scholarly journals Holistic Assessment of Rumen Microbiome Dynamics through Quantitative Metatranscriptomics Reveals Multifunctional Redundancy during Key Steps of Anaerobic Feed Degradation

mSystems ◽  
2018 ◽  
Vol 3 (4) ◽  
Author(s):  
Andrea Söllinger ◽  
Alexander Tøsdal Tveit ◽  
Morten Poulsen ◽  
Samantha Joan Noel ◽  
Mia Bengtsson ◽  
...  

ABSTRACTRuminant livestock is a major source of the potent greenhouse gas methane. The complex rumen microbiome, consisting of bacteria, archaea, and microbial eukaryotes, facilitates anaerobic plant biomass degradation in the cow rumen, leading to methane emissions. Using an integrated approach combining multidomain quantitative metatranscriptomics with gas and volatile fatty acid (VFA) profiling, we aimed at obtaining the most comprehensive picture of the active rumen microbiome during feed degradation to date. Bacterial, archaeal, and eukaryotic biomass, but also methane emissions and VFA concentrations, increased drastically within an hour after feed intake. mRNA profiling revealed a dynamic response of carbohydrate-active enzyme transcripts, transcripts involved in VFA production and methanogenesis. While the relative abundances of functional transcripts did not mirror observed processes, such as methane emissions, transformation to mRNA abundance per gram of rumen fluid echoed ruminant processes. The microbiome composition was highly individual, with, e.g., ciliate,Neocallimastigaceae,Prevotellaceae,Succinivibrionaceae, andFibrobacteraceaeabundances differing between cows. Microbiome individuality was accompanied by inter- and intradomain multifunctional redundancy among microbiome members during feed degradation. This likely enabled the robust performance of the anaerobic degradation process in each rumen.Neocallimastigaceaeand ciliates contributed an unexpectedly large share of transcripts for cellulose- and hemicellulose-degrading enzymes, respectively. Methyl-reducing but not CO2-reducing methanogens were positively correlated with methane emissions. WhileMethanomassiliicoccalesswitched from methanol to methylamines as electron acceptors,Methanosphaerabecame the dominating methanol-reducing methanogen. This study for the first time linked rumen meta-omics with processes and enabled holistic insights into the contribution of all microbiome members to feed degradation.IMPORTANCERuminant animals, such as cows, live in a tight symbiotic association with microorganisms, allowing them to feed on otherwise indigestible plant biomass as food sources. Methane is produced as an end product of the anaerobic feed degradation in ruminants and is emitted to the atmosphere, making ruminant animals among the major anthropogenic sources of the potent greenhouse gas methane. Using newly developed quantitative metatranscriptomics for holistic microbiome analysis, we here identified bacterial, archaeal, and eukaryotic key players and the short-term dynamics of the rumen microbiome during anaerobic plant biomass degradation and subsequent methane emissions. These novel insights might pave the way for novel ecologically and economically sustainable methane mitigation strategies, much needed in times of global climate change.

2018 ◽  
Author(s):  
Andrea Söllinger ◽  
Alexander Tøsdal Tveit ◽  
Morten Poulsen ◽  
Samantha Joan Noel ◽  
Mia Bengtsson ◽  
...  

AbstractBackgroundRuminant livestock is a major source of the potent greenhouse gas methane (CH4), produced by the complex rumen microbiome. Using an integrated approach, combining quantitative metatranscriptomics with gas- and volatile fatty acid (VFA) profiling, we gained fundamental insights into temporal dynamics of the cow rumen microbiome during feed degradation.ResultsThe microbiome composition was highly individual and remarkably stable within each cow, despite similar gas emission and VFA profiles between cows. Gene expression profiles revealed a fast microbial growth response to feeding, reflected by drastic increases in microbial biomass, CH4emissions and VFA concentrations. Microbiome individuality was accompanied by high inter- and intra-domain functional redundancy among pro- and eukaryotic microbiome members in the key steps of anaerobic feed degradation. Methyl-reducing but not CO2-reducing methanogens were correlated with increased CH4emissions during plant biomass degradation.ConclusionsThe major response of the rumen microbiome to feed intake was a general growth of the whole community. The high functional redundancy of the cow-individual microbiomes was possibly linked to the robust performance of the anaerobic degradation process. Furthermore, the strong response of methylotrophic methanogens is suggesting that they might play a more important role in ruminant CH4emissions than previously assumed, making them potential targets for CH4mitigation strategies.


2019 ◽  
Vol 47 (6) ◽  
pp. 1895-1907 ◽  
Author(s):  
Andrea Söllinger ◽  
Tim Urich

Research on methanogenic Archaea has experienced a revival, with many novel lineages of methanogens recently being found through cultivation and suggested via metagenomics approaches, respectively. Most of these lineages comprise Archaea (potentially) capable of methanogenesis from methylated compounds, a pathway that had previously received comparably little attention. In this review, we provide an overview of these new lineages with a focus on the Methanomassiliicoccales. These lack the Wood–Ljungdahl pathway and employ a hydrogen-dependent methylotrophic methanogenesis pathway fundamentally different from traditional methylotrophic methanogens. Several archaeal candidate lineages identified through metagenomics, such as the Ca. Verstraetearchaeota and Ca. Methanofastidiosa, encode genes for a methylotrophic methanogenesis pathway similar to the Methanomassiliicoccales. Thus, the latter are emerging as a model system for physiological, biochemical and ecological studies of hydrogen-dependent methylotrophic methanogens. Methanomassiliicoccales occur in a large variety of anoxic habitats including wetlands and animal intestinal tracts, i.e. in the major natural and anthropogenic sources of methane emissions, respectively. Especially in ruminant animals, they likely are among the major methane producers. Taken together, (hydrogen-dependent) methylotrophic methanogens are much more diverse and widespread than previously thought. Considering the role of methane as potent greenhouse gas, resolving the methanogenic nature of a broad range of putative novel methylotrophic methanogens and assessing their role in methane emitting environments are pressing issues for future research on methanogens.


2017 ◽  
Vol 11 (11) ◽  
pp. 2538-2551 ◽  
Author(s):  
Olov Svartström ◽  
Johannes Alneberg ◽  
Nicolas Terrapon ◽  
Vincent Lombard ◽  
Ino de Bruijn ◽  
...  

2019 ◽  
Author(s):  
Jaire A. Ferreira Filho ◽  
Maria Augusta C. Horta ◽  
Clelton A. dos Santos ◽  
Deborah A. Almeida ◽  
Natália F. Murad ◽  
...  

AbstractBackgroundUnveiling fungal genome structure and function reveals the potential biotechnological use of fungi. Trichoderma harzianum is a powerful CAZyme-producing fungus. We studied the genomic regions in T. harzianum IOC3844 containing CAZyme genes, transcription factors and transporters.ResultsWe used bioinformatics tools to mine the T. harzianum genome for potential genomics, transcriptomics, and exoproteomics data and coexpression networks. The DNA was sequenced by PacBio SMRT technology for multi-omics data analysis and integration. In total, 1676 genes were annotated in the genomic regions analyzed; 222 were identified as CAZymes in T. harzianum IOC3844. When comparing transcriptome data under cellulose or glucose conditions, 114 genes were differentially expressed in cellulose, with 51 CAZymes. CLR2, a transcription factor physically and phylogenetically conserved in T. harzianum spp., was differentially expressed under cellulose conditions. The genes induced/repressed under cellulose conditions included those important for plant biomass degradation, including CIP2 of the CE15 family and a copper-dependent LPMO of the AA9 family.ConclusionsOur results provide new insights into the relationship between genomic organization and hydrolytic enzyme expression and regulation in T. harzianum IOC3844. Our results can improve plant biomass degradation, which is fundamental for developing more efficient strains and/or enzymatic cocktails for the production of hydrolytic enzymes.


Author(s):  
Camila L. Corrêa ◽  
Glaucia E. O. Midorikawa ◽  
Edivaldo Ximenes Ferreira Filho ◽  
Eliane Ferreira Noronha ◽  
Gabriel S. C. Alves ◽  
...  

2009 ◽  
Vol 59 (2) ◽  
pp. 212-213 ◽  
Author(s):  
Mark Morrison ◽  
◽  
Sean C. Daugherty ◽  
William C. Nelson ◽  
Tanja Davidsen ◽  
...  

2018 ◽  
Vol 91 ◽  
pp. 79-99 ◽  
Author(s):  
M.R. Mäkelä ◽  
M. DiFalco ◽  
E. McDonnell ◽  
T.T.M. Nguyen ◽  
A. Wiebenga ◽  
...  

2013 ◽  
Vol 6 (1) ◽  
pp. 24 ◽  
Author(s):  
Aaron Weimann ◽  
Yulia Trukhina ◽  
Phillip B Pope ◽  
Sebastian GA Konietzny ◽  
Alice C McHardy

2017 ◽  
Vol 5 (40) ◽  
Author(s):  
Christian Abendroth ◽  
Sarah Hahnke ◽  
Francisco M. Codoñer ◽  
Michael Klocke ◽  
Olaf Luschnig ◽  
...  

ABSTRACT A new Firmicutes isolate, strain HV4-6-A5C, was obtained from the hydrolysis stage of a mesophilic and anaerobic two-stage lab-scale leach-bed system for biomethanation of fresh grass. It is assumed that the bacterial isolate contributes to plant biomass degradation. Here, we report a draft annotated genome sequence of this organism.


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