A possible case of caprine-associated malignant catarrhal fever in a domestic water buffalo (Bubalus bubalis)in Switzerland
© Dettwiler et al; licensee BioMed Central Ltd. 2011
Received: 11 August 2011
Accepted: 2 December 2011
Published: 2 December 2011
Malignant catarrhal fever (MCF) is a fatal herpesvirus infection, affecting various wild and domestic ruminants all over the world. Water buffaloes were reported to be particularly susceptible for the ovine herpesvirus-2 (OvHV-2) causing the sheep-associated form of MCF (SA-MCF). This report describes the first case of possibly caprine-associated malignant catarrhal fever symptoms in a domestic water buffalo in Switzerland.
The buffalo cow presented with persistent fever, dyspnoea, nasal bleeding and haematuria. Despite symptomatic therapy, the buffalo died and was submitted to post mortem examination. Major findings were an abomasal ulceration, a mild haemorrhagic cystitis and multifocal haemorrhages on the epicardium and on serosal and mucosal surfaces. Eyes and oral cavity were not affected. Histopathology revealed a mild to moderate lymphohistiocytic vasculitis limited to the brain and the urinary bladder. Although these findings are typical for MCF, OvHV-2 DNA was not detected in peripheral blood lymphocytes or in paraffin-embedded brain, using an OvHV-2 specific real time PCR. With the aid of a panherpesvirus PCR, a caprine herpesvirus-2 (CpHV-2) sequence could be amplified from both samples.
To our knowledge, this is the first report of malignant catarrhal fever in the subfamily Bovinae, where the presence of CpHV-2 could be demonstrated. The etiological context has yet to be evaluated.
Malignant catarrhal fever (MCF) is a frequently fatal viral infection, affecting various wild and domestic ruminants and even, as recently reported, pigs . The disease is thought to be caused by herpesviruses of the subfamily gammaherpesvirinae, which cluster within the genus Macavirus . Typical signs of MCF include fever, nasal and ocular discharge, corneal opacity along with erosive lesions on the muzzle, within the oral cavity as well as in the lower gastrointestinal tract, the latter associated with melena and haematuria. Histologically, a lymphohistiocytic vasculitis, sometimes accompanied by fibrinoid necrosis, is present in various organs in most cases . Affected animals normally die, with survivors remaining chronically infected, often displaying persistent eye lesions and arteriopathy . Emaciation and dermal lesions occurring in deer infected with these herpesviruses can also be considered a chronic form of MCF [5–7].
At least six members of the Macaviruses are associated with clinical MCF . The first identified MCF virus was the alcelaphine herpesvirus-1 (AlHV-1) , which persists as a subclinical infection in wildebeest (Connochaetes sp.) and is the causative agent of wildebeest-associated MCF (WA-MCF) or African MCF in susceptible ruminants . The ovine herpesvirus-2 (OvHV-2) is endemic in domestic sheep (Ovis aries) worldwide and causes sheep-associated MCF (SA-MCF), reported in domestic cattle [3, 4, 11], bison (Bison bison) , water buffalos (Bubalus bubalis) [11, 13, 14], various deer species [15–17] and swine (Sus scrofa domesticus) .
Li and colleagues found a new endemic and asymptomatic gammaherpesvirus in domestic goats (Capra hircus), named caprine herpesvirus-2 (CpHV-2) . This virus can cause clinical MCF in several deer species such sika deer (Cervus nippon) [5, 6, 17], roe deer (Capreolus capreolus), moose (Alces alces)  and white-tailed deer (Odocoileus virginianus) [7, 19].
A further gammaherpesvirus with an as yet unknown host reservoir was recovered from white-tailed deer diagnosed with MCF and was named malignant catarrhal fever virus of white-tailed deer (MCFV-WTD) [19, 20].
Alcelaphine herpesvirus-2 (AlHV-2) causes subclinical infection in topi (Damaliscus korrigum)  and hartebeest (Alcelaphus buselaphus) . An AlHV-2-like virus was found as the causative agent of MCF in Barbary red deer (Cervus elaphus barbarus) . In blood samples of healthy zoo or wildlife park ruminants, including Nubian ibex (Capra nubiana), gemsbok (Oryx gazella), muskox (Ovibos moschatus) and aoudad (Ammotragus lervia), several novel homologous gammaherpesvirus sequences have been detected [24, 25]. The viruses were named after their carrier species (MCFV-Ibex, MCFV-Oryx, MCFV-Muskox, MCFV-Aoudad). In 2007, MCFV-Ibex was found in a bongo antelope (Tragelaphus euryceros) with MCF . Furthermore, hippotragine herpesvirus-1 (HiHV-1) has been detected in asymptomatic roan antelopes (Hippotragus equinus) .
This case report describes the clinical, laboratory and postmortem findings of a domestic water buffalo (Bubalus bubalis) with MCF in Switzerland. Surprisingly, the buffalo was PCR-negative for OvHV-2, but was positive for caprine herpesviral DNA. To the authors' knowledge, this is the first reported case of malignant catarrhal fever in a member of the subfamily Bovinae where the presence of CpHV-2 could be demonstrated.
Anamnesis, clinical history and laboratory findings
In January 2011, a 10-year old female domestic water buffalo (Bubalus bubalis) was referred to the Department of Farm Animals, University of Zurich, Switzerland, with a two week history of fever and dyspnoea resistant to therapy with antibiotics, nonsteroidal anti-inflammatory drugs and β2-sympathomimetics. The animal originated from a subalpine farm in Eastern Switzerland that housed 17 adult and 6 juvenile water buffalos, 13 dairy cows, 6 juvenile cattle, 4 suckling calves, 30 ewes, 2 horses and 12 pigs. During the summer months, the buffalos were kept on pasture with intermittent contact to goats and sheep. Cattle and buffalos all tested negative for IBR-IPV (infectious bovine rhinotracheitis) and BVD-MDV (bovine virus diarrhoea/mucosal disease).
The buffalo cow had delivered a healthy calf in June 2010 and was now pregnant in the first trimester.
On arrival at the clinic the animal was in a good body condition. It showed nasal bleeding from the right nostril and a skin lesion on the left fore limb with prolonged bleeding. The rectal temperature was 38.6°C, the skin was cool and had a reduced turgor. Conjunctivae and sclerae were hyperaemic, capillary refill time was prolonged (> 2 sec). The animal was calm, but had an increased heart rate (104/min). Ruminal as well as intestinal motility were absent, food intake was reduced. The quantitatively diminished faeces contained a marked amount of digested blood (melena). Although the peripheral lymph nodes were inconspicuous, the right iliac lymph node was severely enlarged. Catheter urine was brownish to red and contained a maximal amount of haemoglobin/erythrocytes as well as glucose (Combur-Test®, Roche Diagnostics, Basel, Switzerland). In the glutaraldehyde test (Glutal-Test®; Dr. E. Graeub AG, Berne, Switzerland), the blood clotting time was longer than 10 minutes.
Blood parameters of the buffalo cow with MCF
Prothrombin time (PT)
Partial thromboplastin time (PTT)
Thrombin time (TT)
Routine serology for IBR-IPV antibody was negative. DNA was extracted from peripheral blood lymphocytes with the QIAamp DNA Mini Kit® (Qiagen, Hombrechtikon, Switzerland). The DNA was tested by real-time PCR specific for OvHV-2 essentially as described by Hüssy et al.  using the following primers and probe: forward 5'-GAGAACAAGCGCTCCCTACTGA-3', reverse 5'-CGTCAAGCATCTTCATCTCCAG-3', probe FAM-AGTGACTCAGACGATACAGCACGCGACA-TAMRA. No OvHV-2 specific DNA could be detected.
Prolonged clotting parameters, decreased fibrinogen and clotted thrombocytes were suggestive of disseminated intravascular coagulation (DIC) and, as underlying disease, an atypical postparturiant haemoglobinuria or malignant catarrhal fever due to a causative agent other than OvHV-2 was considered. The buffalo cow was treated symptomatically by oral and intravenous administration of electrolytes, glucose and vitamin C.
During the following 36 hours, the rectal temperature rose to 39.4°C. The animal was restless and collapsed several, times resulting in bleeding skin injuries. Nasal bleeding stopped intermittently. A few hours before it died, it became recumbent and shortly before exitus showed severe dyspnoea and acute bleeding arose from nose, vagina and anus.
The tonsils and head lymph nodes were strongly enlarged, red to violet and oedematous. Mediastinal and mesenterial lymph nodes were of normal size, but also dark red and oedematous.
Except for a focally extensive erosion in the pyloric region of the abomasum, no lesions were detectable on the muzzle, in the oral cavity, oesophagus or lower gastrointestinal tract. The eyes showed no macroscopical alterations.
Several organs showed signs of bleeding and thrombus formation. Petechial to ecchymotic haemorrhages were dispersed in the submucosa of the urinary bladder, in the epicardium and myocardium, in the cerebrum and in the lung alveoli. Microthrombi were evident in the kidney, in the abomasum adjacent to the mucosal erosion and in the alveolar capillaries of the lung. Multiple lung venules were obstructed by larger thrombi.
Tonsils and lymph nodes were hyperaemic, oedematous and moderately hyperplastic. A severe hemosiderosis was visible in the spleen despite advanced autolysis. In the bone marrow, activation of erythropoiesis and thrombocytopoiesis was evident.
Cryosections from skin, tongue and thyroid gland were examined with immunohistochemistry for BVD-MD antigen . The result was negative. An immunohistochemical examination of formalin-fixed, paraffin-embedded hippocampus and cerebellum for rabies antigen, using a polyclonal antibody, was negative as well.
No relevant bacteria could be cultured from blood.
The OvHV-2-specific real-time PCR was additionally carried out with DNA extracted from paraffin embedded carotid rete and cerebrum (QIAamp DNA Mini Kit, Qiagen), which was negative. We then performed a panherpesvirus PCR according to Ehlers et al. . The resulting amplicon was sequenced (Microsynth, Balgach, Switzerland) after gel extraction (QiaAmp gel extraction kit; Qiagen) and the sequence was analysed by a BLAST search. The sequence was identical to the corresponding portion of the CpHV-2 polymerase gene.
Buffalo farming is quite uncommon in Switzerland and information on local prevalence of buffalo diseases is sparse. Data from Switzerland concern mainly dairy cattle. To find information about prevalences of buffalo diseases, we can draw conclusions from countries, where buffalos are often kept, like India, Thailand, Indonesia etc., but have to consider that there are differences in housing and feeding, as well as in climate conditions.
The only European report describing an outbreak of sheep-associated MCF in water buffalos occurred in southern Italy . All affected animals were 10-12 months of age and suffered from the "head and eye" form of the disease, characterized by fever, keratoconjunctivitis, oculo-nasal discharge and erosive lesions in the oral cavity and in the laryngo-pharynx. All affected calves had neurological symptoms such as depression and ataxia. In Asian buffalos, however, eye symptoms seemed not to be that severe. Hoffman et al.  and Teankam et al.  noticed an inconsistent presence of corneal opacity, whereas mild to moderate conjunctivitis was a common symptom. In the present case, the eyes were macroscopically normal and a histologic examination was not performed. As has been described in cattle with SA-MCF [3, 4, 11], an ulcerative stomatitis and abomasitis, a diphteric tracheitis and/or pharyngitis and a lung oedema can also be found in affected buffalo [13, 31]. Further common gross pathological findings in buffalo are petechial or ecchymotic haemorrhage on mucosal and serosal surfaces, pericardial and epicardial haemorrhages, serofibrinous epicarditis and myocarditis and oedematous lymph nodes [13, 31]. In the present case, ulceration of the alimentary tract was limited to the abomasal mucosa. Cardial alterations were characterized by a marked hydropericardium and epicardial haemorrhages, most likely due to vascular injury. Other reported findings such as epicarditis, pharyngitis, tracheitis and a lung oedema were absent.
Histologically, the lymphohistiocytic vasculitis and perivascular cuffing was limited to the brain and meningeal vessels, the carotid rete and the urinary bladder wall. Nonpurulent interstitial nephritis and myocarditis, as seen in affected cattle and buffalos [13, 31], were not present. In accordance with Hoffman , but in contradiction to Teankam , fibrinoid necrosis of vessel walls was not evident in any organ examined. Petechial to ecchymotic haemorrhage was distributed multifocally in the myocardium, in the urinary bladder wall, in the white matter of the cerebrum and in the lung alveoli. Especially in the bladder and in the brain, the bleeding was closely associated with inflamed vessels, suggesting a severe vascular injury, whereas in the lung the alveolar haemorrhage can be considered a consequence of circulatory disturbances because of the thrombotic lung venules. This hypercoagulatory state as part of disseminated intravascular coagulation can be explained by the loss of plasma coagulation factors through injured vessel walls and is the most likely cause of death of the buffalo cow.
In summary, the gross and histopathological findings in the present case are consistent with previous descriptions of buffalos succumbing to MCF, albeit in a more discrete manner, although the clinical signs were rather atypical. Possibly, this is related to a different causative agent, as previous cases of MCF in buffalos were associated with OvHV-2, whereas in the present case, CpHV-2 was found in peripheral blood lymphocytes and in brain.
Several authors previously described caprine herpesvirus 2 as a cause of MCF, but exclusively in members of the cervid family. In sika deer, CpHV-2 was found in association with mural folliculitis , extensive alopecia, crusting dermatitis and weight loss [6, 17]. All of these sika deer had a marked lymphocytic meningoencephalitis and adventitial lymphocytic infiltration in several organs including affected skin, consistent with MCF. CpHV-2 associated MCF in white-tailed deer also manifested in weight loss, alopecia and histologically typical alterations . In free-ranging moose and roe deer, the most prominent clinical symptoms were abnormal behaviour, apathy and incoordination. Macroscopically inconspicuous roe deer displayed vascular and perivascular lymphohistiocytic infiltrates in the eye, in the brain and in multiple organs. A moderate erosive stomatitis and rhinitis respectively, was found in moose, together with lymphohistiocytic infiltrates in several organs, including fibrinoid necrosis in brain vessels .
In summary, cervids with CpHV-2 associated MCF presented with rather atypical clinical signs and rather mild to moderate pathological alterations. However, it should be considered, that in most cases these animals did not die a natural death, but were shot by a gamekeeper due to weakness, what might at least partly contribute to reduced severity of the pathological findings.
As in the case of the water buffalo presented here, CpHV-2 associated MCF elicits rather an atypical clinical and gross pathological manifestation in cervids, suggesting that the caprine herpesvirus 2 causes a more atypical form of MCF in other susceptible species.
Unfortunately, further testing on the premises for MCF viruses or MCF virus antibodies was not permitted by the owner. Therefore, it was impossible to unambiguously identify the source of the infection. Specifically, the question, whether or not CpHV-2 was also present in the unaffected buffaloes on the same premises, remained unanswered. However, clinical, pathological, histological, and virological evidence strongly suggests that CpHV-2 may have been the causative agent of the present case of MCF in a water buffalo. Further knowledge about the prevalence of CpHV-2 in other bovids is needed, raising the need to test MCF-affected cattle for CpHV-2, especially if they are negative for OvHV-2 and contact to goats cannot be excluded. A prevalence study on CpHV-2 among cervids and bovids in Switzerland is in preparation (personal communication, A. Stahel).
Consent was obtained from the owner of the animal for publication of this case report and any accompanying images.
Acknowledgements and Funding
We thank Dr. Maja Rütten, Institute of Veterinary Pathology, for her support in the interpretation of the histopathological slides and for her helpful diagnostic proposals. And our thanks go to Prof. Matthias Ackermann, Institute of Veterinary Virology, Zurich, Prof. Lloyd Vaughan and Prof. Franco Guscetti, Institute of Veterinary Pathology, Zurich, for critical reading of the manuscript.
The authors declared that they received no financial support for their research and/or authorship of this article.
- Albini S, Zimmermann W, Neff F, Ehlers B, Häni H, Li H, Hüssy D, Casura C, Engels M, Ackermann M: Porcine malignant catarrhal fever: diagnostic findings and first detection of the pathogenic agent in diseased swine in Switzerland (German). Schweiz Arch Tierheilkd. 2003, 145 (2): 61-68. 10.1024/0036-72184.108.40.206.PubMedView ArticleGoogle Scholar
- Davison AJ, Eberle R, Ehlers B, Haywerd GS, McGeoch DJ, Minson AC, Pellett PE, Roizman B, Studdert MJ, Thiry E: The order Herpesvirales. Arch Virol. 2009, 154: 171-177. 10.1007/s00705-008-0278-4.PubMed CentralPubMedView ArticleGoogle Scholar
- Barker IK, Van Dreumel AA, Palmer N: Malignant catarrhal fever. Pathology of domestic animals. 4th edition. Edited by: Jubb KVF, Kennedy PC and Palmer N. San Diego: Academic Press Inc, 2: 1993, 163-173.Google Scholar
- Müller-Doblies UU, Egli J, Li H, Braun U, Ackermann M: Epidemiology of malignant catarrhal fever in Switzerland (German). Schweiz Arch Tierheilkd. 2001, 143 (4): 173-187.PubMedGoogle Scholar
- Crawford TB, Li H, Rosenburg SR, Norhausen RW, Garner MM: Mural folliculitis and alopecia caused by infection with goat-associated malignant catarrhal fever virus in two sika deer. J Am Vet Med Assoc. 2002, 221 (6): 843-847. 10.2460/javma.2002.221.843.PubMedView ArticleGoogle Scholar
- Keel MK, Patterson JG, Noon TH, Bradley GA, Collins JK: Caprine herpesvirus-2 in association with naturally occurring malignant catarrhal fever in captive sika deer (Cervus nippon). J Vet Diagn Invest. 2003, 15: 179-183. 10.1177/104063870301500215.PubMedView ArticleGoogle Scholar
- Li H, Wunschmann A, Keller J, Hall DG, Crawford TB: Caprine herpesvirus-2-associated malignant catarrhal fever in white-tailed deer (Odocoileus virginianus). J Vet Diagn Invest. 2003, 15: 46-49. 10.1177/104063870301500110.PubMedView ArticleGoogle Scholar
- Cunha CW, Otto L, Taus NS, Knowles DP, Li H: Development of a multiplex real-time PCR for detection and differentiation of malignant catarrhal fever viruses in clinical samples. J Clin Microbiol. 2009, 47: 2586-2589. 10.1128/JCM.00997-09.PubMed CentralPubMedView ArticleGoogle Scholar
- Plowright W, Ferris RD, Scott GR: Blue wildebeest and the aetiological agent of malignant catarrhal fever. Nature. 1960, 188: 1167-1169. 10.1038/1881167a0.PubMedView ArticleGoogle Scholar
- Plowright W: Malignant catarrhal fever virus. Virus infections of ruminants. Edited by: Dinter Z, Morein B. Amsterdam: Elsevier, 1990, 123-150.View ArticleGoogle Scholar
- Tham KM: Molecular and clinicopathological diagnosis of malignant catarrhal fever in cattle, deer and buffalo in New Zealand. Vet Rec. 1997, 141: 303-306. 10.1136/vr.141.12.303.PubMedView ArticleGoogle Scholar
- Schultheiss PC, Collins JK, Spraker TR, DeMartini JC: Epizootic malignant catarrhal fever in three bison herds: differences from cattle and association with ovine herpesvirus-2. J Vet Diagn Invest. 2000, 12: 497-502. 10.1177/104063870001200602.PubMedView ArticleGoogle Scholar
- Teankam K, Tantilertcharoen R, Boonserm T, Suadsong S, Banlunara W: Malignant catarrhal fever in swamp buffaloes (Bubalus bubalis): A retrospective pathological study of outbreaks in Thailand. Thai J Vet Med. 2006, 36 (1): 19-30.Google Scholar
- Martucciello A, Marianelli C, Capuano M, Astarita S, Alfano D, Galiero G: An outbreak of malignant catarrhal fever in mediterranean water buffalo (Bubalus bubalis) (Italian). Large Anim Rev. 2006, 12 (5): 21-24.Google Scholar
- Vikoren T, Li H, Lillehaug A, Monceyron Jonassen C, Bockermann I, Handeland K: Malignant Catarrhal Fever in free-ranging cervids associated with OvHV-2 and CpHV-2 DNA. J Wildlife Dis. 2006, 42 (4): 797-807.View ArticleGoogle Scholar
- Schultheiss PC, Van Campen H, Spraker TR, Bishop C, Wolfe L, Podell B: Malignant catarrhal fever associated with ovine herpesvirus-2 in free-ranging mule deer in Colorado. J Wildlife Dis. 2007, 43 (3): 533-537.View ArticleGoogle Scholar
- Foyle DL, Fuller HE, Higgins RJ, Russell GC, Willoughby K, Rosie WG, Stidworthy MF, Foster AP: Malignant catarrhal fever in sika deer (Cervus Nippon) in the UK. Vet Rec. 2009, 165: 445-447. 10.1136/vr.165.15.445.PubMedView ArticleGoogle Scholar
- Li H, Keller J, Knowles DP, Crawford TB: Recognition of another member of the malignant catarrhal fever virus group: an endemic gammaherpesvirus in domestic goats. J Gen Virol. 2001, 82: 227-232.PubMedView ArticleGoogle Scholar
- Kleiboeker SB, Miller MA, Schommer SK, Ramos-Vara JA, Boucher M, Turnquist SE: Detection and multigenic characterization of a herpesvirus associated with malignant catarrhal fever in white-tailed deer (Odocoileus virginianus) from Missouri. J Clin Microbiol. 2002, 40 (4): 1311-1318. 10.1128/JCM.40.4.1311-1318.2002.PubMed CentralPubMedView ArticleGoogle Scholar
- Li H, Dyer N, Keller J, Crawford TB: Newly recognized herpesvirus causing malignant catarrhal fever in white-tailed deer (Odocoileus virginianus). J Clin Microbiol. 2000, 38: 1313-1318.PubMed CentralPubMedGoogle Scholar
- Mushi EZ, Rossiter PB, Jessett D, Karstad L: Isolation and characterization of a herpesvirus from topi (Damaliscus korrigum, Ogilby). J Comp Pathol. 1981, 91: 63-68. 10.1016/0021-9975(81)90045-1.PubMedView ArticleGoogle Scholar
- Reid HW, Rowe L: The attenuation of a herpes virus (malignant catarrhal fever virus) isolated from hartebeest (Alcelaphus buselaphus cokei Gunther). Res Vet Sci. 1973, 15: 144-146.PubMedGoogle Scholar
- Klieforth R, Maalouf G, Stalis I, Terio K, Jamssem D, Schrenzel M: Malignant catarrhal fever-like disease in Barbary red deer (Cervus elaphus barbarus) naturally infected with a virus resembling alcelaphine herpesvirus 2. J Clin Microbiol. 2002, 40 (9): 3381-3390. 10.1128/JCM.40.9.3381-3390.2002.PubMed CentralPubMedView ArticleGoogle Scholar
- Li H, Gailbreath K, Flach EJ, Taus NS, Cooley J, Keller J, Russell GC, Knowles DP, Haig DM, Oaks JL, Traul DL, Crawford TB: A novel subgroup of rhadinoviruses in ruminants. J Gen Virol. 2005, 86: 3021-3026. 10.1099/vir.0.81238-0.PubMedView ArticleGoogle Scholar
- Li H, Gailbreath K, Bender LC, West K, Keller J, Crawford TB: Evidence of three new members of malignant catarrhal fever virus group in muskox (Ovibos moschatus), Nubian ibex (Capra nubiana), and gemsbok (Oryx gazella). J Wildlife Dis. 2003, 39 (4): 875-880.View ArticleGoogle Scholar
- Okeson DM, Garner MM, Taus NS, Li H, Coke RL: Ibex-associated malignant catarrhal fever in a bongo antelope (Tragelaphus euryceros). J Zoo Wildlife Med. 2007, 38 (3): 460-464. 10.1638/06-046.1.View ArticleGoogle Scholar
- Reid HW, Bridgen A: Recovery of a herpesvirus from a roan antelope (Hippotragus equinus). Vet Microbiol. 1991, 28 (3): 269-279. 10.1016/0378-1135(91)90081-P.PubMedView ArticleGoogle Scholar
- Hüssy D, Stäuber N, Leutenegger CM, Rieder S, Ackermann M: Quantitative fluorogenic PCR assay for measuring ovine herpesvirus 2 replication in sheep. Clin Diagn Lab Immunol. 2001, 8 (1): 123-128.PubMed CentralPubMedGoogle Scholar
- Thür B, Zlinszky K, Ehrensperger F: Immunohistochemical detection of bovine viral diarrhea virus in skin biopsies: A reliable and fast diagnostic tool. J Vet Med Series B. 1996, 43: 163-166.View ArticleGoogle Scholar
- Ehlers B, Borchers K, Grund C, Frölich K, Ludwig H, Buhk HJ: Detection of new DNA polymerase genes of known and potentially novel herpesviruses by PCR with degenerate and deoxyinosine-substituted primers. Virus Genes. 1999, 18 (3): 211-220. 10.1023/A:1008064118057.PubMedView ArticleGoogle Scholar
- Hoffman D, Soeripto S, Sobironingsih S, Campbell RSF, Clarke BC: The clinico-pathology of a malignant catarrhal fever syndrome in the Indonesian swamp buffalo (Bubalus bubalis). Aust Vet J. 1984, 61: 108-112. 10.1111/j.1751-0813.1984.tb07201.x.View ArticleGoogle Scholar
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