نتایج جستجو برای: 16s rdna
تعداد نتایج: 31200 فیلتر نتایج به سال:
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...
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 shiekh.fa@gmail.com 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 ...
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 ...
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...
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...
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...
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...
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...
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...
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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