Pet turtles are a well-recognized source of human salmonellosis, posing a threat to human health, particularly children who commonly keep pet turtles. To date, the genomic characteristics of among pet turtles and children has not been well described. We investigated the prevalence, antimicrobial resistance (AMR) and genomic characteristics of from pet turtles in Beijing, China. In total, 9.6 % (46/480) of pet turtles were positive for with . Thompson being the dominant serovar (19/46) in 2019. Moreover, 80.4 % of were multi-drug resistant (MDR) and 60.7 % were resistant to ampicillin, streptomycin, sulfonamides and tetracycline (ASSuT). We further compared the genomes of . Thompson isolates from pet turtles (=19) with those from children with diarrhoea (=28) in the same region and year, most of which were sequence type (ST)26, with one novel ST7937 identified from a child-associated isolate. . Thompson isolates from children with diarrhoea exhibited less resistance than isolates from pet turtles. Most MDR isolates possessed multiple AMR genes, including the AmpC β-lactamase-encoding genes and which co-occurred with the IncA/C and IncHI plasmid replicon types. To the best of our knowledge, this is the first time that the gene has been detected from . Several pet turtle-associated . Thompson isolates comprised phylogenetically close clusters with those from children with diarrhoea (<20 SNP differences). Bayesian analysis demonstrated that the Chinese ST26 . Thompson strains had a recent evolutionary history and evolved into two major clades, with one clade acquiring various resistant plasmids. Our findings revealed the emergence of MDR among pet turtles in China and provided evidence for the interspecies transmission of . Thompson.
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http://dx.doi.org/10.1099/mgen.0.001164 | DOI Listing |
CD19-directed chimeric antigen receptor-engineered (CD19 CAR) T-cell therapy elicits high response rates but fails to induce durable responses in most adults with relapsed or refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL). In a previous clinical trial (NCT01865617), we observed anti-CAR immune responses associated with impaired in vivo CAR T-cell expansion after second infusions. Because these CD8+ T-cell responses were predominantly directed at peptides derived from the murine single chain variable fragment (scFv) in the CAR, we conducted a clinical trial investigating the safety and efficacy of CD19 CAR T-cells engineered with a CAR incorporating a fully human scFv (JCAR021) in adults with R/R B-ALL (NCT03103971).
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Microplastic Research Interest Group (MRIG), Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia. Electronic address:
This study presents the first evidence of microplastics in natural sea turtle nests at Chagar Hutang Turtle Sanctuary (CHTS) on Redang Island, a crucial habitat for green turtles. Microplastics were detected in all studied turtle nests (0-70 cm depth), with a total abundance of 12,270 microplastic items per kg dry weight of sand. Fibers (80.
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National Institute of Health Doutor Ricardo Jorge, Center for Vectors and Infectious Diseases, Portugal; Institute of Environmental Health (ISAMB), Lisbon, Portugal.
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HUN-REN Veterinary Medical Research Institute, 1143 Budapest, Hungária krt. 21, Hungary. Electronic address:
Conserv Biol
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School of Life Sciences and State Key Laboratory of Biological Control, Sun Yat-sen University, Guangzhou, China.
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