Zoonotic coronavirus disease (COVID) has emerged in the past two decades and caused a pandemic that has produced a significant universal health alarm. Severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome-CoV (MERS-CoV) emerged in 2002 and 2012, respectively, provoking severe lower respiratory infection and deadly pneumonia. COVID-19 is a severe respiratory disease caused by the new strain of novel CoV (SARS-CoV-2). The zoonotic aspects of the SARS-CoV-2 in comparison to SARS-CoV and MERS-CoV are highlighted in this article. COVID-19 has rapidly become a pandemic and has spread and infected millions of people worldwide. As of November 19, 2020, the date of submitting this review, the total CoV cases, deaths, and recovered patients are 56,828,218, 1,359,320, and 39,548,923, respectively. In conclusion, COVID-19 has particularly altered the opinion of the significance of zoonotic diseases and their animal origins and the intermediate reservoirs, which may be unknown wild animals. Genetically, the SARS-CoV-2 is related to the SARS-like bat CoVs and shares 85% identity with the SARS-CoV that is derived from the SARS-like bat CoVs. However, the virus is related to a lesser extent to the MERS-CoV. The SARS-CoV-2 uses the same receptor-binding domain receptor of the SARS-CoV – the angiotensin-converting enzyme 2; conversely, DPP4 (CD26). It has not been proved that the MERS-CoVs primary receptor is the receptor of the SARS-CoV-2.

Aim: Rats are accused in disseminating many zoonotic diseases. This study aimed to isolate and identify bacteria from internal organs of rats captured in Baghdad City, Iraq. Materials and Methods: A total of 120 black rats (R. rattus) were trapped from different areas in Baghdad city. Rats were kept in individual plastic cages for 3 h before euthanizing. Deep pharyngeal swab, intestinal content, urine, and pieces of the liver and spleen, lung, kidney, and brain were obtained aseptically. The specimens were inoculated into peptone water and incubated at 37°C for 24 h for enrichment. A loopful of each specimen was then subcultured onto MacConkey Agar, Blood Agar, and Mannitol Salt Agar. CHROMagar O157 H7 and CHROMagar Listeria were used to detect Escherichia coli 157:7 and Listeria spp., respectively. Biochemical tests on analytical profile index, microscopic examination, and commercial kit for latex agglutination test for serotyping E. coli O157:H7 were used. Results: Mixed bacterial isolates were recorded as 116, 52, 36, 28, 18, 6, and 4 from intestinal contents, deep pharyngeal, liver and spleen, urine, lung, brain, and kidney, respectively. Microorganisms included E. coli, Staphylococcus aureus, Streptococcus spp., Bacillus spp., Pseudomonas aeruginosa, Citrobacter freundii, Proteus vulgaris, E. coli O157:H7, Enterobacter cloacae, Listeria spp., Klebsiella spp., Ochrobactrum anthropi, Aeromonas spp., Brucella spp., Pseudomonas fluorescens, Escherichia fergusonii, Micrococcus spp., Morganella spp., Proteus mirabilis, Pseudomonas luteola, and Streptobacillus spp. The highest bacterial prevalence (88; 73.33%) was recorded for E. coli, where 68 isolates were identified from the intestinal contents. Of these, four isolates were E. coli O157:H7. Conclusion: Rats are important carriers and transmitters of a number of pathogens and can disseminate these microorganisms to humans and animals.

Aim:This study aimed to investigate the role of ticks in transmission of Enterobacteriaceae bacteria in buffaloes in marshes of the south of Iraq.Materials and Methods:This survey included 255 healthy and clinically ill buffaloes in marshes of the south of Iraq (Thi-Qar, Basra, and Misan provinces) between the periods from May 2017 to April 2018. Animals were clinically examined. Ticks, isolated from perineum and under tail, sent to the Department of Parasitology, College of Veterinary Medicine, University of Baghdad and University of Thi-Qar for taxonomy. Ticks were dissected, and all internal organs were removed aseptically by forceps to sterile tubes containing brain heart infusion broth and incubated at 37°C for 36 h and subcultured on blood and MacConkey agars at 37°C for 36 h. Biochemical tests including citrate, methyl red, indole, urease, triple sugar iron (H2S), motility tests, and Gram stain were performed.Results:Two species of ticks were identified. Hyalomma spp. (175; 68.63%) were significantly higher than Rhipicephalus spp. (80; 31.37%). Conversely, pathogenic bacteria in Rhipicephalus spp. (55; 68.75%) was higher than detected from Hyalomma spp. (113; 64.57%), but non-significant. The prevalence of Enterobacteriaceae bacteria in ticks on diseased buffaloes (110; 88.00%) was significantly higher than non-diseased (58; 44.61%). Escherichia coli (123; 73.21%) showed a significantly higher prevalence than Salmonella spp. (25; 14.88%) and Klebsiella spp. (15; 8.92%). There was no significant variation between Salmonella spp. and Klebsiella spp. The latter was significantly higher than Enterobacter spp. (5; 2.97%). The isolation rate of infected tick collected from buffaloes inhabiting marshes was 65 (66.32%), 45 (69.23%), and 58 (63.40%) from Thi-Qar, Basra, and Misan provinces, respectively, with no significant variation. July and August (71.05% and 72.97%) reported the highest among months, while November, December, January, and February recorded nil (0.00%). The summer season was significantly higher (72.72%) followed by autumn (62.06%) and spring (59.77%), while winter reported no any bacterial isolation (0.00%).Conclusion:The high prevalence of Enterobacteriaceae bacteria isolated from hard ticks supports the probability of transmitting these bacteria to buffaloes in marshes of the south of Iraq.

Objectives: The goal of this study is to use polymerase chain reaction (RT-qPCR) and sequencing to assess ovine respiratory syncytial virus (ORSV) infection in Awassi sheep in the middle and south of Iraq (Najaf, Babylon, Wassit, and Dhi-Qar), followed by phylogenetic analyses. Methods: From December 2020 to November 2021, a total of 205 nasal swab samples were taken from sheep of various ages and health situations in Najaf, Babylon, Wassit, and Dhi-Qar, Iraq. During the study, the clinical examinations, and vital clinical signs of disease were recorded. RT-qPCR was used to detect nonstructural protein one (NS1) of ORSV, while nested RT-PCR was used to amplify the NS1 protein gene for sequencing, ORSV's NS1 gene (306-bp). PCR products were sequenced, and MEGA 6 analytic software was utilized. The quantitative findings were given as the mean standard error of the mean, the chi-square test (X2), and T test were used to determine the significance of the observed variations. Results: A total of 205 nasal swabs were taken from Awassi sheep and ORSV had a molecular prevalence of 23.41 % in sheep.

| A study was conducted to identify the prevalence of Cryptosporidium spp. as well as to investigate the effect of the region, age and sex on the infection rate in cattle and their breeders. A total of 288 samples (200 samples for cattle and 88 samples for their breeders) were collected during November 2014 to May 2015. Results showed a significant difference in the prevalence of Cryptosporidium spp. in cattle (57%) and their breeders (32.95%). The effect of age on infection rate in cattle was significant (P<0.01). The highest infection rate (75.68%) was shown in the early age category (less than 1 year), while the lowest (43.47%) was found in age ≥6 years. In general, the infection rate dropped gradually with advanced age until reached the lowest estimation in the older age (≥6 years). On the other hand, the effects of region and sex were not significant. Concerning the cattle breeders all studied effects were not significant.