4.6 Article

Transcriptomic Adjustments in a Freshwater Ectoparasite Reveal the Role of Molecular Plasticity for Parasite Host Shift

期刊

GENES
卷 13, 期 3, 页码 -

出版社

MDPI
DOI: 10.3390/genes13030525

关键词

plasticity; gene expression; host shift; parasite specificity; emerging parasites; rapid adaptation

资金

  1. Agence Nationale de la Recherche (project INCLIMPAR) [ANR-11-JSV7-0010]
  2. BiodivERsA (project PROBIS)
  3. Institut Universitaire de France
  4. French Ministry for Education and Sciences
  5. France Genomique National infrastructure part of Investissement d'avenir program [ANR-10-INBS-09]
  6. Laboratoire d'Excellence (LABEX) entitled TULIP [ANR-10-LABX-41]
  7. Agence Nationale de la Recherche (ANR) [ANR-11-JSV7-0010] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

A parasite's ability to infect alternative host species is influenced by changes in gene expression and molecular pathways, particularly those related to cellular machinery, energetic metabolism, muscle activity, and oxidative stress. This study suggests that molecular plasticity plays a crucial role in facilitating host shift in parasites.
A parasite's lifestyle is characterized by a critical dependency on its host for feeding, shelter and/or reproduction. The ability of parasites to exploit new host species can reduce the risk associated with host dependency. The number of host species that can be infected by parasites strongly affects their ecological and evolutionary dynamics along with their pathogenic effects on host communities. However, little is known about the processes and the pathways permitting parasites to successfully infect alternative host species, a process known as host shift. Here, we tested whether molecular plasticity changes in gene expression and in molecular pathways could favor host shift in parasites. Focusing on an invasive parasite, Tracheliastes polycolpus, infecting freshwater fish, we conducted a transcriptomic study to compare gene expression in parasites infecting their main host species and two alternative host species. We found 120 significant differentially expressed genes (DEGs) between parasites infecting the different host species. A total of 90% of the DEGs were identified between parasites using the main host species and those using the two alternative host species. Only a few significant DEGs (seven) were identified when comparing parasites from the two alternative host species. Molecular pathways enriched in DEGs and associated with the use of alternative host species were related to cellular machinery, energetic metabolism, muscle activity and oxidative stress. This study strongly suggests that molecular plasticity is an important mechanism sustaining the parasite's ability to infect alternative hosts.

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