Yes, you read that right.
A stool culture was s/o to xld and mac. The colonies are buried into the xld and mac agar after 24 hours. Colonies are dug out and g/s. The g/s = GNB. They are lactose fermenters too. They look like little beads in the agar. Dug those out and s/o to
a bap/mac bi plate, and chocolate. The GN broth at 24 hours was s/o to a fresh xld and mac agar.
Today there is ng on the Chochlate, Bi plate and xld/mac (from gn broth).
Dug more colonies out of the primary plates and inoculated then into a Thio broth and a TSB. Re incubated all plates and put the Chocolate one in a CO2 incubator.
Has anyone encounter this before? Will post results of this set up tomorrow.