Literature DB >> 16426012

Reverse line blot assay for direct identification of seven Streptococcus agalactiae major surface protein antigen genes.

Zuotao Zhao1, Fanrong Kong, Gwendolyn L Gilbert.   

Abstract

We developed a multiplex PCR-based reverse line blot hybridization assay (mPCR/RLB) to detect the genes encoding members of the family of variable surface-localized proteins of Streptococcus agalactiae (group B streptococcus [GBS]), namely, Bca (Calpha), Rib, Epsilon (Epsilon/Alp1/Alp5), Alp2, Alp3, and Alp4, and the immunoglobulin A binding protein, Bac (Cbeta). We used the assay to identify these genes in a collection of well-characterized GBS isolates and reference strains. The results showed that mPCR/RLB avoids the common problems of cross-reaction and nontypability associated with protein typing using antisera. It is as sensitive as, but more practical than, separate gene-specific PCRs and would be suitable for large molecular epidemiological studies of GBS.

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Year:  2006        PMID: 16426012      PMCID: PMC1356620          DOI: 10.1128/CVI.13.1.145-149.2006

Source DB:  PubMed          Journal:  Clin Vaccine Immunol        ISSN: 1556-679X


  23 in total

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2.  Simultaneous detection and serotype identification of Streptococcus agalactiae using multiplex PCR and reverse line blot hybridization.

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3.  Molecular profiles of group B streptococcal surface protein antigen genes: relationship to molecular serotypes.

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Journal:  J Clin Microbiol       Date:  2002-02       Impact factor: 5.948

4.  Towards a genotyping system for Streptococcus agalactiae (group B streptococcus): use of mobile genetic elements in Australasian invasive isolates.

Authors:  Fanrong Kong; Diana Martin; Gregory James; Gwendolyn L Gilbert
Journal:  J Med Microbiol       Date:  2003-04       Impact factor: 2.472

5.  GP5+/6+ PCR followed by reverse line blot analysis enables rapid and high-throughput identification of human papillomavirus genotypes.

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Journal:  J Clin Microbiol       Date:  2002-03       Impact factor: 5.948

6.  Serotype identification of group B streptococci by PCR and sequencing.

Authors:  Fanrong Kong; Sonia Gowan; Diana Martin; Gregory James; Gwendolyn L Gilbert
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7.  Origin and utility of the reverse dot-blot.

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8.  Multilocus sequence typing of serotype III group B streptococcus and correlation with pathogenic potential.

Authors:  H Dele Davies; Nicola Jones; Thomas S Whittam; Sameer Elsayed; Naiel Bisharat; Carol J Baker
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9.  Comparison of DNA dot blot hybridization and lancefield capillary precipitin methods for group B streptococcal capsular typing.

Authors:  Stephanie M Borchardt; Betsy Foxman; Donald O Chaffin; Craig E Rubens; Patricia A Tallman; Shannon D Manning; Carol J Baker; Carl F Marrs
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10.  Multilocus sequence typing system for group B streptococcus.

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  10 in total

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2.  Evaluation of a multiplex PCR-based reverse line blot-hybridization assay for identification of serotype and surface protein antigens of Streptococcus agalactiae.

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Journal:  J Clin Microbiol       Date:  2006-10       Impact factor: 5.948

3.  Multiplex PCR-based reverse line blot assay for simultaneous detection of 22 virulence genes in uropathogenic Escherichia coli.

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6.  Expression of group B protective surface protein (BPS) by invasive and colonizing isolates of group B streptococci.

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7.  Serotype IX, a Proposed New Streptococcus agalactiae Serotype.

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8.  Human Streptococcus agalactiae strains in aquatic mammals and fish.

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9.  Antimicrobial susceptibility profiles, serotype distribution and virulence determinants among invasive, non-invasive and colonizing Streptococcus agalactiae (group B streptococcus) from Malaysian patients.

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10.  Status of group B streptococcal vaccine development.

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  10 in total

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