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1.
Mem. Inst. Oswaldo Cruz ; 113(10): e180192, 2018. tab, graf
Article in English | LILACS | ID: biblio-1040581

ABSTRACT

Raoultella planticola is an emerging zoonotic pathogen that is associated with rare but life-threatening cases of bacteremia, biliary tract infections, and urinary tract infections. Moreover, increasing antimicrobial resistance in the organism poses a potential threat to public health. In spite of its importance as a human pathogen, the genome of R. planticola remains largely unexplored and little is known about its virulence factors. Although lipopolysaccharides has been detected in R. planticola and implicated in the virulence in earlier studies, the genetic background is unknown. Here, we report the complete genome and comparative analysis of the multidrug-resistant clinical isolate R. planticola GODA. The complete genome sequence of R. planticola GODA was sequenced using single-molecule real-time DNA sequencing. Comparative genomic analysis reveals distinct capsular polysaccharide synthesis gene clusters in R. planticola GODA. In addition, we found bla TEM-57 and multiple transporters related to multidrug resistance. The availability of genomic data in open databases of this emerging zoonotic pathogen, in tandem with our comparative study, provides better understanding of R. planticola and the basis for future work.


Subject(s)
Polysaccharides, Bacterial/biosynthesis , Genome, Bacterial/genetics , Enterobacteriaceae/genetics , Genes, Bacterial/genetics , Polysaccharides, Bacterial/genetics , Bacterial Capsules/genetics , Enterobacteriaceae/classification
2.
Braz. j. microbiol ; 43(3): 1010-1014, July-Sept. 2012. tab
Article in English | LILACS | ID: lil-656666

ABSTRACT

Staphylococcus aureus (n=157) isolated from intramammary infections in Argentine dairy areas were evaluated for presence of cap5 and cap8 loci. Isolates carrying cap5 and cap8 were serotyped using specific antisera. Sixty four percent of the isolates were genotyped as cap5 or cap8 and 50% of them expressed CP5 or 8.


Subject(s)
Cattle , In Vitro Techniques , Dairy Products/analysis , Mastitis, Bovine/genetics , Phenotype , Polysaccharides, Bacterial/genetics , Polysaccharides, Bacterial/isolation & purification , Polymerase Chain Reaction/methods , Staphylococcus aureus/genetics , Staphylococcus aureus/isolation & purification , Cattle , Genotype , Methods
3.
Hig. aliment ; 20(142): 38-45, jul. 2006.
Article in Portuguese | LILACS | ID: lil-452123

ABSTRACT

Os polissacarídeos de origem microbiana, chamados de biopolímeros ou gomas, apresentam muitas vantagens em relação aos hidrocolóides derivados de algas e plantas. Este trabalho discute a importância dos exopolissacarídeos bacterianos, sua síntese, produção e fatores que afetam esta mesma produção, bem como sua composição química.


Subject(s)
Aeration , Food Technology , Polysaccharides, Bacterial/biosynthesis , Polysaccharides, Bacterial/genetics , Temperature , Culture Media
4.
Yonsei Medical Journal ; : 755-758, 2004.
Article in English | WPRIM | ID: wpr-206343

ABSTRACT

The antigenic similarity between Neisseria meningitidis group B (NMGB) capsular polysaccharide (PS) and human polysialic acid (PSA) has hampered the development of a NMGB PS-based vaccine. But the possibility of a safe vaccine based on NMGB PS has been demonstrated by the existence of the NMGB PS-associated nonautoreactive epitope, which is distinct from those present on human PSA. To obtain peptide mimotopes of NMGB PS, we used HmenB3, a protective and nonautoreactive monoclonal antibody, to screen a phage library with 12 amino acids. We obtained 23 phage clones that bound to HmenB3 but not in the presence of E. coli K1 PS [which is alpha (2-8) -linked PSA like NMGB PS]. The clones contained 3 mimotopes and differed from previously described NMGB PS mimotopes. Immunization with a synthetic peptide of one mimotope elicited anti-NMGB antibodies in BALB/c mice. These mimotopes may be useful in the development of group B meningococcal vaccines.


Subject(s)
Animals , Female , Mice , Amino Acid Sequence , Bacterial Vaccines/immunology , Cloning, Molecular , Meningococcal Infections/immunology , Mice, Inbred BALB C , Molecular Sequence Data , Neisseria meningitidis, Serogroup B/genetics , Polysaccharides, Bacterial/genetics
5.
Journal of Korean Medical Science ; : 779-782, 2004.
Article in English | WPRIM | ID: wpr-27636

ABSTRACT

While ica gene of Staphylococcus epidermidis is known to undergo phase variation by insertion of IS256, the phenomenon in Staphylococcus aureus has not been evaluated. Six biofilm-positive strains were tested for the presence of biofilm-nega-tive phase-variant strains by Congo red agar test. For potential phase-variant strains, pulsed-field gel electrophoresis was done to exclude the possibility of contamination. To investigate the mechanism of the biofilm-negative phase variation, PCR for each ica genes were done. Changes of ica genes detected by PCR were confirmed by southern hybridization, and their nucleotides were analyzed by DNA sequencing. Influence of ica genes and biofilm formation on capacity for adherence to biomedical material was evaluated by comparing the ability of adhering to polyurethane sur-face among a biofilm-negative phase-variant strain and its parent strain. A biofilm-negative phase-variant S. aureus strain was detected from 6 strains tested. icaC gene of the phase-variant strain was found to be inactivated by insertion of additional gene segment, IS256. The biofilm-negative phase-variant strain showed lower adher-ing capacity to polyurethane than its parent strain. This study shows that phase variation of ica gene occurs in S. aureus by insertion of IS256 also, and this biofilm-neg-ative phase variation reduces adhering capacity of the bacteria.


Subject(s)
Bacterial Adhesion/physiology , Biofilms/growth & development , Cell Adhesion Molecules/genetics , Comparative Study , Equipment Contamination/prevention & control , Mutagenesis, Insertional/methods , Mutagenesis, Site-Directed/genetics , Phase Transition , Polysaccharides, Bacterial/genetics , Polyurethanes , Species Specificity , Staphylococcus aureus/cytology , Structure-Activity Relationship
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