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Bed bug deterrence
BMC Biology volume 8, Article number: 117 (2010)
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.
See research article http://www.biomedcentral.com/1741-7007/8/121
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 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 complementary manipulative experiments conducted by Harraca et al. [4] provide convincing evidence of effective communication 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 ectoparasites 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 gland fluids into her body cavity [6–10]. Sperm must migrate through the haemocoel to the female's reproductive 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 excessive 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.
Mating pair (male top) in aggregation of recently fed bed bugs.
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.
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 asymmetrical ectospermalege (right-side only; Figure 3) that channels the sickle-shaped male paramere to puncture the cuticle so that semen is introduced into the mesospermalege, 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 adaptations, 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 its own risks. The evolution of insemination that bypasses the genital system and the subsequent evolution of an extragenital system in the female is an example of the coevolution mediated by sexual conflict [6–11]. Males also have adaptations to avoid injury from homosexual copulation, such as release of a blend of chemicals from the metathoracic gland [9], which in a different context has a putative alarm function [13].
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. Internally the female has a mesospermalege that receives sperm and has a presumed function in the immune responses of the female.
An example to follow?
It remains to be seen if the newer thrusts of basic science research, such as that reported by Harraca and colleagues in BMC Biology, will contribute new approaches to pest control, but certainly the reliance of bed bugs on chemical signalling [13–15] is one avenue that needs to be explored further. Interfering with mating behaviour is an attractive idea, which has shown success with many agricultural pest species, but the longevity of bed bugs (months to a year or more) and our lack of tolerance of their repeated biting, makes the concept much more challenging. Whether interfering with sexual reproduction with 'anti-aphrodiasiac' pheromones is of practical significance or not, ongoing research on bed bug biology is likely to have an impact on the way that we manage this tough pest.
References
- 1.
Potter MF, Rosenberg B, Henriksen M: Bugs without borders: defining the global bed bug resurgence. Pest World. 2010, September/October: 8-20.
- 2.
Romero A, Potter MF, Potter DA, Haynes KF: Insecticide resistance in the bed bug: A factor in the pest's sudden resurgence?. J Med Entomol. 2007, 44: 175-178. 10.1603/0022-2585(2007)44[175:IRITBB]2.0.CO;2.
- 3.
Romero A, Potter MF, Haynes KF: Circadian rhythm of spontaneous locomotor activity in the bed bug, Cimex lectularius L. J Insect Physiol. 2010, 56: 1516-1522. 10.1016/j.jinsphys.2010.04.025.
- 4.
Harraca V, Ryne C, Ignell R: Nymphs of the common bed bug (Cimex lectularius) produce anti-aphrodisiac defence against conspecific males. BMC Biology. 2010, 8: 121-
- 5.
Usinger RL: Monograph of Cimicidae (Hemiptera, Heteroptera). 1966, College Park, MD: Entomological Society of America
- 6.
Morrow EH, Arnqvist G: Costly traumatic insemination and a female counter-adaptation in bed bugs. Proc R Soc B. 2003, 270: 2377-2381. 10.1098/rspb.2003.2514.
- 7.
Reinhardt K, Naylor R, Siva-Jothy MT: Reducing a cost of traumatic insemination: female bedbugs evolve a unique organ. Proc R Soc B. 2003, 270: 2371-2375. 10.1098/rspb.2003.2515.
- 8.
Reinhardt K, Siva-Jothy MT: Biology of the bed bugs (Cimicidae). Annu Rev Entomol. 2007, 52: 351-374. 10.1146/annurev.ento.52.040306.133913.
- 9.
Siva-Jothy MT: Trauma, disease and collateral damage: conflict in cimicids. Phil Trans R Soc Lond B Biol Sci. 2006, 361: 269-275. 10.1098/rstb.2005.1789.
- 10.
Stutt AD, Siva-Jothy MT: Traumatic insemination and sexual conflict in the bed bug Cimex lectularius. Proc Natl Acad Sci USA. 2001, 98: 5683-5687. 10.1073/pnas.101440698.
- 11.
Pfiester M, Koehler PG, Pereira RM: Sexual conflict to the extreme: traumatic insemination in bed bugs. Amer Entomol. 2009, 55: 244-249.
- 12.
Benoit JB, Del Grosso NA, Yoder JA, Denlinger DL: Resistance to dehydration between bouts of blood feeding in the bed bug, Cimex lectularius, is enhanced by water conservation, aggregation, and quiescence. Am J Trop Med Hyg. 2007, 76: 987-993.
- 13.
Levinson HZ, Levinson AR, Maschwitz U: Action and composition of alarm pheromone of bedbug Cimex lectularius L. Naturwissenschaften. 1974, 61: 684-685. 10.1007/BF00606522.
- 14.
Ryne C: Homosexual interactions in bed bugs: alarm pheromones as male recognition signals. Anim Behav. 2009, 78: 1471-1475. 10.1016/j.anbehav.2009.09.033.
- 15.
Siljander E, Gries R, Khaskin G, Gries G: Identification of the airborne aggregation pheromone of the common bed bug, Cimex lectularius. J Chem Ecol. 2008, 34: 708-718. 10.1007/s10886-008-9446-y.
Acknowledgements
We appreciate the support of the University of Kentucky Agricultural Experiment Station and the Kentucky Pest Management Association. MHG was supported by a US National Science Foundation Graduate Research Fellowship.
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Haynes, K.F., Goodman, M.H. & Potter, M.F. Bed bug deterrence. BMC Biol 8, 117 (2010). https://doi.org/10.1186/1741-7007-8-117
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Keywords
- Internal Adaptation
- Gland Fluid
- Untapped Opportunity
- Extra Copulation
- Metathoracic Gland
