# Pathogens as commensals: microbial priming of the immune system and heterologous protection

**Authors:** Thomas Belcher, Emily J. Stevens

PMC · DOI: 10.1099/mic.0.001680 · Microbiology · 2026-02-26

## TL;DR

This review explores how exposure to various microbes, including some pathogens, helps train the immune system and can offer protection against different diseases.

## Contribution

The paper highlights the novel perspective that pathogens and opportunistic microbes can contribute to immune system development and cross-protection.

## Key findings

- Opportunistic pathogens like Staphylococcus aureus can aid in immune system development.
- Attenuated pathogen strains such as BPZE1 and Bacillus Calmette–Guérin show potential clinical benefits.
- Pathogens outside the microbiota can provide cross-protection against infectious and non-infectious diseases in mice.

## Abstract

Exposure to microbes is essential to promote the development of the host’s immune system. Commensal microbes (i.e. the microbiota) which are acquired early in life play a vital role in immune priming. Whilst many organisms within the microbiota are harmless, some can be considered opportunistic pathogens. Examples include Staphylococcus aureus, Streptococcus pneumoniae and Pseudomonas aeruginosa, and these organisms can also contribute to the development of a healthy host immune system. At the extreme end of the spectrum, pathogens which typically do not form part of the microbiota (e.g. Mycobacterium tuberculosis, Bordetella pertussis and Salmonella Typhimurium) have been shown to provide cross-protection against infectious and non-infectious diseases in mice. Attenuated strains of these pathogens, such as BPZE1, could have clinical applications, whilst Bacillus Calmette–Guérin, a live-attenuated Mycobacterium bovis strain, has been shown to have non-specific effects against cancers and other diseases. A wide range of organisms, from harmless microbiota to potentially life-threatening infections, interact with the host immune system and can prime or modulate the immune response in different ways. In this review, we discuss the important role that pathogens, including opportunistic components of the microbiota, play in the development and maintenance of host immunity to a wide range of infectious and non-infectious diseases.

## Linked entities

- **Species:** Staphylococcus aureus (taxon 1280), Streptococcus pneumoniae (taxon 1313), Pseudomonas aeruginosa (taxon 287), Mycobacterium tuberculosis (taxon 1773), Bordetella pertussis (taxon 520)

## Full-text entities

- **Genes:** Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Myd88 (myeloid differentiation primary response gene 88) [NCBI Gene 17874], Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Il2ra (interleukin 2 receptor, alpha chain) [NCBI Gene 16184] {aka CD25, Il2r, Ly-43}, LOC105243590 (Ig heavy chain Mem5-like) [NCBI Gene 105243590] {aka IgH, Igg1}, Itgam (integrin alpha M) [NCBI Gene 16409] {aka CD11b/CD18, CR3, CR3A, Cd11b, F730045J24Rik, Ly-40}, Il13 (interleukin 13) [NCBI Gene 16163] {aka Il-13}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Il1a (interleukin 1 alpha) [NCBI Gene 16175] {aka Il-1a}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Il5 (interleukin 5) [NCBI Gene 16191] {aka Il-5}, Cxcl10 (C-X-C motif chemokine ligand 10) [NCBI Gene 15945] {aka C7, CRG-2, INP10, IP-10, IP10, Ifi10}, Il2 (interleukin 2) [NCBI Gene 16183] {aka Il-2}, Ccl17 (C-C motif chemokine ligand 17) [NCBI Gene 20295] {aka Abcd-2, Scya17, Scya17l, Tarc}, Clstn1 (calsyntenin 1) [NCBI Gene 65945] {aka 1810034E21Rik, Cst-1, Cstn1}, Foxp3 (forkhead box P3) [NCBI Gene 20371] {aka JM2, scurfin, sf}, Il1rn (interleukin 1 receptor antagonist) [NCBI Gene 16181] {aka F630041P17Rik, IL-1ra}, Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Serpinb1-ps1 (serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene) [NCBI Gene 282665] {aka EID, ovalbumin}, Il33 (interleukin 33) [NCBI Gene 77125] {aka 9230117N10Rik, Il-33, Il1f11, NF-HEV}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Cort (cortistatin) [NCBI Gene 12854] {aka CST, PCST}, Ccl11 (C-C motif chemokine ligand 11) [NCBI Gene 20292] {aka Scya11, eotaxin}
- **Diseases:** Salmonella infection (MESH:D012480), C. gattii infection (MESH:D003453), pneumonia (MESH:D011014), non-tuberculosis infectious diseases (MESH:D000073296), pneumococcal pneumonia (MESH:D011018), diarrhoea (MESH:D003967), NOD (MESH:D009765), microbial infections (MESH:D015163), autoimmune diseases (MESH:D001327), staphylococcal (MESH:D011023), lung injury (MESH:D055370), allergic contact dermatitis (MESH:D017449), asthma (MESH:D001249), cancers (MESH:D009369), diabetes (MESH:D003920), asthmatic (MESH:D013224), Giardia (MESH:D005873), influenza (MESH:D007251), AAI (MESH:D007249), bacteraemia (MESH:C531821), diarrhoeal diseases (MESH:D004194), respiratory tract (MESH:D012141), skin and soft tissue infections (MESH:D018461), bladder cancer (MESH:D001749), -infectious diseases (MESH:D003141), sepsis (MESH:D018805), B. pertussis infection (MESH:D014917), stage I (MESH:D062706), MS (MESH:D009103), candidiasis (MESH:D002177), polio (MESH:D011051), CHS (MESH:D003877), HDM (MESH:D000092542), Parasite infection (MESH:D010272), allergic disease (MESH:D004342), vaccinia scar (MESH:D014615), tuberculosis (MESH:D014376), T1D (MESH:D003922), bacterial disease (MESH:D001424), measles (MESH:D008457), type 2 diabetes (MESH:D003924), soil-transmitted helminths (MESH:D005242), cytotoxic (MESH:D064420), weight loss (MESH:D015431), Infection (MESH:D007239), oedema (MESH:C536897), colitis (MESH:D003092), allergic rhinitis (MESH:D065631), COVID-19 (MESH:D000086382), death (MESH:D003643), pneumococcal (MESH:D011008), demyelinating (MESH:D003711)
- **Chemicals:** lipid A (MESH:D008050), blood sugar (MESH:D001786), metformin (MESH:D008687), sugar (MESH:D000073893), DNCB (MESH:D004137), gadolinium (MESH:D005682), methacholine (MESH:D016210), BPZE (-)
- **Species:** H1N1 subtype (serotype) [taxon 114727], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Toxoplasma gondii (species) [taxon 5811], Bordetella bronchiseptica (species) [taxon 518], Streptococcus pneumoniae (species) [taxon 1313], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Schistosoma mansoni (species) [taxon 6183], Bordetella pertussis (species) [taxon 520], Enterococcus faecalis (species) [taxon 1351], Klebsiella pneumoniae (species) [taxon 573], Nematodes (genus) [taxon 333870], Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090], Escherichia coli (E. coli, species) [taxon 562], Bacillus sp. CG (species) [taxon 1196795], Candida albicans (species) [taxon 5476], Cutibacterium acnes (species) [taxon 1747], Cutibacterium granulosum (species) [taxon 33011], Giardia duodenalis (species) [taxon 5741], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282], Corynebacterium accolens (species) [taxon 38284], Staphylococcus aureus (species) [taxon 1280], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mycobacterium tuberculosis (species) [taxon 1773], Dolosigranulum pigrum (species) [taxon 29394], Mycobacterium tuberculosis variant bovis (biotype) [taxon 1765], Respiratory syncytial virus (no rank) [taxon 12814]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12945328/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12945328/full.md

## References

123 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945328/full.md

---
Source: https://tomesphere.com/paper/PMC12945328