TY - JOUR
T1 - Monoclonal antibodies for the detection of Puccinia striiformis urediniospores
AU - Skottrup, Peter
AU - Frøkiær, Hanne
AU - Hearty, Stephen
AU - O'Kennedy, Richard
AU - Hejgaard, Jørn
AU - Nicolaisen, Mogens
AU - Justesen, Annemarie Fejer
PY - 2007
Y1 - 2007
N2 - The fungal pathogen Pst causes yellow rust disease in wheat plants leading to crop losses.
The organism spreads by releasing wind-dispersed urediniospores from infected plants. In
this study a library of novel monoclonal antibodies (mAbs) was developed against Pst urediniospores.
Nine mAb-producing cell lines were cloned and their cross-reactivities characterised
against a panel of airborne fungal spores representing genera commonly found in
the same environment as Pst. Two specific mAbs were used to develop a competitive ELISA
(Pst mAb4) and a subtractive inhibition ELISA (Pst mAb8). Standard curves for both assays
had good intra- and interday reproducibility. The subtractive inhibition ELISA had greater
sensitivity with a detection limit of 1.5 105 spores ml1. Cross-reactivity studies of Pst
mAb8 in the subtractive inhibition ELISA, showed reaction with other Puccinia spores
only, suggesting that common epitopes exist within this genus. The biosensor-compatible
Pst mAb8 assay principle developed in this study has the potential to be implemented in
future ‘label-free’ in-the-field systems for Pst detection.
AB - The fungal pathogen Pst causes yellow rust disease in wheat plants leading to crop losses.
The organism spreads by releasing wind-dispersed urediniospores from infected plants. In
this study a library of novel monoclonal antibodies (mAbs) was developed against Pst urediniospores.
Nine mAb-producing cell lines were cloned and their cross-reactivities characterised
against a panel of airborne fungal spores representing genera commonly found in
the same environment as Pst. Two specific mAbs were used to develop a competitive ELISA
(Pst mAb4) and a subtractive inhibition ELISA (Pst mAb8). Standard curves for both assays
had good intra- and interday reproducibility. The subtractive inhibition ELISA had greater
sensitivity with a detection limit of 1.5 105 spores ml1. Cross-reactivity studies of Pst
mAb8 in the subtractive inhibition ELISA, showed reaction with other Puccinia spores
only, suggesting that common epitopes exist within this genus. The biosensor-compatible
Pst mAb8 assay principle developed in this study has the potential to be implemented in
future ‘label-free’ in-the-field systems for Pst detection.
U2 - 10.1016/j.mycres.2006.11.010
DO - 10.1016/j.mycres.2006.11.010
M3 - Journal article
C2 - 17350244
SN - 0953-7562
VL - 111
SP - 332
EP - 338
JO - Mycological Research
JF - Mycological Research
ER -