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. 1998 Feb;66(2):656–663. doi: 10.1128/iai.66.2.656-663.1998

TABLE 2.

Reactivity of H. influenzae strains with antipilus antisera in a dot blot assaya

hifA RFLP pattern Strain (capsular type)b Hemagglu- tination titer Reactivity with antiserumc
R1 (anti-M43 pili) R19 (anti-Eagan pili)
1 E1ap+ (b) 1:16 0 4+
E1ap (b)d 0 0
R9p+ (b) 1:16 3+ 4+
AA61p+ (b) 1:16 2+ 2+
AAr108p+ (b) 1:16 0 2+
AAr176 (NT) 1:16 0 0
AAr39 (NT) 1:16 0 0
AAr169 (NT) 1:16 0 0
3 M43p+ (b) 1:16 4+ 1+
M42p (b)e 0 0 0
AAr122p+ (b) 1:32 4+ 0
AAr7p+ (b) 1:16 4+ 2+
AAr119p+ (b) 1:32 4+ 0
AAr103p+ (b) 1:32 2+ 4+
SL2p+ (b) 1:32 4+ 0
AAr45 (NT) 1:64 0 0
a

Table generated with data from Gilsdorf et al. (11, 13). 

b

An enrichment technique that depends upon erythrocyte agglutination by piliated H. influenzae type b strains was used to select piliated variants from the clinical isolates. NT, nontypeable H. influenzae. 

c

The reactivities of the antibodies with native pili on the surfaces of intact bacteria were assessed visually with a dot blot assay and compared with reactivities of positive (homologous strains) and negative (nonpiliated variants) controls included in each assay by using a grading scale ranging from 0 (identical to negative controls) to 4+ (identical to homologous strains). 

d

Nonpiliated phase variant of E1ap+

e

Nonpiliated variant of strain M43p+; used as a negative control.