# Genetically Modified Microorganisms: Risks and Regulatory Considerations for Human and Environmental Health

**Authors:** Aaron Lerner, Arnon D. Lieber, Cass Nelson-Dooley, Andre Leu, Michelle Perro, Geoffrey Koch, Carina Benzvi, Jeffrey Smith

PMC · DOI: 10.3390/microorganisms14020467 · 2026-02-14

## TL;DR

This paper reviews the potential risks of genetically modified microorganisms and calls for stronger international regulations to protect human and environmental health.

## Contribution

The paper introduces a decision-based biosafety workflow for GMMs and highlights the need for international regulatory coordination.

## Key findings

- GMMs can disrupt human microbiomes and increase antimicrobial resistance.
- GMMs may destabilize soil carbon cycles and contribute to climate issues.
- Engineered enzymes in food could drive autoimmunity.

## Abstract

Advances in affordable genetic engineering have accelerated the creation and large-scale environmental release of genetically modified microorganisms (GMMs). While beneficial applications exist, GMMs may present unique, long-term risks to human and environmental health. Unlike static chemicals, GMMs are biologically active, self-replicating entities capable of rapid mutation and global dispersal. Current regulatory frameworks place responsibility on each country to regulate GMMs, without a clear, coordinated international policy. This review details critical risk scenarios, including horizontal gene transfer to native species and the possible disruption of vital human microbiomes (gut, oral, and infant), which could increase resistance to degradation, promote traits that expand a microbe’s range of hosts or ecological niches, and enhance the production of novel metabolites with unexpected biological activity. In soil, GMMs may support the emergence of “super bugs” or destabilize carbon sequestration cycles, potentially impacting climate resilience. Engineered microbial enzymes in the food supply may also act as environmental drivers of autoimmunity. Given the limited understanding of microbial ecology, we propose a decision-based biosafety workflow emphasizing pre-release risk assessment and continuous post-release monitoring. We urge national and international regulators to adopt the precautionary principle to better protect human health and the environment from the potential negative outcomes of GMMs.

## Full-text entities

- **Genes:** Mucin [NCBI Gene 100508689], INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, TGM2 (transglutaminase 2) [NCBI Gene 7052] {aka G(h), TG(C), TGC, hTG2, tTG}, PRSS3 (serine protease 3) [NCBI Gene 5646] {aka MTG, PRSS4, T9, TRY3, TRY4}, LAP3 (leucine aminopeptidase 3) [NCBI Gene 51056] {aka HEL-S-106, LAP, LAPEP, PEPS}
- **Diseases:** Autoimmune Disease (MESH:D001327), diarrhea (MESH:D003967), hemolytic (MESH:D006461), celiac disease (MESH:D002446), metabolic syndrome (MESH:D024821), inflammation (MESH:D007249), neurodegenerative (MESH:D019636), injury to (MESH:D014947), lung infections (MESH:D012141), malignant, and autoimmune conditions (MESH:D009369), diabetes (MESH:D003920), gastrointestinal dysbiosis (MESH:D064806), asthma (MESH:D001249), head and neck cancers (MESH:D006258), GM (MESH:C562602), inflammatory bowel disease (MESH:D015212), heart disease (MESH:D006331), allergies (MESH:D004342), infectious disease (MESH:D003141), autoimmune and chronic brain conditions (MESH:D002908), GMMs (OMIM:605429), rheumatoid arthritis (MESH:D001172), drought (MESH:C536747), C. difficile infection (MESH:D003015), gum disease (MESH:C537732), eczema (MESH:D004485), colitis (MESH:D003092), Gastrointestinal Illness (MESH:D005767), brain inflammation (MESH:D004660), infection (MESH:D007239), preterm birth (MESH:D047928), heart attack (MESH:D009203), food allergies (MESH:D005512), toxicity (MESH:D064420), inflammatory joint disease (MESH:D007592)
- **Chemicals:** water (MESH:D014867), PAH (MESH:D011084), nitric oxide (MESH:D009569), Succinate (MESH:D019802), O2 (MESH:D010100), phosphorus (MESH:D010758), nitrate (MESH:D009566), sugar (MESH:D000073893), nitrogen (MESH:D009584), methane (MESH:D008697), lactose (MESH:D007785), lactic acid (MESH:D019344), carbon (MESH:D002244), tricarboxylic acid (MESH:D014233), monosaccharide (MESH:D009005), CO2 (MESH:D002245), fructose (MESH:D005632), nitrous oxide (MESH:D009609), xylose (MESH:D014994), polyethylene terephthalate (MESH:D011093), SCFAs (MESH:D005232), glucose (MESH:D005947), HK44 (-), oligosaccharides (MESH:D009844), TCA (MESH:D014238)
- **Species:** Komagataella pastoris (species) [taxon 4922], Georgenia sp. MMS (species) [taxon 1078391], Aliivibrio fischeri (species) [taxon 668], Streptomyces mobaraensis (species) [taxon 35621], Klebsiella variicola (species) [taxon 244366], Kosakonia sacchari (species) [taxon 1158459], Streptomyces lividans (species) [taxon 1916], Corynebacterium glutamicum (species) [taxon 1718], Bacillus subtilis (species) [taxon 1423], Escherichia coli (E. coli, species) [taxon 562], Yarrowia lipolytica (species) [taxon 4952], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], earthworms (species) [taxon 71170], Metaphire sieboldi (earthworm, species) [taxon 506672], Solanum tuberosum (potatoes, species) [taxon 4113], Bacillus thuringiensis (species) [taxon 1428], Bos taurus (bovine, species) [taxon 9913], PX clade (clade) [taxon 569578], uncultured marine bacterium (species) [taxon 56765], gut metagenome (species) [taxon 749906], Bifidobacterium longum subsp. infantis (subspecies) [taxon 1682], Pseudomonas fluorescens (species) [taxon 294], Viruses (acellular root) [taxon 10239], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606], Clostridioides difficile (species) [taxon 1496], Clostridium (genus) [taxon 1485]
- **Cell lines:** HK44 — Rattus norvegicus (Rat), Rat C-cell carcinoma, Cancer cell line (CVCL_4U24)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12943632/full.md

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Source: https://tomesphere.com/paper/PMC12943632