Identification of new genes involved in biofilm formation is needed to unde
rstand the molecular basis of strain variation and the pathogenic mechanism
s implicated in chronic staphylococcal infections. A biofilm-producing Stap
hylococcus aureus isolate was used to generate biofilm-negative transposon
(Tn917) insertion mutants, Two mutants were found with a significant decrea
se in attachment to inert surfaces (early adherence), intercellular adhesio
n, and biofilm formation. The transposon was inserted at the same locus in
both mutants. This locus (bap [for biofilm associated protein] encodes a no
vel cell wall associated protein of 2,276 amino acids (Bap), which shows gl
obal organizational similarities to surface proteins of gram-negative (Pseu
domonas aeruginosa and Salmonella enterica serovar Typhi) and gram-positive
(Enteroccocus faecalis) microorganisms. Bap's core region represents 52% o
f the protein and consists of 13 successive nearly identical repeats, each
containing 86 amino acids. bap was present in a small fraction of bovine ma
stitis isolates (5% of the 350 S. aureus isolates tested), but it was absen
t from the 75 clinical human S. aureus isolates analyzed. All staphylococca
l isolates harboring bap were highly adherent and strong biofilm producers.
In a mouse infection model bap was involved in pathogenesis, causing a per
sistent infection.