Whole genome and transcriptome analysis reveal MALDI-TOF MS and SDS-PAGE have limited performance for the detection of the key outer membrane protein in carbapenem-resistant Klebsiella pneumoniae isolates

被引:5
作者
Pinto, Naina Adren [1 ,2 ]
D'Souza, Roshan [1 ]
Hwang, In Sik [1 ,2 ]
Choi, Jongrak [1 ]
In, Yong Ha [3 ]
Park, Hyung Soon [3 ]
Ryu, Choong-Min [4 ,5 ]
Yong, Dongeun [1 ]
Lee, Kyungwon [1 ]
机构
[1] Yonsei Univ, Coll Med, Dept Lab Med, Seoul, South Korea
[2] Yonsei Univ, Brain Korea PLUS Project Med Sci 21, Seoul, South Korea
[3] ASTA Corp, Suwon, South Korea
[4] KRIBB, Mol Phytobacteriol Lab, Daejeon, South Korea
[5] Univ Sci & Technol, Sch Sci, Biosyst & Bioengn Program, Daejeon, South Korea
关键词
MALDI-TOF MS; outer membrane protein; transcriptomic analysis; Klebsiella pneumoniae; whole-genome sequencing; Immunology and Microbiology Section; Immune response; Immunity; PORIN GENE; SUSCEPTIBILITY; OMPK35;
D O I
10.18632/oncotarget.19005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To detect the outer membrane protein (OMP), which plays a key role in carbapenem resistance, whole-genome and transcriptome analysis of the clinical carbapenem-resistant Klebsiella pneumoniae was carried out. The index strain lacked both OmpK35 and OmpK36, whereas the other strains lacked only OmpK35. After SDS-PAGE, the putative OMP bands were excised and identified as OmpA and OmpK36. MALDI-TOF MS showed peaks at similar to 36 and similar to 38 kDa that corresponded to OmpA and OmpK36, respectively. In all the strains except YMC2014/03/P345, the similar to 38 kDa peaks were present. The K. pneumoniae ATCC 13883 isolate showed three bands on SDS-PAGE and three corresponding peaks on MALDI-TOF MS. The additional third peak at similar to 37 kDa corresponding to OmpK35 was observed. To verify OmpK35 peak detection in other K. pneumoniae isolates by MALDI-TOF MS, we analyzed six strains from our laboratory's strain bank. Whole genome sequence indicated that only two isolates had intact OmpK35. Both MALDI-TOF MS and SDS-PAGE did not show a similar to 37 kDa peak or an OmpK35 band as observed in the K. pneumoniae ATCC 13883 isolate. Separation using SDS-PAGE showed a single peak representing OmpA. Therefore, both SDS-PAGE and MALDI-TOF MS were not completely reliable for OMP detection because they fail to detect OmpK35. To the best of our knowledge, this is the first report on the performance of SDS-PAGE and MALDI-TOF MS for the detection of OMP's using whole-genome and RNA sequencing analyses.
引用
收藏
页码:84818 / 84826
页数:9
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