Host–Parasite Evolution: General Principles and Avian Models

1998 ◽  
Vol 14 (2) ◽  
pp. 84
Author(s):  
Ben Sheldon
Oikos ◽  
2010 ◽  
Vol 119 (4) ◽  
pp. 669-678 ◽  
Author(s):  
C. Cosseau ◽  
A. Azzi ◽  
A. Rognon ◽  
J. Boissier ◽  
S. Gourbière ◽  
...  

2020 ◽  
Author(s):  
Lisa Freund ◽  
Marie Vasse ◽  
Gregory J. Velicer

Evolutionary diversification can occur in allopatry or sympatry, can be unselected or driven by selection, and can be phenotypically manifested immediately or remain phenotypically latent until later manifestation in a newly encountered environment. Diversification of host-parasite interactions is frequently studied in the context of intrinsically selective coevolution, but the potential for host-parasite interaction phenotypes to diversify latently during parasite-blind evolution is rarely considered. Here we use a social bacterium experimentally adapted to several environments in the absence of phage to analyse allopatric diversification of latent host quality - the degree to which a host population supports a viral epidemic. Phage-blind evolution reduced host quality overall, with some bacteria becoming completely resistant to growth suppression by phage. Selective-environment differences generated only mild divergence in host-quality. However, selective environments nonetheless played a major role in shaping evolution by determining the degree of stochastic diversification among replicate populations within treatments. Ancestral motility genotype was also found to strongly shape patterns of latent hostquality evolution and diversification. These outcomes show that adaptive landscapes can differ in how they constrain stochastic diversification of a latent phenotype and that major effects of selection on biological diversification can be missed by focusing on trait means. Collectively, our findings suggest that latent-phenotype evolution (LPE) should inform host-parasite evolution theory and that diversification should be conceived broadly to include latent phenotypes.


Parasitology ◽  
2019 ◽  
Vol 146 (07) ◽  
pp. 883-896
Author(s):  
Hannah M. Strobel ◽  
Sara J. Hays ◽  
Kristine N. Moody ◽  
Michael J. Blum ◽  
David C. Heins

AbstractRemarkably few attempts have been made to estimate contemporary effective population size (Ne) for parasitic species, despite the valuable perspectives it can offer on the tempo and pace of parasite evolution as well as coevolutionary dynamics of host–parasite interactions. In this study, we utilized multi-locus microsatellite data to derive single-sample and temporal estimates of contemporaryNefor a cestode parasite (Schistocephalus solidus) as well as three-spined stickleback hosts (Gasterosteus aculeatus) in lakes across Alaska. Consistent with prior studies, both approaches recovered small and highly variable estimates of parasite and hostNe. We also found that estimates of hostNeand parasiteNewere sensitive to assumptions about population genetic structure and connectivity. And, while prior work on the stickleback–cestode system indicates that physiographic factors external to stickleback hosts largely govern genetic variation inS. solidus, our findings indicate that stickleback host attributes and factors internal to the host – namely body length, genetic diversity and infection – shape contemporaryNeof cestode parasites.


10.2307/6007 ◽  
1997 ◽  
Vol 66 (6) ◽  
pp. 913
Author(s):  
A. K. Lindholm ◽  
D. H. Clayton ◽  
J. Moore

2012 ◽  
Vol 279 (1741) ◽  
pp. 3234-3240 ◽  
Author(s):  
Alex Best ◽  
Gráinne Long ◽  
Andy White ◽  
Mike Boots

By definition, parasites harm their hosts, but in many infections much of the pathology is driven by the host immune response rather than through direct damage inflicted by parasites. While these immunopathological effects are often well studied and understood mechanistically in individual disease interactions, there remains relatively little understanding of their broader impact on the evolution of parasites and their hosts. Here, we theoretically investigate the implications of immunopathology, broadly defined as additional mortality associated with the host's immune response, on parasite evolution. In particular, we examine how immunopathology acting on different epidemiological traits (namely transmission, virulence and recovery) affects the evolution of disease severity. When immunopathology is costly to parasites, such that it reduces their fitness, for example by decreasing transmission, there is always selection for increased disease severity. However, we highlight a number of host–parasite interactions where the parasite may benefit from immunopathology, and highlight scenarios that may lead to the evolution of slower growing parasites and potentially reduced disease severity. Importantly, we find that conclusions on disease severity are highly dependent on how severity is measured. Finally, we discuss the effect of treatments used to combat disease symptoms caused by immunopathology.


The Auk ◽  
1998 ◽  
Vol 115 (2) ◽  
pp. 546-547
Author(s):  
Marlene Zuk ◽  
George Lozano

2021 ◽  
Vol 288 (1949) ◽  
Author(s):  
Lisa Freund ◽  
Marie Vasse ◽  
Gregory J. Velicer

Evolutionary diversification can occur in allopatry or sympatry, can be driven by selection or unselected, and can be phenotypically manifested immediately or remain latent until manifested in a newly encountered environment. Diversification of host–parasite interactions is frequently studied in the context of intrinsically selective coevolution, but the potential for host–parasite interaction phenotypes to diversify latently during parasite-blind host evolution is rarely considered. Here, we use a social bacterium experimentally adapted to several environments in the absence of phage to analyse allopatric diversification of host quality—the degree to which a host population supports a viral epidemic. Phage-blind evolution reduced host quality overall, with some bacteria becoming completely resistant to growth suppression by phage. Selective-environment differences generated only mild divergence in host quality. However, selective environments nonetheless played a major role in shaping evolution by determining the degree of stochastic diversification among replicate populations within treatments. Ancestral motility genotype was also found to strongly shape patterns of latent host-quality evolution and diversification. These outcomes show that (i) adaptive landscapes can differ in how they constrain stochastic diversification of a latent phenotype and (ii) major effects of selection on biological diversification can be missed by focusing on trait means. Collectively, our findings suggest that latent-phenotype evolution should inform host–parasite evolution theory and that diversification should be conceived broadly to include latent phenotypes.


2019 ◽  
Author(s):  
Maeva A. Techer ◽  
Rahul V. Rane ◽  
Miguel L. Grau ◽  
John M. K. Roberts ◽  
Shawn T. Sullivan ◽  
...  

AbstractMultispecies host-parasite evolution is common, but how parasites evolve after speciating remains poorly understood. Shared evolutionary history and physiology may propel species along similar evolutionary trajectories whereas pursuing different strategies can reduce competition. We test these scenarios in the economically important association between honey bees and ectoparasitic mites by sequencing the genomes of the sister mite species Varroa destructor and Varroa jacobsoni. These genomes were closely related, with 99.7% sequence identity. Among the 9,628 orthologous genes, 4.8% showed signs of positive selection in at least one species. Divergent selective trajectories were discovered in conserved chemosensory gene families (IGR, SNMP), and Halloween genes (CYP) involved in moulting and reproduction. However, there was little overlap in these gene sets and associated GO terms, indicating different selective regimes operating on each of the parasites. Based on our findings, we suggest that species-specific strategies may be needed to combat evolving parasite communities.


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