Table 2.
Transitiona | Host | Symbiont | Association | Condition | Mechanism and evidenceb | Approach | Refs |
---|---|---|---|---|---|---|---|
M → M (−) | Legume (Ensifer medicae) | Rhizobia | Nitrogen-fixing | Host choice blocked | Cheater strains favoured | Experimental | 229 |
M → M (−) | Legume (Trifolium spp.) | Rhizobia | Nitrogen-fixing | Elevated nitrogen | Reduced cooperation under high nitrogen | Experimental | 230 |
M → P | Vertebrate spp. | Coxiella burnetii | Intracellular parasite | Host shift | HGT of virulence-associated genes suggested | Phylogenetic | 30 |
M → P | Jelly fish (Cassiopea xamachana) | Alga (Symbiodinium microadriaticum) | Photosynthate provisioning | HT only | Greater proliferation in host and dispersal rates | Experimental | 109 |
M → P | Plant spp. | Agrobacterium spp. | Plant parasite | NA | HGT of virulence loci | Phylogenetic | 29,231 |
M → P | Plant spp. | Pseudomonas syringae | Plant parasite | NA | HGT of hopZ T3SS effectors | Phylogenetic | 29,79 |
M → P | Escherichia coli | M13 phage | Growth benefit | Host background | Parasitic when shifted to host ancestor | Experimental | 228 |
M → P | E. coli | F1 phage | Parasitic phage | HT allowed | Antagonistic variants favoured | Experimental | 217 |
C → P | Pill bug (Armadillidium vulgare) | Wolbachia (wVulC) | VT endosymbiont | HT only | Titre increased in non-germline-associated tissue | Experimental | 110 |
C → P | In vitro immune envrionment | E. coli | Commensal strain | Macrophage pressure | Heightened macrophage evasion and delayed phagosome maturation, via TE insertion | Experimental | 232 |
C → P | Arabidopsis thaliana | Pseudomonas fluorescens species complex | Rhizophere associated | NA | Gain of putative pathogenicity island | Comparative genomics, phylogenetic | 39 |
C → P | Plant spp. | Rhodococcus spp. | Plant associated | NA | Gain of virulence plasmid (pFID188), host growth inhibition | Experimental, comparative genomics, phylogenetic | 58 |
P → P (+) | Plant spp. | Xanthomonadaceae spp. | Phytopathogen | NA | Gain of hydrolase gene (cbsA); localized parasite become systemic | Comparative genomics, phylogenetic | 54 |
P → P (+) | Barley (Hordeum vulgare) | Barley stripe mosaic virus | Plant parasite | HT only | Increased virulence, independent of titre | Experimental | 111 |
P → P (+) | House finch (Haemorhous mexicanus) | Mycoplasma gallisepticum | Emerging parasite | Adaptation to novel host | Linear increase in virulence since shift | Natural sampling | 83 |
P → P (+) | Mouse (Mus musculus) | Cryptococcus neoformans | Opportunistic parasite | Serial passage | Increased expression of iron reductase and host mortality | Experimental | 233 |
P → P (+) | Amoebae (Acanthamoeba sp.) | Parachlamydia acanthamoebae | Obligate intracellular symbiont | HT only | Enhanced infectivity and virulence, T3SS upregulated | Experimental | 46 |
P → P (+) | Mammal spp. | Yersinia pestis | Enteric parasite | NA | HGT of plasmids (pMT1 and pPCP1), increased transmissibility by fleas and virulence to mammals | Genomic | 65 |
(−), reduced; (+), elevated (for example, P → P (+) indicates transition towards increased parasitism); C, commensalism; HGT, horizontal gene transfer; HT, horizontal transmission; M, mutualism; NA, specific drivers of transition unaccounted for owing to timescale; P, parasitism; T3SS, type III secretion system; TE, transposable element; VT, vertical transmission. aTransitions involve increased virulence or reduced benefit of the symbiotic relationship to hosts over time. bGeneral evidence to support the inferred transition, including the molecular mechanism if known.