A real-time PCR assay for the rapid determination of 16S rRNA genotype in Vibrio vulnificus

2007 ◽  
Vol 68 (2) ◽  
pp. 376-384 ◽  
Author(s):  
Michael C.L. Vickery ◽  
William B. Nilsson ◽  
Mark S. Strom ◽  
Jessica L. Nordstrom ◽  
Angelo DePaola
2013 ◽  
Vol 27 (4) ◽  
pp. 328-332 ◽  
Author(s):  
Stellan Håkansson ◽  
Karin Källén ◽  
Maria Bullarbo ◽  
Per-Åke Holmgren ◽  
Katarina Bremme ◽  
...  

2010 ◽  
Vol 164 (1-2) ◽  
pp. 30-34 ◽  
Author(s):  
Rosana Gainotti ◽  
Carmen Ricarte ◽  
Beatriz Ebekian ◽  
Cristina Videla ◽  
Guadalupe Carballal ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Yousun Chung ◽  
Taek Soo Kim ◽  
Young Gi Min ◽  
Yun Ji Hong ◽  
Jeong Su Park ◽  
...  

Staphylococci are the leading cause of nosocomial blood stream infections. Fast and accurate identification of staphylococci and confirmation of their methicillin resistance are crucial for immediate treatment with effective antibiotics. A multiplex real-time PCR assay that targetsmecA,femAspecific forS. aureus,femAspecific forS. epidermidis,16S rRNAfor universal bacteria, and16S rRNAspecific for staphylococci was developed and evaluated with 290 clinical blood culture samples containing Gram-positive cocci in clusters (GPCC). For the 262 blood cultures identified to the species level with the MicroScan WalkAway system (Siemens Healthcare Diagnostics, USA), the direct real-time PCR assay of positive blood cultures showed very good agreement for the categorization of staphylococci into methicillin-resistantS. aureus(MRSA), methicillin-susceptibleS. aureus(MSSA), methicillin-resistantS. epidermidis(MRSE), methicillin-susceptibleS. epidermidis(MSSE), methicillin-resistant non-S. epidermidisCoNS (MRCoNS), and methicillin-susceptible non-S. epidermidisCoNS (MSCoNS) (κ=0.9313). The direct multiplex real-time PCR assay of positive blood cultures containing GPCC can provide essential information at the critical point of infection with a turnaround time of no more than 4 h. Further studies should evaluate the clinical outcome of using this rapid real-time PCR assay in glycopeptide antibiotic therapy in clinical settings.


2022 ◽  
Author(s):  
Vemula Harshini ◽  
S.M.K. Karthickeyan ◽  
K.G P. Kumarasamy ◽  
Tirumurugaan ◽  
C. Jeevan

Abstract A SYBR green real-time PCR assay was developed to find out the sex skewness in bovine sex-sorted semen samples. The qPCR assay of PLP and SRY genes revealed the mean values of X- and Y-bearing spermatozoa as 50.24 ± 0.65 and 49.75 ± 0.62 per cent in unsorted, and 91.80 ± 0.79 and 8.20 ± 0.73 per cent in X-enriched semen samples respectively.. The amplification efficiencies of the PLP and SRY primers were 99.25 and 98.03 per cent respectively. The method was validated by a series of repeatability and reproducibility assays which revealed low co-efficients of variations as 2.19 and 3.12 per cent respectively Thus becoming a reliable and inexpensive tool to evaluate the sorted semen on routine basis and validation of other sperm sexing technologies.


2007 ◽  
Vol 77 (5) ◽  
pp. 814-817 ◽  
Author(s):  
Narisara Chantratita ◽  
Wasun Chantratita ◽  
Vanaporn Wuthiekanun ◽  
Nicholas P. J. Day ◽  
Direk Limmathurotsakul ◽  
...  

2001 ◽  
Vol 93 (1-2) ◽  
pp. 181-188 ◽  
Author(s):  
Libin Ma ◽  
Hans A.R. Bluyssen ◽  
Marc De Raeymaeker ◽  
Veerle Laurysens ◽  
Niels van der Beek ◽  
...  

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