The aim of the present study was to investigate the efficiency of the gene derived from pv. (Bga) on the identification of Bga from the complex (Bcc) based on the COnsensus-DEgenerate Hybrid Oligonucleotide Primer (CODEHOP) strategy. A set of primers used for the specific amplification of the gene in Bga were designed according to the CODEHOP principle. A total of 1,644 bp of the gene sequence of Bga were acquired by CODEHOP amplification. The sequence was blasted in GenBank and it revealed an average of 86% similarity with the gene of nine genomovars of Bcc. A phylogenetic tree was constructed using the gene sequences. The microarray method was adopted to discriminate Bga from Bcc based on the specific probes designed upon the gene, and five genomovars of Bcc demonstrated a good discrimination from Bga on the microarray chip. CODEHOP strategy succeeded in amplification of the gene of Bga, which made it possible for the identification of Bga from five genomovars of Bcc.
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http://dx.doi.org/10.3892/etm.2018.7137 | DOI Listing |
Diagn Microbiol Infect Dis
February 2023
Facultad de Medicina, Unidad de Medicina Experimental, Universidad Nacional Autónoma de México, Mexico City, Mexico. Electronic address:
Burkholderia cepacia complex (Bcc) species are opportunistic pathogens widely distributed in the environment and often infect people with cystic fibrosis (CF). This study aims to determine which genomovars of the Bcc can cause infections in non-CF patients from a tertiary care hospital in Mexico and if they carry virulence factors that could increase their pathogenicity. We identified 23 clinical isolates that carry the recA gene.
View Article and Find Full Text PDFIndian J Med Microbiol
April 2022
Nitte (Deemed to be University), Division of Infectious Diseases, Nitte University Center for Science Education and Research, Deralakatte, Mangaluru, 575018, Karnataka, India. Electronic address:
Purpose: Burkholderia is a Gram-negative opportunistic bacterium capable of causing severe nosocomial infections. The aim of this study was to characterize Burkholderia cepacia complex and to compare different molecular methods used in its characterization.
Methods: In this study, 45 isolates of Burkholderia cepacia complex (Bcc) isolated from clinical cases were subjected to RAPD (Random amplified polymorphic DNA), recA-RFLP (Restriction fragment length polymorphism), 16SrDNA-RFLP, whole-cell protein analysis, recA DNA sequencing and biofilm assay.
PLoS One
May 2020
J. Craig Venter Institute, San Diego, CA, United States of America.
Transpl Infect Dis
June 2019
Cystic Fibrosis Center, IRCCS Ca' Granda Foundation, Milan, Italy.
Burkholderia cepacia complex (Bcc) includes several phenotypically similar but genotypically distinct gram-negative bacteria (GNB) that can colonize the respiratory tract of Cystic Fibrosis (CF) patients. Pathogens are difficult to treat due to intrinsic resistance to multiple antibiotics and are associated to a more rapid decline in lung function and to increased mortality, particularly after lung transplantation. For all these reasons, chronic infection by Burkholderia (B) cenocepacia is presently considered a relative or absolute contraindication in almost all lung transplant centres.
View Article and Find Full Text PDFExp Ther Med
March 2019
School of Life Sciences, Chongqing University, Shapingba, Chongqing 400030, P.R. China.
The aim of the present study was to investigate the efficiency of the gene derived from pv. (Bga) on the identification of Bga from the complex (Bcc) based on the COnsensus-DEgenerate Hybrid Oligonucleotide Primer (CODEHOP) strategy. A set of primers used for the specific amplification of the gene in Bga were designed according to the CODEHOP principle.
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