What changes for STI targets
- Treatment follows CDC STI treatment guidelines. For targets such as Chlamydia trachomatis, Neisseria gonorrhoeae and Treponema pallidum, the report points to guideline therapy rather than inventing a grade from genotype.
- No cell wall, no beta-lactam. Mycoplasma and Ureaplasma lack a cell wall, so beta-lactams are inactive by definition.
- Not bacteria at all. Trichomonas vaginalis is a protozoan; HSV and HPV are viruses. The report identifies them without pretending an antibacterial grid applies.
Detecting a non-bacterial cause is itself useful: it is one of the clearest arguments against an unnecessary antibiotic.
Molecular detection does not replace confirmatory testing where guidelines require it, and does not replace public-health reporting obligations.
Pathogens on STI panels
Resistance genes relevant to STI
Decision support only. The treating clinician decides. Molecular genotype does not replace phenotypic susceptibility testing, culture, or public-health reporting. Absence of a detected resistance gene does not establish susceptibility. Organism targets vary by panel; CORE-ABR is configured to the assay each laboratory runs.