Abstract

Insect herbivores may undergo genetic divergence on their host plants through host-associated differentiation (HAD). Much of what we know about HAD involves insect species with narrow host ranges (i.e., specialists) that spend part or all their life cycle inside their hosts, and/or reproduce asexually (e.g., parthenogenetic insects), all of which are thought to facilitate HAD. However, sexually reproducing polyphagous insects can also exhibit HAD. Few sexually reproducing insects have been tested for HAD, and when they have insects from only a handful of potential host-plant populations have been tested, making it difficult to predict how common HAD is when one considers the entire species’ host range. This question is particularly relevant when considering insect pests, as host-associated populations may differ in traits relevant to their control. Here, we tested for HAD in a cotton (Gossypium hirsutum) pest, the cotton fleahopper (CFH) (Pseudatomoscelis seriatus), a sexually reproducing, highly polyphagous hemipteran insect. A previous study detected one incidence of HAD among three of its host plants. We used Amplified fragment length polymorphism (AFLP) markers to assess HAD in CFH collected from an expanded array of 13 host-plant species belonging to seven families. Overall, four genetically distinct populations were found. One genetically distinct genotype was exclusively associated with one of the host-plant species while the other three were observed across more than one host-plant species. The relatively low degree of HAD in CFH compared to the pea aphid, another hemipteran insect, stresses the likely importance of sexual recombination as a factor increasing the likelihood of HAD.

Highlights

  • Host-plants play an important role in the diversification of insect populations (Ehrlich and Raven 1964)

  • The percentage of polymorphic loci per host-plant ranged from 45% to 79% with scurvy mallow (SM) and both cotton (CT) and primrose (EP) yielding the lowest and highest polymorphisms, respectively (Table 2)

  • Given that host-associated differentiation (HAD) is known to occur in the cotton fleahopper (CFH) (Barman et al 2012) and that it has an extensive host-plant range of over 160 plants, we predicted that expanded sampling for HAD would reveal additional instances of HAD

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Summary

Introduction

Host-plants play an important role in the diversification of insect populations (Ehrlich and Raven 1964). If reproductive isolation is maintained, this process may end up in the formation of genetically distinct host-associated lineages or host races (Diehl and Bush 1984; Bernays 1991; Carroll and Boyd 1992; Pappers et al 2001; Dres and Mallet 2002). This phenomenon is commonly referred to as host-associated genetic differentiation (HAD) (Bush 1969; Abrahamson et al 2001). Perhaps some of the best-studied cases of insect HAD are those involving apple maggot flies (Rhagoletis pomonella) on apples and hawthorns (Bush 1969; Feder et al 1993; Forbes et al 2010), species associated with goldenrods (Abrahamson et al 2001; Eubanks et al 2003; Stireman et al 2005), pea aphids (Acyrthosiphon pisum) associated with plants in the Fabaceae family

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