نتایج جستجو برای: 16s rdna sequencing

تعداد نتایج: 149926  

Journal: :Journal of clinical microbiology 2004
Carol Iversen Michael Waddington Stephen L W On Stephen Forsythe

The phylogenetic relationships of Enterobacter sakazakii strains were investigated using 16S ribosomal DNA (rDNA) and hsp60 sequencing. Each analysis distributed E. sakazakii strains among four clusters, indicating substantial taxonomic heterogeneity. The E. sakazakii type strain 16S rDNA sequence was 97.8% similar to that of Citrobacter koseri but 97.0% similar to that of Enterobacter cloacae.

Journal: :The new microbiologica 2008
Marco Arosio Francesca Nozza Marco Rizzi Maurizio Ruggeri Pietro Casella Gianluca Beretta Annibale Raglio Antonio Goglio

Gene amplification using 16S rDNA primers has been proposed as a strategy for the diagnosis of bacterial meningitis. The aim of this study was to evaluate the performance of the MicroSeq 500 16S ribosomal DNA test (Applied Biosystems) from patients with suspected bacterial meningitis and CSF negative-culture in comparison to traditional methods. Twelve purulent culture-negative CSF samples were...

2012
Naomi J. Gadsby Alev Onen Sally-Anne Phillips Luke Tysall Steffen J. Breusch Hamish Simpson Jayshree Dave Elzbieta Czarniak Kate E. Templeton

16S rDNA PCR and sequencing are powerful tools for bacterial detection and identification, although their routine use is not currently widespread in the field of clinical microbiology. The availability of pyrosequencing now makes 16S rDNA assays more accessible to routine diagnostic laboratories, but this approach has had limited evaluation in general diagnostic practice. In this study we evalu...

2012
Priit Kasenõmm Jelena Štšepetova

Background: The aim of the study was to analyze the performance of PCR-DGGE based assay and its applicability as a tool for the identification of bacteria in the middle ear of children with otitis media with effusion (OME). Methods: The middle ear effusions from 20 children with OME were analyzed both by bacterial culture and by 16S rDNA-gene-targeted PCR assay, DGGE fingerprinting and sequenci...

Journal: :The Journal of veterinary medical science 2006
Hiraku Sasaki Eiichi Kawamoto Hidehiro Ueshiba Hiromi Amao Takuo Sawada

A 1344 bp fragment of the 16S ribosomal DNA (rDNA) sequence was used to determine the genetic relationship of Pasteurella pneumotropica isolates from laboratory rodents. A total of 30 nucleotide sequences of P. pneumotropica, including 24 wild strains, 3 reference strains, and 3 nucleotide sequences deposited in GenBank, were examined for heterogeneity of their 16S rDNA sequences. Phylogenetic ...

Background: Traditional dairy products are the main sources for probiotic bacteria. This study aimed to isolate and characterize the potentially probiotic Lactobacillus strains isolated from traditional dairy products in Iran. Methods: Microbial population of each dairy product was enriched and screened for acid- and bile- resistant strains. The isolates were ...

Journal: :Journal of medical microbiology 2014
Haiyin Wang Pengcheng Du Juan Li Yuanyuan Zhang Wen Zhang Na Han Patrick C Y Woo Chen Chen

Although 16S rRNA gene (rDNA) sequencing is the gold standard for categorizing bacteria or characterizing microbial communities its clinical utility is limited by bias in metagenomic studies, in either the experiments or the data analyses. To evaluate the efficiency of current metagenomic methods, we sequenced seven simulated samples of ten bacterial species mixed at different concentrations. T...

Journal: :BMC Veterinary Research 2006
M Matsuda A Tazumi S Kagawa T Sekizuka O Murayama JE Moore BC Millar

BACKGROUND At present, six accessible sequences of 16S rDNA from Taylorella equigenitalis (T. equigenitalis) are available, whose sequence differences occur at a few nucleotide positions. Thus it is important to determine these sequences from additional strains in other countries, if possible, in order to clarify any anomalies regarding 16S rDNA sequence heterogeneity. Here, we clone and sequen...

2017
Peggy S Lai Joseph G Allen Diane S Hutchinson Nadim J Ajami Joseph F Petrosino Thomas Winters Christopher Hug Gary R Wartenberg Jose Vallarino David C Christiani

OBJECTIVES To characterize the microbial environment of workers in academic mouse research facilities using endotoxin, 16S qPCR, and 16S amplicon sequencing. To determine whether the work microbiome contributes to the human microbiome of workers. METHODS We performed area air sampling from the animal rooms, dirty, middle, and setup cage wash locations in four academic mouse research facilitie...

Journal: :Journal of clinical pathology 2006
S K P Lau K H L Ng P C Y Woo K-T Yip A M Y Fung G K S Woo K-M Chan T-L Que K-Y Yuen

Using full 16S ribosomal RNA (rRNA) gene sequencing as the gold standard, 20 non-duplicating anaerobic Gram positive bacilli isolated from blood cultures were analysed by the MicroSeq 500 16S rDNA bacterial identification system. The MicroSeq system successfully identified 13 of the 20 isolates. Four and three isolates were misidentified at the genus and species level, respectively. Although th...

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