Sex-related alterations of gut microbiota composition in the BTBR mouse model of autism spectrum disorder

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作者
Lorena Coretti
Claudia Cristiano
Ermanno Florio
Giovanni Scala
Adriano Lama
Simona Keller
Mariella Cuomo
Roberto Russo
Raffaela Pero
Orlando Paciello
Giuseppina Mattace Raso
Rosaria Meli
Sergio Cocozza
Antonio Calignano
Lorenzo Chiariotti
Francesca Lembo
机构
[1] Institute of Endocrinologia ed Oncologia Sperimentale,Department of Pharmacy
[2] IEOS,Department of Medicina Molecolare e Biotecnologie Mediche
[3] Consiglio Nazionale delle Ricerche CNR,Department of Veterinary Medicine and Animal Production
[4] University of Naples Federico II,undefined
[5] University of Naples Federico II,undefined
[6] Istituto Nazionale di Fisica Nucleare,undefined
[7] Sezione di Napoli,undefined
[8] University of Naples Federico II,undefined
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Alterations of microbiota-gut-brain axis have been invoked in the pathogenesis of autism spectrum disorders (ASD). Mouse models could represent an excellent tool to understand how gut dysbiosis and related alterations may contribute to autistic phenotype. In this study we paralleled gut microbiota (GM) profiles, behavioral characteristics, intestinal integrity and immunological features of colon tissues in BTBR T + tf/J (BTBR) inbred mice, a well established animal model of ASD. Sex differences, up to date poorly investigated in animal models, were specifically addressed. Results showed that BTBR mice of both sexes presented a marked intestinal dysbiosis, alterations of behavior, gut permeability and immunological state with respect to prosocial C57BL/6j (C57) strain. Noticeably, sex-related differences were clearly detected. We identified Bacteroides, Parabacteroides, Sutterella, Dehalobacterium and Oscillospira genera as key drivers of sex-specific gut microbiota profiles associated with selected pathological traits. Taken together, our findings indicate that alteration of GM in BTBR mice shows relevant sex-associated differences and supports the use of BTBR mouse model to dissect autism associated microbiota-gut-brain axis alteration.
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