• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

共生体和环境因素对深海热液喷口贻贝基因表达的共轭效应。

Conjugating effects of symbionts and environmental factors on gene expression in deep-sea hydrothermal vent mussels.

机构信息

CNRS, UMR 7144, Adaptation et Diversité en Milieu Marin, Station Biologique de Roscoff, 29682 Roscoff, France.

出版信息

BMC Genomics. 2011 Oct 28;12:530. doi: 10.1186/1471-2164-12-530.

DOI:10.1186/1471-2164-12-530
PMID:22034982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3218092/
Abstract

BACKGROUND

The deep-sea hydrothermal vent mussel Bathymodiolus azoricus harbors thiotrophic and methanotrophic symbiotic bacteria in its gills. While the symbiotic relationship between this hydrothermal mussel and these chemoautotrophic bacteria has been described, the molecular processes involved in the cross-talking between symbionts and host, in the maintenance of the symbiois, in the influence of environmental parameters on gene expression, and in transcriptome variation across individuals remain poorly understood. In an attempt to understand how, and to what extent, this double symbiosis affects host gene expression, we used a transcriptomic approach to identify genes potentially regulated by symbiont characteristics, environmental conditions or both. This study was done on mussels from two contrasting populations.

RESULTS

Subtractive libraries allowed the identification of about 1000 genes putatively regulated by symbiosis and/or environmental factors. Microarray analysis showed that 120 genes (3.5% of all genes) were differentially expressed between the Menez Gwen (MG) and Rainbow (Rb) vent fields. The total number of regulated genes in mussels harboring a high versus a low symbiont content did not differ significantly. With regard to the impact of symbiont content, only 1% of all genes were regulated by thiotrophic (SOX) and methanotrophic (MOX) bacteria content in MG mussels whereas 5.6% were regulated in mussels collected at Rb. MOX symbionts also impacted a higher proportion of genes than SOX in both vent fields. When host transcriptome expression was analyzed with respect to symbiont gene expression, it was related to symbiont quantity in each field.

CONCLUSIONS

Our study has produced a preliminary description of a transcriptomic response in a hydrothermal vent mussel host of both thiotrophic and methanotrophic symbiotic bacteria. This model can help to identify genes involved in the maintenance of symbiosis or regulated by environmental parameters. Our results provide evidence of symbiont effect on transcriptome regulation, with differences related to type of symbiont, even though the relative percentage of genes involved remains limited. Differences observed between the vent site indicate that environment strongly influences transcriptome regulation and impacts both activity and relative abundance of each symbiont. Among all these genes, those participating in recognition, the immune system, oxidative stress, and energy metabolism constitute new promising targets for extended studies on symbiosis and the effect of environmental parameters on the symbiotic relationships in B. azoricus.

摘要

背景

深海热液喷口贻贝 Bathymodiolus azoricus 的鳃中栖息着硫氧化和甲烷氧化共生细菌。虽然这种热液贻贝与其化能自养细菌之间的共生关系已被描述,但共生体之间的分子相互作用过程、共生体的维持、环境参数对基因表达的影响以及个体之间的转录组变化仍知之甚少。为了了解这种双重共生关系是如何以及在多大程度上影响宿主基因表达,我们使用转录组学方法来鉴定可能受共生体特征、环境条件或两者共同调控的基因。这项研究是在来自两个截然不同种群的贻贝上进行的。

结果

消减文库鉴定出约 1000 个可能受共生和/或环境因素调控的基因。微阵列分析显示,120 个基因(所有基因的 3.5%)在梅内兹·格温(MG)和彩虹(Rb)喷口场之间存在差异表达。在共生体含量高的贻贝和共生体含量低的贻贝之间,受调控基因的总数没有显著差异。就共生体含量的影响而言,MG 贻贝中只有 1%的基因受硫氧化(SOX)和甲烷氧化(MOX)细菌含量的调控,而在 Rb 贻贝中则有 5.6%的基因受调控。在两个喷口场中,MOX 共生体也比 SOX 调控更多比例的基因。当根据共生体基因表达分析宿主转录组表达时,它与每个喷口场中的共生体数量有关。

结论

我们的研究初步描述了热液喷口贻贝宿主中同时存在硫氧化和甲烷氧化共生细菌的转录组反应。该模型有助于鉴定参与共生体维持或受环境参数调控的基因。我们的结果提供了共生体对转录组调控影响的证据,并且差异与共生体类型有关,尽管涉及的基因比例仍然有限。在喷口场之间观察到的差异表明,环境强烈影响转录组调控,并且影响每个共生体的活性和相对丰度。在所有这些基因中,那些参与识别、免疫系统、氧化应激和能量代谢的基因构成了对 B. azoricus 共生关系以及环境参数对共生关系影响的进一步研究的新的有希望的靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bd/3218092/043631ed617c/1471-2164-12-530-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bd/3218092/f912a5f117a4/1471-2164-12-530-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bd/3218092/f72e358f1970/1471-2164-12-530-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bd/3218092/043631ed617c/1471-2164-12-530-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bd/3218092/f912a5f117a4/1471-2164-12-530-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bd/3218092/f72e358f1970/1471-2164-12-530-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bd/3218092/043631ed617c/1471-2164-12-530-3.jpg

相似文献

1
Conjugating effects of symbionts and environmental factors on gene expression in deep-sea hydrothermal vent mussels.共生体和环境因素对深海热液喷口贻贝基因表达的共轭效应。
BMC Genomics. 2011 Oct 28;12:530. doi: 10.1186/1471-2164-12-530.
2
Site-related differences in gene expression and bacterial densities in the mussel Bathymodiolus azoricus from the Menez Gwen and Lucky Strike deep-sea hydrothermal vent sites.来自梅内兹格温(Menez Gwen)和幸运打击(Lucky Strike)深海热液喷口的阿氏深海贻贝(Bathymodiolus azoricus)中基因表达和细菌密度的位点相关差异。
Fish Shellfish Immunol. 2014 Aug;39(2):343-53. doi: 10.1016/j.fsi.2014.05.024. Epub 2014 Jun 2.
3
Global host molecular perturbations upon in situ loss of bacterial endosymbionts in the deep-sea mussel Bathymodiolus azoricus assessed using proteomics and transcriptomics.利用蛋白质组学和转录组学评估深海贻贝 Bathymodiolus azoricus 原位丧失细菌内共生体时的全球宿主分子扰动。
BMC Genomics. 2019 Feb 6;20(1):109. doi: 10.1186/s12864-019-5456-0.
4
Transcriptomic response of the hydrothermal mussel Bathymodiolus azoricus in experimental exposure to heavy metals is modulated by the Pgm genotype and symbiont content.热液贻贝阿氏深海贻贝在实验性暴露于重金属时的转录组反应受磷酸葡萄糖变位酶(Pgm)基因型和共生体含量的调节。
Mar Genomics. 2015 Jun;21:63-73. doi: 10.1016/j.margen.2014.11.010. Epub 2014 Dec 24.
5
Vibrio diabolicus challenge in Bathymodiolus azoricus populations from Menez Gwen and Lucky Strike hydrothermal vent sites.对来自梅内兹格温(Menez Gwen)和幸运打击(Lucky Strike)热液喷口区域的阿氏深海贻贝(Bathymodiolus azoricus)种群进行恶魔弧菌(Vibrio diabolicus)挑战。
Fish Shellfish Immunol. 2015 Dec;47(2):962-77. doi: 10.1016/j.fsi.2015.10.038. Epub 2015 Oct 31.
6
Endosymbionts of Metazoans Dwelling in the PACManus Hydrothermal Vent: Diversity and Potential Adaptive Features Revealed by Genome Analysis.后生动物居住在 PACManus 热液喷口的内共生体:通过基因组分析揭示的多样性和潜在的适应特征。
Appl Environ Microbiol. 2020 Oct 15;86(21). doi: 10.1128/AEM.00815-20.
7
Dual symbiosis in a Bathymodiolus sp. mussel from a methane seep on the Gabon continental margin (Southeast Atlantic): 16S rRNA phylogeny and distribution of the symbionts in gills.来自加蓬大陆边缘(东南大西洋)一处甲烷冷泉的一种深海贻贝中的双重共生现象:鳃中16S rRNA系统发育及共生体分布
Appl Environ Microbiol. 2005 Apr;71(4):1694-700. doi: 10.1128/AEM.71.4.1694-1700.2005.
8
Geographical structure of endosymbiotic bacteria hosted by Bathymodiolus mussels at eastern Pacific hydrothermal vents.东太平洋热液喷口处深海贻贝所携带的内共生细菌的地理结构。
BMC Evol Biol. 2017 May 30;17(1):121. doi: 10.1186/s12862-017-0966-3.
9
Identification and gene expression of multiple peptidoglycan recognition proteins (PGRPs) in the deep-sea mussel Bathymodiolus azoricus, involvement in symbiosis?深海贻贝阿氏 Bathymodiolus azoricus 中多种肽聚糖识别蛋白(PGRPs)的鉴定与基因表达,与共生有关吗?
Comp Biochem Physiol B Biochem Mol Biol. 2017 May;207:1-8. doi: 10.1016/j.cbpb.2017.02.002. Epub 2017 Feb 12.
10
High-throughput sequencing and analysis of the gill tissue transcriptome from the deep-sea hydrothermal vent mussel Bathymodiolus azoricus.高通量测序及深海热液喷口贻贝 Bathymodiolus azoricus 鳃组织转录组分析。
BMC Genomics. 2010 Oct 11;11:559. doi: 10.1186/1471-2164-11-559.

引用本文的文献

1
Genome Study of α-, β-, and γ-Carbonic Anhydrases from the Thermophilic Microbiome of Marine Hydrothermal Vent Ecosystems.海洋热液喷口生态系统嗜热微生物群落中α-、β-和γ-碳酸酐酶的基因组研究
Biology (Basel). 2023 May 25;12(6):770. doi: 10.3390/biology12060770.
2
Metatranscriptomics profile of the gill microbial community during aquarium acclimatization at atmospheric pressure.常压下鱼缸驯化过程中鳃微生物群落的宏转录组学特征
AIMS Microbiol. 2018 Mar 20;4(2):240-260. doi: 10.3934/microbiol.2018.2.240. eCollection 2018.
3
Global host molecular perturbations upon in situ loss of bacterial endosymbionts in the deep-sea mussel Bathymodiolus azoricus assessed using proteomics and transcriptomics.

本文引用的文献

1
Use of OmpU porins for attachment and invasion of Crassostrea gigas immune cells by the oyster pathogen Vibrio splendidus.利用 OmpU 孔蛋白附着和入侵牡蛎病原体灿烂弧菌对虾贻贝类免疫细胞。
Proc Natl Acad Sci U S A. 2011 Feb 15;108(7):2993-8. doi: 10.1073/pnas.1015326108. Epub 2011 Jan 31.
2
An i-type lysozyme from the Asiatic hard clam Meretrix meretrix potentially functioning in host immunity.中国蛤蜊(Meretrix meretrix)中的一种 i 型溶菌酶,可能在宿主免疫中发挥作用。
Fish Shellfish Immunol. 2011 Feb;30(2):550-8. doi: 10.1016/j.fsi.2010.11.022. Epub 2010 Dec 4.
3
Insights into metazoan evolution from Alvinella pompejana cDNAs.
利用蛋白质组学和转录组学评估深海贻贝 Bathymodiolus azoricus 原位丧失细菌内共生体时的全球宿主分子扰动。
BMC Genomics. 2019 Feb 6;20(1):109. doi: 10.1186/s12864-019-5456-0.
4
High rates of apoptosis visualized in the symbiont-bearing gills of deep-sea Bathymodiolus mussels.深海贻贝鳃中观察到的共生体高凋亡率。
PLoS One. 2019 Feb 4;14(2):e0211499. doi: 10.1371/journal.pone.0211499. eCollection 2019.
5
Symbiont type and environmental factors affect transcriptome-wide gene expression in the coral .共生体类型和环境因素影响珊瑚全转录组范围的基因表达。
Ecol Evol. 2018 Dec 27;9(1):378-392. doi: 10.1002/ece3.4756. eCollection 2019 Jan.
6
Molecular identification of methane monooxygenase and quantitative analysis of methanotrophic endosymbionts under laboratory maintenance in from the South China Sea.南海来源的甲烷单加氧酶的分子鉴定及实验室培养条件下甲烷营养型内共生菌的定量分析
PeerJ. 2017 Aug 7;5:e3565. doi: 10.7717/peerj.3565. eCollection 2017.
7
Multiple I-Type Lysozymes in the Hydrothermal Vent Mussel Bathymodiolus azoricus and Their Role in Symbiotic Plasticity.热液喷口贻贝阿氏深海贻贝中的多种I型溶菌酶及其在共生可塑性中的作用
PLoS One. 2016 Feb 16;11(2):e0148988. doi: 10.1371/journal.pone.0148988. eCollection 2016.
8
The transcriptome of Bathymodiolus azoricus gill reveals expression of genes from endosymbionts and free-living deep-sea bacteria.深海贻贝(Bathymodiolus azoricus)鳃转录组揭示了共生和自由生活深海细菌基因的表达。
Mar Drugs. 2012 Aug;10(8):1765-1783. doi: 10.3390/md10081765. Epub 2012 Aug 20.
从 Alvinella pompejana cDNA 中洞察后生动物的进化。
BMC Genomics. 2010 Nov 16;11:634. doi: 10.1186/1471-2164-11-634.
4
Response of the Pacific oyster Crassostrea gigas, Thunberg 1793, to pesticide exposure under experimental conditions.太平洋牡蛎(Crassostrea gigas,Thunberg 1793)在实验条件下对农药暴露的反应。
J Exp Biol. 2010 Dec 1;213(Pt 23):4010-7. doi: 10.1242/jeb.048033.
5
High-throughput sequencing and analysis of the gill tissue transcriptome from the deep-sea hydrothermal vent mussel Bathymodiolus azoricus.高通量测序及深海热液喷口贻贝 Bathymodiolus azoricus 鳃组织转录组分析。
BMC Genomics. 2010 Oct 11;11:559. doi: 10.1186/1471-2164-11-559.
6
Scophthalmus maximus cystatin B enhances head kidney macrophage-mediated bacterial killing.大弹涂鱼胱抑素 B 增强头肾巨噬细胞介导的细菌杀伤作用。
Dev Comp Immunol. 2010 Dec;34(12):1237-41. doi: 10.1016/j.dci.2010.07.008. Epub 2010 Aug 12.
7
A new lysozyme from the eastern oyster, Crassostrea virginica, and a possible evolutionary pathway for i-type lysozymes in bivalves from host defense to digestion.一种来自东方牡蛎(Crassostrea virginica)的新溶菌酶,以及双壳类动物中 i 型溶菌酶从宿主防御到消化的可能进化途径。
BMC Evol Biol. 2010 Jul 15;10:213. doi: 10.1186/1471-2148-10-213.
8
Lipopolysaccharides and plant innate immunity.脂多糖与植物先天免疫
Subcell Biochem. 2010;53:387-403. doi: 10.1007/978-90-481-9078-2_17.
9
Proteomic and transcriptional analyses of coral larvae newly engaged in symbiosis with dinoflagellates.与虫黄藻共生的珊瑚幼虫的蛋白质组学和转录组学分析。
Comp Biochem Physiol Part D Genomics Proteomics. 2007 Mar;2(1):63-73. doi: 10.1016/j.cbd.2006.11.003. Epub 2006 Dec 5.
10
Coral host transcriptomic states are correlated with Symbiodinium genotypes.珊瑚宿主转录组状态与共生藻基因型相关。
Mol Ecol. 2010 Mar;19(6):1174-86. doi: 10.1111/j.1365-294X.2010.04534.x. Epub 2010 Feb 8.