TY - JOUR
T1 - Approaches to discern if microbiome associations reflect causation in metabolic and immune disorders
AU - Basic, Marijana
AU - Dardevet, Dominique
AU - Abuja, Peter Michael
AU - Bolsega, Silvia
AU - Bornes, Stephanie
AU - Caesar, Robert
AU - Calabrese, Francesco Maria
AU - Collino, Massimo
AU - De Angelis, Maria
AU - Gerard, Philippe
AU - Gueimonde, Miguel
AU - Leulier, Francois
AU - Untersmayr, Eva
AU - Van Rymenant, Evelien
AU - De Vos, Paul
AU - Savary-Auzeloux, Isabelle
PY - 2022/12/31
Y1 - 2022/12/31
N2 - Our understanding of microorganisms residing within our gut and their roles in the host metabolism and immunity advanced greatly over the past 20 years. Currently, microbiome studies are shifting from association and correlation studies to studies demonstrating causality of identified microbiome signatures and identification of molecular mechanisms underlying these interactions. This transformation is crucial for the efficient translation into clinical application and development of targeted strategies to beneficially modulate the intestinal microbiota. As mechanistic studies are still quite challenging to perform in humans, the causal role of microbiota is frequently evaluated in animal models that need to be appropriately selected. Here, we provide a comprehensive overview on approaches that can be applied in addressing causality of host-microbe interactions in five major animal model organisms (Caenorhabditis elegans, Drosophila melanogaster, zebrafish, rodents, and pigs). We particularly focused on discussing methods available for studying the causality ranging from the usage of gut microbiota transfer, diverse models of metabolic and immune perturbations involving nutritional and chemical factors, gene modifications and surgically induced models, metabolite profiling up to culture-based approached. Furthermore, we addressed the impact of the gut morphology, physiology as well as diet on the microbiota composition in various models and resulting species specificities. Finally, we conclude this review with the discussion on models that can be applied to study the causal role of the gut microbiota in the context of metabolic syndrome and host immunity. We hope this review will facilitate important considerations for appropriate animal model selection.
AB - Our understanding of microorganisms residing within our gut and their roles in the host metabolism and immunity advanced greatly over the past 20 years. Currently, microbiome studies are shifting from association and correlation studies to studies demonstrating causality of identified microbiome signatures and identification of molecular mechanisms underlying these interactions. This transformation is crucial for the efficient translation into clinical application and development of targeted strategies to beneficially modulate the intestinal microbiota. As mechanistic studies are still quite challenging to perform in humans, the causal role of microbiota is frequently evaluated in animal models that need to be appropriately selected. Here, we provide a comprehensive overview on approaches that can be applied in addressing causality of host-microbe interactions in five major animal model organisms (Caenorhabditis elegans, Drosophila melanogaster, zebrafish, rodents, and pigs). We particularly focused on discussing methods available for studying the causality ranging from the usage of gut microbiota transfer, diverse models of metabolic and immune perturbations involving nutritional and chemical factors, gene modifications and surgically induced models, metabolite profiling up to culture-based approached. Furthermore, we addressed the impact of the gut morphology, physiology as well as diet on the microbiota composition in various models and resulting species specificities. Finally, we conclude this review with the discussion on models that can be applied to study the causal role of the gut microbiota in the context of metabolic syndrome and host immunity. We hope this review will facilitate important considerations for appropriate animal model selection.
KW - Gut microbiota
KW - Caenorhabditis elegans
KW - Causality
KW - Drosophila melanogaster
KW - Human
KW - Immunity
KW - Metabolism
KW - Pig
KW - Rodent
KW - Zebrafish
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=researchintelligenceproject&SrcAuth=WosAPI&KeyUT=WOS:000837479100001&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1080/19490976.2022.2107386
DO - 10.1080/19490976.2022.2107386
M3 - (Systematic) Review article
C2 - 35939623
SN - 1949-0976
VL - 14
JO - Gut microbes
JF - Gut microbes
IS - 1
M1 - 2107386
ER -