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1.
Mol Phylogenet Evol ; 188: 107903, 2023 11.
Article in English | MEDLINE | ID: mdl-37574177

ABSTRACT

Yersinia spp. vary significantly in their ability to cause diseases that threaten public health. Their pathogenicity is frequently associated with increasing antimicrobial resistance (AMR) and various virulence factors. The aim of the study was to investigate the AMR genes, virulence factors, and genetic diversity of Yersinia strains isolated from meats and fish in Wenzhou in 2020 by using whole-genome sequencing (WGS). A total of 50 isolates were collected. The phylogenetic relationships among the Yersinia species were also analyzed using multilocus sequence typing (MLST), core genome multi-locus sequence typing (cgMLST), and single nucleotide polymorphism (SNP) analysis. According to the results, all the strains could be classified into five species, with most isolated from beef, followed by poultry, pork, and fish. AMR genes were identified in 23 strains. And the qnrD1 genes were all located in the Col3M plasmid. Virulence genes, such as yaxA, ystB, pla, and yplA, were also found in the 15 Y. enterocolitica strains. And this study also found the presence of icm/dot type IVB-related genes in one Yersinia massiliensis isolate. MLST analysis identified 43 sequence types (STs), 19 of which were newly detected in Yersinia. Moreover, cgMLST analysis revealed that no dense genotype clusters were formed (cgMLST 5341, 5344, 5346-5350, 5353-5390). Instead, the strains appeared to be dispersed over large distances, except when multiple isolates shared the same ST. Isolates Y4 and Y26 were closely related to strains originating from South Korea and Denmark. This study showed considerable diversity in Yersinia spp. isolated from local areas (Wenzhou City). The data generated in our study may enrich the molecular traceability database of Yersinia and provide a basis for the development of more effective antipathogen control strategies.


Subject(s)
Anti-Bacterial Agents , Virulence Factors , Animals , Cattle , Virulence Factors/genetics , Multilocus Sequence Typing/methods , Phylogeny , Drug Resistance, Bacterial/genetics , Yersinia/genetics , Genetic Variation , Genome, Bacterial
2.
Environ Pollut ; 307: 119515, 2022 Aug 15.
Article in English | MEDLINE | ID: mdl-35609842

ABSTRACT

Bibliometric network analysis has revealed that the widespread distribution of microplastics (MPs) has detrimental effects on marine organisms; however, the combined effects of MPs and climate change (e.g., warming) is not well understood. In this study, Prorocentrum donghaiense, a typical red tide species in the East China Sea, was exposed to different MP concentrations (0, 1, 5, and 10 mg L-1) and temperatures (16, 22, and 28 °C) for 7 days to investigate the combined effects of MPs and simulated ocean warming by measuring different physiological parameters, such as cell growth, pigment contents (chlorophyll a and carotenoid), relative electron transfer rate (rETR), reactive oxygen species (ROS), superoxide dismutase (SOD), malondialdehyde (MDA), and adenosine triphosphate (ATP). The results demonstrated that MPs significantly decreased cell growth, pigment contents, and rETRmax, but increased the MDA, ROS, and SOD levels for all MP treatments at low temperature (16 °C). However, high temperatures (22 and 28 °C) increased the pigment contents and rETRmax, but decreased the SOD and MDA levels. Positive and negative effects of high temperatures (22 or 28 °C) were observed at low (1 and 5 mg L-1) and high MP (10 mg L-1) concentrations, respectively, indicating the antagonistic and synergistic effects of combined warming and MP pollution. These results imply that the effects of MPs on microalgae will likely not be substantial in future warming scenarios if MP concentrations are controlled at a certain level. These findings expand the current knowledge of microalgae in response to increasing MP pollution in future warming scenarios.


Subject(s)
Dinoflagellida , Microalgae , Chlorophyll A , Harmful Algal Bloom , Microplastics , Plastics/pharmacology , Reactive Oxygen Species , Superoxide Dismutase
3.
Food Chem ; 194: 12-9, 2016 Mar 01.
Article in English | MEDLINE | ID: mdl-26471521

ABSTRACT

The effects of high hydrostatic pressure processing (HHP at 200, 400 or 600MPa) on non-volatile and volatile compounds of squid muscles during 10-day storage at 4°C were investigated. HHP increased the concentrations of Cl(-) and volatile compounds, reduced the level of PO4(3-), but did not affect the contents of 5'-uridine monophosphate (UMP), 5'-guanosine monophosphate (GMP), 5'-inosine monophosphate (IMP), Na(+) and Ca(2+) in squids on Day 0. At 600MPa, squids had the highest levels of 5'-adenosine monophosphate, Cl(-) and lactic acid, but the lowest contents of CMP and volatile compounds on Day 10. Essential free amino acids and succinic acids were lower on Day 0 than on Day 10. HHP at 200MPa caused higher equivalent umami concentration (EUC) on Day 0, and the EUC decreased with increasing pressure on Day 10. Generally, HHP at 200MPa was beneficial for improving EUC and volatile compounds of squids.


Subject(s)
Decapodiformes/chemistry , Hydrostatic Pressure , Animals
4.
Food Chem Toxicol ; 76: 86-93, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25530105

ABSTRACT

The structural and allergenic modifications of tropomyosin Tod p1 (TMTp1) in fresh squids induced by high hydrostatic pressure (HHP) were investigated. The α-helix in TMTp1 decreased along with increasing pressure from 200 to 600 MPa, where almost 53% α-helix was converted into ß-sheet and random coils at 600 MPa. The free sulfhydryl group dropped significantly as pressure went up, but the surface hydrophobicity increased at 200 and 400 MPa, while it slightly decreased at 600 MPa. Based on in vitro gastrointestinal digestion test, digestibility of TMTp1 was promoted by HHP treatment, in which 400 and 600 MPa were more effective in reducing the allergenicity than 200 MPa based on indirect ELISA. This study suggested that HHP can decrease allergenicity of TMTp1 by protein unfolding and secondary structure modification, thus providing potential for alleviating allergenicity of squid.


Subject(s)
Allergens/immunology , Decapodiformes/chemistry , Tropomyosin/immunology , Allergens/chemistry , Animals , Circular Dichroism , Digestion , Electrophoresis, Polyacrylamide Gel , Food Handling/methods , Food Hypersensitivity/diagnosis , Food Hypersensitivity/therapy , Gastrointestinal Tract/immunology , Gastrointestinal Tract/metabolism , Humans , Hydrophobic and Hydrophilic Interactions , Hydrostatic Pressure , Immunoglobulin E/blood , Immunoglobulin E/immunology , Immunoglobulin G/blood , Immunoglobulin G/immunology , Protein Structure, Secondary , Surface Properties , Tropomyosin/chemistry
5.
Carbohydr Res ; 362: 13-20, 2012 Nov 15.
Article in English | MEDLINE | ID: mdl-23064112

ABSTRACT

Shrimp shell powders (SSPs) were fermented by successive two-step fermentation of Serratia marcescens B742 and Lactobacillus plantarum ATCC 8014 to extract chitin. Taguchi experimental design with orthogonal array was employed to investigate the most contributing factors on each of the one-step fermentation first. The identified optimal fermentation conditions for extracting chitin from SSPs using S. marcescens B742 were 2% SSP, 2h of sonication time, 10% incubation level, and 4d of culture time, while that of using L. plantarum ATCC 8014 fermentation was 2% SSP, 15% glucose, 10% incubation level, and 2d of culture time. Successive two-step fermentation using identified optimal fermentation conditions resulted in chitin yield of 18.9% with the final deproteinization (DP) and demineralization (DM) rate of 94.5% and 93.0%, respectively. The obtained chitin was compared with the commercial chitin from SSP using scanning electron microscopy (SEM), Fourier transform infrared spectrometer (FT-IR) and X-ray diffraction (XRD). Results showed that the chitin prepared by the successive two-step fermentation exhibited similar physicochemical and structural properties to those of the commercial one, while significantly less use of chemical reagents.


Subject(s)
Animal Shells/chemistry , Chitin/isolation & purification , Lactobacillus plantarum/metabolism , Penaeidae/chemistry , Powders/chemistry , Serratia marcescens/metabolism , Animals , Bioreactors , Chitin/biosynthesis , Fermentation , Glucose/metabolism , Microscopy, Electron, Scanning , Sonication , Spectroscopy, Fourier Transform Infrared , X-Ray Diffraction
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