmission 8 ROUTES OF TRANSMISSION • Oral : unpasteurised milk & products, raw milk or meat • Respiratory: lab workers. • Skin: accidental penetration or abrasion – - at risk farmers & veterinarians. • Other routes: Conjunctival, Blood transfusion, Transplacental, person to person.
  • 9. 9
  • 10. 10
  • 11. PATTERN OF DISEASE • It may vary from an acute febrile disease to a chronic low grade disease. • The acute phase is characterized by: pyrexia(up to 40-41deg c) rigors and sweating arthritis/arthralgia involving larger joints. low back pain headache insomnia spleenomegaly and hepatomegaly leucopenia If patient is treated with tetracycline,the symptoms may disappear quickly ,but infection ,being intracellular,may persist giving rise to subacute or relapsing disease. 11
  • 12. 12
  • 13. CONTROL OF BRUCELLOSIS• IN THE ANIMALS The most rational approach for preventing human brucellosis is control and eradication of the infection from animal reservoirs which is based on combination of the following measures: (a)TEST AND SLAUGHTER: case finding done by mass survey. Skin test are available. The complement fixation test is recommended. Those animals infected with brucellosis are slaughtered with full compensation paid to farmers. This is the only satisfactory solution aimed at eradication of the disease. (b)VACCINATION: vaccine of B.abortus strain 19 is commonly used for young animals. a compulsory vaccination programme is given on yearly basis to reduce rate of infection. Systemic vaccination of period of 7-10 years may result in elimination of the disease (c) HYGIENIC MEASURES: these comprise provision of clean sanitary envoirnment for animals sanitary disposal of urine and faeces and health eduction of all those who are occupationaly involved 13
  • 14. • IN THE HUMANS (a) EARLY DIAGNOSIS AND TREATMENT: in uncomplicated case the antibiotic of choice is tetracycline . For adults in the acute stage ,the dose is 500g every 6 hours for 3 weeks. In patients with skeletal or other complication , intramuscular streptomycin 1g daily in addition to tetracycline usually achieves a cure. (b) PASTEURIZATION OF MILK (c) PROTECTIVE MEASURES-prevent direct contact with infected animals. persons at risk should observe high standards of personal hygiene. They should wear protective clothing when handling carcasses. Exposed areas of skin should be washed and soiled clothing renewed 14
  • 15. (d)VACCINATION : human live vaccine of B.abortus strain 19-BA is available. BRUCELLOSIS WOULD DISAPPEAR IF IT WERE ERADICATED FROM ANIMALS. The national and international centre for brucellosis is located at FAO/WHO Brucella reference centre, Indian veterinary research institute ,Izatnagar,(Uttar Pradesh).15
  • 16. HUMAN SALMONELLOSIS • The term ‘salmonellosis’ covers a complex group of food borne infections affecting both man and animals. The disease causes illness and even death in humans as well as economic losses in the animal and food industries. The term ‘food poisoning’ is commonly applied to salmonellosis.
  • 17. PROBLEM STATEMENT • Salmonellosis is a global problem. Human salmonellosis represents 60 to 80% of all reported cases of food borne diseases. • While the incidence of typhoid fever has declined, the incidence of other salmonella infections has increased in the developed countries. The problem is aggrevated by the widespread use of animal feeds containing antimicrobial drugs that favour drug-resistant salmonellae and their potential transmission to humans.
  • 18. EPIDEMIOLOGICAL DETERMINANTS AGENT FACTORS AGENT:- Salmonellae comprises a large and important group of bacteria. This group is now known to comprise more than 2,500 serotypes capable of infecting humans. Compared with other gram-negative rods, salmonellae are relatively resistant to various environmental factors. They have been shown to be resistant to drying, salting, smoking and freezing even for years.
  • 19. Cont.. • As a result, salmonellae have been isolated from divergent foods such as chocolates, biscuits, coconuts and spices. The bacterium is sensitive to heat and will survive temperatures above 70 degree centigrade.
  • 20. Cont.. • From an epidemiological point of view, salmonellae can be classified into three main groups:- (i) Those which infect only man- e.g S. typhi, S. paratyphi A and C. (ii) Those are host- S. cholera-suis , S. Dublin. (iii) Those infect both man and animals- S. typhimurium, S. Enteriditis. 20
  • 21. Cont.. RESERVOIR AND SOURCE OF INFECTION:- (a) FOODS Foods of animal origin, particularly commercially prepared foods such as meat, poultry and egg products are considered to be primary sources of salmonellosis. (b) ANIMALS Animals are the hosts and the principal vectors of zoonotic salmonellosis. E.g cattle, swine, rodents etc. (c) ENVIRONMENT Salmonellae are widely distributed in the environment in dust, water, manure, sewage, sludge, vegetables, insects, birds, fish, rodents and other mammals.
  • 22. MODE OF TRANSMISSION • By ingestion of contaminated food and drink, direct contact with domestic animals especially such as dogs, pigeons, rats, mice and insects. Once man is infected, he becomes a source and the infection may spread to others by the faecal-oral route. • INCUBATION PERIOD:- 6 to 72 hours (usually).
  • 23. 23
  • 24. CLINICAL FEATURES • Clinically, the disease may be manifest by one of the three syndromes: (i) ENTERIC FEVER:- the term ‘enteric fever’ includes both typhoid and paratyphoid fevers. The disease may occur sporadically, epidemically or endemically. (ii) SALMONELLA ENTEROCOLITIS (gastroenteritis) : This is the most common manifestation of Salmonellae infection. 6 to 48 hours of ingestion of Salmonellae there is nausea, headache, vomiting and diarrhoea. Low grade fever is common. Most infections are mild with diarrhoea, in severe cases there may be dehydration.
  • 25. Cont.. (iii) SEPTICAEMIA WITH FOCAL LESION:- Non- typhoid salmonellae may occasionally invade the blood stream leading to generalized or localized infection presenting itself as pyrexia of unknown origin. Focal infection may result in osteomyelitis, pyelonephritis, arthritis, meningitis, cholecystitis and endocarditis.
  • 26. PREVENTON AND CONTROL • Since salmonellosis is zoonotic in origin, preventive measures should begin at the farm and embrace all the elements of the food chain through live animals, animal products, processing, final food preparation to consumption. Approaches indicated at the farm level are : (i) Disease control e.g immunization of farm animals against salmonellosis. (ii) The use of hygienic animal feed. (iii) Ensuring a sanitary environment for the animals
  • 27. LEPTOSPIROSIS Leptospirosis is essentially animal infection by several serotype of liptospira & transmitted to man under certain environmental condition. The disease manifestations are many & varied, ranging severity from a mild febrile illness to severe & sometime fatal disease with liver & kidney involvement. • Leptospirosis is considered to be most widespread of the disease transmissible from animals to man • It has high prevalence in warm humid tropical countries. Out break mostly occur as a result of heavy rain fall. • The global burden of disease in unknown approx 500,000 cases of leptospirosis are estimated to occur worldwide every year
  • 28. EPIDEMOLOGICAL DETERMINATION Agent factor (a) Agent: leptospira are thin & light motile spirochetes 0.1-0.2 µm wide & 5-15µm long & hooked ends. This organisms are visible by dark- field illumination & silver staining. (b) Source of infection: leptospira are excreted in the urine of infections animal for a long time often for an enter life time in case of rodents. (c)Animal reservoirs: leptospirosis effects wild & domestic animal worldwide especially rodents such as rat ,mice etc. most domestic animal including cattle ship , goat, water buffallo, pigs & horse may be infected through pet animal particularly dogs may also be infected.
  • 29. Host factors (a)Age: children acquire the infection from dogs more frequently then do adults. Human infection is only accidental. (b)occupation: human infections are usually due to occupational exposure to the urine of infected animals e.g.- Agriculture,livestocks farmers, workers in rice fields ,sugarcane fields etc. (c)Immunity: A solid serovar specific immunity follows infection.
  • 30. Environmental factors • Leptospirosis infection is unique in that it is acquired through contact with an environment contaminated by urine and faeces from carrier animal or other infected animals. • Leptospira shed in the urine can survive for wks in soil and water, so environmental contamination may reach high levels in areas where carrier animals frequently urinate. • The association of poor housing, limited water supply, inadequate method of water disposal, all combine to make the disease a significant risk for the poor population in both urban and rural areas.
  • 31. Mode of transmission (a)Direct contact: leptospira can enter the body through skin abrasions or through intact mucous membrane by direct contact with urine or tissue of infected animal. (b)Indirect contact :through the contact of the broken skin with soil, water or vegetation contamination by urine of infected animals or through ingestion of food or water contaminated with leptospirosis.
  • 32. (c) Droplet infection: infection may also occur through inhalation as when milking infected cows or goats by breathing air polluted with droplets of urine. Direct man to man infection is rare. • Incubation period: Usually 10 days with a range of 4 to 20 days
  • 33. Diagnosis • It is not possible to diagnose leptospirosis with certainty on clinical grounds alone. Because of the wide spectrum of sign & symptoms, thee diagnosis is made by isolation of leptospires from blood during the acute illness and from urine after the 1 wks. • Early in the disease the organisms may be identified by dark fields examination of the patient’s blood or by culture on a semisolid medium.
  • 34. • The organism may also be grown from the urine from 10th day to 6 wks. • Diagnosis is usually made by means of serological tests , of which several are available. • Agglutination tests & become positive after 7- 8 days of illness and peaks at 3-4 wks & may persist at high level for many yrs. • indirect haemagglutination , immunoflourescent antibody and ELISA tests also available .
  • 35. Control (a) antibiotics: penicillin is the drugs of choice by other antibiotics(tetracycline & doxycycline) are also effective (b) Environmental measures: this includes preventing exposure to potentially contaminated water, reducing contamination by rodent control and protection of workers in hazardous occupation. Measures should be taken to control rodents, proper disposal of wastes & health education etc.
  • 36. vaccination • Immunization of farmers & pets prevent disease. In some countries for instance Italy, USSR & China, where certain occupations carry a high risk of infections, vaccines are available. • It is important that they should incorporate stains of the serotypes that predominant in the particular area since immunity to one type of leptospira may not protect against infection by another.
  • 37. PLAGUE • Plague is primarily and basically a zoonoses, caused by Y. pestis, involving rodents and fleas. It exists in natural foci, and is transmitted by infected flea bites to human living or intruding into the same ecological environment. Plague occurs in many forms- enzootically, epizootically, sporadically and in epidemics of all types including anthroponotic and primary pneumonic forms. 37
  • 38. PROBLEM STATEMENT • WORLD Plague is often seen as problem of the past or an ancient disease that is unlikely to reappear. But continued outbreaks throughout the world attest to its tenacious presence. Although plague is predominantly a rural disease, there have been outbreaks among urban population in Madagascar and the United Republic of Tanzania. 38
  • 39. Cont.. • The data shows that from 2004 to 2009, a total of 12,503 cases of human plague, including 843 deaths, were reported by 16 countries in Africa, Asia and America. The global case-fatality rate was 6.7%. • In 2004, India reported a localized outbreak of bubonic plague (8 cases and 3 deaths) in the Dangud village, District of Uttarkashi. 39
  • 40. EPIDEMIOLOGICAL DETERMINANTS (a) AGENT : The causative agent, Y. pestis is a Gram-negative, non-motile, cocco-bacillus that exhibits bipolar staining with special stains ( Wayson’s stain). The bacilli occur in great abundance in the buboes, blood, spleen, liver and other viscera of infected persons, and in the sputum in cases of pneumonic plague. 40
  • 41. Cont.. (b) RESERVOIR OF INFECTIION : Wild rodents are the natural reservoirs of plague. These are found in mountains, deserts, cultivated areas and forests in temperate and tropical regions. (c) SOURCE OF INFECTION : Infected rodents and fleas and case of pneumonic plague. 41
  • 42. Cont.. HOST FACTORS (a) AGE AND SEX : All ages and both sexes are susceptible. (b) HUMAN ACTIVITIES : Man may come into contact with natural foci in the course of hunting, grazing, cultivation. (c) MOVEMENT OF PEOPLE : Plague is associated with movement of people and cargo by sea or land. Rats and fleas are transported in this way. (d) IMMUNITY : Man has no natural immunity. Immunity after recovery is relative. 42
  • 43. ENVIRONMENTAL FACTORS (a) SEASON : Plague season starts from September until May. The disease tends to die out with the onset of hot weather. (b) TEMPERATURE AND HUMIDITY : A mean temperature of 20 to 25 degree C and a relative humidity of 60% and above are considered favourable for the spread of plague. (c) RAINFALL : Heavy rainfall, especially in the flat fields tend to flood the rat burrows. 43
  • 44. VECTORS OF PLAGUE • The commonest and the most efficient vector of plague is the rat flea, X. cheopis, but other fleas may also transmit the infection, e.g X. astia , X. brasiliensis and Pulex irritants (human flea). Both sexes of the flea bite and transmit the disease. 44
  • 45. BLOCKED FLEA • A flea ingest upto 0.5 cu.mm of blood which may contain as many as 5,000 plague bacilli. The bacilli multiply enormously in the gut of the rat flea and may block the proventriculus so that no food can pass through. Such a flea is called a ‘blocked flea’. 45
  • 46. FLEA INDICES (a) TOTAL FLEA INDEX : the average number of fleas of all species per rat. (b) CHEOPIS INDEX : the average number of X. cheopis per rat. (c) SPECIFIC PERCENTAGE OF FLEAS : the percentage of different species of fleas that are found on rats. (d) BURROW INDEX : the average number of free- living fleas per species per rodent burrow. 46
  • 47. HUMAN PLAGUE MODE OF TRANSMISSION : There are atleast 5 basic types of transmission cycles in plague. 1. Commensal rat rat fleas man. 2. Wild rodentswild rodent fleas or direct contactman. 3. Wild rodents, predomestic rodents, commensal rodentswild rodent fleas, predomestic rodent fleas, commensal rodent fleas man. 4. Manhuman fleasman. 5. Manman. 47
  • 48. DISEASE IN MAN (a) Bubonic plague : most common type of the disease. The infected rat fleas usually bite on the lower extremities and inoculate the bacilli. The bacilli are intercepted by the regional lymphatic glands where they prolifetare. Incubation period-2 to 7 days. (b) Pneumonic plague : Primary pneumonic plague is rare. Pneumonic plague is highly infectious and spreads from man to man by droplet infection. Incubation period – 2 to 7 days. (c) Septicaemic plague : Primary septicaemic plague is rare except for accidental laboratory infections. Incubation period- 1 to 3 days. 48
  • 49. LABORATORY INVESTIGATIONS (a) Staining : it is important to prepare smears of the clinical materials (e.g. bubo fluid, sputum) (b) Culture : blood for culture should be collected from all patients. (c) Serology : acute and convalescent specimens of blood sera should be collected for antibody studies. (d) Other methods : these include inoculation of guinea pigs or mice or immunofluorescent microscopic test. 49
  • 50. PREVENTION AND CONTROL 1) Control of cases (a) Early diagnosis- it is essential that plague-suspected humans and rodents be examined bacteriologically to confirm the presence of plague. (b) Notification- If a human or rodent case is diagnosed, health authorities must be notified promptly. (c) Isolation- all patients with pneumonic plague should be isolated. (d) Treatment- must be started without waiting for confirmation of the diagnosis. 50
  • 51. Cont.. 2) Control of fleas The most effective method to break the chain of transmission (rodentfleaman) is the destruction of rat fleas by the proper application of an effective insecticide. 3) Control of rodents Continuous mass destruction of rodents is an important plague-preventive measure. 51
  • 53. Cont.. 5) Chemoprophylaxis Chemoprophylaxis is a valuable preventive measure, highly recommended. It should be offered to all plague contacts, medical, nursing, and public health personnel exposed to the risk of infection. The drug of choice is tetracycline. For adults, the dose is 500 mg 6 hourly for 5 days. 53