Coxiella burnetii and Borrelia spp. in peripheral blood of dromedary camels in Fars, Iran: molecular characterization, hematological parameters, and acute-phase protein alterations.

Background: Dromedary camels (Camelus dromedarius) are raised in extremely strict ecological conditions of deserts. Camels are vulnerable to many zoonotic infections. There are limited data on the occurrence of Q fever and borreliosis in camels, in Iran. Aims: The current study was focused on the occurrence of Coxiella burnetii and Borrelia spp. infection in the blood samples of Iranian camels using molecular assays. Effect of the presence of these infections on various hematological factors and some acute-phase proteins (Hp, a1AGP, SAA) were also investigated. Methods: Blood samples were collected from 113 clinically healthy camels to investigate the presence of the infections using nested PCR. Moreover, the sequence of positive samples was analyzed phylogenetically. Routine haematological tests were performed and the concentrations of acute-phase proteins were measured in serum using enzyme immunoassay. Results: PCR result showed that 6.19% (95% CI: 2.53-12.35%) (7/113) of camels were positive for C. burnetii. In addition, sequencing results of the corresponding gene of the outer membrane protein (com1) revealed two different genotypes of C. burnetii agent in camels from Southern Iran. In the PCR assay, Borrelia spp. DNA was not detected in the samples. No significant difference was observed in hematological parameters or acute-phase proteins between positive and negative Q fever camels except for mean corpuscular hemoglobin (MCH) and red cell distribution width (RDW). Conclusion: Clinically healthy camels might be very important reservoirs of zoonotic pathogens. Q fever is not considered a notifiable disease in camels of Iran, and clinical cases may scarcely be recognized by the healthcare system. Due to a lack of adequate information, additional studies on the molecular epidemiology and clinical pathology aspects of C. burnetii infection in Iran are needed.

Dynamic and Sex-Specific Changes in Gonadotropin-Releasing Hormone Neuron Activity and Excitability in a Mouse Model of Temporal Lobe Epilepsy.

Reproductive endocrine disorders are prominent comorbidities of temporal lobe epilepsy (TLE) in both men and women. The neural mechanisms underlying these comorbidities remain unclear, but hypothalamic gonadotropin-releasing hormone (GnRH) neurons may be involved. Here, we report the first direct demonstrations of aberrant GnRH neuron function in an animal model of epilepsy. Recordings of GnRH neuron firing and excitability were made in acute mouse brain slices prepared two months after intrahippocampal injection of kainate (KA) or control saline, a well-established TLE model in which most females develop comorbid estrous cycle disruption. GnRH neurons from control females showed elevated firing and excitability on estrus compared with diestrus. By contrast, cells from KA-injected females that developed prolonged, disrupted estrous cycles (KA-long) showed the reverse pattern. Firing rates of cells from KA-injected females that maintained regular cycles (KA-regular) were not different from controls on diestrus, but were reduced on estrus. In KA-injected males, only GnRH neurons in the medial septum displayed elevated firing. In contrast to the diestrus versus estrus and sex-specific changes in firing, GnRH neuron intrinsic excitability was elevated in all KA-injected groups, indicating a role for afferent synaptic and neuromodulatory inputs in shaping overall changes in firing activity. Furthermore, KA-injected females showed cycle-stage-specific changes in circulating sex steroids on diestrus and estrus that also differed between KA-long and KA-regular groups. Together, these findings reveal that the effects of epilepsy on the neural control of reproduction are dynamic across the estrous cycle, distinct in association with comorbid estrous cycle disruption severity, and sex-specific.

Detection of faecal Cryptosporidium parvum antigen in diarrheic Holstein dairy cows.

Over a one-year period, based on a random cluster sampling design, 661 faecal samples from natural cases of diarrheic calves were taken in Fars province of Iran. The samples were taken from the 267 diarrheic calves of high and 394 diarrheic calves of average producing Holstein dairy cows. Faecal samples were collected directly from the rectum. Herd selection was based on geographical location and density of cattle in the region. Samples were collected based on 5 percent of herd population in 4 geographical regions: North, West, East and South of Fars province. The herds were stratified into small, medium and large size. Laboratory investigation consisted of a direct identification test for antigen of Cryptosporidium parvum. All herds had HPDC and APDC Cryptosporidium-infected diarrheic calves in their population. Diarrheic Cryptosporidium infected HPDC calves in southern region of Fars province were at much lower risk (P<0.05) than APDC calves. The rate of Cryptosporidium infection in diarrheic APDC calves in southern region of Fars province was highest when compared to other geographical locations. When considering the effect of age, diarrheic Cryptosporidium affected APDC Holstein calves of younger dams (>2 to 3years) showed a higher rate of infection when compared to diarrheic HPDC Cryptosporidium infected ones. There were no differences among the occurrence of Cryptosporidium infection in diarrheic HPDC and APDC calves of different herd size groups.

Detection of faecal Cryptosporidium parvum antigen in diarrheic Holstein dairy cows

Over a one-year period, based on a random cluster sampling design, 661 faecal samples from natural cases of diarrheic calves were taken in Fars province of Iran. The samples were taken from the 267 diarrheic calves of high and 394 diarrheic calves of average producing Holstein dairy cows. Faecal samples were collected directly from the rectum. Herd selection was based on geographical location and density of cattle in the region. Samples were collected based on 5 percent of herd population in 4 geographical regions: North, West, East and South of Fars province. The herds were stratified into small, medium and large size. Laboratory investigation consisted of a direct identification test for antigen of Cryptosporidium parvum. All herds had HPDC and APDC Cryptosporidium-infected diarrheic calves in their population. Diarrheic Cryptosporidium infected HPDC calves in southern region of Fars province were at much lower risk (P2 to 3years) showed a higher rate of infection when compared to diarrheic HPDC Cryptosporidium infected ones. There were no differences among the occurrence of Cryptosporidium infection in diarrheic HPDC and APDC calves of different herd size groups.

Pulmonary myxoma in a sheep.

Pulmonary myxomas are rare in domestic animals and only two cases have been reported previously in sheep. An 8 x 6 x 4 cm mass was detected in the diaphragmatic lobe of the right lung of a 4-year-old Persian Karakul ewe. The mass was well demarcated, multilobulated, soft in consistency and white in colour. The cut surface exuded a mucoid substance and a distinct capsule was evident. Microscopically, the tumour comprised a hypocellular myxomatous matrix, rich in acid mucopolysaccharides, with scattered spindle-shaped or stellate cells. These cells had uniform, oval-shaped nuclei without visible nucleoli and expressed vimentin and S100 on immunohistochemical examination. These gross, microscopical and immunohistochemical features are characteristics of myxoma.