CBPP
CBPP
Mycoplasmal diseases
( Mycoplasmosis )
Definition
• Mycoplasmosis can be defined as a disease caused by Mycoplasma sp, a
genus of bacteria that lack a cell wall around their cell membranes.
• The main diseases caused by Mycoplasma spp. in animals are listed below:
• Respiratory tract - Contagious bovine pleuro-pneumonia, Contagious
caprine pleuro-pneumonia.
• Joints - Mycoplasmal arthritis.
• Genital tract - Vulvo-vaginitis, endometritis, salpingitis.
• Udder - Contagious agalactia, mastitis.
• Eyes - Pink eye.
Etiology
• CBPP is caused by Mycoplasma mycoides subsp. mycoides (bovine biotype ).
• Mycoplsmas are microorganisms deprived of cell walls and are, therefore, (a)
pleomorphic and (b) resistant to antibiotics of the B-lactamine group, such as penicillin.
• This organism has two types of colonies . small colony type (SC type ) and large colony
type ( LC type ).
• M. m. m. large colony type is pathogenic for sheep and goats but not for cattle.
Etiology
• M. m m. (SC type ) survives well only in vivo and is quickly inactivated when
• This organism does not survive in meat and meat products and does not
survive outside the host in nature for more than a few hours to days.
organisms.
Epidemiology
CBPP is worldwide distributed disease but it has been eradicated from South Africa in 1916, from USA in
It is endemic in most of Africa and it a problem in parts of Asia, especially India and China. Periodically, it
occurs in Europe and outbreaks within the last decade have occurred in Spain, Portugal and Italy.
CBPP is predominantly a disease of the genus Bos, and exotic ( Bos taurus ), zebu ( Bos indicus ) and
rarely water buffalo (Bubalus bubalis ) are susceptible but wild bovids and camels are resistant.
There are many reported breed differences with respect to susceptibility. European breeds tend to be
There does seem to be some age resistance, animals less than 3 years are less resistant.
Morbidity is about 90% and mortality varied and ranges from 10 to 70% in
various outbreaks.
Mortality may depend on other factors such as plane of nutrition, level of
parasitism and general body condition.
Source of infection
Inhalation of droplets.
Convert the animal into an active case.
Transmission
Aerial mostly by direct contact droplets emitted by coughing animals, saliva and urine.
Transplacental infection can occur and inapparent carriers are a major source of infection.
Recovered animals harboring infectious organisms within a pulmonary sequestrum may become active
shedders when stressed. Transmission up to several km has been suspected under favourable climatic
condition.
Clinical findings
The incubation period is variable in natural infection but generally quite long. It has been shown that
healthy animals placed in CBPP-infected herd may begin showing signs of disease 20 to 123 days later.
Experimental infections the incubation period is 2 to 3 weeks.
Sudden onset of moderate fever ( 105 °F ), depressed and inappetent animal with fever.
Coughing followed by evidence of thoracic pain and dyspnoeic, animals are inclined to stand with
elbows abducted in an attempt to decrease thoracic pain and increase chest capacity.
Auscultation of the lung reveals any of a wide variety of sounds, depending upon the pulmonary
parenchyma.
In calves, pneumonia may be accompanied by a polyarthritis. Large joints may be distended and warm
on palpation.
Chronic form is characterized by ill-thrift and recurrent low-grade fever, may be difficult to recognize
pneumonia. Forced exercise may precipitate coughing.
Pathogenesis
• Bovine pleuropneumonia is an acute lobar pneumonia and pleurisy developing by localization of the
• Thrombosis in the pulmonary vessel in an essential part of pathogenesis which develops prior to pneumonic
lesions. The mechanism of thrombosis development is not understood .Death results from anoxia and
Pathogenesis
• Bovine pleuropneumonia is an acute lobar pneumonia and pleurisy developing by localization of the
• Thrombosis in the pulmonary vessel in an essential part of pathogenesis which develops prior to pneumonic
lesions. The mechanism of thrombosis development is not understood .Death results from anoxia and
Necropsy changes
Diagnosis
• Field diagnosis of CBPP can be made on history of contact with infected animals, epidemiologic
features, clinical signs and necropsy examination.
During an outbreak of natural disease, only 33% of animals present symptoms (peracute to acute form
), 46% are infected but have no symptoms ( subclinical forms ) and 21% seem to be resistant.
In adults:
Moderate fever with respiratory, pulmonary and pleuretic symptoms: polypnoea, characteristic attitude
(elbows turned Out, arched back, head extended), cough (at first dry, slight or fitful, becoming moist).
When the animal gets up or after exercise, breathing becomes laboured and grunting can be heared. At
percussion, dull sounds can be noticed in the low areas of the thorax.
In calves:
Pulmonary tropism is not the general rule, and infected calves present arthritis with swelling of the
joints.
Co-existence of pulmonary symptoms in adults and arthritis in young animal should alert the clinician to
a diagnosis of СВРР.
• Significant amount of yellow or turbid exudate in the pleural cavity ( up to 30 liters ) that coagulates to
form large fibrinous clots. Fibrinous pleurisy – thickening and inflammation of the pleura with fibrous
deposits.
• Interlobular edema, marbled appearance due to hepatization and consolidation at different stages of
evolution usually Confined to one lung. Sequestral with fibrous capsule surrounding grey necrotic tissue
in recovered animals.
Laboratory diagnosis
Samples – Live animals, nasal swabs, transtracheal washings or pleural fluid obtained by thoracic puncture.
Dead animals – Affected lung lesions, swabs of major bronchi, tracheo-bronchial or mediastinal lymph nodes
and joint fluids from arthritis cases.
Placed in transport medium ( heart infusion broth, 20% serum, 10% yeast extract, benzyl penicillin at 250 to
1000 iu /ml. Samples should be kept in cool and shipped on wet ice as soon as possible. Blood should be
collected for sera.
Isolation and identification of the causative agents by metabolic and growth inhibition tests and by ELISA.
Serology – Sub-acute and chronic forms can be diagnosed by Complement fixation tes ,Hemagglutination and
Agglutination test.
Treatment
Small colony type organisms are susceptible to streptomycin, oxytetracycline and chloramphenicol antibiotics.
Oxytetracycline @ 2-5 mg/kg body weight IM daily for 5 days may be used.
Rolitetracycline @ 10 mg/kg body weight daily for 5 to 7 days IM or IV found 95.36% effective.
Tylosin tartrate @ 10 mg/kg body weight at 12 hourly for 6 IM injections is highly effective.
1. Sanitary prophylaxis
In disease free-areas : Quarantine, serological test (CFT) and slaughter of all animals of the herd in which
positive animals have been found.
Control of cattle movements is the most efficient way of limiting the spread of CBPP.
2. Medical prophylaxis
In infected areas: a modified live vaccine is available for use in enzootic areas.
It generates an unpredictable local reaction – so given in the tail tip, which may become necrotic and
slough.
Immunity last for 12 months. Sometimes it is given in combination with Rinderpest.
Serological testing of importation is a recommended safeguard.
A model Prescription
1. Client’s Information:
a) Client’s name: Md Abdul Haque