» Articles » PMID: 7512093

PCR Primers and Probes for the 16S RRNA Gene of Most Species of Pathogenic Bacteria, Including Bacteria Found in Cerebrospinal Fluid

Overview
Specialty Microbiology
Date 1994 Feb 1
PMID 7512093
Citations 167
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Tea seedlings growth promotion by widely distributed and stress-tolerant PGPR from the acidic soils of the Kangra valley.

Thakur R, Rahi P, Gulati A, Gulati A BMC Microbiol. 2025; 25(1):102.

PMID: 40021986 PMC: 11869635. DOI: 10.1186/s12866-025-03811-0.


An environmental isolate of , 20EI1, reduces growth in an iron-dependent manner and alters secondary metabolism.

Wyman E, Grayburn W, Gilbert M, Lebar M, Lohmar J, Cary J Front Microbiol. 2025; 15:1514950.

PMID: 39902287 PMC: 11788345. DOI: 10.3389/fmicb.2024.1514950.


Methicillin-resistant Staphylococci in canine pyoderma in Thailand.

Putriningsih P, Phuektes P, Jittimanee S, Kampa J Vet World. 2023; 16(11):2340-2348.

PMID: 38152262 PMC: 10750743. DOI: 10.14202/vetworld.2023.2340-2348.


Possible Molecular Targeting of Biofilm-Associated Genes by Nano-Ag in Candida albicans.

Esfahani M, Khodavandi A, Alizadeh F, Bahador N Appl Biochem Biotechnol. 2023; 196(7):4205-4233.

PMID: 37922031 DOI: 10.1007/s12010-023-04758-6.


Molecular Characterization of spp., , and in Dairy Goat Kids with Diarrhea in Partial Regions of Shaanxi Province, China.

Yang X, Wang J, Huang S, Song J, Fan Y, Zhao G Animals (Basel). 2023; 13(18).

PMID: 37760322 PMC: 10526037. DOI: 10.3390/ani13182922.


References
1.
WILSON K, Blitchington R, GREENE R . Amplification of bacterial 16S ribosomal DNA with polymerase chain reaction. J Clin Microbiol. 1990; 28(9):1942-6. PMC: 268083. DOI: 10.1128/jcm.28.9.1942-1946.1990. View

2.
Woese C, Stackebrandt E, Macke T, Fox G . A phylogenetic definition of the major eubacterial taxa. Syst Appl Microbiol. 1985; 6:143-51. DOI: 10.1016/s0723-2020(85)80047-3. View

3.
Collins M, Wallbanks S, Lane D, Shah J, Nietupski R, Smida J . Phylogenetic analysis of the genus Listeria based on reverse transcriptase sequencing of 16S rRNA. Int J Syst Bacteriol. 1991; 41(2):240-6. DOI: 10.1099/00207713-41-2-240. View

4.
Bentley R, Leigh J, Collins M . Intrageneric structure of Streptococcus based on comparative analysis of small-subunit rRNA sequences. Int J Syst Bacteriol. 1991; 41(4):487-94. DOI: 10.1099/00207713-41-4-487. View

5.
Aguirre M, Collins M . Phylogenetic analysis of Alloiococcus otitis gen. nov., sp. nov., an organism from human middle ear fluid. Int J Syst Bacteriol. 1992; 42(1):79-83. DOI: 10.1099/00207713-42-1-79. View