Literature DB >> 2469620

Broad range DNA probes for detecting and amplifying eubacterial nucleic acids.

K Chen1, H Neimark, P Rumore, C R Steinman.   

Abstract

In this report we describe and characterize two oligomer probes that are broadly homologous to conserved eubacterial 16S ribosomal RNA (rRNA) sequences not present in human 18 rRNA or human mitochondrial 12S rRNA. One or both of the probes can detect all of 23 phylogenetically diverse eubacterial nucleic acids against which they were tested by dot blot hybridization. A sensitivity of about 1 bacterium per 10 eukaryotic cells was achieved. By using these oligomer sequences or their complements as primers in the polymerase chain reaction (PCR), the equivalent of 1 pg of E. coli DNA was detected in the presence of a large excess of eukaryotic DNA. Information useful for partial phylogenetic classification of detected organisms may be obtained by direct sequence analysis of the amplified DNA and comparison with known sequences or catalogs. Such broadly homologous probes offer advantages over more narrowly specific probes for detecting organisms whose identity is unknown. They could thus be employed for recognizing infection by organisms that cannot be cultured as may occur, for example, in tissue culture or in plant or animal diseases of unknown cause, provided the probes fail to hybridize with host nucleic acids.

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Year:  1989        PMID: 2469620     DOI: 10.1016/0378-1097(89)90139-0

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  29 in total

1.  High-density microarray of small-subunit ribosomal DNA probes.

Authors:  Kenneth H Wilson; Wendy J Wilson; Jennifer L Radosevich; Todd Z DeSantis; Vijay S Viswanathan; Thomas A Kuczmarski; Gary L Andersen
Journal:  Appl Environ Microbiol       Date:  2002-05       Impact factor: 4.792

2.  Real-time PCR for detection and differentiation of gram-positive and gram-negative bacteria.

Authors:  Sven Klaschik; Lutz E Lehmann; Ansgar Raadts; Malte Book; Andreas Hoeft; Frank Stuber
Journal:  J Clin Microbiol       Date:  2002-11       Impact factor: 5.948

3.  Comparison of different decontamination methods for reagents to detect low concentrations of bacterial 16S DNA by real-time-PCR.

Authors:  Sven Klaschik; Lutz E Lehmann; Ansgar Raadts; Andreas Hoeft; Frank Stuber
Journal:  Mol Biotechnol       Date:  2002-11       Impact factor: 2.695

4.  Amplification of bacterial 16S ribosomal DNA with polymerase chain reaction.

Authors:  K H Wilson; R B Blitchington; R C Greene
Journal:  J Clin Microbiol       Date:  1990-09       Impact factor: 5.948

Review 5.  Impact of 16S rRNA gene sequence analysis for identification of bacteria on clinical microbiology and infectious diseases.

Authors:  Jill E Clarridge
Journal:  Clin Microbiol Rev       Date:  2004-10       Impact factor: 26.132

6.  Endocarditis caused by culture-negative organisms visible by Brown and Brenn staining: utility of PCR and DNA sequencing for diagnosis.

Authors:  M B Wilck; Y Wu; J G Howe; J Y Crouch; S C Edberg
Journal:  J Clin Microbiol       Date:  2001-05       Impact factor: 5.948

7.  Polymerase chain reaction in the diagnosis of bacterial endophthalmitis.

Authors:  K L Therese; A R Anand; H N Madhavan
Journal:  Br J Ophthalmol       Date:  1998-09       Impact factor: 4.638

8.  Comparison of phenotypic and genotypic techniques for identification of unusual aerobic pathogenic gram-negative bacilli.

Authors:  Y W Tang; N M Ellis; M K Hopkins; D H Smith; D E Dodge; D H Persing
Journal:  J Clin Microbiol       Date:  1998-12       Impact factor: 5.948

Review 9.  Sequence-based identification of microbial pathogens: a reconsideration of Koch's postulates.

Authors:  D N Fredricks; D A Relman
Journal:  Clin Microbiol Rev       Date:  1996-01       Impact factor: 26.132

10.  Restriction fragment length polymorphism analysis of 16S ribosomal DNA of Streptococcus and Enterococcus species of bovine origin.

Authors:  B M Jayarao; J J Doré; S P Oliver
Journal:  J Clin Microbiol       Date:  1992-09       Impact factor: 5.948

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