Chronology of parasite-induced alteration of fish behaviour: effects of parasite maturation and host experience

被引:29
|
作者
Shirakashi, S [1 ]
Goater, CP [1 ]
机构
[1] Univ Lethbridge, Dept Biol Sci, Lethbridge, AB T1K 3M4, Canada
关键词
parasite-induced host behaviour; fitness; rheotaxis; optomotor; host manipulation hypothesis;
D O I
10.1017/S0031182004006432
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
We monitored temporal changes in the magnitude of altered host behaviour in minnows (Pimephales promelas) experimentally infected with metacercariae of a brain-encysting trematode (Ornithodiplostomum ptychocheilus). This parasite develops and then encysts in a region of the brain that mediates the optomotor response (OMR), an innate behaviour that links visual stimuli with motor performance. The OMR of infected and uninfected minnows was evaluated between 0 and 10 weeks post-infection (p.i.), an interval spanning the development period of metacercariae to infectivity in birds. Trials involved monitoring the time an individual minnow spent following a spinning drum that had been painted with alternating black and white stripes. At 2 and 4 weeks p.i., infected minnows followed the drum 40% less often than controls. Differences between controls and infected fish declined thereafter, and were undetectable by 10 weeks p.i. Both control and infected fish habituated equally rapidly to the spinning drum. However, the difference in performance between controls and infected fish was 29% for experienced fish and 48% for fish that: had never experienced the drum. Because maximum parasite induced reduction in OMR coincided with the period of maximum parasite development, the behavioural effects are most likely due to unavoidable pathology in the brain associated with developing larvae.
引用
收藏
页码:177 / 183
页数:7
相关论文
共 50 条
  • [41] Parasite-induced leucomyelopathy in llamas (Lama glama)
    Barnett, J. E. F.
    Preston, G. D.
    Steele, L. M.
    Gibbons, L. M.
    Scholes, S. F. E.
    Schock, A.
    Higgins, R. J.
    VETERINARY RECORD, 2008, 163 (17) : 516 - 517
  • [42] Parasite-induced vulnerability to predation in larval anurans
    DeBlieux, Turner S.
    Hoverman, Jason T.
    DISEASES OF AQUATIC ORGANISMS, 2019, 135 (03) : 241 - 250
  • [43] Chemokines as markers for parasite-induced inflammation and tumors
    Trakatelli, C
    Frydas, S
    Hatzistilianou, M
    Papadopoulos, E
    Simeonidou, I
    Founta, A
    Paludi, D
    Petrarca, C
    Castellani, ML
    Papaioannou, N
    Salini, V
    Conti, P
    Kempuraj, D
    Vecchiet, J
    INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 2005, 20 (04): : 197 - 203
  • [44] Finding the cause of parasite-induced abortions in cattle
    Lindsay, DS
    Dubey, JP
    Blagburn, BL
    VETERINARY MEDICINE, 1996, 91 (01) : 64 - 71
  • [45] Drug Development for Parasite-Induced Diarrheal Diseases
    Debnath, Anjan
    McKerrow, James H.
    FRONTIERS IN MICROBIOLOGY, 2017, 8
  • [46] A mosquito mediator of parasite-induced immune priming
    Simoes, Maria L.
    Dimopoulos, George
    TRENDS IN PARASITOLOGY, 2015, 31 (09) : 402 - 404
  • [47] The influence of non-host predators on parasite-induced behavioral changes in a freshwater snail
    Levri, EP
    OIKOS, 1998, 81 (03) : 531 - 537
  • [48] Effects of a parasite-induced nephritis on osmoregulation in the common carp Cyprinus carpio
    Meyer, C
    Ganter, M
    Körting, W
    Steinhagen, D
    DISEASES OF AQUATIC ORGANISMS, 2002, 50 (02) : 127 - 135
  • [49] Parasite-induced variation in host morphology: Brain-encysting trematodes in fathead minnows
    Sandland, GJ
    Goater, CP
    JOURNAL OF PARASITOLOGY, 2001, 87 (02) : 267 - 272
  • [50] Parasite-induced change in host behavior of a freshwater snail: parasitic manipulation or byproduct of infection?
    Levri, EP
    BEHAVIORAL ECOLOGY, 1999, 10 (03) : 234 - 241