Staphylococci are a worldwide cause of human and animal infection and are considered to be of the most common causes of infections in birds. Enterotoxins produced by some staphylococcal species were recognized as a causative agent of staphylococcal food poisoning (SFP). Only enterotoxins produced by Staphylococcus aureus were as yet well characterized. Much less is known about enterotoxigenic potential of coagulase-negative species of genus Staphylococcus (CNS). It has been reported that enterotoxigenic CNS strains have been associated with human and animal infections and food poisoning. Samples collected from chicken production cycle (un hatched eggs, baby chicks, broilers, chicken meat and table eggs) in Luxor, Egypt were tested to investigate the presence of Staphylococcus species and detection of their enterotoxines genes with more special attention for detection of methicillin resistance gene (mec A). Samples were tested for S. aureus and CNS on the basis of cultural and biochemical properties and confirmed by PCR amplification of 16S rRNA and clfa gene. Results showed that the presence of Staphylococci were 50/150 (33.3%), 14% of the samples were S. aureus (21/150), while, 19.33% were CNS (29/150). mecA gene was detected in 66.7% and 51.7% among S. aureus and CNS respectively. Enterotoxins genes (seb, sec and see) were found in 5 (23.8%) of S. aureus with a percent of (9.5%) for seb and sec and (4.8%) for see, while sec and see were found in 6 (20.6%) of CNS. With a percent (10.3%) for each.

The current study was achieved to designate the accessory sex glands, ampullae and urethra of 25 healthy male donkeys using the ultrasonography. Animals were classified according to their age into young peri-mature (i.e. =2 years; n=7) and old mature (>3 years; n=18). The examination was done per rectum by using Magic 2200 scanner with a 6 MHz linear transrectal transducer. The position of each gland was allocated, and length and width were measured. The dimensions of prostate gland lobes and ampulla ductus deferens significantly differed between the examined groups. The echo-pattern analysis of vesicular gland and ampulla ductus deferens, in terms of mean pixel value (MPV), pixel intensity (PI) and pixel number (PN), significantly differed between premature and mature donkeys. Age was significantly correlated with all sex glands measurements. There was a substantial confident relationship between MPV and PI and the dimensions of vesicular and ampulla ductus deferens. In the meantime, PN was clearly negatively correlated with vesicular gland length and width. In conclusions, ultrasound is a feasible non-invasive diagnostic tool that could be used to characterize the accessory glands along the course of the pelvic urethra of male donkeys reared in Egypt. The addressed measures as well as acoustic physiognomies of the secondary sex organs are considered a promising guide in fertility potential prediction and/or the discrimination of the pathological conditions of male reproductive organs.

Cryptosporidium sp. is predominant universally and sheep are an imperative zoonotic supply of the disease. Owing to the little information presented with respect to Cryptosporidium sp. infecting sheep, this study was directed to survey the predominance and molecular characterization of Cryptosporidium sp. among sheep of different ages and sexes in Qalyubia governorate, Egypt. The fecal specimens were gathered from 432 sheep of various ages (=1 to <6, 6-12 and >12 months) and sexes. The samples were microscopically examined after staining by modified Zeihl- Neelsen technique and the intestinal mucosa was scanned by electron microscopy. A nested PCR was connected to amplify a 830 bp of 18S rRNA sequence of Cryptosporidium. RFLP (restriction fragment length polymorphism) technique using SspI and VspI enzymes for digestion of the secondary product of PCR for species identification was applied. The total infection rate was 25.93%. The parasite was more prevalent in males than females of different age groups. Two zoonotic Cryptosporidium species were distinguished after RFLP-PCR sequencing: C. parvum and C. ubiquitum (identified previously as Cervine genotype). The finding recommends that sheep must be considered as a noteworthy potential source of human cryptosporidiosis. A strict reconnaissance of zoonotic cryptosporidiosis must be set up to counteract human infection and to assess forthcoming disease when applying control programs.

This work aimed to detect, identify and study the epidemiology of Arcobacter species in avian species in Upper Egypt. A total 600 samples, including cloacal swabs and intestinal samples were collected from chickens, turkeys and ducks in Assiut Governorate in Upper Egypt. Using conventional phenotypic methods for isolation and identification, Arcobacter species could be isolated and identified with percentage 25.5% in chickens, 9.5% in turkeys and 14% in ducks. Sixteen randomly selected phenotypically identified Arcobacter species isolates were confirmed using one step multiplex PCR assay. In conclusion, Arcobacter species could be detected and identified from various avian species with variable incidence. Conventional phenotypic methods for detection and differentiation of Arcobacter species are often hampered by many limitations, while molecular methods, and PCR, in particular can provide a sensitive and rapid alternative method for detection and identification of Arcobacter species in different domestic poultry species.

Cryptosporidium spp. are common intestinal protozoan parasites that causes diarrhoea in neonates and young calves. This longitudinal study was conducted at two large dairy cattle farms in central Ethiopia during February/2014 to June/2015 to determine the age-related distribution of Cryptosporidium species, to identify risk factors of the disease and to assess the public health significance of the parasite. Thirty calves born to these dairy farms were followed-up from birth to three months of age, and 270 faecal samples were collected and examined by the Modified Ziehl-Neelsen, PCR-RFLP and Sequencing. Cryptosporidium was detected from week 1 to 3 months of age with an overall prevalence of 14.8%, Peak of the infection was at two weeks of age when 12 of the 30 calves (40%) shedded oocysts. Cryptosporidium parvum and C. andersoni were identified in pre-weaned and post-weaned calves, respectively. Phylogenetic analysis showed clustering of the C. parvum isolates from this study with GenBank sequences for C. parvum bovine genotype IIa and IId subtypes. This study showed the predominance of the zoonotic C. parvum species in pre-weaned calves and demonstrated that this age group of calves pose the greatest risk for human infection. Due attention on the management of pre-weaned calves is recommended to prevent transmission of the infection to humans and lessen contamination of the environment by oocysts.