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Background Besnoitia darlingi , B. neotomofelis and B. oryctofelisi are closely related coccidian parasites with felids as definitive hosts. These parasites use a variety of animal species as intermediate hosts. North American opossums ( Didelphis virginiana ), North American southern plains woodrats ( Neotoma micropus ) and South American domestic rabbits ( Oryctolagus cuniculus ) are intermediate hosts of B. darlingi , B. neotomofelis and B. oryctofelisi , respectively. Based on conserved regions in the internal transcribed spacer-1 (ITS1) sequence of the ribosomal DNA (rDNA), a real-time PCR for a sensitive detection of these Besnoitia spp. in tissues of intermediate hosts and faeces of definitive hosts has recently been established. Available sequence data suggest that species such as B. akodoni and B. jellisoni are also covered by this real-time PCR. It has been hypothesised that additional Besnoitia spp. exist worldwide that are closely related to B. darlingi or B. darlingi -like parasites ( B. neotomofelis , B. oryctofelisi , B. akodoni or B. jellisoni ). Also related, but not as closely, is B. besnoiti , the cause of bovine besnoitiosis. Methods Faecal samples from two free-ranging cheetahs ( Acinonyx jubatus ) from Namibia that had previously tested positive for coccidian parasites by coproscopy were used for this study. A conventional PCR verified the presence of coccidian parasite DNA. To clarify the identity of these coccidia, the faecal DNA samples were further characterised by species-specific PCRs and Sanger sequencing. Results One of the samples tested positive for B. darlingi or B. darlingi -like parasites by real-time PCR, while no other coccidian parasites, including Toxoplasma gondii , Hammondia hammondi , H. heydorni , B. besnoiti and Neospora caninum , were detected in the two samples. The rDNA of the B. darlingi -like parasite was amplified and partially sequenced. Comparison with existing sequences in GenBank revealed a close relationship to other Besnoitia spp., but also showed clear divergences. Conclusions Our results suggest that a so far unknown Besnoitia species exists in Namibian wildlife, which is closely related to B. darlingi , B. neotomofelis , B. oryctofelisi , B. akodoni or B. jellisoni. The cheetah appears to be the definitive host of this newly discovered parasite, while prey species of the cheetah may act as intermediate hosts. Graphical Abstract

Sexual differences in physiology are widely regarded as potential proximate mechanisms that underlie sex differences in mortality, life history and disease risk of vertebrates. However, little is known about the causes of sex‐specific variation in physiology. Sexual selection and parental workload are two key components suggested to play a role. Theory predicts that, within males, species with stronger male sexual selection (greater sexual dichromatism and more frequent social polygyny) and higher male parental effort should have lower immune capacity and stronger oxidative imbalance. Within females, a weak or no direct effect of male sexual selection on physiology is expected, but species where females invest more in parental care should have lower immune capacity and higher oxidative imbalance. We tested these predictions by phylogenetic comparative analyses conducted separately for the two sexes and based on 11,586 physiological measurements of samples collected in the field from 2048 individuals of 116 and 106 European bird species for males and females, respectively. For males, we found that the degree of dichromatism, polygyny and male parental effort correlated negatively with multiple immune indices, and the level of antioxidant glutathione correlated positively with polygyny score. In contrast, female immune and oxidative variables were unrelated or weakly related to both male sexual selection and female parental effort. We conclude that sex roles can drive inter‐specific variation in immune function (primarily in male birds), but less so in oxidative physiology. These findings support earlier claims that males pay higher physiological costs of sexual selection than females, but apparently also of caregiving. We discuss how females might avoid such costs. Our comparative analyses explored across‐species variation in physiology to evaluate the role of sexual selection and parental care in the evolution of immune and oxidative physiology. Our results highlight that male sexual selection and parental effort are powerful factors shaping male but not female immunity, but have no effect on oxidative physiology in either sex.

Immune defenses are crucial for survival but costly to develop and maintain. Increased immune investment is therefore hypothesized to trade-off with other life-history traits. Here, we examined innate and adaptive immune responses to environmental heterogeneity in wild Antarctic fur seals. In a fully crossed, repeated measures design, we sampled 100 pups and their mothers from colonies of contrasting density during seasons of contrasting food availability. Biometric and cortisol data as well as blood for the analysis of 13 immune and oxidative status markers were collected at two key life-history stages. We show that immune responses of pups are more responsive than adults to variation in food availability, but not population density, and are modulated by cortisol and condition. Immune investment is associated with different oxidative status markers in pups and mothers. Our results suggest that early life stages show greater sensitivity to extrinsic and intrinsic effectors, and that immunity may be a strong target for natural selection even in low-pathogen environments such as Antarctica. An investigation into the immune profiles of Antarctic fur seals provides detailed insights into how organisms manage the allocation of and trade-offs among resources in a variable environment.

Immunological responses of hibernating mammals are suppressed at low body temperatures, a possible explanation for the devastating effect of the white-nose syndrome on hibernating North American bats. However, European bats seem to cope well with the fungal causative agent of the disease. To better understand the immune response of hibernating bats, especially against fungal pathogens, we challenged European greater mouse-eared bats (Myotis myotis) by inoculating the fungal antigen zymosan. We monitored torpor patterns, immune gene expressions, different aspects of the acute phase response, and plasma oxidative status markers and compared them with sham-injected control animals at 30 min, 48 h and 96 h after inoculation. Torpor patterns, body temperatures, body masses, white blood cell counts, expression of immune genes, reactive oxygen metabolites, and non-enzymatic antioxidant capacity did not differ between groups during the experiment. However, zymosan injected bats had significantly higher levels of haptoglobin than the control animals. Our results indicate that hibernating greater mouse-eared bats mount an inflammatory response to a fungal challenge, with only mild to negligible consequences for the energy budget of hibernation. Our study gives a first hint that hibernating European bats may have evolved a hibernation-adjusted immune response in order to balance the trade-off between competent pathogen elimination and a prudent energy-saving regime.

Hibernation is a physiological adaptation to overcome extreme environmental conditions. It is characterized by prolonged periods of torpor interrupted by temporary arousals during winter. During torpor, body functions are suppressed and restored rapidly to almost pre-hibernation levels during arousal. Although molecular studies have been performed on hibernating rodents and bears, it is unclear how generalizable the results are among hibernating species with different physiology such as bats. As targeted blood proteomic analysis are lacking in small hibernators, we investigated the general plasma proteomic profile of European Myotis myotis and hibernation associated changes between torpid and active individuals by two-dimensional gel electrophoresis. Results revealed an alternation of proteins involved in transport, fuel switching, innate immunity and blood coagulation between the two physiological states. The results suggest that metabolic changes during hibernation are associated with plasma proteomic changes. Further characterization of the proteomic plasma profile identified transport proteins, coagulation proteins and complement factors and detected a high abundance of alpha-fetoprotein. We were able to establish for the first time a basic myotid bat plasma proteomic profile and further demonstrated a modulated protein expression during torpor in Myotis myotis , indicating both novel physiological pathways in bats in general and during hibernation in particular.

Feathers play an important role in many aspects of avian life histories, for exampling acting in thermoregulation, communication and flight. Damaged feathers may reduce the ability to perform these functions, so there are likely fitness costs for individuals possessing damaged plumage. Recently, descriptive studies provided evidence that birds carry featherdegrading bacteria on their plumage. These bacteria have the ability to degrade feathers, rapidly under laboratory conditions, more slowly under field conditions. If such feather-degrading bacteria reduce avian fitness, natural selection should favour the evolution of anti-bacterial defences. Moult has been suggested as one such defence. Here we test this prediction with mallards, Anas platyrhynchos, and the use of repeated measures of total cultivable and feather-degrading bacterial loads on the same birds before, during and after moult. We found that moult had no significant effect on total cultivable and feather-degrading bacterial loads on feathers. Our results show that the bacterial contamination that takes place after moult overrides the potential role of moult as a mechanism to reduce feather bacterial loads.

Background Knowledge about parasitic infections is crucial information for animal health, particularly of free-ranging species that might come into contact with livestock and humans. Methods We investigated the seroprevalence of three tissue-cyst-forming apicomplexan parasites ( Toxoplasma gondii , Neospora caninum and Besnoitia besnoiti ) in 506 individuals of 12 wildlife species in Namibia using in-house enzyme linked immunosorbent assays (indirect ELISAs applying purified antigens) for screening and immunoblots as confirmatory tests. We included six species of the suborder Feliformia, four species of the suborder Caniformia and two species of the suborder Ruminantia. For the two species for which we had most samples and life-history information, i.e. cheetahs ( Acinonyx jubatus , n  = 250) and leopards ( Panthera pardus , n  = 58), we investigated T. gondii seroprevalence in relation to age class, sex, sociality (solitary, mother-offspring group, independent sibling group, coalition group) and site (natural habitat vs farmland). Results All but one carnivore species (bat-eared fox Otocyon megalotis , n  = 4) were seropositive to T. gondii , with a seroprevalence ranging from 52.4% (131/250) in cheetahs to 93.2% (55/59) in African lions ( Panthera leo ). We also detected antibodies to T. gondii in 10.0% (2/20) of blue wildebeest ( Connochaetes taurinus ). Adult cheetahs and leopards were more likely to be seropositive to T. gondii than subadult conspecifics, whereas seroprevalence did not vary with sex, sociality and site. Furthermore, we measured antibodies to N. caninum in 15.4% (2/13) of brown hyenas ( Hyaena brunnea ) and 2.6% (1/39) of black-backed jackals ( Canis mesomelas ). Antibodies to B. besnoiti were detected in 3.4% (2/59) of African lions and 20.0% (4/20) of blue wildebeest. Conclusions Our results demonstrate that Namibian wildlife species were exposed to apicomplexan parasites at different prevalences, depending on parasite and host species. In addition to serological work, molecular work is also needed to better understand the sylvatic cycle and the clear role of wildlife in the epidemiology of these parasites in southern Africa.

Reproduction is one of the costliest processes in the life of an animal. Life history theory assumes that when resources are limiting allocation to reproduction will reduce allocation to other essential processes thereby inducing costs of reproduction. The immune system is vital for survival. If reproduction reduces investment in immune function, this could increase the risk of disease, morbidity and mortality. We here test in the guinea pig, if even under ad libitum food conditions, pregnancy and lactation reduce the activity of the adaptive and innate immune system compared to the reaction of non-reproducing animals. In response to a challenge with keyhole limpet haemocyanin the antibody-mediated adaptive immunity during (pregnancy and) lactation was reduced. Pregnant and lactating females showed higher levels of bacterial killing activity, an integrated measure of innate immunity, than non-reproducing females. However, two major effectors of the innate immunity, the natural antibody and the complement of pregnant and lactating females showed lower levels than in non-reproducing females. Pregnant and lactating females did not differ significantly in the expressed levels of innate immunity. Our results indicate that changes in the immune response during reproduction are physiological adjustments to predictable allocation problems, because they happen even under ad libitum food availability.

Maintaining a competent immune system is energetically costly and thus immunity may be traded against other costly traits such as seasonal migration. Here, we tested in long-distance migratory Nathusius’ pipistrelles ( Pipistrellus nathusii ), if selected branches of immunity are expressed differently in response to the energy demands and oxidative stress of aerial migration. During the migration period, we observed higher baseline lymphocyte and lower neutrophil levels than during the pre-migration period, but no stronger response of cellular effectors to an antigen challenge. Baseline plasma haptoglobin, as a component of the humoral innate immunity, remained similar during both seasons, yet baseline plasma haptoglobin levels increased by a factor of 7.8 in migratory bats during an immune challenge, whereas they did not change during the pre-migration period. Oxidative stress was higher during migration than during pre-migration, yet there was no association between blood oxidative status and immune parameters, and immune challenge did not trigger any changes in oxidative stress, irrespective of season. Our findings suggest that humoral effectors of the acute phase response may play a stronger role in the first-line defense against infections for migrating bats compared to non-migrating bats. We conclude that Nathusius’ pipistrelles allocate resources differently into the branches of their immune system, most likely following current demands resulting from tight energy budgets during migration.