Effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite system

<p>Abstract</p> <p>Background</p> <p>Ecological factors play an important role in the evolution of parasite exploitation strategies. A common prediction is that, as shorter host life span reduces future opportunities of transmission, parasites compensate with an evoluti...

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Main Authors: Koella Jacob C, Nidelet Thibault, Kaltz Oliver
Format: Article
Language:English
Published: BMC 2009-03-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/9/65
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spelling doaj-4a8b239e8f4f465893c141eb03f791672021-09-02T09:43:37ZengBMCBMC Evolutionary Biology1471-21482009-03-01916510.1186/1471-2148-9-65Effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite systemKoella Jacob CNidelet ThibaultKaltz Oliver<p>Abstract</p> <p>Background</p> <p>Ecological factors play an important role in the evolution of parasite exploitation strategies. A common prediction is that, as shorter host life span reduces future opportunities of transmission, parasites compensate with an evolutionary shift towards earlier transmission. They may grow more rapidly within the host, have a shorter latency time and, consequently, be more virulent. Thus, increased extrinsic (i.e., not caused by the parasite) host mortality leads to the evolution of more virulent parasites. To test these predictions, we performed a serial transfer experiment, using the protozoan <it>Paramecium caudatum </it>and its bacterial parasite <it>Holospora undulata</it>. We simulated variation in host life span by killing hosts after 11 (<it>early </it>killing) or 14 (<it>late </it>killing) days post inoculation; after killing, parasite transmission stages were collected and used for a new infection cycle.</p> <p>Results</p> <p>After 13 cycles (≈ 300 generations), parasites from the <it>early-killing </it>treatment were less infectious, but had shorter latency time and higher virulence than those from the <it>late-killing </it>treatment. Overall, shorter latency time was associated with higher parasite loads and thus presumably with more rapid within-host replication.</p> <p>Conclusion</p> <p>The analysis of the means of the two treatments is thus consistent with theory, and suggests that evolution is constrained by trade-offs between virulence, transmission and within-host growth. In contrast, we found little evidence for such trade-offs across parasite selection lines within treatments; thus, to some extent, these traits may evolve independently. This study illustrates how environmental variation (experienced by the host) can lead to the evolution of distinct parasite strategies.</p> http://www.biomedcentral.com/1471-2148/9/65
collection DOAJ
language English
format Article
sources DOAJ
author Koella Jacob C
Nidelet Thibault
Kaltz Oliver
spellingShingle Koella Jacob C
Nidelet Thibault
Kaltz Oliver
Effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite system
BMC Evolutionary Biology
author_facet Koella Jacob C
Nidelet Thibault
Kaltz Oliver
author_sort Koella Jacob C
title Effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite system
title_short Effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite system
title_full Effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite system
title_fullStr Effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite system
title_full_unstemmed Effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite system
title_sort effects of shortened host life span on the evolution of parasite life history and virulence in a microbial host-parasite system
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2009-03-01
description <p>Abstract</p> <p>Background</p> <p>Ecological factors play an important role in the evolution of parasite exploitation strategies. A common prediction is that, as shorter host life span reduces future opportunities of transmission, parasites compensate with an evolutionary shift towards earlier transmission. They may grow more rapidly within the host, have a shorter latency time and, consequently, be more virulent. Thus, increased extrinsic (i.e., not caused by the parasite) host mortality leads to the evolution of more virulent parasites. To test these predictions, we performed a serial transfer experiment, using the protozoan <it>Paramecium caudatum </it>and its bacterial parasite <it>Holospora undulata</it>. We simulated variation in host life span by killing hosts after 11 (<it>early </it>killing) or 14 (<it>late </it>killing) days post inoculation; after killing, parasite transmission stages were collected and used for a new infection cycle.</p> <p>Results</p> <p>After 13 cycles (≈ 300 generations), parasites from the <it>early-killing </it>treatment were less infectious, but had shorter latency time and higher virulence than those from the <it>late-killing </it>treatment. Overall, shorter latency time was associated with higher parasite loads and thus presumably with more rapid within-host replication.</p> <p>Conclusion</p> <p>The analysis of the means of the two treatments is thus consistent with theory, and suggests that evolution is constrained by trade-offs between virulence, transmission and within-host growth. In contrast, we found little evidence for such trade-offs across parasite selection lines within treatments; thus, to some extent, these traits may evolve independently. This study illustrates how environmental variation (experienced by the host) can lead to the evolution of distinct parasite strategies.</p>
url http://www.biomedcentral.com/1471-2148/9/65
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