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1.
Curr Microbiol ; 79(12): 354, 2022 Oct 11.
Article in English | MEDLINE | ID: mdl-36219324

ABSTRACT

Clostridioides difficile is the main pathogen responsible for antibiotic-associated diarrhea in adults. Besides its challenging diagnosis, C. difficile infection (CDI) causes substantial morbidity and mortality. Commercially, there are assays with different targets and performances in sensitivity and specificity. The objectives of this study were to: (1) evaluate the prevalence and seasonal variability of CDI rates at a tertiary hospital in southern Brazil over 12 years and (2) determine the impact of using a two-step algorithm test in the laboratory diagnosis. Between January 2007 and May 2019, fecal samples from 2275 patients were analyzed in a cross-sectional study. Four commercial tests were adopted for the diagnosis of CDI, the immunochromatographic test for toxin A from 2007 to 2010; the enzyme-linked immunosorbent assay method for toxins A and B from 2011 to March 2017; and the rapid enzyme immunoassay (EIA) for GDH and toxins A and B, associated with a Polymerase Chain Reaction (PCR) for the toxin B gene from June 2017 to 2019. The annual prevalence was 8.7% from 2007 to March 2017, increasing between June 2017 and 2019 to 14.7% when the C. diff Quik Chek Complete + GeneXpert C. difficile (two-step algorithm) test was adopted. The number of samples (691) and percentage of CDI cases (10.5%) were higher in winter, but the difference has no statistical significance (P > 0.05). An accurate diagnosis and adequate knowledge of the local seasonality of CDI allow the effective implementation of prevention and control strategies for nosocomial CDI, in addition to effective treatment for patients.


Subject(s)
Bacterial Toxins , Clostridioides difficile , Clostridium Infections , Adult , Anti-Bacterial Agents/analysis , Bacterial Proteins/analysis , Bacterial Proteins/genetics , Bacterial Toxins/genetics , Brazil/epidemiology , Clostridioides difficile/genetics , Clostridium Infections/diagnosis , Clostridium Infections/epidemiology , Cross-Sectional Studies , Feces/chemistry , Glutamate Dehydrogenase/analysis , Humans , Prevalence , Sensitivity and Specificity , Tertiary Care Centers
2.
Bol. Centro Pesqui. Process. Aliment ; 31(01): 25-38, jan. 2013.
Article in English | LILACS | ID: biblio-915764

ABSTRACT

This work has studied the application of the osmo-convective dehydration on yacon roots, regarding its composition and quality attributes. Slices of yacon were submitted to osmotic treatment with sucralose solution followed by convective dry. The experiments followed a complete 23 factorial design to assessthe effect of three variables of the process (temperature, stirring rate of the osmotic solution and drying temperature) over four quality attributes (moisture content, color, luminosity and soluble solid content). The application of the osmotic treatment before convective drying provided quality gains to the dried product, such as low browning and shrinkage rates, and reduction of the structural damages towards angular distortions and fissures, in comparison to the samples dried directly on the tray dryer. The effect of osmotic treatment over the centesimal composition of yacon have resulted on absorption of sucralose and water loss without a significance compromise of its nutritional attributes. The obtained product presented different contents of moisture, but similar levels of darkening and color alteration at diverse experimental conditions.


Investigou-se a aplicação da desidratação osmo-convectiva em raízes de yacon, com relação à sua composição centesimal e atributos de qualidade. Fatias de yacon foram submetidas ao tratamento osmótico em solução de sucralose e depois à secagem convectiva. Os experimentos seguiram planejamento fatorial completo (2


Subject(s)
Maillard Reaction , Food Composition , Food Preservation , Plant Roots
3.
Food Microbiol ; 28(5): 936-41, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21569936

ABSTRACT

This is the first report on the screening of shellfish from Portugal for the presence of human enteropathogenic viruses. Approximately 2000 shellfish (Curbicula fluminea, Ruditapes decussatus, Tellina crassa, Spisula solida, Dosinia exoleta, Ensis spp., Mytilus spp., Ostrea edulis and Cerastoderma edule), organized in 49 batches, were collected between March 2008 and February 2009. They were tested for norovirus (NoV), hepatitis A virus (HAV) and enterovirus (EV) by RT-PCR followed by nucleotide sequencing. Bacterial contamination was also evaluated by Escherichia coli counts. Viral contamination was detected throughout the year in all shellfish species and in all collection areas, independently of their harvesting areas classification. Overall, 67% of all analyzed batches were contaminated by at least one of the studied viruses while the simultaneous presence of two and three viruses was detected in 22% and 6% batches, respectively. Of the three viruses, NoV was detected in 37% of the batches, followed by EV in 35%, and HAV in 33%. Nucleotide sequencing of the NoV and HAV RT-PCR products demonstrated that all strains belonged to NoV genotype GII.4 and HAV subgenotype 1B. The presence of NoV and HAV in shellfish from "A class" harvesting areas of Portugal can represent a potential health risk.


Subject(s)
Enterovirus/isolation & purification , Food Contamination/analysis , Hepatitis A virus/isolation & purification , Mollusca/microbiology , Mollusca/virology , Norovirus/isolation & purification , Shellfish/microbiology , Shellfish/virology , Animals , Enterovirus/classification , Enterovirus/genetics , Hepatitis A virus/classification , Hepatitis A virus/genetics , Molecular Sequence Data , Norovirus/classification , Norovirus/genetics , Phylogeny , Portugal
4.
Int J Food Microbiol ; 129(1): 50-8, 2009 Jan 31.
Article in English | MEDLINE | ID: mdl-19081155

ABSTRACT

This work had as main objectives to characterize two bacteriocins produced by lactic acid bacteria (LAB) previously isolated from non-fermented seafood, in order to evaluate their potential as new food protective agents. The two bacteriocinogenic isolates were identified by Polymerase Chain Reaction (PCR) using genus- and species-specific primers, and confirmed by 16S rDNA sequencing, as Enterococcus faecium and Pediococcus pentosaceus. The antimicrobial spectrum of each strain included several indicator microorganisms, some of them also isolated from seafood. Growth of Listeria innocua, L. monocytogenes, Staphylococcus aureus, Bacillus cereus and other LAB species were inhibited, although no inhibition of Gram-negative microorganisms was observed. Proteolytic, but not lipolytic or glycolytic enzymes, completely inactivated the antimicrobial effect of both cell-free supernatants confirming the proteinaceous nature of the inhibitors. The antimicrobial activity was maintained after treatment with NaCl, SDS, Triton X-100, Tween 20, Tween 80 and EDTA after 2 h or 5 h of exposure and both bacteriocins were stable over a wide range of pH and temperatures. Production of bacteriocin by E. faecium (bacALP7) was detected initially at exponential phase and reached a maximum activity of 25,600 AU/ml in the early stationary phase, whereas bacteriocin production by P. pentosaceus ALP57 (bacALP57) reached the maximum at exponential phase with 12,800 AU/ml. The bacteriocins did not kill L. monocytogenes ESB54 nor L. innocua 2030c however, cellular growth was reduced. The partially purified bacteriocins, bacALP7 and bacALP57, were below 6.5 kDa in size as determined by Tricine-SDS gel electrophoresis. E. faecium and P. pentosaceus contained DNA fragments corresponding in size to those recorded for enterocin B and pediocin PA-1, respectively. Sequencing of the fragments from both bacteriocins confirmed the homology. To our knowledge, for the first time two LAB producing bacteriocins similar to pediocin PA-1 and enterocin B, were isolated from non-fermented shellfish. The adaptation of the cultures to seafood matrices may be advantageous in terms of application as a biopreservation strategy for reduction of L. monocytogenes levels in seafood products.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacteriocins/pharmacology , Food Preservation/methods , Listeria/drug effects , Shellfish/microbiology , Animals , Anti-Bacterial Agents/biosynthesis , Anti-Bacterial Agents/isolation & purification , Antibiosis , Bacteriocins/biosynthesis , Bacteriocins/genetics , Bacteriocins/isolation & purification , Consumer Product Safety , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal , Enterococcus faecium/genetics , Enterococcus faecium/metabolism , Food Microbiology , Humans , Kinetics , Listeria/growth & development , Microbial Sensitivity Tests , Pediocins , Pediococcus/genetics , Pediococcus/metabolism , Species Specificity
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