Publication:
Bioassay for spore polar tube extrusion of shrimp Enterocytozoon hepatopenaei (EHP)

dc.contributor.authorDiva January Aldama-Canoen_US
dc.contributor.authorPiyachat Sanguanruten_US
dc.contributor.authorNatthinee Munkongwongsirien_US
dc.contributor.authorJosé Cuauhtémoc Ibarra-Gámezen_US
dc.contributor.authorOrnchuma Itsathitphaisarnen_US
dc.contributor.authorRapeepun Vanichviriyakiten_US
dc.contributor.authorTimothy W. Flegelen_US
dc.contributor.authorKallaya Sritunyalucksanaen_US
dc.contributor.authorSiripong Thitamadeeen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherThailand National Science and Technology Development Agencyen_US
dc.contributor.otherInstituto Tecnológico de Sonoraen_US
dc.date.accessioned2019-08-23T10:19:54Z
dc.date.available2019-08-23T10:19:54Z
dc.date.issued2018-01-04en_US
dc.description.abstract© 2018 The microsporidian Enterocytozoon hepatopenaei (EHP) is an intracellular spore-forming parasite, which has recently become a serious threat of cultivated penaeid shrimp in Asia. These studies were aimed to generate comprehensive study on EHP infection as well as establishing innovative strategies to reduce its viability and potential infectivity in shrimp farms. The EHP spore purification method by using Percoll gradient separation with ultracentrifugation step at 15 °C has been developed. The viability of the purified spores has been evaluated by its polar tube extrusion with Phloxin B staining. The active EHP spores were exposed to different temperature (−20 °C, 4 °C and 33 °C) and chemical treatments including calcium hypochlorite, formalin, potassium permanganate (KMnO4) and ethanol to identify the conditions that can be used to inhibit the extrusion of the polar tube. Complete inhibition of activity was demonstrated either by freezing the spores at −20 °C for at least 2 h or by treating them with chemicals. The chemicals that yielded 100% inhibition were 15 ppm KMnO4 for 15 min, 40 ppm of 65% active chlorine for 15 min or 10 ppm of 65% active chlorine for 24 h and 20% ethanol for 15 min. However 200 ppm formalin resulted in a maximum reduction of 95.33%. Taken together, our protocol demonstrates for the first time that living EHP spores can be isolated and purified, providing a potential platform for future testing and development of EHP's control strategies.en_US
dc.identifier.citationAquaculture. Vol.490, (2018), 156-161en_US
dc.identifier.doi10.1016/j.aquaculture.2018.02.039en_US
dc.identifier.issn00448486en_US
dc.identifier.other2-s2.0-85042498695en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/44832
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85042498695&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleBioassay for spore polar tube extrusion of shrimp Enterocytozoon hepatopenaei (EHP)en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85042498695&origin=inwarden_US

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