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Alpha smooth muscle actin (α-SMA) localization was investigated in the utero-vagina of the one-humped camel during the follicular and luteal phases. A total of 86 dromedary she-camels brought to the Maiduguri municipal abattoir for slaughter were used for this study. Blood was collected prior to slaughter, and the corresponding genitalia was also collected immediately after slaughter. The ovarian structures and serum progesterone levels were evaluated and used to categorize the animals into the follicular (FP) and luteal phases (LP). The utero-vaginal tissues were also subjected to immunohistochemistry for the localization of alpha smooth muscle actin. The serum P4 levels ranged from 0.6 to 2.5 ng/ml with means of 0.89 ± 0.16 and 1.61 ± 0.81 ng/ml for camels in the follicular and luteal phases, respectively. Immunohistochemistry result demonstrated the localization of α-SMA in the smooth muscle cells of the uterus and vagina during both reproductive phases. Alpha-SMA reactions were intense in the tunica muscularis and the smooth muscles of the blood vessels, with mild evidence of α-SMA localization within the epithelial linings of the vagina and uterine glands. There were no differences (p > 0.05) in the distribution of high positive, low positive, and negative percentages in both uterine and vaginal sections. However, there were differences (p

Contagious ecthyma (Orf) is a viral skin condition caused by a parapoxvirus. It results in cutaneous lesions that destroy the hides and skin of the infected host. In this study, the pathogenicity of Malaysian isolates of Orf virus (UPM 1/14 and UPM 2/14) was evaluated in a rat model using different inoculation sites with/without dexamethasone administration. A total of 50 rats were used in this study. For the first part of the study, 35 rats were divided into three groups; group 1 (n = 15) was inoculated with 0.5 mL of UPM 1/14 (tissue culture infective dose 50% (TCID50) 108.1/mL) while group 2 (n = 15) was inoculated with 0.5 mL of UPM 2/14 (TCID50 107.2/mL) each at the dorsum (n = 5), ear pinna (n = 5), and labial commissure (n = 5). Group 3 (n = 5) served as the control and was administered 0.5 mL of phosphate-buffered saline in all the sites mentioned above. In the second study, 15 rats were divided into three groups: a dexamethasone group (n = 5) which was given 10 mg/kg of dexamethasone once daily for 3 days, a non-dexamethasone group (n = 5), and a control (n = 5). Intradermal inoculation of 0.5 mL of UPM 1/14 was administered to each rat in the dexamethasone and non-dexamethasone groups at the dorsum, ear pinna, and labial commissure, respectively. Clinical signs and histopathological changes were evaluated for 14 days post inoculation for the first experiment and 7 days for the second experiment. Mild hyperemia was observed in the dorsum, ear pinna, and labial commissures of all inoculation groups. Group 1 (ORFV UPM 1/14) had a higher (P 0.05) in the mean thickness of the stratum basale of the ear pinna and labial commissure between the dexamethasone and non-dexamethasone groups. Orf virus was detected by PCR from the skin tissues of rats with lesions using F1L and B2L viral genes. In conclusion, Malaysian isolates of Orf virus were seen to be mildly pathogenic to rats. The difference in inoculation sites and the induction of immune suppression were observed to present varying pathological responses in rats.

Lead acetate (PbAC) toxicity can occur by either ingestion or inhalation from contaminated surfaces or from the environment. Nigella sativa is a natural product with immense pharmacological properties, which include antioxidant, antibacterial, and antianemia properties. It has been showed to counter the effect of PbAC-induced hematological and biochemical changes in short-term studies. This study hypothesized that the N. sativa (NS) administration will ameliorate the deleterious effects of chronic PbAC toxicity in rats. A total of 75 Sprague Dawley rats were divided into three groups of 25 rats, and each group was further sub-divided into five groups of five rats each. Group 1 rats (negative control) were given distilled water, group 2 (positive control; PC) were given 10 mg/kg of lead acetate (PbAC) daily, and groups 3 (T1), 4 (T2), and 5 (T3) were each given 10 mg/kg of PbAC followed by graded concentrations of powdered seeds of NS; 100, 150, and 200 mg/kg, respectively. Five rats in each group were euthanized at 30, 60, and 90 days for collection of whole blood and selected organs. Whole blood was collected after euthanized via cardio puncture and used to evaluate the complete blood profile, while plasma was used for biochemical analysis. Tissue samples of the liver and kidney were fixed with 10% buffered formalin, processed, and stained with H&E and periodic acid–Schiff (PAS) for the liver. Aggression and fear were increased in the PbAC-exposed group and absent in the T3 group. There was a lower (p

Orf is an infectious disease that affects the skin of sheep and goats resulting in lesions that reduce animal productivity. This study was aimed to determine the status of orf infection among small ruminants from selected farms in the state of the Selangor based on IgM antibody detection. Serum samples were collected from 90 goats and 90 sheep and subjected to qualitative enzyme-linked immunosorbent assay (ELISA) to measure IgM antibodies followed by chi-square analysis of the data. The result from this study showed that 33 goats (36.7%) and 7 sheep (7.8%) were positive for orf IgM antibodies, indicating higher seroprevalence among goats as compared to sheep. The risk factors such as species, breed, farm location, and history of orf, age, gender, presence of clinical signs, and farm location were shown to significantly affect the seropositivity of IgM antibodies in these species. In conclusion, this study showed that a significant number of goat populations in Selangor, Malaysia, harbor active orf infection in comparison to sheep.

Lead acetate (LA) is a toxic compound that has detrimental effects on the male reproductive system, such as decreased testicular size and function, low androgen hormone concentration, and altered testicular histology. While Nigella sativa (NS) has been shown to possess a handful of therapeutic benefits, few studies have shown its effect on damage caused by lead acetate toxicity in the male reproductive system. In this study, 75 Sprague-Dawley rats were divided into 3 groups of 25 rats, which were further subdivided into 5 subgroups each. Group 1 (negative control) was given distilled water, group 2 (positive control (PC)) administered 10 mg/kg of lead acetate (LA) orally/daily, while groups 3 (T1), 4 (T2), and 5 (T3) were given LA 10 mg/kg and graded concentrations (100, 150, and 200 mg/kg) each of NS. One group each, comprising of 25 rats, was euthanized at days 30, 60, and 90 for collection of blood plasma, epididymis, and organ tissues fixed in 10 % buffered formalin at each time interval. The right caudal epididymis was homogenized and used for the determination of spermiogram. Plasma was used for the determination of testosterone (TS), follicle stimulating hormone (FSH), and luteinizing hormone (LH) and estradiol (EST) using radioimmunoassay kits. There was reduced number of spermatogenic cells and epididymal sperm reserves in the PC group in comparison to the treatment groups. The level of TS was lower (p

Iridovirus is the causative agent of grouper iridovirus infection (GIV), which causes severe epizootics resulting in large-scale mortalities and huge economic losses in cultured and marine fishes worldwide. The current study evaluated the gross and histopathological lesions, and molecular detection of GIV in naturally infected grouper farms in Malaysia. A total of 150 moribund fish showing different clinical signs, presented to the Aquatic unit were used for this study. The fish were necropsied and visceral organs (spleen, kidney, heart, liver, intestine, brain, eyes, gills, and some parts of skin with ulcer) were collected and fixed in 10 % buffered formalin for histopathological processing and evaluation. Molecular detection of the virus was done by polymerase chain reaction (PCR). Grossly, the groupers had ulceration on the operculum and close to the caudal fin with hemorrhages on the margin of the caudal fin. In some fish, there was necrosis of the caudal fin, sloughing of the epidermis, dermal ulceration and popeyes Histological sections showed large basophilic cytoplasmic inclusions and vacuolations in the cytoplasm of hepatocytes. Basophilic or eosinophilic enlarged cells with the presence of mononuclear cellular infiltrations were seen in the kidney, liver, eye and gills, which is the distinctive feature of this disease. PCR detection showed positive amplification from 27 groupers. Based on the gross, histopathological and molecular detection GIV infection was established.

Pasteurella multocida is responsible for one of the major animal diseases with economic importance in both developed and developing countries. P. multocida B:2 causes haemorrhagic septicemia (HS) in cattle and buffaloes, which result in heavy economic losses through direct effect, resulting in high mortality rates and indirect effects through impairment of the animal productivity. It is well known that HS affects mainly the respiratory and digestive tracts of host animals. However, involvement of the reproductive system in the pathogenesis of HS has not been reported previously. This study was designed to present detailed detection and histopathological changes of the reproductive system and mammary glands of buffaloes experimentally infected with P. multocida B:2. Briefly, nine healthy buffalo calves aged 8-month-old were divided into three groups of three calves each. Calves from groups 1 and 2 were inoculated subcutaneously and orally with 10 mL of 1 × 1012 cfu/mL of P. multocida B:2, respectively, while calves of group 3 were inoculated orally with 10 mL of phosphate buffer saline as a sham control. All the calves in group 1 had to be euthanized after 12 h post-infection, while calves in group 2 were euthanized after day 21 post-infection. Successful isolation and PCR confirmation of P. multocida B:2 was achieved from different parts of the reproductive system, including ovary, oviduct, uterine horn, uterine body and vagina as well as mammary glands and supramammary lymph nodes of the buffaloes in group 1 after 12 h post-infection. However, P. multocida B:2 was not detected in the reproductive organs of buffaloes in group 2 and group 3 after 21 days post-infection. Significant differences (P

Gonado-hypophyseal lesions and reproductive hormonal changes in Brucella melitensis-infected mice and its lipopolysaccharide (LPS) were investigated. Forty-eight mice (24 males and 24 females) were used as infection models in this study, and they were divided into three equal separate groups of eight mice based on their sex: M1, M2, and M3 and F1, F2, and F3 (M = Male, F = Female). Groups M1 and F1 were orally inoculated with sterile phosphate-buffered saline (PBS) and served as the negative control. Groups M2 and F2 were orally inoculated with 0.4 ml of 109 colony-forming units (cfu) of B. melitensis, while groups M3 and F3 were orally inoculated with 0.4 ml of LPSs from 109 cfu of B. melitensis. All the groups were observed for 10 days for changes in clinical signs or signs of mortality and then euthanized. Whole blood was collected via cardiac puncture, while tissues were fixed in 10 % formalin for histopathological processing. Histopathological lesions in the male and female reproductive tracts ranged from mild to moderate degenerative, inflammatory, and necrotic lesions. These changes were moderate in M2 than in M3 in males and in F3 than in F2 groups in females. Lesions in the pituitary gland ranged from mild to moderate inflammation and necrosis with astrogliosis. F2 and M2 groups had more lesion distribution in the pituitary gland than F3 and M3 groups. There was a 13 % decline in progesterone concentration in F2 and a 44 % decline in F3. Estradiol level declined by 33 % in F2 and slightly increased by 4.2 % in F3. Progesterone-estrogen ratio (P/E) increased by 31 % in F2 and declined by 46 % in F3. Testosterone concentration increased by 74 % in M2 and decreased by 56 % in M3. The study showed that oral administration of B. melitensis affects the pituitary gland and may alter the hypothalamic-pituitary-gonadal axis.

Fertility of unilateral cryptorchid Sahel buck in uncontrolled breeding depends on sperm output of the scrotal testis. Semen evaluation and testicular and epididymal sperm head counts of cryptorchid and normal bucks were carried out at comparable age, body weight and testicular size. Mean semen volume and sperm cell count of the cryptorchids were not different from those of normal bucks, but the percentage of sperm cell abnormalities in semen was higher than normal consisting of narrow and big sperm heads, bent mid-piece, curved tails and tailless heads. Scrotal testes and epididymides of the cryptorchids had comparable mean size parameters and sperm head counts as those of the normal bucks. In conclusion, the scrotal testis of the cryptorchid produces as much sperm as the testis of the normal buck, but probably contributes more sperm to the ejaculate than normal with increased sperm cell abnormalities that may reduce fertility of the cryptorchid.

This study was designed to evaluate the uteri of camels and cows slaughtered in north-eastern Nigeria with the aim of determining the reproductive efficiency of these species. Three hundred and twenty-two (322) camelids and 180 bovine uteri were examined bacteriologically and pathologically using standard protocols. The result showed that there were 86 bacteria isolated from camels with Staphylococcus aureus (46.5 %), Escherichia coli (33.8 %), and other coliform species (18.6 %) being the most prominent isolates; while in the cow, there were 92 isolates, with E. coli (57.6 %), S. aureus (15.2 %), and Streptococcus pyogenes (12.0 %) being the most frequently isolated. The major isolates from both species were similar, but higher isolation rate (p

Concurrent outbreak of staphylococcal pneumonia with infectious bursal disease (IBD) occurred in 29-day-old broiler chickens. The outbreak started after a flock of 279 birds was decongested by moving 121 birds to another pen. The birds were depressed and weak before death and carcasses were cyanotic. At necropsy, the lungs were dark red, congested and consolidated; the bursa of Fabricius (BF) was enlarged; the liver was pale and the intestinal mucosa was hyperaemic. Histopathological examination of the lungs, BF and liver revealed fibrinopurulent pneumonia, purulent inflammation of the BF and hepatic lipidosis, respectively. Staphylococcus aureus was isolated from the teased tissue of the lungs. The mortality was 35.8% within 5 days of the outbreak. The circumstances of the outbreak suggested that immunosuppression due to stress associated with crowding and transferring of the birds from one pen to another and poor seroconversion to previous infectious bursal disease virus vaccination, favoured the clinical establishment of the bacterial and IBD viral infections.