Using Bacteriophages to Characterize Gut Microbe Interactions In Situ

2021 ◽  
pp. 110715
Author(s):  
Tyler Alexander Cookson
2019 ◽  
Author(s):  
Benedikt K Geier ◽  
Emilia Sogin ◽  
Dolma Michellod ◽  
Moritz Janda ◽  
Mario Kompauer ◽  
...  

Spatial metabolomics describes the location and chemistry of small molecules involved in metabolic phenotypes, defense molecules and chemical interactions in natural communities. Most current techniques are unable to spatially link the genotype and metabolic phenotype of microorganisms in situ at a scale relevant to microbial interactions. Here, we present a spatial metabolomics pipeline (metaFISH) that combines fluorescence in situ hybridization (FISH) microscopy and high-resolution atmospheric pressure mass spectrometry imaging (AP-MALDI-MSI) to image host-microbe symbioses and their metabolic interactions. metaFISH aligns and integrates metabolite and fluorescent images at the micrometer-scale for a spatial assignment of host and symbiont metabolites on the same tissue section. To illustrate the advantages of metaFISH, we mapped the spatial metabolome of a deep-sea mussel and its intracellular symbiotic bacteria at the scale of individual epithelial host cells. Our analytical pipeline revealed metabolic adaptations of the epithelial cells to the intracellular symbionts, a variation in metabolic phenotypes in one symbiont type, and novel symbiosis metabolites. metaFISH provides a culture-independent approach to link metabolic phenotypes to community members in situ - a powerful tool for microbiologists across fields.


2020 ◽  
Vol 34 (8) ◽  
pp. 10682-10698
Author(s):  
Chuanhai Zhang ◽  
Xiaoyun He ◽  
Yao Sheng ◽  
Cui Yang ◽  
Jia Xu ◽  
...  

2020 ◽  
Author(s):  
Hugo R. Barajas ◽  
Shamayim Martínez-Sánchez ◽  
Miguel F. Romero ◽  
Cristóbal Hernández-Álvarez ◽  
Luis Servín-González ◽  
...  

AbstractThe two-step model for plant root microbiomes considers soil as the primary microbial source. Active selection of the plant’s bacterial inhabitants results in a biodiversity decrease towards roots. We collected in situ ruderal plant roots and their soils and used these soils as the main microbial input for single genotype tomatoes grown in a greenhouse. We massively sequenced the 16S rRNA and shotgun metagenomes of the soils, in situ plants, and tomato roots. Tomato roots did follow the two-step model, while ruderal plants did not. Ruderal plants and their soils are closer than tomato and its soil, based on protein comparisons. We calculated a metagenomic tomato root core of 51 bacterial genera and 2,762 proteins, which could be the basis for microbiome-oriented plant breeding programs. The tomato and ruderal metagenomic differences are probably due to plant domestication trade-offs, impacting plant-microbe interactions.


2020 ◽  
Vol 33 (2) ◽  
pp. 124-134 ◽  
Author(s):  
Bridget S. O’Banion ◽  
Lindsey O’Neal ◽  
Gladys Alexandre ◽  
Sarah L. Lebeis

Although the influence of microbiomes on the health of plant hosts is evident, specific mechanisms shaping the structure and dynamics of microbial communities in the phyllosphere and rhizosphere are only beginning to become clear. Traditionally, plant–microbe interactions have been studied using cultured microbial isolates and plant hosts but the rising use of ‘omics tools provides novel snapshots of the total complex community in situ. Here, we discuss the recent advances in tools and techniques used to monitor plant–microbe interactions and the chemical signals that influence these relationships in above- and belowground tissues. Particularly, we highlight advances in integrated microscopy that allow observation of the chemical exchange between individual plant and microbial cells, as well as high-throughput, culture-independent approaches to investigate the total genetic and metabolic contribution of the community. The chemicals discussed have been identified as relevant signals across experimental spectrums. However, mechanistic insight into the specific interactions mediated by many of these chemicals requires further testing. Experimental designs that attempt to bridge the gap in biotic complexity between single strains and whole communities will advance our understanding of the chemical signals governing plant–microbe associations in the rhizosphere and phyllosphere.


2020 ◽  
Author(s):  
Juliana Gil Loaiza ◽  
Laura Meredith ◽  
Jordan Krechmer ◽  
Megan Claflin ◽  
Rob Roscioli ◽  
...  

<p>Microbial metabolic functions and biogeochemical pathways of the complex rhizosphere-soil-microbe interactions change with aboveground vegetation and the ecosystem response to environmental changes. Soil trace gases and current genomic approaches have been valuable to characterize in-situ microbial activity. However, there is a lack of understanding of the complexity of the belowground processes, the time frame of microbial community responses to environmental changes and the degree to which microbial activity can be inferred current -omics approaches. In the nitrogen cycling at a field scale, microbial diversity or gene abundance sometimes does not explain N<sub>2</sub>O emissions or even gene expression, there some bacteria that cannot be cultivated, and in general –omics involve destructive soil sampling that is prone to changes of the in-situ soil conditions. Additionally, field soil sampling may not capture the heterogeneity of the soil or specific area of study.</p><p>Volatile Organic Compounds (VOCs) produced in the rhizosphere play an important role in microbial nutrient cycling. VOCs are produced by plants and microorganisms as a response to biotic or biotic stressors or the type of carbon sources available.</p><p>Here, we present how subsurface soil gas measurements in an enclosed ecosystem during the Water, Atmosphere, and Life Dynamics experiment (B2-WALD) at the Tropical Rainforest biome of Biosphere 2 (Arizona, USA) during an induced controlled drought. We present initial results of a unique non-destructive approach that simultaneously couples a) new hydrophobic-porous subsurface soil probes, b) high-resolution Tunable Infrared Laser Direct Absorption Spectrometers (TILDAS) to analyze in situ trace gas isotopomers, and c) a proton transfer reaction mass spectrometer (VOCUS, high resolution volatile organic compound gas analyzer) for VOC quantification. We measured soil gas isotopic composition of N<sub>2</sub>O and VOCs-- comparing rhizosphere and control areas before and during the drought. We will focus our discussion on VOCs and its potential as makers of microbial interactions and signaling as a response to an environmental stressor like drought.</p><p>In this project, we demonstrate the feasibility of online coupling of soil probes with high-resolution instrumentation to measure products from nitrogen cycling and nonmethane VOC production in soils as a response to soil-plant microbe interactions. In addition, this approach could be a potential tool to constraint inferences derived from different –omics approaches.</p>


mSystems ◽  
2018 ◽  
Vol 3 (2) ◽  
Author(s):  
Melissa M. Galey ◽  
Laura M. Sanchez

ABSTRACT Microbial communities contribute to a wide variety of biological functions in hosts and have the ability to specifically influence the health of those organisms through production of specialized metabolites. However, the structures or molecular mechanisms related to health or disease in host-microbe interactions represent a knowledge gap. In order to close this gap, we propose that a combinatory approach, pulling from microbiology and analytical chemistry, be considered to investigate these interactions so as to gain a better understanding of the chemistry being produced. We hypothesize that bacteria alter their chemistry in order to survive and induce specific states in their host organisms. Our lab makes use of imaging mass spectrometry and other analytical techniques to study this chemistry in situ , which provides actionable information to test hypotheses.


iScience ◽  
2021 ◽  
pp. 103216
Author(s):  
Jürgen W. Schönborn ◽  
Fiona A. Stewart ◽  
Kerstin Maas Enriquez ◽  
Irfan Akhtar ◽  
Andrea Droste ◽  
...  

2019 ◽  
Author(s):  
Anja Røyne ◽  
Yi Jing Phua ◽  
Simone Balzer Le ◽  
Ina Grosås Eikjeland ◽  
Kjell Domaas Josefsen ◽  
...  

AbstractThe production of concrete for construction purposes is a major source of anthropogenic CO2 emissions. One promising avenue towards a more sustainable construction industry is to make use of naturally occurring mineral-microbe interactions, such as microbial-induced carbonate precipitation (MICP), to produce solid materials. In this paper, we present a new process where calcium carbonate in the form of powdered limestone is transformed to a binder material (termed BioZEment) through microbial dissolution and recrystallization. For the dissolution step, a suitable bacterial strain, closely related to Bacillus pumilus, was isolated from soil near a limestone quarry. We show that this strain produces organic acids from glucose, inducing the dissolution of calcium carbonate in an aqueous slurry of powdered limestone. In the second step, the dissolved limestone solution is used as the calcium source for MICP in sand packed syringe moulds. The amounts of acid produced and calcium carbonate dissolved are shown to depend on the amount of available oxygen as well as the degree of mixing. Precipitation is induced through the pH increase caused by the hydrolysis of urea, mediated by the enzyme urease, which is produced in situ by the bacterium Sporosarcina pasteurii DSM33. The degree of successful consolidation of sand by BioZEment was found to depend on both the amount of urea and the amount of glucose available in the dissolution reaction.


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