It is widely accepted that, in order to prevent and control antimicrobial resistance (AMR), surveillance systems across human, animal and environmental sectors need to be integrated, in a One Health approach. Currently, in Europe, there are surveillance networks established only for the human and food sector and, until now, there has been no organized effort to monitor AMR in bacterial pathogens derived from diseased animals in Europe. Since 2017, efforts to fill this gap have taken place by the European Antimicrobial Resistance Surveillance network in a veterinary medicine (EARS-Vet) initiative, included in the EU Joint Action on AMR and Healthcare-Associated Infections (EU-JAMRAI). EARS-Vet is designed to complement and integrate with existing European monitoring systems for AMR as well as constitute a European network of national monitoring systems. As Greece has no national AMR surveillance system for pathogens of animal origin currently in place, in the context of the development of EARS-Vet, an initiative took place for the organization of such a system by competent agencies and other stakeholders. In this article, the steps to organize a first AMR national surveillance network in Greece are presented and a Strengths, Weaknesses, Opportunities, and Threats (SWOT) analysis is performed to present main characteristics of the approach implemented.

Ticks are temporary ectoparasites that serve as vectors for a wide range of pathogens affecting both wildlife and humans. In Greece, research on the prevalence of tick-borne pathogens in wildlife is limited. This study investigates the presence of pathogens, including Anaplasma spp., Babesia spp., Bartonella spp., Rickettsia spp., as well as tick-borne encephalitis (TBE), and Crimean–Congo hemorrhagic fever (CCHF) viruses, in ticks collected from 28 wild animals across 10 different animal species. Ticks were manually harvested and identified using molecular methods, with sequencing confirming the presence of Hyalomma aegyptium, H. marginatum, H. anatolicum, Ixodes frontalis, and I. ventalloi. Among the pathogens detected, R. aeschlimannii was the most prevalent, particularly in H. aegyptium ticks from tortoises. Additionally, R. africae was identified in H. aegyptium from tortoises, marking the first report of this pathogen in this tick species in Greece. Hemolivia mauritanica, an apicomplexan parasite commonly found in Testudo tortoises, was also detected. No evidence of Babesia spp., Anaplasma spp., Bartonella spp., or viral nucleic acid was found. Phylogenetic analysis revealed close genetic relationships between the detected Rickettsia species and those previously reported in neighboring regions. These findings underscore the role of wildlife in the epidemiology of tick-borne pathogens in Greece and highlight the need for comprehensive surveillance to prevent future outbreaks.

Background/Objectives: Over the past decade, extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli have emerged as a significant public health concern due to their potential to spread beyond clinical settings and healthy carriers, in various environments, including in animal source foods. This study seeks to investigate the molecular characteristics of ESBL-producing E. coli strains isolated from food of animal origin, with a focus on chromosomal typing, plasmid typing, and the description of the associated resistance genes’ genetic environment. Methods: Ninety-seven food of animal origin samples were tested for E. coli isolates resistant to cefotaxime. The resulting isolates were then subjected to antimicrobial susceptibility testing and PCR analysis to detect beta-lactamase genes. Additional assays, encompassing mating-out procedures, molecular typing utilizing Pulsed-Field Gel Electrophoresis, Multilocus Sequence Typing Analysis, and Oxford Nanopore Technology Lite whole plasmid sequencing, were also conducted. Results: E. coli was detected in 26 raw food specimens, generating a percentage of 27%. Fourteen of the current isolates (14%) were resistant to third generation cephalosporins, producing CTX-M-1, CTX-M-15, CTX-M-55, and SHV-12 beta-lactamases. The respective genes were accompanied by Insertion Sequences ISEcp1 and IS26, facilitating their transfer. Among plasmids harboring ESBL genes, representatives belonging to incI1 incompatibility group prevailed (5/8), followed by IncY and IncX3. Most plasmids proved conjugative. Diversity of molecular fingerprints of ESBL producing E. coli was revealed. Conclusions: To the best our knowledge, this study is the first to describe the molecular characteristics of E. coli isolates producing ESBLs sourced from foods of animal origin in Greece. The prevalence of ESBLs in our confined food collection is primarily associated with the very successful IncI1 plasmids, which were not linked to a specific E. coli genetic background. This lack of association confirms that horizontal plasmid transfer plays a more significant role than clonal dissemination in the spread of ESBL-mediated cephalosporin resistance.

The objective of this report is to present a case of canine cutaneous reactive histiocytosis with a high number of dendritic cells. A 7‐year‐old male pit bull terrier was presented with a 5‐month history of skin nodules and plaques on the trunk of varying diameter, along with corneal oedema and anterior uveitis. No other clinical signs were observed. Histopathological findings showed that the main cell type of the dermal subcutaneous infiltrate was histiocytoid cells, with a high number of dendritic cells. Treatment with systemic use of cyclosporine A for 6 weeks was effective.

An 11‐year‐old female Persian cat was presented with a 4‐week history of anorexia, exercise intolerance, weight loss and difficulty in ambulation. Plain radiographs and CT revealed diffuse symmetric hyperostosis of the appendicular skeleton and multiple, space‐occupying masses in the lungs along with bronchial consolidation of the caudal lung lobe. The lung masses were labelled strongly by pan‐cytokeratin but not by vimentin and diagnosed as lepidic pulmonary adenocarcinoma by histopathological examination. The cat did not respond to chemotherapy and was euthanized 77 days later. Post‐mortem examination of bone sample confirmed the diagnosis of new bone formation (hypertrophic osteopathy).

Wild birds are increasingly recognized as contributors to the circulation and environmental dissemination of zoonotic pathogens, yet data from Greece remain limited, particularly for raptors, corvids, and water birds. This study investigated selected parasitic, mycotic, and bacterial pathogens of public health relevance in free-living wild birds originating from various regions of Greece and admitted to two animal health care facilities. Between November 2023 and May 2025, cloacal swabs from 212 injured or sick birds were analyzed using quantitative PCR for Cryptococcus spp., Chlamydia psittaci, Giardia duodenalis, Cryptosporidium spp., and Mycobacterium avium. At least one pathogen was detected in 37 samples (17.5%), with Cryptococcus spp. being the most frequent agent (11.8%), followed by C. psittaci (3.8%), G. duodenalis (0.9%), and Cryptosporidium spp. (0.9%). M. avium was not detected. Pathogen occurrence varied by bird category, genus, and region, and was associated with health status. To the best of our knowledge, this study provides the first molecular evidence worldwide of G. duodenalis in Ardea spp., Cryptosporidium spp. in Asio otus, and C. psittaci in Botaurus stellaris and Plegadis falcinellus. These findings highlight wild birds as potential zoonotic reservoirs and support the implementation of One Health–oriented surveillance programs.