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. 2000 Mar;182(5):1364–1373. doi: 10.1128/jb.182.5.1364-1373.2000

TABLE 4.

Adherence of recombinant H. influenzae cells to Chang conjunctival epithelial cells in vitro and detection of recombinant proteins on the bacterial cell surface

Recombinant plasmid M. catarrhalis proteina Adherenceb Detection of protein on cell surfacec
pACYC184 (vector) 0.2 ± 0.1 918 ± 276
pELU112 012E-UspA1 35.1 ± 8.7 13,870 ± 2,132
pELU212 012E-UspA2 0.4 ± 0.2 5,557 ± 1,546
pELU135 035E-UspA1 17.4 ± 7.3 5,050 ± 1,184
pELU235 035E-UspA2 0.2 ± 0.1 7,175 ± 3,201
pELU171 V1171-UspA1 12.3 ± 7.2 6,425 ± 1,049
pELU271 V1171-UspA2 0.4 ± 0.2 4,111 ± 1,333
pELU137 TTA37-UspA1 0.9 ± 0.4 1,286 ± 206
pELU237 TTA37-UspA2H 16.9 ± 6.3 11,630 ± 1,351
pELU146 046E-UspA1 0.8 ± 0.2 703 ± 221
pELU246 046E-UspA2H 52.6 ± 15.17 28,980 ± 1,703
pELU266 V1166-UspA2H 62.3 ± 16.6 5,632 ± 199
a

The M. catarrhalis protein expressed by the H. influenzae DB117 clone containing this recombinant plasmid. 

b

Adherence of M. catarrhalis organisms to Chang cells is expressed as the mean (± standard deviation) percentage of the inoculum which adhered to the monolayers. 

c

Counts per minute (mean ± standard deviation) of radioiodinated goat anti-mouse immunoglobulin bound to MAb 17C7 on the surface of recombinant cells. The indirect antibody-accessibility assay was performed as described previously (2). 

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