نتایج جستجو برای: 16s rdna

تعداد نتایج: 31200  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه کردستان - دانشکده کشاورزی 1391

سوختگی برگی باکتریایی درختچه سیاه تلو (christ’s thorn)، بیماری جدیدی است که تاکنون جایگاه دقیق تاکسونومیکی عامل بیماری مشخص نشده است. تحقیق حاضر به منظور تعیین جایگاه تاکسونومیکی باکتری عامل بیماری، از طریق بررسی ژن 16s rdnaو آنالیز پروفیل اسیدچرب باکتری عامل بیماری و مقایسه آن با جدایه های استاندارد صورت گرفت. در این بررسی از 15 جدایه که در طی بهار و تابستان سال های 86 و 87، از برگ های درختچه...

2012
Farooq A Shiekh

Correspondence: Farooq A Shiekh URMITE, Faculté de Médecine, 27 Bd Jean Moulin, 13385 Marseille Cedex 5, France Tel +33 4 91 32 44 80 Fax +33 4 91 38 77 72 Email [email protected] Dear editor With great interest, I read a recent article published in the International Journal of Nanomedicine by Guo et al. This study involved an analysis of calcifying nanoparticles to determine the presence of ...

2009
F Gu Y Li C Zhou D.T.W Wong C.M Ho F Qi W Shi

Human saliva can be separated by centrifugation into cell pellet and cell-free supernatant, which are called cellular phase and liquid phase in this study. While it is well documented that the cellular phase of saliva contains hundreds of oral bacteria species, little is known whether the liquid phase of saliva contains any information related to oral microbiota. In this study, we analyzed the ...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2012
Mouhamad Al Masalma Michel Lonjon Hervé Richet Henry Dufour Pierre-Hugues Roche Michel Drancourt Didier Raoult Pierre-Edouard Fournier

BACKGROUND The bacterial flora involved in brain abscess is often complex. In a previous study, using a metagenomic approach based on 16S ribosomal DNA (rDNA) amplification, we demonstrated that the diversity of the microbial flora involved in these infections was underestimated. METHODS We performed a 16S rDNA-based metagenomic analysis of cerebral abscesses from patients diagnosed from 2006...

Journal: :International journal of systematic and evolutionary microbiology 2004
Bozena Korczak Henrik Christensen Stefan Emler Joachim Frey Peter Kuhnert

Sequences of the gene encoding the beta-subunit of the RNA polymerase (rpoB) were used to delineate the phylogeny of the family Pasteurellaceae. A total of 72 strains, including the type strains of the major described species as well as selected field isolates, were included in the study. Selection of universal rpoB-derived primers for the family allowed straightforward amplification and sequen...

Journal: :FEMS microbiology letters 1997
A Ibrahim W Liesack A G Steigerwalt D J Brenner E Stackebrandt R M Robins-Browne

Thirty-eight bacterial isolates from raw milk samples in Queensland, Australia were identified as members of the genus Yersinia on the basis of biochemical profile, ability to hybridize with a genus-specific DNA probe, comparative 16S rDNA sequence analysis, and the presence of characteristic 16S rDNA signature nucleotides which occur in all Yersinia spp. Twenty-five of these isolates reacted w...

Journal: :PLoS ONE 2007
Lam Tran-Hung Ny Tran-Thi Gérard Aboudharam Didier Raoult Michel Drancourt

BACKGROUND Dental pulp is used for PCR-based detection of DNA derived from host and bacteremic microorganims. Current protocols require odontology expertise for proper recovery of the dental pulp. Dental pulp specimen exposed to laboratory environment yields contaminants detected using universal 16S rDNA-based detection of bacteria. METHODOLOGY/PRINCIPAL FINDINGS We developed a new protocol b...

Journal: :Environmental microbiology 2014
Ramiro Logares Shinichi Sunagawa Guillem Salazar Francisco M Cornejo-Castillo Isabel Ferrera Hugo Sarmento Pascal Hingamp Hiroyuki Ogata Colomban de Vargas Gipsi Lima-Mendez Jeroen Raes Julie Poulain Olivier Jaillon Patrick Wincker Stefanie Kandels-Lewis Eric Karsenti Peer Bork Silvia G Acinas

Sequencing of 16S rDNA polymerase chain reaction (PCR) amplicons is the most common approach for investigating environmental prokaryotic diversity, despite the known biases introduced during PCR. Here we show that 16S rDNA fragments derived from Illumina-sequenced environmental metagenomes (mi tags) are a powerful alternative to 16S rDNA amplicons for investigating the taxonomic diversity and s...

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...

2014
Fumika Hotta Hiroshi Eguchi Takeshi Naito Yoshinori Mitamura Kohei Kusujima Tomomi Kuwahara

BACKGROUND In clinical settings, bacterial infections are usually diagnosed by isolation of colonies after laboratory cultivation followed by species identification with biochemical tests. However, biochemical tests result in misidentification due to similar phenotypes of closely related species. In such cases, 16S rDNA sequence analysis is useful. Herein, we report the first case of an Achromo...

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