Sensitivity and specificity of methods for the identification of toxigenic
strains of Pasteurella multocida were compared. The production of dermonecr
otoxin was determined by a skin test in guinea pigs, a cell culture test us
ing bovine embryonic lung cells, and PCR. The highest sensitivity and speci
ficity were found for PCR that allows the identification of strains produci
ng only small amounts of the toxin in vitro that are not detectable by biol
ogical methods. However, strains producing structurally different toxins wi
th the same biological effect are not identifiable by this technique owing
to its high specificity. Therefore, biological and particularly cell cultur
e tests are necessary for a comprehensive assessment of toxigenicity of ind
ividual strains.