Literature DB >> 7512093

PCR primers and probes for the 16S rRNA gene of most species of pathogenic bacteria, including bacteria found in cerebrospinal fluid.

K Greisen1, M Loeffelholz, A Purohit, D Leong.   

Abstract

A set of broad-range PCR primers for the 16S rRNA gene in bacteria were tested, along with three series of oligonucleotide probes to detect the PCR product. The first series of probes is broad in range and consists of a universal bacterial probe, a gram-positive probe, a Bacteroides-Flavobacterium probe, and two probes for other gram-negative species. The second series was designed to detect PCR products from seven major bacterial species or groups frequently causing meningitis: Neisseria meningitidis, Haemophilus influenzae, Streptococcus pneumoniae, S. agalactiae, Escherichia coli and other enteric bacteria, Listeria monocytogenes, and Staphylococcus aureus. The third series was designed for the detection of DNA from species or genera commonly considered potential contaminants of clinical samples, including cerebrospinal fluid (CSF): Bacillus, Corynebacterium, Propionibacterium, and coagulase-negative Staphylococcus spp. The primers amplified DNA from all 124 different species of bacteria tested. Southern hybridization testing of the broad-range probes with washes containing 3 M tetramethylammonium chloride indicated that this set of probes correctly identified all but two of the 102 bacterial species tested, the exceptions being Deinococcus radiopugnans and Gardnerella vaginalis. The gram-negative and gram-positive probes hybridized to isolates of two newly characterized bacteria, Alloiococcus otitis and Rochalimaea henselii, as predicted by Gram stain characteristics. The CSF pathogen and contaminant probe sequences were compared with available sequence information and with sequencing data for 32 different species. Testing of the CSF pathogen and contaminant probes against DNA from over 60 different strains indicated that, with the exception of the coagulase-negative Staphylococcus probes, these probes provided the correct identification of bacterial species known to be found in CSF.

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Year:  1994        PMID: 7512093      PMCID: PMC263034          DOI: 10.1128/jcm.32.2.335-351.1994

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  26 in total

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Authors:  C R Woese; E Stackebrandt; T J Macke; G E Fox
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Authors:  K H Wilson; R B Blitchington; R C Greene
Journal:  J Clin Microbiol       Date:  1990-09       Impact factor: 5.948

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Authors:  R W Bentley; J A Leigh; M D Collins
Journal:  Int J Syst Bacteriol       Date:  1991-10

4.  Isolation and restriction endonuclease analysis of mycobacterial DNA.

Authors:  R Patel; J T Kvach; P Mounts
Journal:  J Gen Microbiol       Date:  1986-02

5.  Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries.

Authors:  W I Wood; J Gitschier; L A Lasky; R M Lawn
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

6.  Rapid identification of cell wall components as a guide to the classification of aerobic coryneform bacteria from human skin.

Authors:  D G Pitcher
Journal:  J Med Microbiol       Date:  1977-11       Impact factor: 2.472

7.  Phylogenetic analysis of the genus Listeria based on reverse transcriptase sequencing of 16S rRNA.

Authors:  M D Collins; S Wallbanks; D J Lane; J Shah; R Nietupski; J Smida; M Dorsch; E Stackebrandt
Journal:  Int J Syst Bacteriol       Date:  1991-04

8.  Phylogenetic analysis of Alloiococcus otitis gen. nov., sp. nov., an organism from human middle ear fluid.

Authors:  M Aguirre; M D Collins
Journal:  Int J Syst Bacteriol       Date:  1992-01

9.  Quantitation of bacteria in cerebrospinal fluid and blood of children with meningitis and its diagnostic significance.

Authors:  L J La Scolea; D Dryja
Journal:  J Clin Microbiol       Date:  1984-02       Impact factor: 5.948

10.  An unusual Neisseria isolated from conjunctival cultures in rural Egypt.

Authors:  H Mazloum; P A Totten; G F Brooks; C R Dawson; S Falkow; J F James; J S Knapp; J M Koomey; C J Lammel; D Peters
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  159 in total

1.  Fluorescent In situ hybridization allows rapid identification of microorganisms in blood cultures.

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Review 2.  Molecular bacteriology: a diagnostic tool for the millennium.

Authors:  T L Pitt; N A Saunders
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3.  Contamination and sensitivity issues with a real-time universal 16S rRNA PCR.

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4.  Comparison of 16S rRNA gene PCR and BACTEC 9240 for detection of neonatal bacteremia.

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5.  One-step heminested PCR for amplification of Neisseria meningitidis DNA in cerebrospinal fluid.

Authors:  J H Atobe; M H Hirata; S Hoshino-Shimizu; M R Schmal; E M Mamizuka
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6.  Rapid detection of sepsis complicating acute necrotizing pancreatitis using polymerase chain reaction.

Authors:  W Z Zhang; T Q Han; Y Q Tang; S D Zhang
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Review 7.  PCR in diagnosis of infection: detection of bacteria in cerebrospinal fluids.

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8.  Rapid detection of Shigella species in environmental sewage by an immunocapture PCR with universal primers.

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9.  Direct identification of bacteria from positive blood cultures by amplification and sequencing of the 16S rRNA gene: evaluation of BACTEC 9240 instrument true-positive and false-positive results.

Authors:  Q Qian; Y W Tang; C P Kolbert; C A Torgerson; J G Hughes; E A Vetter; W S Harmsen; S O Montgomery; F R Cockerill; D H Persing
Journal:  J Clin Microbiol       Date:  2001-10       Impact factor: 5.948

Review 10.  Molecular detection of antimicrobial resistance.

Authors:  A C Fluit; M R Visser; F J Schmitz
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