Probo

I have not done any because the pandemic suspended the lab practices before I could have contact with it, but I imagine that speading would sort of mixture the colonies, and the results would be less accurate, but I am not certain if that is the case.

Why, in this method, when compared to "Spread plate", does it have less tendency of interference between one colony and another?

We all know that most heterotroph bacteria are not considered patogens, but why is it important for its density to be kept under control? If there is something wrong, sorry for my bad English. It is not my main language.