Publication:
Transcriptomic analysis of male and female Schistosoma mekongi adult worms

dc.contributor.authorOrawan Phuphisuten_US
dc.contributor.authorPravech Ajawatanawongen_US
dc.contributor.authorYanin Limpanonten_US
dc.contributor.authorOnrapak Reamtongen_US
dc.contributor.authorSupaporn Nuamtanongen_US
dc.contributor.authorSumate Ampawongen_US
dc.contributor.authorSalisa Chaimonen_US
dc.contributor.authorParon Dekumyoyen_US
dc.contributor.authorDorn Watthanakulpanichen_US
dc.contributor.authorBrett E. Swierczewskien_US
dc.contributor.authorPoom Adisakwattanaen_US
dc.contributor.otherArmed Forces Research Institute of Medical Sciences, Thailanden_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2019-08-23T11:17:54Z
dc.date.available2019-08-23T11:17:54Z
dc.date.issued2018-09-10en_US
dc.description.abstractBACKGROUND: Schistosoma mekongi is one of five major causative agents of human schistosomiasis and is endemic to communities along the Mekong River in southern Lao People's Democratic Republic (Laos) and northern Cambodia. Sporadic cases of schistosomiasis have been reported in travelers and immigrants who have visited endemic areas. Schistosoma mekongi biology and molecular biology is poorly understood, and few S. mekongi gene and transcript sequences are available in public databases. RESULTS: Transcriptome sequencing (RNA-Seq) of male and female S. mekongi adult worms (a total of three biological replicates for each sex) were analyzed and the results demonstrated that approximately 304.9 and 363.3 million high-quality clean reads with quality Q30 (> 90%) were obtained from male and female adult worms, respectively. A total of 119,604 contigs were assembled with an average length of 1273 nt and an N50 of 2017 nt. From the contigs, 20,798 annotated protein sequences and 48,256 annotated transcript sequences were obtained using BLASTP and BLASTX searches against the UniProt Trematoda database. A total of 4658 and 3509 transcripts were predominantly expressed in male and female worms, respectively. Male-biased transcripts were mostly involved in structural organization while female-biased transcripts were typically involved in cell differentiation and egg production. Interestingly, pathway enrichment analysis suggested that genes involved in the phosphatidylinositol signaling pathway may play important roles in the cellular processes and reproductive systems of S. mekongi worms. CONCLUSIONS: We present comparative transcriptomic analyses of male and female S. mekongi adult worms, which provide a global view of the S. mekongi transcriptome as well as insights into differentially-expressed genes associated with each sex. This work provides valuable information and sequence resources for future studies of gene function and for ongoing whole genome sequencing efforts in S. mekongi.en_US
dc.identifier.citationParasites & vectors. Vol.11, No.1 (2018), 504en_US
dc.identifier.doi10.1186/s13071-018-3086-zen_US
dc.identifier.issn17563305en_US
dc.identifier.other2-s2.0-85056287141en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/45965
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85056287141&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleTranscriptomic analysis of male and female Schistosoma mekongi adult wormsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85056287141&origin=inwarden_US

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