Development of monoclonal antibodies against Perkinsus olseni using whole cells

The genus Perkinsus is comprised of multiple species, notably P. olseni and P. marinus that are on the list of notifiable pathogens of the World Organisation for Animal Health. These protozoans are responsible for mass mortalities in mollusc populations worldwide. Current diagnostic tests for these...

Full description

Saved in:
Bibliographic Details
Published inAquaculture reports Vol. 24; p. 101179
Main Authors Hanrio, Eliot, Batley, Jacqueline, Davern, Kathleen, Dang, Cécile
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.06.2022
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The genus Perkinsus is comprised of multiple species, notably P. olseni and P. marinus that are on the list of notifiable pathogens of the World Organisation for Animal Health. These protozoans are responsible for mass mortalities in mollusc populations worldwide. Current diagnostic tests for these parasites include incubation in Ray’s fluid thioglycollate medium associated with microscopy, and molecular assays such as PCR or qPCR using species-specific primers, which can be time and labour consuming. To simplify the detection of Perkinsus spp. infections, the current study developed monoclonal antibodies with strong potential for diagnostic use in immunoassays. Mice were immunised with a mix of P. olseni SA-00978–12 T isolate cell types, and multiple promising antibodies were produced through different immunoassays. The immunoglobulins developed seem to be specific to P. olseni and recognise trophozoite and hypnospore cell types. The study also highlighted the difficulty of developing antibodies against Perkinsus spp. and their different cell types and geographical isolates. •P. olseni is a parasite responsible of mass mortalities in mollusc populations worldwide and is on the list of notifiable pathogens of the OIE.•Current diagnostic tests used are molecular assays and microscopy.•Monoclonal antibodies were developed that could be used in an immunoassay for the rapid and inexpensive detection of all cell types of .P. olseni.
ISSN:2352-5134
2352-5134
DOI:10.1016/j.aqrep.2022.101179