Longitudinal study of ESBL/AmpC-producing Enterobacterales strains sharing between cohabiting healthy companion animals and humans in Portugal and in the United Kingdom.

Extended-spectrum beta-lactamase (ESBL)- and plasmid-mediated cephalosporinase (AmpC)-producing Enterobacterales (ESBL/AmpC-E) are an increasing healthcare problem in both human and veterinary medicine. The aim of this study was to investigate the possible sharing of ESBL/AmpC-E strains between healthy companion animals and humans of the same household in Portugal (PT) and the United Kingdom (UK). In a prospective longitudinal study, between 2018 and 2020, faecal samples were collected from healthy dogs (n=90), cats (n=20) and their cohabiting humans (n=119) belonging to 41 PT and 44 UK households. Samples were screened for the presence of ESBL/AmpC-E and carbapenemase-producing bacteria. Clonal relatedness between animal and human strains was established by using REP-PCR fingerprinting method, followed by whole-genome sequencing (WGS) of selected strains. ESBL/AmpC-E strains were detected in companion animals (PT=12.7%, n=8/63; UK=8.5%, n=4/47) and humans (PT=20.7%, n=12/58; UK=6.6%, n=4/61) in at least one timepoint. REP-PCR identified paired multidrug-resistant ESBL/AmpC-producing Escherichia coli strains from companion animals and owners in two Portuguese households (4.8%) and one UK household (2.3%). WGS analysis of nine E. coli strains from these three households confirmed that interhost sharing occurred only between the two animal-human pairs from Portugal. Three shared strains were identified: one CTX-M-15-producing E. coli strain in a cat-human pair (O15-H33-ST93) and two CTX-M-15- and CTX-M-55/CMY-2-producing E. coli strains, in a dog-human pair (O8:H9-ST410 and O11:H25-ST457, respectively) at different timepoints. These E. coli clonal lineages are human pandemic, highlighting the role of companion animals living in close contact with humans in the dissemination and persistence of antimicrobial resistance in the household environment.

Ammonia sensitivity of the glass eel (Anguilla anguilla L.): salinity dependence and the role of branchial sodium/potassium adenosine triphosphatase.

Eel aquaculture is capture based and thus dependent on the fishery for juvenile glass eels. This fishery typically takes place in estuaries where salinity varies and ammonia levels can be elevated. Also, during capture and transport glass eels are kept at high densities and ammonia from endogenous production can increase to toxic levels. Ammonia is known to have detrimental effects on fish growth and survival. In the present study, the salinity dependence of ammonia sensitivity in glass eels acclimated to either seawater or freshwater was determined, and the possible role of branchial sodium/potassium adenosine triphosphatase (Na+/K+ -ATPase) was investigated. Freshwater-acclimated glass eels were found to be more sensitive to ammonia with a lethal concentration to 50% of the test organisms (LC50) value for 96 h of 3.30 mM for total ammonia nitrogen (TAN) and 117 microM for un-ionized ammonia (UIA), versus values of 4.95 mM and 138 microM, respectively, for seawater-acclimated animals. Freshwater glass eels also had significantly lower body TAN levels than seawater-acclimated glass eels, although body accumulation profiles during exposure were similar. The higher branchial Na+/K+ -ATPase activities in seawater glass eels might explain this difference in sensitivity; however, activities decreased significantly with increasing ammonia levels. There was also no salinity dependence of net ammonia flux rates (0.388 micromol of TAN/g/h). Holding glass eels at high densities characteristic of transport conditions resulted in elevated ammonia concentrations to approximately 3 mM, which coincidently approaches to the freshwater LC50 value and may therefore contribute to mortality.