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. 2004 Apr;72(4):1939–1945. doi: 10.1128/IAI.72.4.1939-1945.2004

TABLE 2.

Adhesion of A. caviae strain Sch3 wild-type and mutant strains to HEp-2 and intestinal cell linesa

Strain Mutation Presence of polar flagellumb Presence of lateral flagellab Mean no. of bacteria per cell ± SD (% decrease from wild type)c
HEp-2 Henle 407 Caco-2
Wild-type A. caviae Sch3 + + 15.5 ± 6.2 19.5 ± 7.4 20.9 ± 5.1
AAR6 lafA1::CmrlafA2::Kmr + − 5.9 ± 3.2 (62) 8.3 ± 2.1 (58) 9.2 ± 3.6 (56)
AAR194d flgH::mini-Tn5Cmr − + 5.9 ± 3.2 (62) 12.4 ± 3.6 (37) 8.6 ± 3.9 (59)
AAR31 flaA::CmrflaB::Kmr − ± 0.5 ± 0.9 (97) 0.2 ± 0.7 (99) 2.9 ± 2.5 (88)
AAR31C AAR31 plus pARP1266 (flA+flaB+flaG+flaH+flaJ+) + + 14.8 ± 4.0 (4) 16.9 ± 2.7 (13) 17.5 ± 2.8 (17)
AAR400d cheA::mini-Tn5Cmr + + 8.8 ± 5.5 (43) 9.9 ± 6.9 (49) 8.9 ± 3.9 (57)
a

Strains were tested on triplicate coverslips in 23, 16, and 10 separate experiments for HEp-2, Henle, and Caco-2 cells, respectively.

b

Flagellar expression was determined by transmission electron microscopy and Western blotting with whole-cell preparations (2, 8).

c

For the mutant strains AAR6, AAR194, AAR31, and AAR400, all adherence values were significantly reduced compared to the wild-type strain (P < 0.001). For two of the three cell lines (HEp-2 and Henle 407), adherence by the complemented mutant strain was not significantly different from adherence by the wild-type strain.

d

These mutants were unable to swim or swarm in agar motility assays.