Manipulative parasites with complex life cycles are known to induce behavioural and physiological changes in their intermediate hosts. Cyathocephalus truncatus is a manipulative parasite which infects Gammarus pulex as intermediate host. G. pulex males display pre-copulatory mate guarding as a response to male-male competition for access to receptive females. In this paper, we tested the influence that C. truncatus-infection might have on male G. pulex sperm number and pairing success. We considered 3 classes of G. pulex males in our experiments: (i) uninfected males found paired in the field, (ii) uninfected males found unpaired in the field, or (iii) infected males found unpaired in the field. Both infected males and uninfected unpaired males paired less with a new female than uninfected paired males did. Furthermore, infected males appear to be at a strong disadvantage when directly competing for females with a healthy rival male, and had fewer sperm in their testes. We discuss the potential effect of male and female mating strategies on such male host mating alteration.

Some parasites with complex life-cycles are able to manipulate the behaviour of their intermediate hosts in a way that increases their transmission to the next host. Gammarids infected by the tapeworm Cyathocephalus truncatus (Cestoda: Spathebothriidea) are known to be more predated by fish than uninfected ones, but potential behavioural manipulation by the parasite has never been investigated. In this study, we tested the hypothesis that C. truncatus is able to manipulate the behaviour of one of its intermediate hosts, Gammarus pulex (Crustacea: Amphipoda). To assess if any behavioural change was linked to other phenotypic alterations, we also measured the immunity of infected and uninfected individuals and investigated the pathogenic effects of the parasite. Infected gammarids were significantly less photophobic than uninfected ones, but no effect of infection on the level of immune defence was found. The results on survival, swimming activity and oxygen consumption suggest that the parasite also has various pathogenic effects. However, the alteration in host phototaxis was not correlated to some of these pathogenic effects. Therefore, we propose that the modification in host reaction to light is a behavioural manipulation, explaining the previously observed increase of gammarid predation rate.

Nosema sp. naturally occurred in both Spodoptera littoralis (Boisd.) and S. exigua (Hübner) laboratory colonies in Alexandria, Egypt (since November 1984). It was responsible for the dramatic suppression of their laboratory populations. Both young (3-day-old) and old (9-day-old) larvae of S. littoralis were susceptible to Nosema sp. However, the pathogen was more effective against the young larvae, especially at high doses, than the old ones. The estimated LC50 was 4.0 × 107 spores'ml, for 3-day-old larvae. The slope value was low (1.2) as typical of protozoan insect pathogens. Heavily infected 9-day-old larvae tended to die as larvae; while less infected ones either pupate or produce larval-pupal intermediate forms (12–23%). The developmental period of both infected larvae and pupae was increased by 4–6 and 3–5 days, respectively. The number of infected insects that reached the adult stage was decreased as the concentration of Nosema sp. spores was increased. Furthermore, infection was shown to reduce adult longevity and fecundity, and viability of the eggs. Larval faecal pellets harboured large numbers of viable spores. Transovum transmission of infection occurred. Two dipterous species, Culex pipiens and Aedes aegypti, were not susceptible to Nosema sp.