This randomized clinical trial involved two research centers—The Karolinska Institute in Sweden (KI) and Helperby Therapeutics Ltd. in the United Kingdom (HP). Each study was approved by the respective institutional boards and the respective national competent authorities and was registered with the European Union Clinical Trials Register (for details, see Text S1 in the supplemental material). Each center involved healthy volunteers, randomized into two test groups and one control group. At KI, 30 volunteers were randomly assigned to either the ciprofloxacin (Cipro), the clindamycin (Clinda), or the placebo (Plac KI) group. At HP, 44 volunteers were randomly assigned to the amoxicillin (Amox, n = 15), the minocycline (Minoc, n = 15), or the placebo (Plac HP, n = 14) group. Saliva and fecal samples were collected on 6 occasions: immediately before administration of the antibiotic (baseline), immediately after the treatment course was completed (week 1), and 1 month, 2 months, 4 months, and 12 months postdosing. Sample DNA was extracted, 16S rRNA gene amplicons were sequenced, and data were processed as described previously (36 (link)– (link)38 (link)) (see Text S1).