TY - JOUR
T1 - Nonrepresentative PCR amplification of variable gene sequences in clinical specimens containing dilute, complex mixtures of microorganisms
AU - Wright, C. J.
AU - Jerse, A. E.
AU - Cohen, M. S.
AU - Cannon, J. G.
AU - Seifert, H. S.
PY - 1994
Y1 - 1994
N2 - PCR amplification and DNA sequencing of the expression locus from Neisseria gonorrhoeae contained in urine sediments collected from experimentally infected human subjects produced two observations. First, different pilin sequences were obtained when separate aliquots of the same sample were amplified and sequenced. In contrast, the same pilin sequence was obtained when repeated amplifications were performed on individual colonies grown from the clinical samples. Second, mixed sequences (i.e., more than one nucleotide at variable positions in the pilin gene sequence) were observed in both the direct clinical isolates and individual cultures grown from the isolates. These results suggest that when clinical samples are directly examined by PCR amplification and sequencing, multiple amplifications may be required to detect sequence variants in the sample and minority variant sequences will not always be detected.
AB - PCR amplification and DNA sequencing of the expression locus from Neisseria gonorrhoeae contained in urine sediments collected from experimentally infected human subjects produced two observations. First, different pilin sequences were obtained when separate aliquots of the same sample were amplified and sequenced. In contrast, the same pilin sequence was obtained when repeated amplifications were performed on individual colonies grown from the clinical samples. Second, mixed sequences (i.e., more than one nucleotide at variable positions in the pilin gene sequence) were observed in both the direct clinical isolates and individual cultures grown from the isolates. These results suggest that when clinical samples are directly examined by PCR amplification and sequencing, multiple amplifications may be required to detect sequence variants in the sample and minority variant sequences will not always be detected.
UR - http://www.scopus.com/inward/record.url?scp=0028012213&partnerID=8YFLogxK
U2 - 10.1128/jcm.32.2.464-468.1994
DO - 10.1128/jcm.32.2.464-468.1994
M3 - Article
C2 - 7908674
AN - SCOPUS:0028012213
SN - 0095-1137
VL - 32
SP - 464
EP - 468
JO - Journal of Clinical Microbiology
JF - Journal of Clinical Microbiology
IS - 2
ER -