Why the gut microbiome is critical for the success of checkpoint inhibitor cancer therapy is a question that remains unanswered, but progress has slowed. We argue that this lack of advancement is due to an unappreciated biological detail. Here, we show that the antibiotic cocktail used in seminal publications-all of which have used the C57BL/6_mouse strain-are bitter and not tolerated by other common mouse strains (ie, BALB/c and DBA/2). We write to alert readers of this important biological limitation that must be considered when planning cancer experiments investigating the gut microbiota, to prevent the unnecessary dehydration of experimental animals, and to save our colleagues valuable experimental time and resources.

Author Info: (1) Research School of Biology, College of Science, Australian National University, Canberra, ACT, Australia. (2) Research School of Biology, College of Science, Australian Nationa l University, Canberra, ACT, Australia. (3) Biological Data Science Institute, College of Science, Australian National University, Canberra, ACT, Australia. (4) John Curtin School of Medical Research, College of Health and Medicine, Australian National University, Canberra, ACT, Australia. (5) Research School of Biology, College of Science, Australian National University, Canberra, ACT, Australia aude.fahrer@anu.edu.au.