A comparison of the effects of organophosphate insecticide exposure and temperature stress on fluctuating asymmetry and life history traits in Culex quinquefasciatus
Introduction
Environmental or genetic stress has been shown many times to cause an increase in the fluctuating asymmetry (FA) of bilaterally morphological traits (Parsons, 1990; Clarke and McKenzie, 1992; Markow, 1995). FA can be defined as the random non-directional deviation from perfect bilateral symmetry with a normal distribution around a mean of zero (Palmer and Strobeck, 1986; Møller and Swaddle, 1997). An increase in FA is interpreted as an indication of increased developmental instability or reduced developmental homeostasis (Clarke and McKenzie, 1992; Markow, 1995). Environmental stressors shown to increase FA include temperature extremes, larval density, chemical pollution and nutrition deficiency.
The present study was designed to look at the effects of a non-chemical (temperature) and chemical (insecticide) stress on the development of Culex quinquefasciatus mosquitoes (C. pipiens sp. complex) by using levels of FA and more conventional life history traits as indicators of environmental stress. Temperature is an important environmental determinant for ectothermic organisms since it affects all biological processes. Many organisms operate optimally within a very narrow temperature range and deviations from this could impose stress during development (Parsons, 1987, Parsons, 1989; Imasheva et al., 1997). At the molecular level, temperature stress directly affects biological molecules such as enzymes, which are crucial for the survival of the organism, whereas at the population level it may result in chronic effects within the genetic architecture of the population (Imasheva et al., 1997). Temperature per se is a general stressor, which impacts upon the whole developmental homeostasis of an ectothermic organism, mainly by affecting crucial biological pathways and systems pivotal to survival (Parsons, 1961). On the other hand, xenobiotic compounds are often more specific because they generally affect individual pathways within the organism (Parsons, 1990). Since these stressors have different modes of action on the organism, it is of interest to compare their effects on developmental homeostasis. Effects of exposure to these stressors on the development of the C. quinquefasciatus mosquitoes, with particular reference to phenotypic variation of life history characters such as survival of different life stages, development time, adult body size and developmental instability of fitness-related traits, were measured.
Section snippets
Insect strain
A standard insecticide susceptible laboratory strain of C. quinquefasciatus named SLab was used (Georghiou et al., 1966). The mosquitoes were reared in a constant temperature humidity room (CTH, temperature 25±0.2°C, RH 70±5%, 12:12 light to dark) using standard techniques.
Insecticide exposure
The insecticide was prepared by dissolving analytical grade temephos in ethanol. Three insecticide concentrations were prepared: 0.00011, 0.00025 and 0.00032 mg/l in 140 ml total volume of water by the addition of
Life history measurements
Elevated temperature significantly influenced development time measured as the mean number of days from hatching to adult eclosion (F2,32=257,P<0.001) (Fig. 1(a)). Development time decreased as temperature increased. Exposure to temephos had no effect on development time (F3,32=1.45,P=0.247) (Fig. 1(a)). Survival was influenced by both temperature (F2,36=71.72,P<0.001) and insecticide dose (F3,36=9.97,P<0.001), with highest survival at 25°C, and lowest survival at 37°C (Fig. 1(b)). No
Discussion
Insect wing lengths are routinely used in studies of developmental stability (Clarke and Ridsdill-Smith, 1990; Agnew and Koella, 1997; Crespi and Vanderkist, 1997; Hardersen and Wratten, 1998) and are thought to be adequately suited for such studies. The reason for their choice is the ease with which they can be measured and also they are usually measured with sufficient accuracy and are highly repeatable. Numerous studies correlated the level of wing FA with the degree of chemical stress due
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2022, Infection, Genetics and EvolutionCitation Excerpt :In this regard, previous works had explored wing morphology effects as indicators of instability during development, in environments with variable food supply, such as preserved and anthropized environments (Márquez and Saldamando-Benjumea, 2013; Nouvellet et al., 2011). Other studies had also reported the effect of insecticides on vectors' FA where it has been found that such compounds are important sources of stress (Alves et al., 2020; Bourguet et al., 2004; Mpho et al., 2001; Nattero et al., 2017b, 2019). In the triatomine Triatoma infestans, for example, exposure to pyrethroids induced high levels of FA, but asymmetry decreases after several generations (Nattero et al., 2019).
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2020, Science of the Total EnvironmentCitation Excerpt :As symmetric sides of an organism are under the same environmental and genetic influences, FA is considered to result from random developmental perturbations and is interpreted as a sign of altered developmental stability and homeostasis (Markow, 1995; Palmer and Strobeck, 2003; Estes et al., 2006; Graham et al., 2010; Beasley et al., 2013). Evidence has shown that FA can be increased when individuals develop under suboptimal conditions (Mpho et al., 2001; Chang et al., 2007a) or as a result of exposure to environmental contaminants (Görür, 2006; Görür, 2009). Yet, evidence with respect to the effects of EDCs is inconsistent: some studies have shown positive associations between FA and exposure to substances with endocrine disrupting properties (Valentine and Soule, 1973; Borisov et al., 1997; Custer et al., 2001; Maul and Farris, 2005; Estes et al., 2006; Chang et al., 2007b; Bustnes et al., 2008; Jenssen et al., 2010; Bradley et al., 2019), while others have found no relationship (Knopper and Mineau, 2004; Green and Lochmann, 2006; Arambourou et al., 2017).
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2019, Infection, Genetics and EvolutionCitation Excerpt :The environmental stress imposed by insecticide applications in genetically variable populations may select for certain alleles that ameliorate the immediate stress, but which may also disturb developmental processes and lead to an increased asymmetry (McKenzie and Clarke, 1988; McKenzie and O'Farrell, 1993). For example, resistant strains of the mosquito Culex quinquefasciatus (Mpho et al., 2001) and the moth Heliothis virescens (Gulzar and Wright, 2014) exhibited increasing levels of FA compared with susceptible strains. Subsequent selection for background modifier genes ameliorated the negative impacts of resistance genes, reducing asymmetry scores to those levels present in susceptible genotypes (McKenzie and O'Farrell, 1993).
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2016, Pesticide Biochemistry and PhysiologyCitation Excerpt :There have been some investigations into the effects of abiotic stressors on variation in wing morphometry in Culex species. The results of those studies showed that temperature and different concentrations of pesticide produced significant effects on the wing characters in this organism [44–46]. The evolutionary dynamics of xenobiotic resistance rely on how resistance mutations affect the fitness of their bearers, both in the presence and absence of xenobiotic selection pressure [47].