» Articles » PMID: 19375316

Host Mixing and Disease Emergence

Overview
Journal Curr Biol
Publisher Cell Press
Specialty Biology
Date 2009 Apr 21
PMID 19375316
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Recent cases of emergent diseases have renewed interest in the evolutionary and ecological mechanisms that promote parasite adaptation to novel hosts [1-6]. Crucial to adaptation is the degree of mixing of original, susceptible hosts, and novel hosts. An increase in the frequency of the original host has two opposing effects on adaptation: an increase in the supply of mutant pathogens with improved performance on the novel host [7-9]; and reduced selection to infect novel hosts, caused by fitness costs commonly observed to be associated with host switching [10-17]. The probability of disease emergence will therefore peak at intermediate frequencies of the original host. We tested these predictions by following the evolution of a virus grown under a range of different frequencies of susceptible (original) and resistant (novel) host bacteria. Viruses that evolved to infect resistant hosts were only detected when susceptible hosts were at frequencies between 0.1% and 1%. Subsequent experiments supported the predictions that there was reduced selection and mutation supply at higher and lower frequencies, respectively. These results suggest that adaptation to novel hosts can occur only under very specific ecological conditions, and that small changes in contact rates between host species might help to mitigate disease emergence.

Citing Articles

Emergence failure of early epidemics: A mathematical modeling approach.

Breban R PLoS One. 2024; 19(5):e0301415.

PMID: 38809831 PMC: 11135784. DOI: 10.1371/journal.pone.0301415.


Bacteriophage specificity is impacted by interactions between bacteria.

Bisesi A, Mobius W, Nadell C, Hansen E, Bowden S, Harcombe W mSystems. 2024; 9(3):e0117723.

PMID: 38376179 PMC: 11237722. DOI: 10.1128/msystems.01177-23.


Gut Fungal Communities Are Influenced by Seasonality in Captive Baikal Teal () and Common Teal ().

Sakda P, Xiang X, Wu Y, Zhang X, Xu W, Zhou L Animals (Basel). 2023; 13(18).

PMID: 37760348 PMC: 10525870. DOI: 10.3390/ani13182948.


Bacteria-phage coevolution with a seed bank.

Schwartz D, Shoemaker W, Magalie A, Weitz J, Lennon J ISME J. 2023; 17(8):1315-1325.

PMID: 37286738 PMC: 10356755. DOI: 10.1038/s41396-023-01449-2.


The Coincidental Evolution of Virulence Partially Explains the Virulence in a Generalist Entomopathogenic.

Trejo-Melendez V, Mendez-Lopez T, Contreras-Garduno J Acta Parasitol. 2023; 68(2):293-303.

PMID: 36806112 PMC: 10281897. DOI: 10.1007/s11686-023-00663-4.


References
1.
Parrish C, Holmes E, Morens D, Park E, Burke D, Calisher C . Cross-species virus transmission and the emergence of new epidemic diseases. Microbiol Mol Biol Rev. 2008; 72(3):457-70. PMC: 2546865. DOI: 10.1128/MMBR.00004-08. View

2.
Gupta S, Anderson R, May R . Networks of sexual contacts: implications for the pattern of spread of HIV. AIDS. 1989; 3(12):807-17. View

3.
Jones K, Patel N, Levy M, Storeygard A, Balk D, Gittleman J . Global trends in emerging infectious diseases. Nature. 2008; 451(7181):990-3. PMC: 5960580. DOI: 10.1038/nature06536. View

4.
Cleaveland S, Laurenson M, Taylor L . Diseases of humans and their domestic mammals: pathogen characteristics, host range and the risk of emergence. Philos Trans R Soc Lond B Biol Sci. 2001; 356(1411):991-9. PMC: 1088494. DOI: 10.1098/rstb.2001.0889. View

5.
Woolhouse M, Gowtage-Sequeria S . Host range and emerging and reemerging pathogens. Emerg Infect Dis. 2006; 11(12):1842-7. PMC: 3367654. DOI: 10.3201/eid1112.050997. View