# Methanogenic activities signatures in broilers fed black soldier fly (Hermetia illucens) larvae-based diets

**Authors:** Deborah Oluwaferanmi Ibiwoye, Opeyemi Adetola Oladejo, Oluwatomisin Aderonke Akinsola, Aruna Olasekan Adekiya, Olufemi Mobolaji Alabi, Ayantade Dayo Ayansina, Samuel Olatunde Dahunsi

PMC · DOI: 10.1016/j.bbrep.2026.102441 · Biochemistry and Biophysics Reports · 2026-01-08

## TL;DR

This study explores how feeding black soldier fly larvae to broilers affects methane-producing microbes in their gut, with implications for fermentation efficiency and greenhouse gas emissions.

## Contribution

The study reveals how varying levels of black soldier fly larvae meal in broiler diets alter methanogenic enzyme activity and microbial pathways.

## Key findings

- Methanogenic enzymes like FMD and MCR were strongly detected at 25% BSFLM inclusion.
- At 100% BSFLM, methylotrophic enzymes were strongly detected while hydrogenotrophic enzymes declined.
- Methanogenesis-related pathways were present in all treatments but varied with BSFLM levels.

## Abstract

Methanogenic archaea in the avian gut contribute to hydrogen turnover and thus play a role in fermentative efficiency and greenhouse gas emission. While black soldier fly larvae meal (BSFLM) has been explored as a replacement for fishmeal in broiler diets, less is known about how varying BSFLM inclusion levels affect methanogenesis pathways and enzyme activities in the gut microbial community. This study investigated the presence, relative abundance, and shifts in methanogenesis enzyme pathways in broilers fed diets with increasing levels of BSFLM. Arbor Acre Plus broiler chicks were allocated to five dietary treatments over 8 weeks. Diets replaced fishmeal with BSFLM at 0 % (control), 25 %, 50 %, 75 %, and 100 % levels. Cecal samples were collected post-mortem, DNA extracted, and the bacterial 16S rRNA (V1–V9) region sequenced on PacBio Sequel IIe. Functional predictions via PICRUSt2 were used to identify KEGG orthologs associated with methanogenesis (e.g. K00200–K00205 for FMD, K00399 etc. for MCR, methyltransferases, etc.). Enzyme detection across treatments was assessed qualitatively and semi-quantitatively (e.g. “low”, “moderate”, “strong”) based on relative abundance. Key methanogenic enzymes (including FMD, MCH, MTD, F420-dependent enzymes, methyltransferases, and MCR) were profiled, and their activity compared across treatments. Correlations were examined and predicted functional capacity via PICRUSt2. Methanogenesis-related pathways were detectable in all dietary treatments. In the control (0 % BSFLM), enzyme levels were minimal, reflecting low background methanogenic potential. At 25 % BSFLM inclusion (T2), there was strong detection of hydrogenotrophic pathway enzymes (FMD, coenzyme F420 hydrogenase, MCR) and moderate presence of methylotrophic methyltransferases, suggesting dominance of hydrogenotrophic methanogenesis. In the 50 % BSFLM treatment (T3), enzyme levels declined somewhat: hydrogenotrophic enzyme activity was moderate, and methylotrophic components were weaker. With 100 % BSFLM (T5), methylotrophic pathway enzymes (methanol- and methylamine-corrinoid protein Co-methyltransferases) were strongly detected, while hydrogenotrophic enzymes persisted but at low levels. These shifts have implications for gut fermentation efficiency, substrate (hydrogen and methyl compound) availability, nitrogen metabolism, and possibly GHG emission. Optimization of BSFLM inclusion levels may help balance production performance and environmental sustainability.

•Methanogenic archaea were detected in the caeca of broilers fed BSFLM.•The PICRUSt2 tool was used to identify KEGG orthologs associated with methanogenesis.•Key methanogenic enzymes (including FMD, MCH, MTD, F420-dependent enzymes, methyltransferases, and MCR) were profiled.•Methanogenesis-related pathways were detectable in all dietary treatments with variations.•These shifts have implications for gut fermentation efficiency, substrate availability, nitrogen metabolism, and GHG emission.

Methanogenic archaea were detected in the caeca of broilers fed BSFLM.

The PICRUSt2 tool was used to identify KEGG orthologs associated with methanogenesis.

Key methanogenic enzymes (including FMD, MCH, MTD, F420-dependent enzymes, methyltransferases, and MCR) were profiled.

Methanogenesis-related pathways were detectable in all dietary treatments with variations.

These shifts have implications for gut fermentation efficiency, substrate availability, nitrogen metabolism, and GHG emission.

## Linked entities

- **Proteins:** FLNA (filamin A), NR3C2 (nuclear receptor subfamily 3 group C member 2), PMCH (pro-melanin concentrating hormone), MT1E (metallothionein 1E)
- **Species:** Hermetia illucens (taxon 343691)

## Full-text entities

- **Genes:** mtd (mustard) [NCBI Gene 45467] {aka CG10196, CG10199, CG32464, Dmel\CG32464, L(3)82Fd, L82}, mch (minute chaetae) [NCBI Gene 249741], Mcr (Macroglobulin complement-related) [NCBI Gene 44071] {aka CG7586, DmTEP6, Dmel\CG7586, E(br)155, TEP6, TEP6mel}
- **Chemicals:** hydrogen (MESH:D006859), GHG (-), nitrogen (MESH:D009584)
- **Species:** Hermetia illucens (black soldier fly, species) [taxon 343691], fungal sp. M-D (species) [taxon 1074441]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12816829/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12816829/full.md

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Source: https://tomesphere.com/paper/PMC12816829