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Anaplasma phagocytophilum is a Gram-negative obligate intracellular bacterium that replicates in neutrophil granulocytes. It is transmitted by ticks and causes tick-borne fever in domestic ruminants such as sheep, cattle and goats. However, in contrast to sheep and cattle little is known about the clinical course of infection in goats. We report here on three cases of symptomatic infection with A. phagocytophilum in two goats (Capra aegagrus hircus) and one water buffalo (Bubalus bubalis). The animals showed symptoms and laboratory findings similar to sheep and cattle. To our knowledge, this is the first report on the symptomatic infection of water buffalos with A. phagocytophilum. The infecting strains were genetically characterized by 16S rRNA gene, ankA gene and multilocus sequence typing (MLST). Four other strains from asymptomatically infected goats were also included. The ankA sequences from five goats were part of the formerly described ankA gene clusters I and IV that are known to contain A. phagocytophilum strains from sheep and cattle. However, the sequences from one goat and from the water buffalo belonged to ankA gene cluster II that was formerly described to be restricted to roe deer. A similar observation was made for MLST as three goats clustered with sequences from sheep and cattle, whereas three other goats and the water buffalo were found to be part of the roe deer cluster. However, since most of the strains from sheep and cattle were distinct from the roe deer strains, roe deer might not represent major reservoir hosts for tick-borne fever in domestic ruminants. When differing parts of the 16S rRNA gene were used for typing the results were conflicting. This shows that the use of a standardized typing method such as MLST is highly desirable to generate easily comparable results.

The metastrongyloid nematode Aelurostrongylus abstrusus is a worldwide occurring feline lungworm. The spectrum of clinical signs in infected cats ranges from mild (e.g. nasal discharge or cough) to severe respiratory distress. The aim of this seroepidemiological study was to define prevalence and risk factors for A. abstrusus infections in Swiss cats, to assess the biogeographic distribution and to investigate the influence of temperature and altitude on the occurrence of this parasite. Sera of 4067 domestic cats were collected from all over Switzerland, tested for the presence of antibodies against A. abstrusus by a novel ELISA and the results correlated with biogeographic aspects. A subsample of 1000 datasets was used for risk factor analyses. Overall, 10.7% (434/4067, 95% confidence intervals [CI]: 9.7-11.7%) of the cats were tested positive, with variations from 0.0% to 20.0% among ten different biogeographic regions. Differences were significant between the Western (13.9%, CI: 11.4-16.7%) and the Eastern (9.2%, CI: 8.0-10.5%) Swiss Plateau, possibly attributable to the suitability of the areas for intermediate hosts. In total 90.3% (392/434) of the seropositive cats originated from regions lower than 700 m above sea level. Correspondingly, 98.9% (429/434) of positive samples were obtained from regions with a mean temperature higher than -2 °C in January, suggesting altitude and temperature being limiting factors for A. abstrusus infections in Switzerland. Concerning individual risk factors, prevalence was higher in intact (15.5%, CI: 9.5-23.4%) than in neutered cats (5.8%, CI: 7.9-10.4%). Young adult cats (aged 11-22 months) were significantly more often seropositive (10/76, 13.2%, CI: 6.5-22.9%) than kittens aged 1-10 months (1/34, 2.9%, CI: 0.1-15.3%) or adult and senior cats > 22 months (58/889, 6.5%, CI: 5-8.4%). Outdoor cats and cats presenting respiratory signs tend to be more often positive than indoor cats (p = 0.077) and animals without respiratory signs (p = 0.086), respectively. We here confirm that the use of a serological test can contribute to improve the identification of infected animals, through evaluation of risk factors on a population level and for a better management on an individual level, overcoming the challenges represented by faecal examinations and the correlated underestimation of the occurrence of A. abstrusus in cats.

In 2011 and 2012, outbreaks of clinical canine babesiosis were observed in 2 areas of the Swiss Midlands that had no history of this disease so far. In one area, cases of canine babesiosis occurred over 2 consecutive tick seasons. The outbreaks involved 29 dogs, 4 of which died. All dogs were infected with large Babesia sp. as diagnosed in Giemsa-stained blood smears and/or PCR. These were identified as B. canis (formerly known as B. canis canis) by subsequent partial sequencing of the 18S rRNA gene of Babesia sp. Interestingly, the sequence indicated either a genotype with heterogeneity in the ssrRNA gene copies or double infection with different B. canis isolates. None of the dogs had a recent travel history, but one had frequently travelled to Hungary and had suffered twice from clinical babesiosis 18 and 24 months prior to the outbreak in autumn 2011. Retrospective sequencing of a stored blood DNA sample of this dog revealed B. canis, with an identical sequence to the Babesia involved in the outbreaks.For the first time in Switzerland, the partial 18S rRNA gene of B. canis could be amplified from DNA isolated from 19 out of 23 adult Dermacentor reticulatus ticks flagged in the same area. The sequence was identical to that found in the dogs. Furthermore, one affected dog carried a female D. reticulatus tick harbouring B. canis DNA. Our findings illustrate that, under favourable biogeographic and climatic conditions, the life-cycle of B. canis can relatively rapidly establish itself in previously non-endemic areas. Canine babesiosis should therefore always be a differential diagnosis when dogs with typical clinical signs are presented, regardless of known endemic areas., NM and CFF are both supported by the Swiss National Science Foundation (grants nos. PBBEP3_139398 and PBBEP3_141435, respectively).