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Plant-based enteral nutrition outperforms ultra-processed formulas in mitigating consequences of antibiotic-induced dysbiosis
Mona Chatrizeh, Jianmin Tian, Matthew Rogers, Firuz Feturi, Guojun Wu, Brian Firek, Roman Nikonov, Lauren Cass, Alexandra Sheppeck, Lavnish Ojha, Ali Carroll, Matthew Henkel, Justin Azar, Rajesh K. Aneja, Brian Campfield, Dennis Simon, Michael J. Morowitz
Mona Chatrizeh, Jianmin Tian, Matthew Rogers, Firuz Feturi, Guojun Wu, Brian Firek, Roman Nikonov, Lauren Cass, Alexandra Sheppeck, Lavnish Ojha, Ali Carroll, Matthew Henkel, Justin Azar, Rajesh K. Aneja, Brian Campfield, Dennis Simon, Michael J. Morowitz
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Research Article Gastroenterology Immunology

Plant-based enteral nutrition outperforms ultra-processed formulas in mitigating consequences of antibiotic-induced dysbiosis

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Abstract

Malnutrition, gut inflammation, and antibiotic-induced dysbiosis are well-recognized risk factors for poor clinical outcomes among critically ill patients. We previously showed that commercially available plant-based enteral nutrition (PBEN) preserves a commensal microbiome compared with commonly used artificial enteral nutrition (AEN). In this study, PBEN was superior to AEN in promoting recovery from antibiotic-induced dysbiosis in mice and humans. PBEN effectively mitigated anemia and leukopenia, restored naive lymphocyte populations, and reduced bone marrow myeloid expansion. Animals randomized to PBEN also exhibited improved responses to infectious gastrointestinal challenges following antibiotic exposure. A pilot clinical study validated these findings, demonstrating increased gut commensals, reduced pathogens, and improved leukocyte balance in critically ill children receiving PBEN compared with AEN. Together, these results suggest that PBEN offers a practical dietary approach to mitigate antibiotic-associated complications and potentially improve clinical outcomes among hospitalized patients requiring supplemental nutrition.

Authors

Mona Chatrizeh, Jianmin Tian, Matthew Rogers, Firuz Feturi, Guojun Wu, Brian Firek, Roman Nikonov, Lauren Cass, Alexandra Sheppeck, Lavnish Ojha, Ali Carroll, Matthew Henkel, Justin Azar, Rajesh K. Aneja, Brian Campfield, Dennis Simon, Michael J. Morowitz

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Figure 3

PBEN but not AEN mitigates signs of intestinal inflammation due to ABX exposure.

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PBEN but not AEN mitigates signs of intestinal inflammation due to ABX e...
(A) Disease activity index (DAI) following antibiotic treatment and dietary intervention (n = 5 per group). (B) Cecal/body weight ratio in PBEN (n = 5) versus AEN (n = 4) mice with representative cecal images. (C) Fecal Lcn2 levels (n = 11 per group). (D) Heatmap of relative expression of 32 cytokines from colon tissue lysates (n = 6–11 per group); X denotes undetectable cytokines. Selected cytokines (IL-6, TNF-α, IFN-γ) are shown as pg/mg protein. (E) Splenic bacterial burden (n = 5–7 per group) with representative images. (F) Ileal Reg3g protein and mRNA expression (n = 5–11 per group). Data represent mean ± SEM. Significance: 2-tailed Student’s t test comparing ABX-naive vs. ABX-treated and PBEN vs. AEN after ABX. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001.

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