# Rhodotorula mucilaginosa JAASSRY1 Ameliorates Cyclophosphamide-Induced Immunosuppression by Regulating Gut Microbiota and Activation of Spleen TLR4/MyD88/NF-κB Pathway

**Authors:** Min Yang, Yuguang He, Xinyu Miao, Mubai Sun, Honghong Niu, Mei Hua, Da Li, Hongyan Xu, Jinghui Wang

PMC · DOI: 10.4014/jmb.2510.10031 · Journal of Microbiology and Biotechnology · 2026-01-21

## TL;DR

A yeast called Rhodotorula mucilaginosa helps reverse immune damage in mice caused by a chemotherapy drug by improving gut bacteria and boosting immune function.

## Contribution

JAASSRY1 ameliorates CTX-induced immunosuppression via gut microbiota modulation and spleen pathway activation.

## Key findings

- JAASSRY1 reversed CTX-induced weight loss and immune organ atrophy in mice.
- The yeast suppressed pro-inflammatory cytokines and restored immunoglobulin levels.
- JAASSRY1 modulated gut microbiota and the TLR4/MyD88/NF-κB pathway to reduce spleen injury.

## Abstract

The present study was designed to evaluate the ameliorative effects of Rhodotorula mucilaginosa JAASSRY1 (JAASSRY1) on cyclophosphamide (CTX)-induced immunosuppression in mice. Immunocompromised mice were established by intraperitoneal injection of CTX (80 mg/kg/bw) for three consecutive days, followed by JAASSRY1 orally administered of JAASSRY1 for 21 days. Various immunological parameters, including immune organ indices, spleen cytokine levels, and immunoglobulin profiles, were evaluated. JAASSRY1 prevented CTX-induced immune damage by reversing weight loss and immune organ atrophy, suppressing the expression of IL-6, IL-17, and IFN-γ in the spleen (P< 0.01), and restoring levels of IgA and IgG, while up-regulating IL-4 (P< 0.01). Furthermore, JAASSRY1 attenuated immunosuppressive spleen injury by modulating the TLR4/MyD88/NF-κB pathway and regulating the Bax/Bcl-2 ratio. JAASSRY1 also alleviated CTX-induced dysbiosis by enhancing the abundance of Colidextribacter and reducing the levels of Parabacteroides and Bacteroides. A significant association was observed between specific gut microbiome Bacteroides and immune parameters (P< 0.01). Above all, JAASSRY1 demonstrates efficacy in ameliorating immunosuppression through the modulation of the “gut microbiota-spleen” axis, providing a basis for the development of probiotic formulations with immunomodulatory properties.

## Linked entities

- **Genes:** TLR4 (toll like receptor 4) [NCBI Gene 7099], MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596]
- **Chemicals:** cyclophosphamide (PubChem CID 2907), IL-6 (PubChem CID 165368475), IgA (PubChem CID 76900), IL-4 (PubChem CID 171905173)
- **Species:** Rhodotorula mucilaginosa (taxon 5537), Colidextribacter (taxon 1980681), Parabacteroides (taxon 375288), Bacteroides (taxon 816)

## Full-text entities

- **Genes:** Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, Bcl2 (B cell leukemia/lymphoma 2) [NCBI Gene 12043] {aka Bcl-2, C430015F12Rik, D630044D05Rik, D830018M01Rik}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, GLS2 (glutaminase 2) [NCBI Gene 27165] {aka GA, GLS, LGA, hLGA}, Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, Igha (immunoglobulin heavy constant alpha) [NCBI Gene 238447] {aka IgA, Igh-2}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970] {aka AIF3BL3, CMCU, NFKB3, p65}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Igh-V7183 (immunoglobulin heavy chain (V7183 family)) [NCBI Gene 16059] {aka B9-scFv, IgG, IgH, IgVH1(VSG), VH7183, VI24H}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, Bax (BCL2-associated X protein) [NCBI Gene 12028], Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, Nfkbia (nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha) [NCBI Gene 18035] {aka Nfkbi}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, Myd88 (myeloid differentiation primary response gene 88) [NCBI Gene 17874]
- **Diseases:** metabolic disorders (MESH:D008659), inflammation (MESH:D007249), immunodeficiency (MESH:D007153), intestinal injury (MESH:D007410), immune dysfunction (MESH:D007154), weight loss (MESH:D015431), dysbiosis (MESH:D064806), CTX (MESH:D019294), spleen damage (MESH:D013160), cancer (MESH:D009369), IBD (MESH:D015212), liver fibrosis (MESH:D008103), polycystic ovary syndrome (MESH:D011085), atrophy (MESH:D001284), hyperuricemia (MESH:D033461), NASH (MESH:D005235), hypertension (MESH:D006973), gut ecological disorder (MESH:C536735)
- **Chemicals:** beta-carotene (MESH:D019207), paraffin (MESH:D010232), PBS (MESH:D007854), levamisole hydrochloride (MESH:D007978), polysaccharides (MESH:D011134), oil (MESH:D009821), LPS (MESH:D008070), saline (MESH:D012965), paraformaldehyde (MESH:C003043), polyunsaturated fatty acids (MESH:D005231), carnosic acid (MESH:C018381), HES (MESH:D006569), H&amp;E (MESH:D006371), PVDF (MESH:C024865), Colidextribacter (-), RH (MESH:D012238), carotenoids (MESH:D002338), beta-glucan (MESH:D047071), lutein (MESH:D014975), SDS (MESH:D012967), CTX (MESH:D003520), lycopene (MESH:D000077276), DAPI (MESH:C007293), Genistein (MESH:D019833), PC (MESH:C053518)
- **Species:** Homo sapiens (human, species) [taxon 9606], Bacteroides (genus) [taxon 816], Lactobacillus (genus) [taxon 1578], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Rhodotorula mucilaginosa (species) [taxon 5537], Rattus norvegicus (brown rat, species) [taxon 10116], Bos taurus (bovine, species) [taxon 9913], Mus musculus (house mouse, species) [taxon 10090], Parabacteroides (genus) [taxon 375288], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Gallus gallus (bantam, species) [taxon 9031], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Cell lines:** HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320)

## Full text

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12868951/full.md

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Source: https://tomesphere.com/paper/PMC12868951