Difference between revisions of "Feline Infectious Anaemia"
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==Aetiology== | ==Aetiology== | ||
Mhf is one of a group of organisms known as haemotropic mycoplasmas which infect several other domestic animal species. The causative organism was previously called Haemobartonella felis and thus the disease was known as haemobartonellosis. Polymerase chain reaction (PCR) assays allowing DNA analysis resulted in the reclassification of the organism in 2001<sup>1</sup>. Two other haemotropic mycoplasmas (''Candidatus M. haemominutum'' and ''Candidatus M. turicensis'') have been identified in cats but appear to be less pathogenic<sup>2</sup>. | Mhf is one of a group of organisms known as haemotropic mycoplasmas which infect several other domestic animal species. The causative organism was previously called Haemobartonella felis and thus the disease was known as haemobartonellosis. Polymerase chain reaction (PCR) assays allowing DNA analysis resulted in the reclassification of the organism in 2001<sup>1</sup>. Two other haemotropic mycoplasmas (''Candidatus M. haemominutum'' and ''Candidatus M. turicensis'') have been identified in cats but appear to be less pathogenic<sup>2</sup>. | ||
| + | |||
Mhf can vary in shape from cocci to rods and are sometimes present in chains on the cell surface. | Mhf can vary in shape from cocci to rods and are sometimes present in chains on the cell surface. | ||
| − | The mode of transmission of Mhf is poorly understood. It is thought that it may be transmitted through biting and fighting activities, although this has not been able to be demonstrated experimentally. | + | |
| + | The mode of transmission of Mhf is poorly understood. It is thought that it may be transmitted through biting and fighting activities, although this has not been able to be demonstrated experimentally. As transmission has been shown to occur through blood transfusion, it is recommended that blood donors been screened<sup>3</sup>. | ||
==Signalment== | ==Signalment== | ||
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==Differential diagnosis== | ==Differential diagnosis== | ||
| − | There are multiple causes of both regenerative and non-regenerative anaemia in cats which must be considered as differential diagnoses. | + | There are multiple causes of both regenerative and non-regenerative anaemia in cats which must be considered as differential diagnoses when investigating anaemia in cats. |
| + | |||
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| + | For cats showing signs of regeneration, causes of blood loss or haemolysis must be considered: | ||
| + | *primary immune-mediated haemolytic anaemia | ||
| + | *Heinz body haemolytic anaemia (onions, garlic,propofol) | ||
| + | *other infectious causes such as "Babesia felis" and "Cytauxzoon felis" | ||
| + | *neoplasia | ||
| + | |||
| − | + | Major differential diagnoses for cats with non-regenerative anaemia include: | |
| − | * | + | *neoplasia |
| − | * | + | *chronic inflammatory conditions |
| − | * | + | *underlying conditions such as diabetes mellitus and renal disease |
| + | *Feline Immunodeficiency Virus (FIV) and FeLV infections | ||
| + | *bone marrow diseases | ||
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The most commmon findings from complete blood counts from cats with Mhf infections are a marcocytic, hypochromic regenerative anaemia. Reticulocytes and Howell-Jolly bodies may be identified on cytologic examination. | The most commmon findings from complete blood counts from cats with Mhf infections are a marcocytic, hypochromic regenerative anaemia. Reticulocytes and Howell-Jolly bodies may be identified on cytologic examination. | ||
| + | |||
Mhf infection can be definitvely diagnosed by identification of organisms on a blood smear, appearing as cocci or rods and sometimes forming short chains of organisms. However, examination of a single blood smear is less than 50% sensitive <sup>5</sup> as the animal's immune response causes organisms to disappear from the blood stream for several days, often to reappear a few days later. It was found in one study that smears should be examined every four days over a minimum of three four day cycles<sup>5</sup>. As there could be eight days between presentation and diagnosis this is clearly not an ideal means of diagnosis. It also has the potential for misidentification. | Mhf infection can be definitvely diagnosed by identification of organisms on a blood smear, appearing as cocci or rods and sometimes forming short chains of organisms. However, examination of a single blood smear is less than 50% sensitive <sup>5</sup> as the animal's immune response causes organisms to disappear from the blood stream for several days, often to reappear a few days later. It was found in one study that smears should be examined every four days over a minimum of three four day cycles<sup>5</sup>. As there could be eight days between presentation and diagnosis this is clearly not an ideal means of diagnosis. It also has the potential for misidentification. | ||
| + | |||
| + | |||
| + | The gold standard for diagnosis of Mhf infection is polymerase chain reaction (PCR), which detects the 16S RNA gene. The test is widely available through veterinary diagnostic laboratories. | ||
==Treatment== | ==Treatment== | ||
Revision as of 21:41, 1 April 2012
Previously known as: Haemobartonellosis
Caused by: Mycoplasma haemofelis , previously known as Haemobartonella felis
Introduction
Feline Infectious Anaemia, caused by Mycoplasma haemofelis (Mhf), is a regenerative anaemia of cats. The disease occurs worldwide and should be considered as a differential diagnosis for any cat presenting with anaemia.
Aetiology
Mhf is one of a group of organisms known as haemotropic mycoplasmas which infect several other domestic animal species. The causative organism was previously called Haemobartonella felis and thus the disease was known as haemobartonellosis. Polymerase chain reaction (PCR) assays allowing DNA analysis resulted in the reclassification of the organism in 20011. Two other haemotropic mycoplasmas (Candidatus M. haemominutum and Candidatus M. turicensis) have been identified in cats but appear to be less pathogenic2.
Mhf can vary in shape from cocci to rods and are sometimes present in chains on the cell surface.
The mode of transmission of Mhf is poorly understood. It is thought that it may be transmitted through biting and fighting activities, although this has not been able to be demonstrated experimentally. As transmission has been shown to occur through blood transfusion, it is recommended that blood donors been screened3.
Signalment
The major group at risk for Mhf infection are young male cats who spend time outdoors. In many areas of the world an association has been shown between Mhf and retroviral infections2. It has been demonstrated that cats infected with Mhf and feline leukaemia virus (FeLV) are likely to develop more severe anaemia that cats infected only with Mhf3.
Pathogenesis
The pathogenesis of Mhf is not fully understood. It is thought that the presence of the parasite on the surface of the red blood cells may induce antibody production4. The anaemia, which is primarily extravascular, may be due to direct damage of erythrocytes by the organism or as a result of the antibodies produced by the infected animal 2.
Clinical signs
Infected cats most commonly present for lethargy and decreased appetite. Physical examination findings are non-specific and can include signs of anaemia, such as mucous membrane pallor, tachypnoea and tachycardia, pyrexia and occasionally splenomagaly and jaundice. Pyrexia is frequently intermittent and spikes when parasite numbers are highest 3. The anaemia can be severe and rapidly fatal in some cases.
Differential diagnosis
There are multiple causes of both regenerative and non-regenerative anaemia in cats which must be considered as differential diagnoses when investigating anaemia in cats.
For cats showing signs of regeneration, causes of blood loss or haemolysis must be considered:
- primary immune-mediated haemolytic anaemia
- Heinz body haemolytic anaemia (onions, garlic,propofol)
- other infectious causes such as "Babesia felis" and "Cytauxzoon felis"
- neoplasia
Major differential diagnoses for cats with non-regenerative anaemia include:
- neoplasia
- chronic inflammatory conditions
- underlying conditions such as diabetes mellitus and renal disease
- Feline Immunodeficiency Virus (FIV) and FeLV infections
- bone marrow diseases
Diagnosis
The most commmon findings from complete blood counts from cats with Mhf infections are a marcocytic, hypochromic regenerative anaemia. Reticulocytes and Howell-Jolly bodies may be identified on cytologic examination.
Mhf infection can be definitvely diagnosed by identification of organisms on a blood smear, appearing as cocci or rods and sometimes forming short chains of organisms. However, examination of a single blood smear is less than 50% sensitive 5 as the animal's immune response causes organisms to disappear from the blood stream for several days, often to reappear a few days later. It was found in one study that smears should be examined every four days over a minimum of three four day cycles5. As there could be eight days between presentation and diagnosis this is clearly not an ideal means of diagnosis. It also has the potential for misidentification.
The gold standard for diagnosis of Mhf infection is polymerase chain reaction (PCR), which detects the 16S RNA gene. The test is widely available through veterinary diagnostic laboratories.
Treatment
Infected cats should be treated with doxycycline for 3 weeks twice daily. Enrofloxacin is also a good treatment choice especially in refractory cases when combined with doxycycline.
A blood transfusion may also be required in cases of severe anaemia.
As blood sucking endoparasites, such as Fleas, are thought to spread disease the animal should also receive flea treatment.
Prednisolone is also advised to treat the immune mediated mechanisms and to prevent further erythrophagocytosis.
Prognosis
Varied prognosis depending on the severity of the anaemia at presentation. If not treated 1/3 of affected animals will die. Antibiotics do not clear the infection so many cats become carriers of the organism however relapses are uncommon.
| Feline Infectious Anaemia Learning Resources | |
|---|---|
 Test your knowledge using flashcard type questions |
Small Animal Emergency and Critical Care Medicine Q&A 12 |
 Search for recent publications via CAB Abstract (CABI log in required) |
Mycoplasma haemofelis publications |
Full text articles available from CAB Abstract (CABI log in required) |
Diagnosis and management of Hemoplasma infections. Lappin, M. R.; The North American Veterinary Conference, Gainesville, USA, Small animal and exotics. Proceedings of the North American Veterinary Conference, Orlando, Florida, USA, 17-21 January, 2009, 2009, pp 655-656, 23 ref. |
References
- Niemark H, Johansson KE, Rikihisa Y, et al (2001) Proposal to transfer some members of the genera Haemobartonella and Eperythrozoon to the genus Mycoplasma with descriptions of Candidatus Mycoplasma haemofelis, Candidatus Mycoplasma haemomuris, Candidatus Mycoplasma haemosuis and Candidatus Mycoplasma wenyonii Int J Sys Evol Microbiol 51(3) pp891-9
- Sykes, JE (2010) Feline Hemotropic Mycoplasmas Vet Clinics of North America: Small Animal Practice pp. 1157-1170
- Wardrop J, Reine N, Birkenheuer A et al (2005) Canine and feline blood donor screening for infectious disease J Vet Intern Med 19(1) pp.135-42
- Hagiwara, MK (2009) Anemia in Cats: Is It Mycoplasma? Proceedings of the 34th World Small Animal Veterinary Congress
- Ettinger, S.J, Feldman, E.C. (2005) Textbook of Veterinary Internal Medicine (6th edition, volume 2)W.B. Saunders Company
- Czerski A, Gnus J, Agnieszka Rusiecka A, et al (2009) Usefulness of blood films for the feline infectious anaemia diagnosis Acta Sci. Pol., Medicina Veterinaria 9(4)pp. 21-28
Merck & Co (2008) The Merck Veterinary Manual (Eighth Edition) Merial
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