TY - JOUR
T1 - The Fecal Microbiome and Metabolome of Pitt Hopkins Syndrome, a Severe Autism Spectrum Disorder
AU - Dilmore, Amanda H.
AU - McDonald, Daniel
AU - Nguyen, Tanya T.
AU - Adams, James B.
AU - Krajmalnik-Brown, Rosa
AU - Elijah, Emmanuel
AU - Dorrestein, Pieter C.
AU - Knight, Rob
N1 - Funding Information:
We thank the Pitt Hopkins Research Foundation for their generous support and the families who took part in the research. We thank Gail Ackermann for metadata support; Greg Humphrey, Tara Schwartz, MacKenzie Bryant, Karenina Sanders, and Rodolfo Salido Benitez for 16S and metagenomics preparation; and Dominic Nguyen for microbiome kit support. T.T.N. is supported by NIH grant K23 MH118435.
Publisher Copyright:
© 2021 Dilmore et al.
PY - 2021/12
Y1 - 2021/12
N2 - Alterations to the gut microbiome have been reported between children with autism spectrum disorders (ASDs) and typically developing (TD) children. Characterizing these differences has led to the proposal of new treatments for ASD, such as probiotic interventions and fecal matter transplants. However, no study to date has characterized the gut microbiome or metabolome in Pitt Hopkins syndrome (PTHS), a severe ASD with a high incidence of gastrointestinal (GI) disturbances such as constipation. Here, we surveyed the gut microbiome and metabolome in a cohort of PTHS individuals and their unaffected parents. We focused our analysis on Clostridium bolteae, a microbe previously associated with ASD known to chemically modify bile acids in the gut. PTHS individuals carry a higher load of C. bolteae than their parents as well as both ASD and non-ASD individuals from the American Gut Project cohort. Specific metabolites were associated with PTHS, including bile acids and sphingosines. With a metadata reanalysis tool, we found that PTHS-associated metabolites have previously been identified in inflammatory bowel disease and obesity patients. These results suggest microbial involvement in PTHS, but further research must be performed to clarify the exact mechanisms through which microbes may act. Furthermore, new associations between PTHS-specific metabolites and other conditions may lead to additional therapeutic options for PTHS individuals.
AB - Alterations to the gut microbiome have been reported between children with autism spectrum disorders (ASDs) and typically developing (TD) children. Characterizing these differences has led to the proposal of new treatments for ASD, such as probiotic interventions and fecal matter transplants. However, no study to date has characterized the gut microbiome or metabolome in Pitt Hopkins syndrome (PTHS), a severe ASD with a high incidence of gastrointestinal (GI) disturbances such as constipation. Here, we surveyed the gut microbiome and metabolome in a cohort of PTHS individuals and their unaffected parents. We focused our analysis on Clostridium bolteae, a microbe previously associated with ASD known to chemically modify bile acids in the gut. PTHS individuals carry a higher load of C. bolteae than their parents as well as both ASD and non-ASD individuals from the American Gut Project cohort. Specific metabolites were associated with PTHS, including bile acids and sphingosines. With a metadata reanalysis tool, we found that PTHS-associated metabolites have previously been identified in inflammatory bowel disease and obesity patients. These results suggest microbial involvement in PTHS, but further research must be performed to clarify the exact mechanisms through which microbes may act. Furthermore, new associations between PTHS-specific metabolites and other conditions may lead to additional therapeutic options for PTHS individuals.
KW - Autism spectrum disorders
KW - Computational biology
KW - Microbiome
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U2 - 10.1128/mSystems.01006-21
DO - 10.1128/mSystems.01006-21
M3 - Article
AN - SCOPUS:85122632771
SN - 2379-5077
VL - 6
JO - mSystems
JF - mSystems
IS - 6
M1 - e01006-21
ER -