Rapid and sensitive detection of Yersinia pestis using amplification of plague diagnostic bacteriophages monitored by real-time PCR

• Published in: PloS one 2010-06, Vol.5 (6), p.e11337-e11337
• Main Authors: Sergueev, Kirill V, He, Yunxiu, Borschel, Richard H, Nikolich, Mikeljon P, Filippov, Andrey A
• Format: Article
• Language: English
• Subjects: Amplification; Bacteria; Bacterial infections; Bacteriophages - genetics; Bacteriophages - isolation & purification; Base Sequence; Deoxyribonucleic acid; Diagnostic software; Diagnostic systems; DNA; DNA Primers; DNA, Viral - analysis; Ethylenediaminetetraacetic acids; Genomes; Humans; Infections; Lysis; Medical diagnosis; Medical laboratories; Medical research; Meningitis; Microbiology; Microbiology/Applied Microbiology; Microbiology/Environmental Microbiology; Microbiology/Medical Microbiology; Mutagenesis; Pathogens; Phages; Plague; Plague - diagnosis; Polymerase chain reaction; Polymerase Chain Reaction - methods; Primers; Public health; Quantum dots; Real time; Sensitivity and Specificity; Studies; Yersinia pestis; Yersinia pestis - genetics; Yersinia pestis - isolation & purification; Yersinia pestis - virology
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0011337

Yersinia pestis, the agent of plague, has caused many millions of human deaths and still poses a serious threat to global public health. Timely and reliable detection of such a dangerous pathogen is of critical importance. Lysis by specific bacteriophages remains an essential method of Y. pestis detection and plague diagnostics. The objective of this work was to develop an alternative to conventional phage lysis tests--a rapid and highly sensitive method of indirect detection of live Y. pestis cells based on quantitative real-time PCR (qPCR) monitoring of amplification of reporter Y. pestis-specific bacteriophages. Plague diagnostic phages phiA1122 and L-413C were shown to be highly effective diagnostic tools for the detection and identification of Y. pestis by using qPCR with primers specific for phage DNA. The template DNA extraction step that usually precedes qPCR was omitted. phiA1122-specific qPCR enabled the detection of an initial bacterial concentration of 10(3) CFU/ml (equivalent to as few as one Y. pestis cell per 1-microl sample) in four hours. L-413C-mediated detection of Y. pestis was less sensitive (up to 100 bacteria per sample) but more specific, and thus we propose parallel qPCR for the two phages as a rapid and reliable method of Y. pestis identification. Importantly, phiA1122 propagated in simulated clinical blood specimens containing EDTA and its titer rise was detected by both a standard plating test and qPCR. Thus, we developed a novel assay for detection and identification of Y. pestis using amplification of specific phages monitored by qPCR. The method is simple, rapid, highly sensitive, and specific and allows the detection of only live bacteria.