Abstract
AbstractThe preparation of Erwinia amylovora isolations by different treatments or from different sources is shown to influence the results obtained by immunofluorescent microscopical examination. Where absorption of antisera is impracticable, serial dilutions of the antiserum involved when using constant numbers of the bacterium to be tested, can result in a reduction of cross‐reactions. Emphasis is made on standardization of such procedures in order to increase the chances of more accurate diagnosis.
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