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Contagious bovine pleuropneumonia (CBPP)
Synonym(s): CBPP
Introduction
- Cause: contagious bovine pleuropneumonia (CBPP) is caused by a bacterium called Mycoplasma mycoides subsp. mycoides Small Colony (MmmSCSC).
- Signs:
- CBPP is characterized by nonspecific signs of fever, loss of appetite, depression and a drop in milk production, followed by respiratory signs, which may include coughing, purulent or mucoid nasal discharges, and rapid respiration.
- Pregnant animals may abort the fetus or give birth to stillborn calves Abortion and stillbirths: overview.
- Severely affected cattle often die, typically within three weeks.
- In calves up to six months of age respiratory signs of CBPP are less common and the primary sign is polyarthritis, especially of the carpal and tarsal joints, and resultant edema. Pain in the affected joint results in the animal being reluctant to move.
- Diagnosis:
- Isolation and identification of MmmSC from clinical samples.
- Polymerase Chain Reaction (PCR) based assays are commonly used for confirmation of the identity of the bacteria.
- Less commonly older biochemical and serologic methods are used (growth inhibition, immunofluorescence, dot immunobinding on a membrane filter [MF-dot] test, agar gel immunodiffusion).
- Post-mortem investigation Post-mortem on-farm will reveal abnormalities within the chest cavity, including; gross pathologic lesions of the lung (often affecting only one lung), the accumulation of a large volume of yellow fluid (often containing large fibrinous clots) and enlarged lymph nodes.
- Treatment:
- Antibiotics of the tetracycline Oxytetracycline, macrolide Erythromycin and fluoroquinolone families can be effective in treatment; however in some cases the bacteria is not completely eliminated and subclinically infected carriers can develop.
- Prognosis:
- The mortality rate of CBPP rate ranges from 10% to 80%, although mortality greater than 50% is rare unless in naïve herds.
- Animals that recover are frequently weak and emaciated, and may remain chronically infected.
- Euthanasia Euthanasia: techniques, on welfare grounds, should be considered for some cases.
- CBPP is a notifiable disease Notifiable diseases in the UK.
Geographic incidence
- CBPP is widespread throughout the whole of sub-Saharan Africa; with outbreaks reported in Ethiopia, Angola, Namibia, Tanzania, Zambia, DRC and Kenya.
- Outbreaks have also been reported in Asia (India, Bangladesh and Myanmar) and the Middle East, probably derived from importation of infected cattle from Africa.
- The USA has been free from CBPP since 1892.
- The UK has been free of CBPP since 1898.
- The disease was introduced to South Africa in 1853 and eliminated by 1924.
- Australia has been free from CBPP since the 1970s.
- China has been free from CBPP since the 1980s.
- CBPP was eliminated from Europe in the nineteenth century, but there were outbreaks in Portugal (1951), Spain (1957), France (1984), Italy (1990) and Portugal (1999).
Age predisposition
- The more severe respiratory forms of CBPP are observed in adult animals, whilst the polyarthritic forms are more commonly observed in calves under 6 months of age.
Breed/Species predisposition
- Cattle (Bos Taurus Bos Taurus), Zebu (Bos indicus) and Asian buffalo (Bubalus bubalis) are the primary hosts for MmmSC under natural conditions. To a lesser degree yak (Bos grunniens) are also a host species and one single case has been reported in American buffaloes (Bison bison).
Public health considerations
- There is no evidence that humans are infected by MmmSC.
Cost considerations
- CBPP is one of the most important infectious diseases of cattle in Africa. Naïve herds can experience losses of up to 80%.
- Animals that recover can be weak and emaciated and may remain chronically infected. This can result in underdeveloped adults and also recurrent infections within the herd.
- In the UK, affected herds may be liable to compulsory slaughter under the Animal Health Act 1981.
Pathogenesis
Etiology
- The causative agent of CBPP is the bacterium MmmSC.
- Studies have shown that the disease originated in Europe in the 1700s and was spread to other continents during colonization.
- Molecular epidemiology studies have shown that there are two distinct subtypes; those isolated from European outbreaks (post 1980) and those isolated from African outbreaks.
Predisposing factors
General
- Subclinical bovine carriers with chronic infection can retain viable bacteria within sequestra in the lungs for up to two years. These carriers are a major source of infection as they can shed viable bacteria when they become stressed or immunosuppressed.
- Outbreaks usually begin as the result of animal movements and contact of an infected animal with a naive herd.
Pathophysiology
- The disease causing mechanisms are not well elucidated. Two of the main factors in the disease formation of CBPP are the capsular polysaccharide, galactan and the membrane protein, L-alpha-glycerophosphate oxidase (GlpO).
- Galactan has cytopathic and vaso-active effects and results in pulmonary edema, capillary thrombosis and collagen deposition.
- The membrane protein L-alpha-glycerophosphate oxidase (GlpO) plays central role in cytotoxicity by catalyzing the oxidation of glycerol-3-phosphate, to release hydrogen peroxide (H2O2) which causes direct damage to cells and tissues and, in addition, triggers an inflammatory response.
Timecourse
- Under natural conditions the incubation period of the disease is usually 1–4 months, but can be longer.
Epidemiology
- The main form of transmission of MmmSC is through respiratory aerosols and close, repeated contact is generally required for infection. However, MmmSC might be spread over longer distances (up to 200 meters) under favorable climatic conditions.
- The organism also occurs in saliva, urine, fetal membranes and uterine discharges.
- Subclinical carriers with chronic infection can retain viable bacteria within sequestra (lesions) in the lungs for up to two years. These carriers are a major source of infection as they can shed viable bacteria when they become stressed or immunosuppressed.
Diagnosis
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Treatment
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Prevention
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Outcomes
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Further Reading
Publications
Refereed Papers
- Recent references from PubMed and VetMedResource.
- Di Teodoro G, Marruchella G, Di Provvido A et al (2020) Contagious bovine pleuropneumonia: A comprehensive overview. Vet Pathol 57 (4), 476-489 PubMed.
- Kairu-Wanyoike S W, Kiara H, Heffernan C et al (2014) Control of contagious bovine pleuropneumonia: Knowledge, attitudes, perceptions and practices in Narok district of Kenya. Prev Vet Med 115 (3-4), 143-156 PubMed.
- Dupuy V, Manso-Silván L, Barbe V, Thebault P, Dordet-Frisoni E et al (2012) Evolutionary history of contagious bovine pleuropneumonia using next generation sequencing of Mycoplasma mycoides Subsp. mycoides “Small Colony”. PLOS one 7 (10) PubMed.
- Pilo P, Frey J & Vilei E M (2007) Molecular mechanisms of pathogenicity of Mycoplasma mycoides subsp. mycoides SC. Vet J 174 (3-3), 513–521 PubMed.
- Huebschle O J, Ayling R D, Godinho K, Lukhele O, Tjipura-Zaire G, Rowan T G & Nicholas R A (2006) Danofloxacin (Advocin) reduces the spread of contagious bovine pleuropneumonia to healthy in-contact cattle. Res Vet Sci 81 (3), 304-309 PubMed.
Other sources of information
- Legislation.gov.uk (2020) Animal Health Act 1981. SCHEDULE 3 - Power to Slaughter in Relation to Certain Diseases - Cattle plague. Website: www.legislation.gov.uk
- United States Department of Agriculture (2017) Foreign Animal Disease Preparedness & Response Plan. Website: www.aphis.usda.gov (pdf download).
- EUR-Lex (2013) EU Directive 82/894. Council Directive on the notification of animal diseases within the community. Website: www.eur-lex.europa.eu.
- World Organisation for Animal Health (online) Contagious Bovine Pleuropneumonia. Website: www.woah.org.