Table 14.1.
Quick reference guide to infectious diseases
| Disease | Incubation period | Route of transmission | Clinical signs | Diagnostic tests | Treatment | Comments |
|---|---|---|---|---|---|---|
| Fleas | Life cycle takes 30–35 days for rabbit flea | Direct contact | Pruritus Hair loss Dermatitis |
Visualization of fleas. Flea combing | Imidacloprid, selamectin | Spilopsyllus cuniculi is the rabbit flea; however, most infestations are Ctenocephalides spp. |
| Lice | Life cycle takes 14–21 days | Direct contact | Visualization of lice or nits | Avermectins | Haemodipsus ventricosus may act as a vector for myxomatosis | |
| Mites Psoroptes cuniculi (Leporacarus, Cheyletiella, etc.) |
Life cycle 21 days, eggs hatch after 4 days | Direct contact | Intensely painful and pruritic otitis externa (skin flaking/hairloss) |
Clinical signs, visualization of mites in exudate/crust | Selamectin, ivermectin, moxidectin are suitable for all mite infestations |
May get aberrant infestations on other parts of the body |
| Warbles Cuterebra spp. |
28 days to 11 months | Not contagious | Masses around head and over back | Finding the warble within a mass | Mechanical removal of the warble; treat any concurrent infection | USA only, do not occur in UK |
| Passalurus ambiguus | 18 days | Faecal oral contamination | None in adults, possible contribution to enteritis complex of weanlings | Faecal flotation, zinc sulphate flotation | Often not required. Piperazine and fenbendazole are effective |
Ivermectin is not effective |
| Obeliscoides cuniculi | 16–22 days | Faecal oral contamination | Possibly none | Faecal flotation | May not be required; fenbendazole is effective | Can affect a variety of other species. Rare in the UK |
| Tapeworms Several species |
Rabbits often act as intermediate hosts | Oral intake of eggs from infected pasture | Cysts cause pain and signs related to area in the body in which they are found | Visualization of scolices from cyst fluid | There are tapeworms where rabbit is the primary host | |
| Coccidiosis | 7–8 days, complex life cycle | Faecal oral contamination | Diarrhoea, inappetence, weight loss, can be fatal | Faecal flotation, histopathology of gut wall | Eimeria stiedae causes hepatic coccidiosis, leading to jaundice, weight loss, ascites, diarrhoea, hepatomegaly | |
| Encephalitozoonosis | 30–70 days, variable, may be much longer | Oral intake of spores from infected urine | Vestibular signs, seizures, signs of renal disease. Rarely myocarditis | Serology, PCR of suitable tissue or urine, exclusion of differential diagnoses | Fenbendazole, albendazole, fluoroquinolones, lufenuron(?) |
Encephalitozoon cuniculi does not fulfill Koch’s postulates and it is uncertain whether it can cause disease in and of itself |
| Toxoplasmosis | 7–8 days | Ingestion of infected cat faeces | Sudden anorexia, pyrexia and death, possibly CNS signs | Serology Histopathology |
Not reported | The rabbit is not the final host; therefore it is not infectious to other rabbits. No cysts are found in rabbit faeces. Can infect humans eating undercooked rabbit meat |
| Pasteurellosis | 8–21 days | Direct contact and airborne spread. May be a commensal. Fomite spread possible | Many possible: rhinitis, pneumonia, abscesses, otitis media | Culture and sensitivity, serology | Antibiotics in accordance with sensitivities | Not all manifestations of these clinical signs are due to Pasteurella, so culture is mandatory |
| Bordetella bronchiseptica | 3–10 days | Direct contact, airborne spread | Suppurative bronchopneumonia, may be relatively non-pathogenic | Culture and sensitivity | Antibiotics in accordance with sensitivities | Can cause potentially serious disease in guinea pigs housed with rabbits |
| Tyzzer’s disease | 3–7 days | Faecal oral contamination, ingestion of spores from environment | Acute diarrhoea, sudden death, intestinal fibrosis | Serology | Reduce stress, increase dietary fibre, antibiosis and supportive care. Generally unrewarding | Usually weanling rabbits 6–12 weeks old |
| Salmonellosis | 6–24 hours | Intake of contaminated food or water | Diarrhoea, emaciation, death. May get asymptomatic carriers | Faecal culture | No successful treatment reported. Questionable whether anything other than supportive care should be employed | Rare |
| Colibacillosis | 12–24 hours | Intake of contaminated food or water, or infected faeces | Enteritis and death, particularly in colony situations | Faecal culture | Antibiosis and supportive care | With some strains mortality can be 25–75% |
| Clostridial enterotoxaemia | 12 hours or more after alterations in bacterial flora | Carbohydrate overload, inappropriate antibiotic treatment | Severe enteric disease | PCR for clostridial toxins on faeces | Supportive care, fluids, cholestyramine resin | Clostridia are present in small numbers in normal rabbit gut flora |
| Treponematosis | 3–6 weeks | Sexually transmitted, or from dam during birthing process | Crusty lesions around, eyes, mouth/nose and on genitalia | Serology, dark field microscopy on material from lesions, histopathology | Penicillin, × 3 doses at 5- to 7-day intervals | Can get clinically normal infected carriers |
| Listeriosis | 3–70 days reported in humans and animals reported to be similar | Intake of contaminated food | Abortion, sudden death | Culture, post-mortem examination and culture | Not reported | Rare, organism appears to have predilection for gravid uterus |
| Paratuberculosis | Variable, up to several years | Ingestion of contaminated food or water | Intermittent diarrhoea | Histopathology (post-mortem?) | Not reported | Incidence higher in wild rabbits geographically close to farms with a history of Johne's disease. |
| Pseudotuberculosis (yersiniosis) |
15 days or more | Oral intake of infected faeces from wildlife or vermin | Wasting, diarrhoea, dull coat, nodules palpable on the liver | Histopathology (post-mortem) | Not reported clinically. Vermin control required | |
| Tulareemia | 1–14 days | Vector (tick) borne | Pyrexia, lethargy | Post-mortem histopathology, serology (not commercially in UK) | Supportive care, antibiosis | Zoonotic |
| Lyme disease | Unknown in rabbits, 3–32 days in other species | Tick-borne | Causes polyarthritis in other species, knowledge of recent tick bite | Serology (not available commercially for rabbits) | Not reported | Serological surveys indicate higher prevalence in areas where rabbit-feeding tics are abundant |
| Myxomatosis | At least 5 days, but varies according to strain | Vector spread, although direct contact possible | Swellings around eyelids/face viraemia and death | Clinical signs | Supportive care, depending on strain is frequently fatal | Rabbits that have been vaccinated previously can get atypical myxomatosis, which presents as subcutanoues plaques/masses. This form is unlikely to be fatal |
| Viral haemorrhagic disease | 3–4 days | Direct contact, fomite spread possible | Severe necrotizing hepatitis, disseminated intravascular coagulation, death | Clinical signs, serology, histopathology | Almost universally fatal. Supportive care | |
| Shopes fibroma virus | 1–5 days | Vector spread (mosquitos) | Fibromatous swellings over body | Clinical signs, histopathology of masses | Swellings usually regress within 3 weeks, so supportive care only if required | Recovery from Shopes fibroma virus confers cross-immunity against myxomatosis |
| Shopes papilloma virus | 7 days | Arthropod vector | Malignant masses resembling squamous cell carcinomas in European rabbits, benign swellings in cotton tails | Histopathology | Supportive care, will likely fail | |
| Papillomatosis | 9–38 days experimentally, natural infection unknown | Direct contact | Small wart-like growths inside the mouth | Clinical signs, histopathology | As the rabbit ages, immunity occurs and the warts regress. Treatment only indicated if lesions are causing problems | Primarily young rabbits 6–9 months of age |
| Rabbit corona virus | 2–5 days for acute, 6–12 days for less acute signs | Pyrexia, pulmonary oedema, enteritis in weanling rabbits. FIP lie syndrome also reported | Histopathology, serology (not available in UK) | None reported, supportive care addresses clinical problems identified | May not be a naturally occurring pathogen. Unlikely to be seen in general practice | |
| Dermatophytosis | 1–2 weeks | Direct and fomite spread | Lesions at base of ears and around muzzle | Culture, fluorescence with Wood’s lamp | As for other species | May get asymptomatic carriers |
| Aspergillosis | Variable dependent on dose taken in | From environment or food | Pulmonary granulomas have been reported, rhinitis seen anecdotally | Culture, histopathology | Itraconazole, terbinafine | Reports rare in literature, likely more common clinically |