Bacterial strains, experimental reagents and instruments
The bacterial strains used were provided by the Laboratory of Peking University People's Hospital (Table S1), and the reagents and instruments used were provided by the laboratory of Tsinghua University (Tables S2 and S3).
Extraction of bacterial nucleic acid
The bacterial strains were propagated and cultured in 100 ml Luria broth . Nucleic acids were extracted from the four bacteria using the QIAamp cador Pathogen Mini Kit (QIAGEN, Germany) according to the methods suggested in manufacturer’s instructions. We used Nanodrop to measure the extracted nucleic acid concentrations and stored samples at –20 °C.
Design of primers and probes
The specific genes of bacterial strains were selected according to the GenBank database. The specific genes of E. coli and S. aureus were SWG-9 and coagulase COA gene, respectively. Primers and probes were designed for conserved regions in SWG-9 and coagulase COA gene sequences (Table S4 and S5). We used Oligo 7.0 and Primer Express 3.0 software to design and evaluate primers and probes for the nucleic acid sequence containing the site to be detected. The sequences were delivered to Thermo Fisher Scientific (CN) to synthesize the primers and probes. The 5 'end of the E. coli probe was labeled with 6-FAM fluorescent molecule, the 5' end of the S. aureus probe was labeled with VIC fluorescent molecule.
Workflow of the ddPCR system
We carried out ddPCR using the QX200 ddPCR system (Bio-Rad, CA) according to the manufacturer’s instructions. The QX200 ddPCR system (Bio-Rad, CA) consists of four steps: (1) preparation of the reaction mixture using a ddPCR amplification volume 20 µL (Table S6); (2) droplet generation; (3) ddPCR amplification (Table S7); and (4) droplet reading and analysis of results using QuantaSoft 3.0 software.
Detection of bacterial strains using a real-time quantitative PCR system
The SYBR Green real-time quantitative PCR system and the MGB probe real-time quantitative PCR system were used to quantify the gradient-diluted nucleic acid of E. coli standard strain (ATCC25922) to determine the sensitivity range of the two real-time quantitative PCR. The template dilution gradient (copies/µL) of ATCC25922 was 106, 105, 104, 103, 102, 101, 1, and 0. Each group of experiments was repeated three times in parallel.
Detection of bacterial strains by ddPCR system
We used the ddPCR system to quantify the gradient-diluted nucleic acid of E. coli (ATCC25922) to determine the sensitivity range of the ddPCR system. The template dilution gradient (copies/20 μl) of ATCC25922 were 105, 104, 103, 102, 25, 1.5625, and 0. Each group of experiments was repeated three times in parallel.
The ddPCR system simultaneously detects two bacterial strains
Various numbers of DNA templates, specific primers and probes (ATCC25922: 5'-FAM/3'MGB, ATCC25923: 5'-VIC/3'MGB) of the two bacterial strains were added to a ddPCR reaction system (Group A, bacteria counts of E. coli: bacteria counts of S. aureus = 10:1, Group B, bacteria counts of E. coli∶ bacteria counts of S. aureus = 1:10). We counted DNA template numbers of E. coli and S. aureus, and calculated the detection rate of the two bacteria.
Detection of blood samples of simulated bacteremia blood sample using the ddPCR system
The blood samples were obtained from the Department of Gastroenterological Surgery, Peking University People’s Hospital. All of the blood samples donors included in this study provided their informed consent. The study was approved by the Human Ethics Committee of the Peking University People’s Hospital (China). All methods were carried out in “accordance” with the approved guidelines and regulations. The blood collection tube were pretreated with EDTA anticoagulation. Three simulations of bacteremic blood samples were prepared, Group A: 100 μL of the serially-diluted suspensions of E. coli (ATCC25922) were injected into 400 μL of blood treated with EDTA . Group B: 100 μL of the serially diluted suspension of the S. aureus strain (ATCC25923) was injected into the 400 μL blood treated with EDTA . Group C: 100 µL of the ATCC25922 and ATCC25923 suspensions were diluted into gradients, then added to the blood samples with 400 µL EDTA. Extraction of nucleic acid from bacterial blood specimens was performed as follows: nucleic acid from bacterial blood specimens was extracted using a bacterial nucleic acid kit (Qiagen, Germany) We used 50 µl of solution buffer to elute DNA from the column and store at 80 °C. The extracted nucleic acid was detected using the ddPCR system. Repeat the test three times in parallel.
The detection results were statistically analyzed using SPSS 22.0, GraphPad Prism 5 and OriginPro 2016 software, and the linear dynamic range of the method was measured by R2 value.