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Targeted gut microbiota manipulation attenuates seizures in a model of infantile spasms syndrome
Chunlong Mu, Naghmeh Nikpoor, Thomas A. Tompkins, Anamika Choudhary, Melinda Wang, Wendie N. Marks, Jong M. Rho, Morris H. Scantlebury, Jane Shearer
Chunlong Mu, Naghmeh Nikpoor, Thomas A. Tompkins, Anamika Choudhary, Melinda Wang, Wendie N. Marks, Jong M. Rho, Morris H. Scantlebury, Jane Shearer
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Research Article Metabolism

Targeted gut microbiota manipulation attenuates seizures in a model of infantile spasms syndrome

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Abstract

Infantile spasms syndrome (IS) is a devastating early-onset epileptic encephalopathy associated with poor neurodevelopmental outcomes. When first-line treatment options, including adrenocorticotropic hormone and vigabatrin, are ineffective, the ketogenic diet (KD) is often employed to control seizures. Since the therapeutic impact of the KD is influenced by the gut microbiota, we examined whether targeted microbiota manipulation, mimicking changes induced by the KD, would be valuable in mitigating seizures. Employing a rodent model of symptomatic IS, we show that both the KD and antibiotic administration reduce spasm frequency and are associated with improved developmental outcomes. Spasm reductions were accompanied by specific gut microbial alterations, including increases in Streptococcus thermophilus and Lactococcus lactis. Mimicking the fecal microbial alterations in a targeted probiotic, we administered these species in a 5:1 ratio. Targeted probiotic administration reduced seizures and improved locomotor activities in control diet–fed animals, similar to KD-fed animals, while a negative control (Ligilactobacillus salivarius) had no impact. Probiotic administration also increased antioxidant status and decreased proinflammatory cytokines. Results suggest that a targeted probiotic reduces seizure frequency, improves locomotor activity in a rodent model of IS, and provides insights into microbiota manipulation as a potential therapeutic avenue for pediatric epileptic encephalopathies.

Authors

Chunlong Mu, Naghmeh Nikpoor, Thomas A. Tompkins, Anamika Choudhary, Melinda Wang, Wendie N. Marks, Jong M. Rho, Morris H. Scantlebury, Jane Shearer

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Figure 3

Effects of antibiotics on the gut microbiota composition.

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Effects of antibiotics on the gut microbiota composition.
(A) Animals we...
(A) Animals were given diets without (CDE, KDE) or with antibiotics (CDE + Abx; KDE + Abx) after epilepsy induction from P5 to P7 following the timeline shown (left); effect of antibiotic treatment on seizure frequency (right). (n = 9, 11, 8, and 15 for CDE, CDE + Abx, KDE, and KDE + Abx, respectively). The data were analyzed using 1-way ANOVA with Tukey’s post hoc. (B) Body weight gain (n = 14, 17, 20, and 17 for CDE, CDE + Abx, KDE, and KDE + Abx, respectively). (C) Quantitative PCR analysis of fecal 16S rRNA gene copies (n = 6, 6, 12, 11, 12, and 10 for CDS, KDS, CDE, CDE + Abx, KDE, and KDE + Abx, respectively). (D) Relative abundances of Streptococcus and Lactococcus (n = 6, 6, 12, 10, 12, and 10 for CDS, KDS, CDE, CDE + Abx, KDE, and KDE + Abx, respectively). (E) Relative abundances of Streptococcus thermophilus and Lactococcus lactis (n = 6, 6, 12, 11, 12, and 10 for CDS, KDS, CDE, CDE + Abx, KDE, and KDE + Abx, respectively). (A and B) values are mean ± SEM. (C–E) The data are presented as box and whisker plots (minimum to maximum values). (A, D, and E) *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, #0.1 < P < 0.05. (B and C) Labeled means without a common superscript letter differ, P < 0.05. CDE, CDE + Abx are control diet, epilepsy induction without and with antibiotics; KDE, KDE + Abx are ketogenic diet, epilepsy induction without and with antibiotics.

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