Accurate identification and epidemiological characterization of Burkholderia cepacia complex: an update

被引:58
|
作者
Ragupathi, Naveen Kumar Devanga [1 ]
Veeraraghavan, Balaji [1 ]
机构
[1] Christian Med Coll & Hosp, Dept Clin Microbiol, Vellore 632004, Tamil Nadu, India
关键词
Burkholderia cepacia complex; Cystic fibrosis; Hospital acquired infections; recA; hisA; rpsU; DESORPTION IONIZATION-TIME; CYSTIC-FIBROSIS PATIENTS; RALSTONIA-PICKETTII; PSEUDOMONAS-CEPACIA; STENOTROPHOMONAS-MALTOPHILIA; RESPIRATORY SECRETIONS; ANTIBIOTIC-RESISTANCE; POLYPHASIC TAXONOMY; PANDORAEA-SPUTORUM; BETA-LACTAMASES;
D O I
10.1186/s12941-019-0306-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacteria belonging to the Burkholderia cepacia complex (Bcc) are among the most important pathogens isolated from cystic fibrosis (CF) patients and in hospital acquired infections (HAI). Accurate identification of Bcc is questionable by conventional biochemical methods. Clonal typing of Burkholderia is also limited due to the problem with identification. Phenotypic identification methods such as VITEK2, protein signature identification methods like VITEK MS, Bruker Biotyper, and molecular targets such as 16S rRNA, recA, hisA and rpsU were reported with varying level of discrimination to identify Bcc. rpsU and/or 16S rRNA sequencing, VITEK2, VITEK MS and Bruker Biotyper could discriminate between Burkholderia spp. and non-Burkholderia spp. Whereas, Bcc complex level identification can be given by VITEK MS, Bruker Biotyper, and 16S rRNA/rpsU/recA/hisA sequencing. For species level identification within Bcc hisA or recA sequencing are reliable. Identification of Bcc is indispensable in CF patients and HAI to ensure appropriate antimicrobial therapy.
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页数:10
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