2014
DOI: 10.1590/s0036-46652014000100004
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Evaluation of Four Different Dna Extraction Methods in Coagulase-Negative Staphylococci Clinical Isolates

Abstract: Currently there are several methods to extract bacterial DNA based on different principles. However, the amount and the quality of the DNA obtained by each one of those methods is highly variable and microorganism dependent, as illustrated by coagulase-negative staphylococci (CoNS) which have a thick cell wall that is difficult to lyse. This study was designed to compare the quality and the amount of CoNS DNA, extracted by four different techniques: two in-house protocols and two commercial kits. DNA amount an… Show more

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Cited by 33 publications
(26 citation statements)
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“…qnrS plasmidresistance genes was performed using polymerase chain reaction specific primers (Table 1) [24]. Plasmid DNA was extracted by boiling [25]. PCR amplifications were performed in a thermocycler (Gene Amp PCR System 9700, Applied Biosystems, USA) as follows: 94°C for 5 minutes and 35 cycles of 5 minutes at 72°C, 1 minute at specific annealing temperature for each primer, and 1 minute at 72°C.…”
Section: Detection Of Qnr-mentioning
confidence: 99%
“…qnrS plasmidresistance genes was performed using polymerase chain reaction specific primers (Table 1) [24]. Plasmid DNA was extracted by boiling [25]. PCR amplifications were performed in a thermocycler (Gene Amp PCR System 9700, Applied Biosystems, USA) as follows: 94°C for 5 minutes and 35 cycles of 5 minutes at 72°C, 1 minute at specific annealing temperature for each primer, and 1 minute at 72°C.…”
Section: Detection Of Qnr-mentioning
confidence: 99%
“…Deoxyribonucleic acid (DNA) for PCR was extracted using the QIAamp DNA mini kit (Qiagen) as described by Oliveira et al (25) .The SCCmec types and subtypes I, II, III, IVa, IVb, IVc, IVd, and V and mecA were investigated using the multiplex PCR designed by Zhang et al (26) with the following modifications: the PCR reaction mixtures contained 1.5mM MgCl 2 and 1.15 unit of Platinum Taq . Methicillin-resistant isolates that did not produce PCR products using any of the primers tested were considered nontypable.…”
Section: Determination Of the Sccmec Types Among All The Consmentioning
confidence: 99%
“…Since population densities were very low even for symptomatic stalk samples, the extraction protocol needs be one that maintain the maximum range of DNA total on samples instead of to try keep it clean and purified. Oliveira et al (2014) stated that the quality of extracted DNA is important when sequencing the samples, or when a long sample storage time is required, or when constructing genomic libraries for future use. Furthermore it's common to extract DNA just boiling when the bacteria is gram-negative, Nogueira et al (2004), did not find positive results on RAPD-PCR when extracted DNA of Gram-positive bacteria by boiling while when they did the same method for Gram-negative the results were positive in PCR.…”
Section: Resultsmentioning
confidence: 99%