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. 2022 Feb 10;16(2):e0010181. doi: 10.1371/journal.pntd.0010181

Table 1. Primer and probes used to detect B. anthracis in two outbreaks of anthrax in Amhara region, northern Ethiopia, 2018-2019. Primers were supplied by the United States Centers for Disease Control and Prevention.

Primer/probe Sequence (5’-3’) Target gene Reference
PA-forward CGG ATC AAG TAT ATG GGA ATA TAG CAA pagA [50]
PA-reverse CCG GTT TAG TCG TTT CTA ATG GAT pagA [50]
PA-probe 6FAM-CTC GAA CTG GAG TGA AGT GTT ACC GCA AAT-BHQ1 pagA [50]
CAP-forward ACG TAT GGT GTT TCA AGA TTC ATG capB [50]
CAP-reverse ATT TTC GTC TCA TTC TAC CTC ACC capB [50]
CAP-probe 6FAM-CCA CGG AAT TCA AAA ATC TCA AAT GGC AT-BHQ1 capB [50]
RNP-forward AGA TTT GGA CCT GCG AGC G RNase P [51]
RNP-reverse GAG CGG CTG TCT CCA CAA GT RNase P [51]
RNP-probe 6FAM-TTC TGA CCT GAA GGC TCT GCG CG-BHQ1 RNase P [51]

Probes were labeled at the 5’-end with the reporter molecule 6-carboxyfluorescein (6FAM) and at the 3’- end with the quencher, Black Hole Quencher-1 (BHQ1).