Ej. Hansen et al., DETECTION OF HAEMOPHILUS-DUCREYI LIPOOLIGOSACCHARIDE BY MEANS OF AN IMMUNOLIMULUS ASSAY, Journal of immunological methods, 185(2), 1995, pp. 225-235
A murine monoclonal antibody (MAb) directed against a surface-exposed
epitope of the lipooligosaccharide (LOS) of Haemophilus ducreyi strain
35000 was shown to be reactive with all 37 strains of this pathogen t
ested in a colony blot-radioimmunoassay. The LOS epitope bound by this
MAb appeared to be stably expressed by H. ducreyi growing in vitro. T
he use of this MAb in the immunolimulus system revealed that it could
detect purified H. ducreyi LOS at a level of 25 pg/ml. Similarly, this
immunolimulus system could detect as few as 1000 colony forming units
of in vitro-grown H. ducreyi cells per mi of buffer. When this MAb wa
s utilized in the immunolimulus system together with lesion material f
rom rabbits infected with two different H. ducreyi strains, a positive
reaction was obtained with every sample tested, even when no viable o
rganisms were present in the lesion material. In contrast, this MAb yi
elded consistently negative results when used in the immunolimulus sys
tem with lesion material from animals infected with Staphylococcus aur
eus.