Comparative analysis of different methods used for molecular characterization of Burkholderia cepacia complex isolated from noncystic fibrosis conditions

被引:2
|
作者
Modapathi, Shraddha Rani [1 ]
Rohit, Anusha [2 ]
Aditya, Vankadari [1 ]
Shetty, Varsha Prakash [1 ]
Kotian, Akshatha [1 ]
Mohanapriya [2 ]
Rai, Praveen [1 ]
Karunasagar, Indrani [1 ]
Deekshit, Vijaya Kumar [1 ]
机构
[1] Nitte Deemed Univ, Nitte Univ, Div Infect Dis, Ctr Sci Educ & Res, Mangaluru 575018, Karnataka, India
[2] Madras Med Mission, Dept Microbiol, Chennai 600037, Tamil Nadu, India
关键词
Burkholderia cepacia complex; recA sequencing; Biofilm; Antimicrobial resistance; Microbial pathogenesis; CYSTIC-FIBROSIS; PSEUDOMONAS-AERUGINOSA; BIOFILM FORMATION; IDENTIFICATION; GENOMOVARS; VIETNAMIENSIS; CENOCEPACIA;
D O I
10.1016/j.ijmmb.2021.09.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. Results: Of the 45 isolates tested, 97.7% were sensitive to ceftazidime, 82.2% were sensitive to Cotrimoxazole, 73.3% were sensitive to meropenem, 55.5% were sensitive to minocycline and 42.2% were sensitive to levofloxacin. Majority of the isolates harbored all the tested virulence genes except bpeA and cblA. The RAPD generated 11 groups (R1-R11), recA-RFLP 10 groups (A1-A10), 16SrRNA-RFLP 5 groups (S1-S5) and SDS-PAGE (Sodium Dodecyl Sulphate-Polyacrylamide gel electrophoresis) whole cell protein analysis revealed 12 groups (C1-C12). recA sequencing revealed that most of the isolates belonging to the genomovar III Burkholderia cenocepacia. Though all the methods are found to be efficient in differentiating Burkholderia spp., recA-RFLP was highly discriminatory at 96% similarity value. The study also identified a new strain Burkholderia pseudomultivorans for the first time in the country. Further, recA sequencing could identify the strains to species level. Majority of the multidrug-resistant strains also showed moderate to strong biofilm-forming ability, which further contributes to the virulence characteristics of the pathogens. Conclusions: The study highlights the importance of combination of molecular methods to characterize Burkholderia cepacia complex. Molecular typing of these human pathogens yields important information for the clinicians in order to initiate the most appropriate therapy in the case of severe infections and to implement preventive measures for the effective control of transmission of Burkholderia spp.
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页码:74 / 80
页数:7
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