# Alleviation of Ulcerative Colitis in Mice by Individual Fermentation of Periplaneta americana Powder with L. bulgaricus SN22 and S. thermophilus SN05

**Authors:** Qingqing Zhang, Cheng Chen, Xiaoqin Mu, Zihan Zhang, Cuiling Luo, Chenjuan Zeng, Bisong Yue, Zhenxin Fan, Lianming Du

PMC · DOI: 10.3390/microorganisms14020301 · 2026-01-27

## TL;DR

Fermenting Periplaneta americana powder with specific bacteria reduced inflammation in mice with ulcerative colitis and showed anti-cancer effects in lab tests.

## Contribution

A novel microbial fermentation strategy using L. bulgaricus and S. thermophilus to enhance the anti-inflammatory properties of insect-derived materials for UC treatment.

## Key findings

- Fermented PA supernatant reduced pro-inflammatory cytokines IL-1β and TNF-α in a DSS-induced colitis mouse model.
- Fermentation enriched metabolites like 3-anisic acid and vitamin U, which have anti-inflammatory and antioxidant properties.
- The fermented supernatant suppressed HT-29 colon cancer cell proliferation and induced apoptosis in vitro.

## Abstract

The escalating global incidence of ulcerative colitis (UC) underscores the demand for novel therapeutic strategies. This study investigated the fermentation of Periplaneta americana (PA) powder using two conventional dairy starter strains, Lactobacillus delbrueckii subsp. bulgaricus SN22 and Streptococcus thermophilus SN05, to enhance its functional properties, particularly anti-inflammatory activity, via microbial processing. Both strains demonstrated favourable safety and antimicrobial activity. Untargeted metabolomics revealed that fermentation significantly altered the metabolite profile of the PA supernatant, enriching compounds with potential bioactivities, notably anti-inflammatory (e.g., 3-anisic acid) and antioxidant (e.g., vitamin U) properties. In the DSS-induced mouse colitis model, treatment with the fermented supernatant alleviated intestinal inflammation compared to the unfermented group. This was demonstrated by significantly reduced levels of the pro-inflammatory cytokines IL-1β and TNF-α, along with improved maintenance of intestinal barrier integrity. Further in vitro assays showed that the fermented supernatant significantly suppressed proliferation and clonogenicity in human HT-29 colon cancer cells, while also inducing reactive oxygen species accumulation and apoptosis. Results demonstrate these strains are multifunctional starters possessing superior antimicrobial and anti-inflammatory efficacy. This study employed LAB fermentation of insect-derived matrices to derive bioactive components. The fermentation products exhibited anti-inflammatory potential, offering a potential microbial transformation strategy for developing functional products for adjunctive UC intervention.

## Linked entities

- **Chemicals:** 3-anisic acid (PubChem CID 11461), vitamin U (PubChem CID 16217806)
- **Diseases:** ulcerative colitis (MONDO:0005101), colon cancer (MONDO:0002032)
- **Species:** Periplaneta americana (taxon 6978), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** CECR (cat eye syndrome chromosome region) [NCBI Gene 1055] {aka CES}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, GHS (Goldenhar syndrome) [NCBI Gene 7971], Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, GTS (Gilles de la Tourette syndrome) [NCBI Gene 2973], Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** Hemolysis (MESH:D006461), burns (MESH:D002056), bleeding (MESH:D006470), fibroplasia (MESH:D012178), diarrhea (MESH:D003967), cancer (MESH:D009369), inflammation (MESH:D007249), injury to (MESH:D014947), necrosis (MESH:D009336), UC (MESH:D003093), mucosal damage (MESH:D052016), IBD (MESH:D015212), Colitis (MESH:D003092), gastrointestinal diseases (MESH:D005767), Cytotoxicity (MESH:D064420), weight loss (MESH:D015431), lethargy (MESH:D053609), colon cancer (MESH:D015179)
- **Chemicals:** glutamate (MESH:D018698), gentamicin (MESH:D005839), TPP (MESH:D013835), allantoin (MESH:D000481), pyrimidine (MESH:C030986), clindamycin (MESH:D002981), water (MESH:D014867), phospholipid (MESH:D010743), tyrosine (MESH:D014443), CCK-8 (MESH:D012844), terpenoids (MESH:D013729), 5-hydroxytryptophan (MESH:D006916), AA (MESH:D016718), stearic acid (MESH:C031183), phenolic acids (MESH:C017616), iron (MESH:D007501), lyso-phosphatidylethanolamine (MESH:C008301), DCFH-DA (MESH:C029569), indoles (MESH:D007211), vancomycin (MESH:D014640), nitrogen (MESH:D009584), uric acid (MESH:D014527), prostaglandins (MESH:D011453), Vitamin U (MESH:D014814), alanine (MESH:D000409), 2',7'-dichlorodihydrofluorescein diacetate (MESH:C110400), Triton X-100 (MESH:D017830), chitin (MESH:D002686), agar (MESH:D000362), fructooligosaccharides (MESH:C116580), Azole (MESH:D001393), linoleic acid (MESH:D019787), methanol (MESH:D000432), clarithromycin (MESH:D017291), inosine (MESH:D007288), pyruvate (MESH:D019289), thioether (MESH:D013440), glycerophospholipid (MESH:D020404), phosphorus (MESH:D010758), 4-oxoproline (MESH:C036784), lanthionine (MESH:C001520), guanosine (MESH:D006151), membrane lipid (MESH:D008563), tryptophan (MESH:D014364), oleic acid (MESH:D019301), lyso-phosphatidylcholine (MESH:D008244), calcium (MESH:D002118), ROS (MESH:D017382), magnesium (MESH:D008274), chloramphenicol (MESH:D002701), steroid (MESH:D013256), PAP (MESH:D010724), ATP (MESH:D000255), DSS (MESH:D016264), ampicillin (MESH:D000667), SN22 (MESH:C051891), sterol (MESH:D013261), nucleosides (MESH:D009705), purine (MESH:C030985), PFA (MESH:C003043)
- **Species:** Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Panax ginseng (Asiatic ginseng, species) [taxon 4054], Mus musculus (house mouse, species) [taxon 10090], Lactobacillus delbrueckii subsp. bulgaricus (subspecies) [taxon 1585], Yersinia enterocolitica (species) [taxon 630], Astragalus membranaceus (species) [taxon 649199], Periplaneta americana (American cockroach, species) [taxon 6978], Streptococcus thermophilus (species) [taxon 1308], Paenisporosarcina antarctica (species) [taxon 417367], Artemisia argyi (species) [taxon 259893], Leptospira sp. AB (species) [taxon 103236], Shigella dysenteriae (species) [taxon 622], Streptomyces sp. N22 (species) [taxon 1508664], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C-65  C
- **Cell lines:** SN05 — Homo sapiens (Human), Melanoma, Cancer cell line (CVCL_W876), ATCC 14028 — Homo sapiens (Human), Transformed cell line (CVCL_FD91), ATCC 23715 — Homo sapiens (Human), Duchenne muscular dystrophy, Finite cell line (CVCL_5T15), ATCC 51334 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320), SN22 — Mus musculus (Mouse), Hybridoma (CVCL_C7JA), NCM460 — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0460)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943602/full.md

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Source: https://tomesphere.com/paper/PMC12943602