Rapid and Sensitive Detection of Yersinia pestis Using Amplification of Plague Diagnostic Bacteriophages Monitored by Real-Time PCR
Figure 4
Dynamics of growth of phages φA1122 and L-413C on different concentrations of Y. pestis cells detected by qPCR.
The starting points of phage infection correspond to 100 PFU per 1 µl sample and are normalized to 1. A. The titer rise of φA1122. B. L-413C amplification.