Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/70022
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dc.contributor.authorRujipas Yongsawasen_US
dc.contributor.authorVeeranan Chaimaneeen_US
dc.contributor.authorJeffery S. Pettisen_US
dc.contributor.authorHumberto Freire Boncristiani Junioren_US
dc.contributor.authorDawn Lopezen_US
dc.contributor.authorAmmarin In-Onen_US
dc.contributor.authorPanuwan Chantawannakulen_US
dc.contributor.authorTerd Disayathanoowaten_US
dc.date.accessioned2020-10-14T08:23:05Z-
dc.date.available2020-10-14T08:23:05Z-
dc.date.issued2020-07-01en_US
dc.identifier.issn20754450en_US
dc.identifier.other2-s2.0-85087926908en_US
dc.identifier.other10.3390/insects11070439en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85087926908&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70022-
dc.description.abstract© 2020 by the authors. Licensee MDPI, Basel, Switzerland. In this study, we examined the impact of Sacbrood virus (SBV), the cause of larval honeybee (Apis mellifera) death, producing a liquefied a larva sac, on the gut bacterial communities on two larval honeybee species, Apis mellifera and Apis cerana. SBV was added into a worker jelly food mixture and bee larvae were grafted into each of the treatment groups for 24 h before DNA/RNA extraction. Confirmation of SBV infection was achieved using quantitative reverse transcription polymerase chain reaction (RT-qPCR) and visual symptomology. The 16S rDNA was sequenced by Illumina sequencing. The results showed the larvae were infected with SBV. The gut communities of infected A. cerana larvae exhibited a dramatic change compared with A. mellifera. In A. mellifera larvae, the Illumina sequencing revealed the proportion of Gilliamella, Snodgrassella and Fructobacillus was not significantly different, whereas in A. cerana, Gilliamella was significantly decreased (from 35.54% to 2.96%), however, with significant increase in Snodgrassella and Fructobacillus. The possibility of cross-infection should be further investigated.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleImpact of sacbrood virus on larval microbiome of apis mellifera and apis ceranaen_US
dc.typeJournalen_US
article.title.sourcetitleInsectsen_US
article.volume11en_US
article.stream.affiliationsKing Mongkuts University of Technologyen_US
article.stream.affiliationsMaejo Universityen_US
article.stream.affiliationsUniversity of Floridaen_US
article.stream.affiliationsUSDA Agricultural Research Service, Washington DCen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsPettis and Associates LLCen_US
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