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. 2022 Jan;149(1):35-43.
doi: 10.1017/S0031182021001529. Epub 2021 Sep 9.

Allee effect in a manipulative parasite within poikilothermic host under temperature change

Affiliations

Allee effect in a manipulative parasite within poikilothermic host under temperature change

Ekaterina Mironova et al. Parasitology. 2022 Jan.

Abstract

Temperature and intraspecific competition are important factors influencing the growth of all organisms, including parasites. The temperature increase is suggested to stimulate the development of parasites within poikilothermic hosts. However, at high parasite densities, this effect could be diminished, due to stronger intraspecific competition. Our study, for the first time, addressed the joint effects of warming and parasite abundances on parasite growth in poikilothermic hosts. The growth of the common fish parasite larvae (trematode Diplostomum pseudospathaceum) within the rainbow trout at different infection intensities and temperatures (15°C and 18°C) was experimentally investigated. The results showed that temperature was positively correlated with both parasite infection success and growth rates. The growth rates increased much more compared to those in many free-living poikilothermic animals. Atypically for a majority of parasites, D. pseudospathaceum larvae grow faster when abundant (Allee effect). The possible causes for this phenomenon (manipulation cost sharing, etc.) are discussed in this study. Importantly, limited evidence of the interaction between temperature and population density was found. It is likely that temperature did not change the magnitude of the Allee effect but affected its timing. The impact of these effects is supposed to become more pronounced in freshwater ecosystems under current climate changes.

Keywords: Crowding effect; Diplostomum pseudospathaceum; Oncorhynchus mykiss; eye fluke; infection intensities; metacercariae; parasite growth; size variation; thermal response.

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Conflict of interest statement

The authors declare there are no conflicts of interest.

Figures

None
Graphical abstract
Fig. 1.
Fig. 1.
Within-eye infection intensity vs metacercariae size taken separately for each metacercariae age × temperature treatment. The shaded area represents the 95% confidence intervals.
Fig. 2.
Fig. 2.
Difference in metacercariae sizes at different temperatures. ‘Boxes’ represent a median with the interquartile range (IQR), whiskers extend from the highest to lower values within 1.5*IQR.
Fig. 3.
Fig. 3.
Difference in infection intensities at different temperatures (A). The relationship between fish weight and infection intensity taking into account different infection doses is presented in the residual plot (B). ‘Boxes’ represent a median with the IQR, whiskers extend from the highest to lower values within 1.5*IQR, the shaded area represents the 95% confidence intervals.
Fig. 4.
Fig. 4.
Mean metacercariae length vs log(CV) of metacercariae length in fish dissected on the 12th (A) and 17th (B) day after infection. (C) Variability of metacercariae length in fish from different temperature treatments. The shaded area represents the 95% confidence intervals.

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