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We note the recent article by Koenig et al. (3) which de- scribes discordance between results obtained with the BD ProbeTEC ET System (BDPT) and a cppB gene-based PCR assay for the detection of Neisseria gonorrhoeae. Overall, 22.6% of BDPT-positive assays were not confirmed by the cppB gene- based PCR, but agreement was particularly low in those sam- ples producing a reduced method-other-than-acceleration score with the BDPT PCR. The BDPT PCR has been found to cross-react with commensal Neisseria species (5), but such cross-reactions may not adequately explain the high level of nonconfirmed BDPT PCR-positive results obtained in this study. Even with samples with method-other-than-acceleration scores in higher ranges (20,000), between 6 and 15.5% of positive BDPT PCR results could not be confirmed with the cppB gene-based assay. The authors discussed, among a num- ber of potential reasons for the discrepancy, the possibility that the presence of gonococci lacking the cryptic plasmid where the cppB gene is located may account for this difference. This possibility was disregarded on the basis of studies reporting that 96% of gonococci contained a cryptic plasmid and that even where this plasmid was absent, amplification of a cppB gene sequence replicated in the chromosome may produce the required positive result. Recent studies suggest this confidence in cppB gene-based assays may be misplaced. We have recently reported that 10% of culture-positive gonococci were cppB gene-based PCR neg- ative but positive in other assays, including the BDPT PCR (4;

journal of clinical microbiology

Cryptic-Plasmid-Free Gonococci May Contribute to Failure of <i>cppB</i> Gene-Based Assays To Confirm Results of BD ProbeTEC PCR for Identification of <i>Neisseria gonorrhoeae</i>

Cryptic-Plasmid-Free Gonococci May Contribute to Failure of cppB Gene-Based Assays To Confirm Results of BD ProbeTEC PCR for Identification of Neisseria gonorrhoeae