Matthew C. I. Medeiros

Host compatibility rather than vector- host-encounter rate determines the host range of avian Plasmodium parasites

Blood-feeding arthropod vectors are responsible for transmitting many parasites between vertebrate hosts. While arthropod vectors often feed on limited subsets of potential host species, little is known about the extent to which this influences the distribution of vector-borne parasites in some systems. Here, we test the hypothesis that different vector species structure parasite–host relationships by restricting access of certain parasites to a subset of available hosts. Specifically, we investigate how the feeding patterns of Culex mosquito vectors relate to distributions of avian malaria parasites among hosts in suburban Chicago, IL, USA. We show that Plasmodium lineages, defined by cytochrome b haplotypes, are heterogeneously distributed across avian hosts. However, the feeding patterns of the dominant vectors (Culex restuans and Culex pipiens) are similar across these hosts, and do not explain the distributions of Plasmodium parasites. Phylogenetic similarity of avian hosts predicts similarity in their Plasmodium parasites. This effect was driven primarily by the general association of Plasmodium parasites with particular host superfamilies. Our results suggest that a mosquito-imposed encounter rate does not limit the distribution of avian Plasmodium parasites across hosts. This implies that compatibility between parasites and their avian hosts structure Plasmodium host range.

Species formation by host shifting in avian malaria parasites

Significance Emerging infectious diseases pose threats to humans and livestock, but little is known about the general propensity of parasitic organisms to shift between hosts or the role of host shifting in the diversification of parasite lineages. The malaria parasites of contemporary vertebrate species descended from a common ancestor, likely after the diversification of their major host taxa, requiring rapid speciation and shifting between hosts across large host–taxonomic distances. Examination of sister lineages of avian malaria parasites in the New World suggests that such host shifting is common and often leads to the origin of new evolutionary lineages of parasites. The malaria parasites (Apicomplexa: Haemosporida) of birds are believed to have diversified across the avian host phylogeny well after the origin of most major host lineages. Although many symbionts with direct transmission codiversify with their hosts, mechanisms of species formation in vector-borne parasites, including the role of host shifting, are poorly understood. Here, we examine the hosts of sister lineages in a phylogeny of 181 putative species of malaria parasites of New World terrestrial birds to determine the role of shifts between host taxa in the formation of new parasite species. We find that host shifting, often across host genera and families, is the rule. Sympatric speciation by host shifting would require local reproductive isolation as a prerequisite to divergent selection, but this mechanism is not supported by the generalized host-biting behavior of most vectors of avian malaria parasites. Instead, the geographic distribution of individual parasite lineages in diverse hosts suggests that species formation is predominantly allopatric and involves host expansion followed by local host–pathogen coevolution and secondary sympatry, resulting in local shifting of parasite lineages across hosts.

Local host specialization, host-switching, and dispersal shape the regional distributions of avian haemosporidian parasites

Significance Within eastern North America, distributions of vector-transmitted haemosporidian blood parasites of birds, commonly known as “avian malaria parasites,” are associated with the distributions of their host species independently of direct effects of climate on potential vectors. Spatial analyses additionally indicated an absence of dispersal limitation for these parasites. Finally, host-breadth, ranging continuously from specialist to generalist, varies among parasite lineages and is dynamic within parasite assemblages over space and time. The distributions of avian haemosporidian parasites emphasize the ability of parasites to disperse across broad regions and to switch readily between hosts to become emerging infectious diseases. The drivers of regional parasite distributions are poorly understood, especially in comparison with those of free-living species. For vector-transmitted parasites, in particular, distributions might be influenced by host-switching and by parasite dispersal with primary hosts and vectors. We surveyed haemosporidian blood parasites (Plasmodium and Haemoproteus) of small land birds in eastern North America to characterize a regional parasite community. Distributions of parasite populations generally reflected distributions of their hosts across the region. However, when the interdependence between hosts and parasites was controlled statistically, local host assemblages were related to regional climatic gradients, but parasite assemblages were not. Moreover, because parasite assemblage similarity does not decrease with distance when controlling for host assemblages and climate, parasites evidently disperse readily within the distributions of their hosts. The degree of specialization on hosts varied in some parasite lineages over short periods and small geographic distances independently of the diversity of available hosts and potentially competing parasite lineages. Nonrandom spatial turnover was apparent in parasite lineages infecting one host species that was well-sampled within a single year across its range, plausibly reflecting localized adaptations of hosts and parasites. Overall, populations of avian hosts generally determine the geographic distributions of haemosporidian parasites. However, parasites are not dispersal-limited within their host distributions, and they may switch hosts readily.

Explosive Increase in Ectoparasites in Hawaiian Forest Birds

Ectoparasites, particularly chewing lice in the Phthiraptera (Insecta), affect the ecology of numerous host species. Most lice are highly host-specific, and there are no documented cases of major increases of chewing lice, within populations, over years. During continuous study from 1987–2005 at upper elevation forests on the island of Hawaii, chewing lice were exceedingly rare and, until 2003, were found in just 2 of 12 species of native and introduced birds. From 2003–2005, there was an explosive increase in the prevalence of chewing lice in all host species. There was no change in humidity, or in behavior of hosts, that could have caused an ecological release of existing lice. Based on reduced fat levels and increases in broken wing and tail feathers for most host species, there was apparently a food limitation that preceded the increase. The increase coincided temporally with detection of a nonnative bird that had recently been found in elevations below the study sites. Although there were isolated sightings of this bird on the study sites, seasonal movements and behavior of some species of native birds could also have allowed greater transmission to study sites. Both prevalence and intensity of infection, indexed by number of body regions parasitized, were lower in native species with greater bill overlap, a character that could help birds control lice. Seasonality of prevalence indicated that low prevalence preceded molt and high prevalence occurred after molting of hosts. The number of major fault bars in wing and tail feathers, a sign of nutritive stress, was correlated with intensity of infection, indicating an indirect cost to the hosts of being parasitized. In addition, birds with lice were less likely to be recaptured than birds without lice.

Specialized avian Haemosporida trade reduced host breadth for increased prevalence

Parasite specialization on one or a few host species leads to a reduction in the total number of available host individuals, which may decrease transmission. However, specialists are thought to be able to compensate by increased prevalence in the host population and increased success in each individual host. Here, we use variation in host breadth among a community of avian Haemosporida to investigate consequences of generalist and specialist strategies on prevalence across hosts. We show that specialist parasites are more prevalent than generalist parasites in host populations that are shared between them. Moreover, the total number of infections of generalist and specialist parasites within the study area did not vary significantly with host breadth. This suggests that specialists can infect a similar number of host individuals as generalists, thus compensating for a reduction in host availability by achieving higher prevalence in a single host species. Specialist parasites also tended to infect older hosts, whereas infections by generalists were biased towards younger hosts. We suggest that this reflects different abilities of generalists and specialists to persist in hosts following infection. Higher abundance and increased persistence in hosts suggest that specialists are more effective parasites than generalists, supporting the existence of a trade‐off between host breadth and average host use among these parasites.

A Fledgling-Mass Threshold Greatly Affects Juvenile Survival in the Hawaii Akepa (Loxops Coccineus Coccineus)

ABSTRACT. Offspring quality is an important issue in avian life-history theory, particularly with regard to birds that have low reproductive rates and extended parental care. Offspring mass has been identified as an indicator of quality in several bird species. These studies have shown that nestling mass is predictive of offspring survival outside the nest, but few studies have considered the role of fledgling mass. Mass during the fledgling period may change and influence juvenile survival. Fledgling mass may be especially relevant for tropical birds that have very long fledgling periods during which food conditions randomly or seasonally change. Here, we show that fledgling mass predicts juvenile survival in the Hawaii Akepa (Loxops coccineus coccineus), an endangered Hawaiian Honeycreeper with high annual adult survival and a two-egg clutch. Juvenile survival of Hawaii Akepa approximated a trimodal pattern of no survival, low survival, and high survival that corresponded to ascending mass classes. Fledglings in the highest mass class had an apparent juvenile survival probability that was more than double that of fledglings of the lower mass classes and that was statistically indistinguishable from survival rates of adults. This mass-dependent juvenile survival has important implications for understanding the life-history evolution and population biology of the Hawaii Akepa and perhaps of other tropical birds. RESUMEN. La calidad de las crías es un aspecto importante de la teoría sobre las historias de vida de las aves, particularmente para las que presentan tasas reproductivas bajas y cuidado parental extendido. La masa de las crías ha sido identificada como un indicador de la calidad en varias especies de aves. Esos estudios han mostrado que la masa de los pichones predice la supervivencia de las crías fuera del nido, pero pocos estudios han considerado el papel de la masa de los volantones al momento de abandonar el nido. La masa durante el período de emplumamiento puede cambiar e influenciar la supervivencia de las aves jóvenes. La masa de los volantones podría ser especialmente relevante para las aves tropicales que tienen períodos de emplumamiento muy largos, durante los cuales las condiciones cambian aleatoria o estacionalmente. En este estudio demostramos que la masa de emplumamiento predice la supervivencia de las aves jóvenes en Loxops coccineus coccineus, una especie de mielero hawaiano amenazada que presenta una supervivencia anual de los adultos alta y una nidada de dos huevos. La supervivencia de los jóvenes se aproximó a un patrón trimodal de no supervivencia, supervivencia baja y supervivencia alta, que correspondió a una escala creciente de clases de masa. Los volantones en la clase de masa más alta presentaron una probabilidad de supervivencia aparente de más del doble en comparación con la de los volantones de las clases de masa menores, y su tasa de supervivencia fue estadisticamente indistinguible de la de las aves adultas. Esta supervivencia dependiente de la masa en las aves jóvenes tiene implicaciones importantes para entender la evolución de la historia de vida y la biología poblacional de L. c. coccineus y quizás de otras aves tropicales.

Plasmodium prevalence across avian host species is positively associated with exposure to mosquito vectors.

The prevalence of vector-borne parasites varies greatly across host species, and this heterogeneity has been used to relate infectious disease susceptibility to host species traits. However, a few empirical studies have directly associated vector-borne parasite prevalence with exposure to vectors across hosts. Here, we use DNA sequencing of blood meals to estimate utilization of different avian host species by Culex mosquitoes, and relate utilization by these malaria vectors to avian Plasmodium prevalence. We found that avian host species that are highly utilized as hosts by avian malaria vectors are significantly more likely to have Plasmodium infections. However, the effect was not consistent among individual Plasmodium taxa. Exposure to vector bites may therefore influence the relative number of all avian Plasmodium infections among host species, while other processes, such as parasite competition and host-parasite coevolution, delimit the host distributions of individual Plasmodium species. We demonstrate that links between avian malaria susceptibility and host traits can be conditioned by patterns of exposure to vectors. Linking vector utilization rates to host traits may be a key area of future research to understand mechanisms that produce variation in the prevalence of vector-borne pathogens among host species.

An inverse association between West Nile virus serostatus and avian malaria infection status

BackgroundVarious ecological and physiological mechanisms might influence the probability that two or more pathogens may simultaneously or sequentially infect a host individual. Concurrent infections can have important consequences for host condition and fitness, including elevated mortality risks. In addition, interactions between coinfecting pathogens may have important implications for transmission dynamics.MethodsHere, we explore patterns of association between two common avian pathogens (West Nile virus and avian malaria parasites) among a suburban bird community in Chicago, IL, USA that share mosquito vectors. We surveyed 1714 individual birds across 13 species for both pathogens through established molecular protocols.ResultsField investigations of haemosporidian and West Nile virus (WNV) infections among sampled birds yielded an inverse association between WNV serostatus and Plasmodium infection status. This relationship occurred in adult birds but not in juveniles. There was no evidence for a relationship between Haemoproteus infection and WNV serostatus. We detected similar prevalence of Plasmodium among birds captured with active WNV infections and spatiotemporally paired WNV-naïve individuals of the same species, demonstrating that the two pathogens can co-infect hosts.ConclusionsMechanisms explaining the negative association between WNV serostatus and Plasmodium infection status remain unclear and must be resolved through experimental infection procedures. However, our results highlight potential interactions between two common avian pathogens that may influence their transmission among hosts. This is especially relevant considering that West Nile virus is a common zoonotic pathogen with public health implications. Moreover, both pathogens are instructive models in infectious disease ecology, and infection with either has fitness consequences for their avian hosts.

Prevalence of avian haemosporidian parasites is positively related to the abundance of host species at multiple sites within a region.

Parasite prevalence is thought to be positively related to host population density owing to enhanced contagion. However, the relationship between prevalence and local abundance of multiple host species is underexplored. We surveyed birds and their haemosporidian parasites (genera Plasmodium and Haemoproteus) at multiple sites across eastern North America to test whether the prevalence of these parasites in a host species at a particular site is related to that host’s local abundance. Prevalence was positively related to host abundance within most sites, although the effect was stronger and more consistent for Plasmodium than for Haemoproteus. In contrast, prevalence was not related to variation in the abundance of most individual host species among sites across the region. These results suggest that parasite prevalence partly reflects the relative abundances of host species in local assemblages. However, three nonnative host species had low prevalence despite being relatively abundant at one site, as predicted by the enemy release hypothesis.

Dispersal of male and female Culex quinquefasciatus and Aedes albopictus mosquitoes using stable isotope enrichment

The dispersal patterns of mosquito vectors are important drivers of vector-borne infectious disease dynamics and understanding movement patterns is pivotal to devise successful intervention strategies. Here, we investigate the dispersal patterns of two globally important mosquito vectors, Aedes albopictus and Culex quinquefasciatus, by marking naturally-occurring larvae with stable isotopes (13C or 15N). Marked individuals were captured with 32 CDC light trap, 32 gravid trap, and 16 BG Sentinel at different locations within two-kilometer radii of six larval habitats enriched with either 13C or 15N. In total, 720 trap nights from July to August 2013 yielded a total of 32,140 Cx. quinquefasciatus and 7,722 Ae. albopictus. Overall, 69 marked female mosquitoes and 24 marked male mosquitoes were captured throughout the study period. The distance that Cx. quinquefasciatus females traveled differed for host-seeking and oviposition-seeking traps, with females seeking oviposition sites traveling further than those seeking hosts. Our analysis suggests that 41% of Cx. quinquefasciatus females that were host-seeking occurred 1–2 kilometer from their respective natal site, while 59% remained within a kilometer of their natal site. In contrast, 59% of Cx. quinquefasciatus females that were seeking oviposition sites occurred between 1–2 kilometer away from their larval habitat, while 15% occurred > 2 kilometer away from their natal site. Our analysis estimated that approximately 100% of Ae. albopictus females remained within 1 km of their respective natal site, with 79% occurring within 250m. In addition, we found that male Ae. albopictus dispersed farther than females, suggesting male-biased dispersal in this Ae. albopictus population. This study provides important insights on the dispersal patterns of two globally relevant vector species, and will be important in planning next generation vector control strategies that mitigate mosquito-borne disease through sterile insect techniques, novel Wolbachia infection, and gene drive strategies.