Rapid bacterial detection and antibiotic susceptibility testing in whole blood using one-step, high throughput blood digital PCR

被引:86
作者
Abram, Timothy J. [1 ]
Cherukury, Hemanth [2 ,3 ]
Ou, Chen-Yin [1 ]
Tam Vu [2 ,4 ]
Toledano, Michael [2 ]
Li, Yiyan [2 ,5 ]
Grunwald, Jonathan T. [1 ]
Toosky, Melody N. [1 ]
Tifrea, Delia F. [6 ]
Slepenkin, Anatoly [6 ]
Chong, Jonathan [2 ]
Kong, Lingshun [2 ]
Del Pozo, Domenica Vanessa [2 ]
Kieu Thai La [2 ]
Labanieh, Louai [2 ]
Zimak, Jan [2 ]
Shen, Byron [1 ]
Huang, Susan S. [7 ]
Gratton, Enrico [4 ,8 ]
Peterson, Ellena M. [6 ]
Zhao, Weian [2 ,3 ,4 ,9 ,10 ,11 ]
机构
[1] Velox Biosyst, 5 Mason,Suite 160, Irvine, CA 92618 USA
[2] Univ Calif Irvine, Sue & Bill Gross Stein Cell Res Ctr, 845 Hlth Sci Rd,Suite 3027, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Pharmaceut Sci, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[5] Ft Lewis Coll, Dept Phys & Engn, Durango, CO 81301 USA
[6] Univ Calif Irvine, Dept Pathol & Lab Med, Irvine, CA 92697 USA
[7] UCI Sch Med, Div Infect Dis, Irvine, CA 92697 USA
[8] Univ Calif Irvine, Lab Fluorescence Dynam, Irvine, CA 92697 USA
[9] Univ Calif Irvine, Chao Family Comprehens Canc Ctr, Irvine, CA 92697 USA
[10] Univ Calif Irvine, Edwards Life Sci Ctr Adv Cardiovasc Technol, Irvine, CA 92697 USA
[11] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
关键词
STREAM INFECTIONS; ANTIMICROBIAL THERAPY; IDENTIFICATION; RESISTANCE; AMPLIFICATION; DROPLETS; IMPACT;
D O I
10.1039/c9lc01212e
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sepsis due to antimicrobial resistant pathogens is a major health problem worldwide. The inability to rapidly detect and thus treat bacteria with appropriate agents in the early stages of infections leads to excess morbidity, mortality, and healthcare costs. Here we report a rapid diagnostic platform that integrates a novel one-step blood droplet digital PCR assay and a high throughput 3D particle counter system with potential to perform bacterial identification and antibiotic susceptibility profiling directly from whole blood specimens, without requiring culture and sample processing steps. Using CTX-M-9 family ESBLs as a model system, we demonstrated that our technology can simultaneously achieve unprecedented high sensitivity (10 CFU per ml) and rapid sample-to-answer assay time (one hour). In head-to-head studies, by contrast, real time PCR and BioRad ddPCR only exhibited a limit of detection of 1000 CFU per ml and 50100 CFU per ml, respectively. In a blinded test inoculating clinical isolates into whole blood, we demonstrated 100% sensitivity and specificity in identifying pathogens carrying a particular resistance gene. We further demonstrated that our technology can be broadly applicable for targeted detection of a wide range of antibiotic resistant genes found in both Gram-positive (vanA, nuc, and mecA) and Gram-negative bacteria, including ESBLs (bla(CTX-M-1) and bla(CTX-M-2) families) and CREs (bla(OXA-48) and bla(KPC)), as well as bacterial speciation (E. coli and Klebsiella spp.) and pan-bacterial detection, without requiring blood culture or sample processing. Our rapid diagnostic technology holds great potential in directing early, appropriate therapy and improved antibiotic stewardship in combating bloodstream infections and antibiotic resistance.
引用
收藏
页码:477 / 489
页数:13
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