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. 2004 Sep;10(9):1585–1592. doi: 10.3201/eid1009.030933

Table 2. Location of primers used for PCR amplification and sequencing of eight intergenic spacers in Yersinia pestisa.

Spacer Upstream gene (N)
Downstream gene (N) Primer sequence
(5´ → 3´)
YP1 ace K (YP03724)
ace A (YP03725) AATCCCTGCAAAATGGTCTG
CTGATGGGAAGCAAAGGTGT
YP3 glg P (YP03938)
glg A (YP03939) TCAGTGCATCCACACTGACA
CGTATCGCCTTCACTAAGGC
YP4 gene ID 1176814 (YP03976)
gor (YP03977) TAATCCGCCGTGGAAATTAG
ACGATTATCTGGCAATTGGC
YP5 Gene ID 1175557 (YP02727)
Gene ID 1175558 (YP02728) GCATGCGCTGTTTGATATTG
TTATGACTCACGGACGATGC
YP7 lex A (YP00314)
Gene ID 1173160 (YP00315) GTAACGGGGACTGGATCTGA
ATAAACCGTGTGCTTCCACC
YP8 Gene ID 1175559 (YP02729)
Gene ID 1175560 (YP02730) ACGGAAATTGCCAGATTCA
GACTTGAGCTTCATTTGGCC
YP9 mrd F (YP02648)
mrd E (YP02649) GCGCTGATACGTGTTATTGG
TTGTTAATATCGCGGGTGGTA
YP10 bio D (YP02269)
Gene ID 1175101 (YP02270) ATGCTGAAACAATCGCAATG
CAATAAGGTGTACTCGCCGG

aNumbering according to the Y. pestis CO92 strain genome, GenBank accession no. NC-223143). PCR, polymerase chain reaction.

HHS Vulnerability Disclosure