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African swine fever is one of the most serious threats to the world pig industry due to high infectivity and mortality rates among pigs. To date, no effective means of active prevention of the infection have been developed. The only effective method of control is passive monitoring of the spread of the pathogen among the population of domestic and wild pigs, detection of infected animals and their depopulation. The study analyzes the spread of African swine fever in Ukraine from 2012 to 2024 and compares it with the countries that share a common border – Poland, Romania, Hungary, Slovakia and Moldova. In Ukraine, the first outbreaks were recorded in 2012 in Zaporizhzhia region among domestic pigs. In total, 619 outbreaks were detected during the study period: 482 among domestic pigs and 137 among wild pigs. The largest number of outbreaks was recorded in Odesa (64), Poltava (54), Mykolaiv (52) and Kyiv (46) regions. In Eastern European countries, African swine fever was detected later: in Poland – since 2014 (1304 among domestic and 17871 among wild pigs), Romania – since 2017 (6729 and 3649, respectively), Hungary and Slovakia – since 2018 (0 and 7875; 72 and 3645). In Moldova, the first outbreak was in 2020 (39 among domestic and 45 among wild pigs). The highest total number of outbreaks was recorded in Poland (19175), mainly among wild boars (93.2%). In Hungary, all detected cases involved wild animals. The analysis revealed a statistically significant difference in the number of African swine fever outbreaks between the analyzed countries. There is also a difference in the number of outbreaks within the analyzed time period. If we analyze the number of cases since 2018, there is no statistically significant difference. Prevention and control of African swine fever are complicated by the circulation of the pathogen among wild boars, non-compliance with biosecurity measures by owners of small pig farms and the movement of infected animals. Comprehensive monitoring with early detection of outbreaks and timely destruction of infected animals plays a key role.

Coagulase-positive staphylococci are an important infectious agentcausing numerous infections in animals. Staphylococcus aureus andStaphylococcus pseudintermedius share a number of similar cultural andbiochemical characteristics, which makes their differentiation difficult.Since these species have different zoonotic potential, it is advisable todevelop rapid and specific schemes for species differentiation of pathogens.We have studied the cultural and biochemical characteristics ofStaphylococcus spp. isolated from dogs, cats and cows. In total, 103halophilic coccal cultures were isolated from companion animals and45 from cows, of which 55 and 30 cultures were coagulase-positivestaphylococci, respectively. The reactions that can be used to differentiateS. pseudintermedius and S. aureus were studied. Growth inhibition zonesaround the disk with polymyxin B antibiotic for S. pseudintermediuswere statistically higher (p

The results of optimization of the Staphylococcus spp. identification protocol by polymerase chain reaction with agarose gel detection and approbation of the protocol with wild strains selected from dogs are presented. Determination of the parameters of specificity and sensitivity of the method was performed on museum strains of cocci S. epidermidis ATCC 14990, S. aureus ATCC 25923, S. aureus subsp. aureus UKM B-918, S. pneumoniae ATCC 49619 and E. faecalis ATCC 194433. DNA extraction was performed using the IndiSpin Pathogen Kit. The ready PCR mix NEB OneTaq® 2X Master Mix with Standard Buffer was used to prepare the reaction mixture. Primers targeted to the tuf gene region using an amplification product of 370 bp were used for the study. The reaction results were recorded in a 2% agronomic gel with the addition of ethidium bromide at a concentration of 0.5%. The optimal annealing temperature was determined by the temperature gradient method. In a study of the specificity of the method, three museum strains of staphylococci were identified as positive, while strains of other cocci did not give reaction products. The sensitivity study of the method was to detect the amplification product in seven dilutions of bacterial suspension that meet McFarland turbidity standards, the lowest concentration was further diluted 10, 100 and 1,000 times. The last dilution, which showed the presence of the amplification product corresponds to 2×106 CFU in 200 μl of saline used for DNA isolation. PCR protocol was tested on wild staphylococcal strains. Ear and nasal swabs of dogs, as well as washes from the transfer cage were selected for the study. The primary inoculation of the material was carried out on mannitol salt agar, on this medium only the growth of halophilic microorganisms is possible. Growth was found on 17 Petri dishes. The PCR washings of these cups indicated the presence of staphylococci in the test materials. The results of in-laboratory PCR testing indicate that the primer we used gives high indicators of specificity and sensitivity. Our tested technique can be used to confirm the presence of Staphylococcus spp. bacteria in the primary culture of smears taken from dogs.

Staphylococcus spp. a common genus of bacteria that colonizes the body of dogs. Some families of this genus are pathogenic and are involved in the development of diseases of various systems and organs, especially the skin and outer ear. One of the main signs of the most pathogenic families of this genus is the secretion of the enzyme coagulase. They are grouped into the group of coagulase-positive Staphylococcus (CoPS). S. pseudintermedius most often is isolated from a dog, about 10-60% isolates. S. aureus is identified less frequently, in 4-15% of cases, but it is associated with people who are its natural carriers. S. schleiferi subsp. coagulans is another family that can be identified in the pathological material obtained from dogs. However, coagulase is one of much different pathogenicity factors in this family. Also, microorganisms of this family can exist both in the form of a planktonic culture and in the structure of a biofilm, on which the effect of antibacterial agents is weakened. Some strain of CoPS carry genes of resistance to various antibacterial agents and may occupy a dominant position in the pathogenic process. Such strains can colonize the environment in places where animals congregate, which leads, for example, to the occurrence of clinical infections. Also resistant are strains of this family that can colonize other animals or humans. Owners and specialists working with animals are constantly at risk. To date, the issue of the emergence of resistance to beta-lactam antibiotics (methicelin-resistant strains) and the acquisition of resistance to several groups of antibacterial agents is acute. In the countries of the European Union, a fairly large number of studies are conducted aimed at studying the spread of Staphylococcus spp. analysis of virulence and pathogenicity factors, as well as mechanisms of acquiring antibacterial resistance. Programs to control the prevalence of resistant strains are also being developed there. Different authors show resistance to a large number of antibacterial agents, the profile of antibacterial resistance may differ both within different groups and between different drugs of the same pharmaceutical group. In Ukraine, there are no systematic studies of the spread of resistant strains of microorganisms among small animals.

Marina Shevchenko,1 Ekaterina Servuli,1,2 Zarema Albakova,1,3 Leonid Kanevskiy,1 Alexander Sapozhnikov1,3 1Department of Immunology, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia; 2Department of Experimental Physiology, Institute of Biomedical Problems, Russian Academy of Sciences, Moscow, Russia; 3Department of Biology, Lomonosov Moscow State University, Moscow, RussiaCorrespondence: Marina ShevchenkoDepartment of Immunology, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya Street 16/10, Moscow 117997, RussiaTel/Fax +74953304011Email mshevch@gmail.comAbstract: Asthma is a complex chronic disorder of the airways, affecting immune and structural cells and inducing both protein and tissue remodeling. Heat shock proteins 70 kDa (HSP70s) are highly conserved members of the stress-induced family, possessing precisely described chaperone activity. There is growing evidence of a tight relationship between inflammatory diseases of different origins and the elevation of local HSP70 expression and secretion. Although extracellular HSP70 does not serve as a common marker of asthma, elevated HSP70 levels have been detected in the peripheral blood serum and sputum of patients with asthma, as well as in the bronchoalveolar lavage fluid of mice with induced allergic airway inflammation. Possessing diverse immunomodulating properties, extracellular HSP70 can manifest different activities in airway inflammatory processes and asthma, acting either as a pro-inflammatory trigger, or an anti-inflammatory agent. This review will discuss the effects and possible mechanisms concerning HSP70 implication in airway inflammation regulation in asthma. We examine ATPase and chaperone activities of HSP70 as potential modulators of immune responses in asthma. Given the crucial role of a chronic inflammatory response in asthma, understanding the effects of HSP70 on immune and structural cells may reveal new perspectives for the therapeutic control of inflammation.Keywords: heat shock protein 70 kDa, asthma, allergic airway inflammation, immune cells, ATP