The black-eared opossum (Didelphis aurita) is a South American synanthropic marsupial. The presence of opossums in domestic spaces is relevant in the One-Health context since they are hosts of pathogens and ectoparasites that may affect the health of domestic animals and humans. In this study, we aim to determine the occurrence of hemoplasmas and selected tick-borne pathogens in free-ranging black-eared opossums, along with their molecular characterization, hematological and biochemical evaluation and factors associated with infection, in the municipality of Viçosa, State of Minas Gerais, southeastern Brazil. Thirty black-eared opossums were trapped between March 2021 and June 2022. Ectoparasites were collected. Hematological and biochemical analyses were performed. DNA from EDTA-blood samples were analyzed by PCR and qPCR assays. By molecular analyses, ‘Candidatus Mycoplasma haemoalbiventris’ was the most prevalent hemoparasite (73.3%), followed by Hepatozoon sp. (22.2%). Significant differences were observed in the number of platelets, and in the concentration of protein and globulins in the animals infected by ‘Ca. M. haemoalbiventris’ when compared with the negative group. This is the first report of ‘Ca. M. haemoalbiventris’ infection in D. aurita.

Hemotropic mycoplasmas (hemoplasmas) are small pleomorphic bacteria that parasitize the surface of red blood cells of mammals. Hemoplasmas have been described in different species from the Camelidae Family, such as llamas and alpacas (South American camelids), but data on dromedary camels (Camelus dromedarius) are limited to a few reports. Somalia has one of the world’s largest dromedary camel populations, and studies on hemoplasmas and tick-borne pathogens are lacking. Accordingly, this study aimed to screen dromedaries from Somalia for hemoplasmas by PCR-based assays. A total of 155 dromedary camel blood samples from 2 different areas of Mogadishu (n = 104) and the Lower Shabelle Region (n = 51) of the country were collected. All blood DNA samples were screened for hemoplasmas using a SYBR Green Universal Real-Time PCR (qPCR), nested PCR (nPCR), and conventional PCR (cPCR) assays targeting the 16S rRNA gene of hemoplasmas. Five out of 155 animals (3.23%; 95% confidence interval [CI]: 1.39–7.33%) were positive for hemoplasmas. A total of 346 (228 M, 117 F, and 1 nymph) ticks were collected from 79/155 (50.9%; 95% CI: 42.8–59.1%) dromedary camels with a mean of 4.4 ticks per animal. Ticks were identified as Rhipicephalus pulchellus (174/346; 50.3%), Hyalomma dromedarii (103/346; 29.8%), Hyalomma rufipes (35/346; 10.1%), Hyalomma marginatum (16/346; 4.6%), Rhipicephalus humeralis (14/346; 4.0%), Amblyomma lepidum (2/346; 0.6%), Amblyomma gemma (1/346; 0.3%), and Ornithodoros sp. (1/185; 0.5). This is the first study on the molecular screening for hemoplasmas in dromedary camels from Somalia and the first report of A. lepidum and R. humeralis in Somali dromedary camels.

In Veterinary Education, non-harmful alternatives methods have been explored in order to replace the use of animals as a teaching resource. The objective of this study was to analyze the students' opinion regarding the use of a low cost model for training ovariaosalpingohisterectomy in small animals before in vivo performance. There were 21 veterinary medicine students from a Veterinary Surgical Teaching class enrolled in the study. They underwent training in the model before performing the surgery on the animal and then answered a questionnaire regarding the use of the model, including team organization, emotional safety and technique training. Among the students, 95.2% considered that the training improved the flow of tasks, 85.7% felt safer in performing the surgery on the live animal after training with the model and 76.2% considered that the training resulted in an improvement in the surgical ability to perform the surgery. There was also a 23.2% decrease (32 minutes) in surgical time in the live animal, compared to the previous year's group without training in the model. The use of the model had positive results, because besides being well accepted by the students, it brought greater confidence and technical skill during the surgery, reducing the time of the procedure.

The present study aimed to investigate the occurrence of Leishmania spp., hemotropic Mycoplasma spp., tick-borne pathogens (TBP), and co-infection in dogs with clinical signs suggestive of visceral leishmaniasis (VL). It also aimed to determine the factors associated with infection and to map the distribution of co-infected dogs in an endemic area in the Northeast region of Brazil. Blood samples from 168 dogs were evaluated for serological analysis to Leishmania spp., Anaplasma spp., Ehrlichia spp., Babesia spp., and molecular assays to Leishmania spp., Anaplasma platys, Ehrlichia canis, Babesia spp., and hemotropic Mycoplasma spp. In serological and molecular analysis, 29.8% and 5.9% of dogs were co-infected. In the regression analysis, seropositivity for Ehrlichia spp., Babesia spp., and Leishmania spp. was significantly associated with the presence of petechiae, young dogs, and weight loss. Serology revealed that co-exposure with Babesia spp. and Ehrlichia spp. was associated with fever and thrombocytopenia, and there was an association between seropositivity for Ehrlichia spp. and Babesia spp. in dogs seropositive for Leishmania spp. The presence of hemotropic Mycoplasma spp. DNA was associated with anorexia. Thus, dogs with clinical VL have co-infection with other pathogens, reinforcing the importance of this study for a better understanding of these co-infections in dogs from endemic areas.

Ehrlichioses, caused by Ehrlichia species, are tick-borne diseases (TBDs) that affect animals and humans worldwide. This study aimed to investigate the molecular occurrence of Ehrlichia spp. in 530 animals (155 Dromedary camels, 199 goats, 131 cattle, and 45 sheep) in the Benadir and Lower Shabelle regions of Somalia. Blood DNA samples were tested for PCR targeting dsb and sodB genes of Ehrlichia spp. and PCS20 and map1 genes of E. ruminantium. The obtained sequences were submitted for phylogenetic analyses. Ehrlichia spp. were detected in 26.4% (140/530) of animals by dsb-PCR, with the highest prevalence in dromedary camels (54.8%), followed by cattle (29.8%), goats (7.0%), and sheep (4.4%). Dromedary camels, cattle, and goats had significantly higher infection odds compared to sheep (p < 0.05). Among dsb-PCR-positive samples, 76.9% (30/39) of cattle tested sodB-positive, while other species were negative. E. ruminantium was detected in 13.7% (18/131) of cattle by pCS20-PCR, but none were positive for the map1 gene. Phylogenetic analysis confirmed E. minasensis in camels, sheep, and goats and E. ruminantium in cattle, marking the first molecular evidence of E. minasensis in dromedary camels, sheep, and goats globally, and E. ruminantium in cattle from Somalia. These findings emphasize the need for further research on its economic and public health impact.