Proteus mirabilis (P. mirabilis) is a Gram-negative, motile opportunistic pathogen with a broad host range. It causes both community- and hospital-acquired infections and is increasingly detected in poultry and food chains, raising food-safety concerns. This study systematically evaluated the prevalence, antimicrobial-susceptibility profiles, and the distribution of resistance genes, virulence-associated genes (VAGs), and metal-tolerance genes in chicken-derived P. mirabilis in Hunan Province. From June 2022 to January 2025, 1,679 chicken cloacal swabs were collected in Hunan; 192 P. mirabilis isolates were recovered (prevalence 11.44%). Antimicrobial-susceptibility testing (AST) was performed on a simple random sample of 118 isolates (118/192, 61.5%) using CLSI-recommended disk diffusion. The results showed that the MDR rate was 72.0% (85/118). Resistance was most frequent to Trimethoprim - Sulfamethoxazole (SXT) (81.4%), Ampicillin (AMP) (79.7%), Ciprofloxacin (CIP) (78.0%), and Gentamicin (GEN) (75.4%), followed by Neomycin (NEO) (63.6%) and Chloramphenicol (CHL) (61.0%). Carbapenem resistance was detected in a subset of isolates, including meropenem (MEM) (6.8%) and imipenem (IPM) (11.0%). Resistance-gene screening identified high prevalence of plasmid-mediated quinolone resistance (PMQR) determinants qnrA 58.9% (113/192) and aac(6')-Ib-cr 59.9% (115/192). The carbapenemase gene blaNDM-1 was detected in 10.4% (20/192) of isolates, and 24.0% (46/192) were positive for vanA. Markers associated with class 1 integrons, including qacEΔ1 and the integrase intI1, were detected in 71.9% and 49.5% of isolates, respectively. Furthermore, copper-tolerance genes copB and pcoA were detected in 49.5% and 10.4% of isolates, respectively. In summary, poultry-derived P. mirabilis in Hunan demonstrated high MDR prevalence and frequent carriage of resistance-, virulence-, and environment-related markers. Our findings enrich the epidemiological data on Proteus mirabilis at the farm level and provide scientific guidance for the prevention and control of this disease.
Salmonella enterica is a major foodborne pathogen associated with poultry, representing a critical challenge for food safety worldwide. Accurate identification of serovar diversity is essential for designing control strategies; however, conventional culture-based methods often underestimate this complexity. In this study, we report the first application of CRISPR-SeroSeq in Ecuador to characterize Salmonella serovar diversity in commercial broilers. A total of 76 flocks (one hose of one farm in different cycles) originated across 19 broiler farms were sampled. All flocks belonged to an integrated poultry company. From all samples, 77.6% tested positive for Salmonella. CRISPR-SeroSeq analysis revealed a clear dominance of serovar Infantis, even within mixed populations. Importantly, serovars of significant public health concern, including Enteritidis and Typhimurium, were detected at low frequencies that would likely be missed by conventional methods. These findings highlight the utility of high-resolution serotyping approaches, providing valuable insights for targeted interventions to improve poultry production biosecurity and food safety.
We examined the antimicrobial resistance of commensal Escherichia coli and occurrence of extended-spectrum beta-lactamase (ESBL)-/AmpC-producing E. coli in organic meat chicken flocks of three different fattening types using a longitudinal study design. Fourteen German small scale meat chicken farms fattening either slow-growing broiler, dual-purpose cockerels or male layer hybrids were sampled between 2023 and 2025. Throughout the fattening period, four consecutive flocks per farm were sampled five times each. Three isolates per sampling time point were picked from MacConkey agar (MCA). Additionally, MCA + 1mg/L cefotaxime (MCA+CTX) was used to selectively screen for ESBL-/AmpC-producing E. coli. In total, 696 commensal E. coli from MCA and 51 ESBL-/AmpC-producing E. coli from MCA+CTX were isolated. Antimicrobial resistance was determined using broth microdilution and minimum inhibitory concentrations were evaluated using epidemiological cut-off values. Throughout the fattening period, most commensal E. coli were susceptible in slow-growing broilers (63.0-80.0%), male layer hybrids (76.9-97.6%) and dual-purpose cockerels (69.0-89.6%). Resistance to ampicillin (11.1%; 77/696), ciprofloxacin (9.9%; 69/696), tetracycline (9.5%; 66/696), and nalidixic acid (8.3%; 58/696) was overall most prevalent in resistant commensal isolates regardless of sampling time point and fattening type. Whole genome sequencing revealed a diverse population among resistant commensal E. coli, with most resistant strains belonging to ST10 or ST155. Clonal dissemination of resistant strains was shown both within flocks or between subsequent flocks of a farm and between different farms. The providing hatchery was shown to have an influence (p < 0.001) on the recovery of resistant isolates. Only 27.5% of all flocks were positive for ESBL-/AmpC-producing E. coli for at least one sampling time point, with none of the flocks being positive throughout the whole fattening period and a high diversity of sequence types. blaCTX-M-1 (29.2%, 7/24) was the most prevalent ESBL gene identified. This study is the first to describe antimicrobial resistance in different organic meat chicken fattening types in Germany in a longitudinal approach.

