Comparative transcriptomics and host-specific parasite gene expression profiles inform on drivers of proliferative kidney disease.
Comparative transcriptomics and host-specific parasite gene expression profiles inform on drivers of proliferative kidney disease.
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比较转录组学和宿主特异性寄生虫基因表达谱为增殖性肾病的驱动因素提供信息
DOI:
10.1038/s41598-020-77881-7
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发表时间:
2021-01-25
影响因子:
4.6
通讯作者:
Holland JW
中科院分区:
文献类型:
--
作者:
Faber M;Shaw S;Yoon S;de Paiva Alves E;Wang B;Qi Z;Okamura B;Hartikainen H;Secombes CJ;Holland JW
The myxozoan parasite, Tetracapsuloides bryosalmonae has a two-host life cycle alternating between freshwater bryozoans and salmonid fish. Infected fish can develop Proliferative Kidney Disease, characterised by a gross lymphoid-driven kidney pathology in wild and farmed salmonids. To facilitate an in-depth understanding of T. bryosalmonae-host interactions, we have used a two-host parasite transcriptome sequencing approach in generating two parasite transcriptome assemblies; the first derived from parasite spore sacs isolated from infected bryozoans and the second from infected fish kidney tissues. This approach was adopted to minimize host contamination in the absence of a complete T. bryosalmonae genome. Parasite contigs common to both infected hosts (the intersect transcriptome; 7362 contigs) were typically AT-rich (60–75% AT). 5432 contigs within the intersect were annotated. 1930 unannotated contigs encoded for unknown transcripts. We have focused on transcripts encoding proteins involved in; nutrient acquisition, host–parasite interactions, development, cell-to-cell communication and proteins of unknown function, establishing their potential importance in each host by RT-qPCR. Host-specific expression profiles were evident, particularly in transcripts encoding proteases and proteins involved in lipid metabolism, cell adhesion, and development. We confirm for the first time the presence of homeobox proteins and a frizzled homologue in myxozoan parasites. The novel insights into myxozoan biology that this study reveals will help to focus research in developing future disease control strategies.
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影响因子:
16.6
作者:
Berthelot, Camille;Brunet, Frederic;Chalopin, Domitille;Juanchich, Amelie;Bernard, Maria;Noel, Benjamin;Bento, Pascal;Da Silva, Corinne;Labadie, Karine;Alberti, Adriana;Aury, Jean-Marc;Louis, Alexandra;Dehais, Patrice;Bardou, Philippe;Montfort, Jerome;Klopp, Christophe;Cabau, Cedric;Gaspin, Christine;Thorgaard, Gary H.;Boussaha, Mekki;Quillet, Edwige;Guyomard, Rene;Galiana, Delphine;Bobe, Julien;Volff, Jean-Nicolas;Genet, Carine;Wincker, Patrick;Jaillon, Olivier;Roest Crollius, Hugues;Guiguen, Yann
通讯作者:
Guiguen, Yann
影响因子:
1.3
作者:
Foox, Jonathan;Siddall, Mark E.
通讯作者:
Siddall, Mark E.
DOI:
10.1073/pnas.1819976116
发表时间:
2019-04-02
影响因子:
11.1
作者:
Dorrell, Richard G.;Azuma, Tomonori;Kamikawa, Ryoma
通讯作者:
Kamikawa, Ryoma
影响因子:
2.9
作者:
Bailey, Christyn;Strepparava, Nicole;Segner, Helmut
通讯作者:
Segner, Helmut
影响因子:
3.1
作者:
Bai, Zhiyi;Lin, Jingyun;Li, Jiale
通讯作者:
Li, Jiale