TY - JOUR
T1 - Color-coded molecular beacons for multiplex PCR screening assays
AU - Marras, Salvatore A.E.
AU - Tyagi, Sanjay
AU - Antson, Dan Oscar
AU - Kramer, Fred Russell
N1 - Funding Information:
This research was supported by National Institutes of Health Grant R01 EB000277 and by National Institutes of Health Grant R01 CA227291. The open access charge for the publication of this paper was supported by the laboratory’s (Public Health Research Institute, Rutgers University) share of the income received from the nonexclusive licensing of molecular beacons technology by PHRI Properties, Inc., which is a nonprofit corporation wholly owned by Rutgers University. Neither PHRI Properties, Inc., nor any of the approximately 75 molecular beacons licensees, had any role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors are grateful to Diana Vargas-Gold for thoughtful discussions and critical review of the manuscript.
Publisher Copyright:
© 2019 Marras et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2019/3
Y1 - 2019/3
N2 - The number of different fluorescent colors that can be distinguished in a PCR screening assay restricts the number of different targets that can be detected. If only six colors can be distinguished, and the probe for each target is labeled with a unique color, then only six different targets can be identified. Yet, it is often desirable to identify more targets. For instance, the rapid identification of which bacterial species (if any) is present in a patient’s normally sterile blood sample, out of a long list of species, would enable appropriate actions to be taken to prevent sepsis. We realized that the number of different targets that can be identified in a screening assay can be increased significantly by utilizing a unique combination of two colors for the identification of each target species. We prepared a demonstration assay in which 15 different molecular beacon probe pairs were present, each pair specific for the same identifying sequence in the 16S ribosomal RNA gene of a different bacterial species, and each pair labeled with a unique combination of two fluorophores out of the six differently colored fluorophores that our PCR instrument could distinguish. In a set of PCR assays, each containing all 30 color-coded molecular beacons, and each containing DNA from a different bacterial species, the only two colors that arose in each real-time assay identified the species-specific target sequence that was present. Due to the intrinsic low background of molecular beacon probes, these reactions were specific and extremely sensitive, and the threshold cycle reflected the abundance of the target sequence present in each sample.
AB - The number of different fluorescent colors that can be distinguished in a PCR screening assay restricts the number of different targets that can be detected. If only six colors can be distinguished, and the probe for each target is labeled with a unique color, then only six different targets can be identified. Yet, it is often desirable to identify more targets. For instance, the rapid identification of which bacterial species (if any) is present in a patient’s normally sterile blood sample, out of a long list of species, would enable appropriate actions to be taken to prevent sepsis. We realized that the number of different targets that can be identified in a screening assay can be increased significantly by utilizing a unique combination of two colors for the identification of each target species. We prepared a demonstration assay in which 15 different molecular beacon probe pairs were present, each pair specific for the same identifying sequence in the 16S ribosomal RNA gene of a different bacterial species, and each pair labeled with a unique combination of two fluorophores out of the six differently colored fluorophores that our PCR instrument could distinguish. In a set of PCR assays, each containing all 30 color-coded molecular beacons, and each containing DNA from a different bacterial species, the only two colors that arose in each real-time assay identified the species-specific target sequence that was present. Due to the intrinsic low background of molecular beacon probes, these reactions were specific and extremely sensitive, and the threshold cycle reflected the abundance of the target sequence present in each sample.
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U2 - 10.1371/journal.pone.0213906
DO - 10.1371/journal.pone.0213906
M3 - Article
C2 - 30883590
AN - SCOPUS:85063284784
VL - 14
JO - PLoS One
JF - PLoS One
SN - 1932-6203
IS - 3
M1 - e0213906
ER -