Bed bug deterrence

Haynes et al. BMC Biology 2010, 8:117 http://www.biomedcentral.com/1741-7007/8/117 CO M M E N TA R Y Open Access Bed bug deterrence Kenneth F Haynes*, Mark H Goodman and Michael F Potter See research article http://www.biomedcentral.com/1741-7007/8/121 Abstract A recent study in BMC Biology has determined that the immature stage of the bed bug (the nymph) signals its reproductive status to adult males using pheromones and thus avoids the trauma associated with copulation in this species. The success of this nymphal strategy of deterrence is instructive. Against the background of increasing problems with bed bugs, this research raises the question whether pheromones might be used to control them. Bed bug resurgence A global resurgence of bed bugs, a once common household pest that had nearly disappeared for 50 years, has renewed scientific interest in these fascinating insects. Pest control companies from every part of the world are reporting many more encounters now than 10 years ago [1]. Undoubtedly, many factors have led to this outbreak, but evolved resistance to some of the most commonly used insecticides is a contributor [2]. Unlike many other blood-feeding arthropods, such as mosquitoes, tstetse flies, ticks, and sand flies, bed bugs are not known to effectively vector any human pathogen. However, bed bugs inhabit our beds, and return repeatedly at night [3] for blood meals required to complete each stage of development (five immature stages) and each cycle of egg production. Recent research by Harraca and colleagues presented in BMC Biology provides new insights into the reproduction of bed bugs that may offer an untapped opportunity for pest control [4]. Anti-aphrodisiac pheromones defend vulnerable nymphs Harraca and colleagues have demonstrated that bed bug nymphs (Cimex lectularius) produce a chemical signal that interrupts the attempts of adult males to mate with *Correspondence: Department of Entomology, S-225 Agricultural Science Center, University of Kentucky, Lexington KY 40546, USA them [4]. Because adult males, females, nymphs and eggs are found in aggregations around where the host sleeps (in the case of humans, our beds), encounters between males and nymphs are common. Copulation between an adult and a nymph is reproductively ineffective, but can be very costly to the nymph and the male; rupture of the cuticle for the nymph, and loss of sperm and other components of the ejaculate for males. As a result the reproductive fitness of the male and survival of the nymphs are parallel interests. These are exactly the circumstances that should favour the evolution of communication, because both signaller and receiver benefit from the information transfer. Two complemen tary manipulative experiments conducted by Harraca et al. [4] provide convincing evidence of effective commu nication between nymphs and males. When the glandular source of the scent that is unique to nymphs is blocked, males will copulate with them. When a nymph-specific compound or nymph-specific ratio of compounds were puffed on male-female pairs, mating was disrupted. Furthermore, males have sensory neurons that respond to the nymph odours. Thus, the chemical signal translates into the simple received message that the source nymph is not a reproductive female. The nature of copulation, known as traumatic or hypodermic insemination, may help to explain the evolution of communication between nymphs and males. Traumatic insemination Reproductive modes of insects are remarkably diverse, as one might expect from a class of animals with millions of species, with some found in every terrestrial habitat, and most aquatic environments as well. Within that diversity, traumatic insemination stands out as an evolutionary enigma. It is a characteristic of the family Cimicidae, a family to which C. lectularius (the bed bug or the human bed bug), C. hemipterus (the tropical bed bug, another human parasite), and over 70 species that are ecto parasites of birds and bats belong [5]. During copulation the male curls his abdomen under the female (Figure 1), punctures her cuticle with a rigid, sickle-shaped paramere (Figure 2) and introduces sperm and accessory © 2010 Haynes et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Haynes et al. BMC Biology 2010, 8:117 http://www.biomedcentral.com/1741-7007/8/117 Figure 1. Mating pair (male top) in aggregation of recently fed bed bugs. gland fluids into her body cavity [6-10]. Sperm must migrate through the haemocoel to the female’s repro ductive system. The extragenital adaptations seen in females greatly reduce the costs that would be associated with punctures of the cuticle [6]. Even with these modifications, mating is costly, occurring with an exces sive frequency that is roughly 20 times that necessary for fertilization of eggs [9]. Each copulation increases risk of infection or physical damage and because nymphs are immature and lack the external and internal adaptations they are at even greater risk. Adaptations to traumatic insemination in mature bedbugs In sexually reproducing organisms, the reproductive interests of males and females are not necessarily congruous. Often males can increase their fitness by mating with many females, but female success may be optimized by mating with high quality sires. Traumatic insemination represents an extreme in the conflict of interests of males and females [11]. Primicimex cavernis resembles a common ancestor of all Cimicidae with respect to copulation; it has traumatic insemination, but not the female counter-adaptations seen in most other species [5]. In contrast, C. lectularius has an asym metrical ectospermalege (right-side only; Figure 3) that channels the sickle-shaped male paramere to puncture the cuticle so that semen is introduced into the meso spermalege, which is an internal structure with presumed immunological function. The internal adaptations are even more extensive in other species of Cimicidae. In addition to morphological and immunological adapta tions, females reduce extra copulations by dispersing from aggregations [11]. For an insect that benefits from proximity to host and microhabitat humidity control, which is enhanced by aggregation [12], dispersal carries Page 2 of 3 Figure 2. The sickle-shaped paramere at the end of the males abdomen penetrates the cuticle of the female and introduces sperm and accessory gland fluids into her body cavity. Ventral view. Horizontal bar is 5 mm. Figure 3. The ectospermalege (inverted V-shape) is an extragenital cuticular structure only on the right side of female. By channelling the male paramere to this part of the abdomen it limits the damage done. Ventral view. Horizontal bar is 5 mm. Int (...truncated)