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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.

We amplified Ehrlichia and Anaplasma DNA from Amblyomma dubitatum tick-infested capybaras (Hydrochoerus hydrochaeris) in southern Brazil. Sequencing of 16S rRNA, sodB, and groEL indicated a novel Ehrlichia species, and sequencing of 16S rRNA from 2 capybaras indicated a novel Anaplasma species. The tick vectors remain unknown.

The purpose of this study was to carry out a descriptive investigation of the Azara's agouti (Dasyprocta azarae) eye and to establish reference values of select ophthalmic diagnostic tests and physiologic parameters. A total of 19 healthy agoutis were used. Select ophthalmic diagnostic tests were performed, including Schirmer tear test type I (STTI), analysis of the conjunctival bacterial microflora, corneal esthesiometry, and tonometry. B-mode ultrasonic biometry, fundus photography, optical coherence tomography, and gross and histologic analysis of two eyes were also performed. Reference range parameters found for the ocular diagnostic tests were esthesiometry, 4.50 ± 0.36 cm (0.7 ± 0.01 g/mm2); tonometry, 11.61 ± 0.44 mm Hg; palpebral fissure length, 1.70 ± 0.25 mm; STTI, 9.73 ± 0.47 mm/min; corneal thickness, 0.8 ± 0.003 mm; anterior chamber depth, 1.71 ± 0.07 mm; lens thickness, 5.03 ± 0.05 mm; vitreous chamber depth, 5.12 ± 0.01 mm; and globe axial length, 14.02 ± 0.01 mm. A paurangiotic, retinal, vascular pattern with a conspicuous pigment-laden optic disc was observed. The most frequent bacteria isolated were nonhemolytic Streptococcus sp. (36.84%), followed by Enterobacter harfinia (31.58%) and Escherichia coli (28.95%). No significant differences between genders or between left and right eyes were found for any of the results. Gross and histologic evaluation of two eyes confirmed the presence of melanocytic pigment granules between optic nerve fibers. The diagnostic values and the morphologic observations described here provide a reference to veterinarians to aid in the diagnosis of ocular disease.

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.