The occurrence of Listeria monocytogenes in marine fish and fish market areas was investigated. Two hundred and eighty-eight samples (123 environmental samples—siphons, knives, cutting boards, floor, sinks, water, and ice—and 165 marine fish samples) were examined. Twenty-four isolates were characterized as Listeria monocytogenes (five from environmental samples (4.0%) and 19 from fish samples (11.5%)). The strains were further characterized according to their antibiotic resistance, pathogenicity, and biofilm formation ability. They were molecularly serotyped as IIc (n = 22) and IVb (n = 2) and possessed all the virulence genes tested (inlA, inlB, inlC, inlJ, actA, hlyA, iap, plcA, and prfA), except for two strains lacking the hlyA and iap genes, respectively. All strains showed strong (41.7%) or moderate biofilm-producing ability (58.3%) and almost all showed resistance to at least one antibiotic, with the highest rates being observed against clindamycin and vancomycin. The proteomic analysis by MALDI-TOF revealed two distinct clusters that involved strains from fish only and those from both fish and the environment. The presence of Listeria monocytogenes in the fish-market environment and marine fish, along with the pathogenicity and persistence characteristics of the seafood-related strains, emphasize the need for vigilance concerning the spread of this notorious foodborne pathogen.

Listeria monocytogenes, the leading cause of fatalities among foodborne pathogens, exhibits remarkable resilience in food industry environments. This study aims to isolate and characterize L. monocytogenes strains along the beef production chain of a vertically integrated industry. Sampling included carcass, hide, and environmental samples collected from a cattle unit and partner slaughterhouse. The samples were examined for the presence of Listeria monocytogenes. The isolates were characterized via molecular serotyping and MALDI-TOF proteomic analysis. Further analyses included antimicrobial susceptibility testing, biofilm formation assessment, and virulence gene investigation. A total of 24 L. monocytogenes strains were isolated. The prevalence in carcasses, hide and slaughterhouse environment was 21.7%, 6.7% and 8.8% respectively. Molecular serogroup IIc predominated, followed by serogroups IIa, IIb, and IVb. Almost all strains showed a moderate or strong ability to produce biofilms and resistance to at least one antimicrobial, with clindamycin, vancomycin, and tetracycline demonstrating the highest rates of resistance. Three strains were also characterized as multidrug-resistant, while all strains possessed at least six virulence genes. The proteomic analysis organized the isolated strains in three clusters, whereas the transmission pathways primarily implicated carcass washing water and hides. Understanding L.monocytogenes dissemination along the beef production chain is vital for preventing transmission to humans and emergence of a listeriosis outbreak.

Antimicrobial resistance is considered a topic of utmost interest under the concept of “One Health”, having severe implications in both human and veterinary medicine. Among the antibiotic-resistant bacteria, gram-negative bacteria, especially those belonging to the order of Enterobacterales (such as Escherichia coli), hold a prominent position in terms of both virulence and possessing/disseminating antimicrobial resistance (AMR) traits. The aim of this study was to examine the presence of extended-spectrum β-lactamase producing E. coli isolates in raw poultry carcasses collected from a university club. Five hundred raw poultry skin samples were collected from the Aristotle University of Thessaloniki (AUTh) club in Thessaloniki, Greece. A total of 64% of the samples were positive for the presence of extended-spectrum β-lactamase (ESBL)-producing E. coli. The isolates were further examined for their susceptibility to selected antibiotics by the disc diffusion method and were characterized as true ESBL, as producing class C cephalosporinases (AmpC) or “of unknown etiology” by the combination disc test. The 86 of the 120 isolates (71.67%) were classified as true ESBL, 24 (20.00%) as AmpC, and 10 (8.33%) as “of unknown etiology”. The isolates were screened for the occurrence of β-lactamase genes (bla_TEM, bla_CTX-M, bla_SHV, and bla_OXA). Thirty-six isolates (32 ESBL- and 4 AmpC-phenotype) harbored both bla_TEM and bla_CTX-M genes, twenty-two isolates (among which 19 ESBL-phenotype and 2 AmpC-phenotype) harbored bla_CTX-M only, whereas twenty-six (14 ESBL- and 12 AmpC-phenotype) isolates harbored bla_TEM alone. No isolate harboring bla_SHV or bla_OXA was detected. The results demonstrate the existence of E. coli isolates producing extended-spectrum β-lactamases in poultry carcasses from Greece, pausing a risk for antibiotic resistance transfer to humans.

The quality changes of Mediterranean horse mackerel skinned fillets kept under vacuum during 20 months of frozen storage at −18°C were studied. Analyses included physicochemical and chemical changes and sensory acceptance. Attribute scores (appearance, texture, odor, flavor) were found to be at a level of acceptance for almost 16 months. Water holding capacity decreased significantly over the first 8 months of frozen storage, while pH values did not lead to good correlation with the storage time. Lipid hydrolysis developed gradually up to 8 months and then remained relatively constant between 10 and 18 months. There were some fluctuations in malondialdehyde (MDA) values (μg malondialdehyde/kg sample) throughout frozen storage, reaching maximum but still acceptable levels at the 14th month. Although a proportional increase in TVB-N (total volatile base-nitrogen) with storage time was observed, the values never exceeded the upper limit for frozen fish products.