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1.
Bull Math Biol ; 86(11): 131, 2024 Sep 23.
Article in English | MEDLINE | ID: mdl-39311987

ABSTRACT

In this work, we obtained a general formulation for the mating probability and fertile egg production in helminth parasites, focusing on the reproductive behavior of polygamous parasites and its implications for transmission dynamics. By exploring various reproductive variables in parasites with density-dependent fecundity, such as helminth parasites, we departed from the traditional assumptions of Poisson and negative binomial distributions to adopt an arbitrary distribution model. Our analysis considered critical factors such as mating probability, fertile egg production, and the distribution of female and male parasites among hosts, whether they are distributed together or separately. We show that the distribution of parasites within hosts significantly influences transmission dynamics, with implications for parasite persistence and, therefore, with implications in parasite control. Using statistical models and empirical data from Monte Carlo simulations, we provide insights into the complex interplay of reproductive variables in helminth parasites, enhancing our understanding of parasite dynamics and the transmission of parasitic diseases.


Subject(s)
Helminths , Host-Parasite Interactions , Mathematical Concepts , Models, Biological , Monte Carlo Method , Animals , Female , Helminths/physiology , Male , Host-Parasite Interactions/physiology , Fertility/physiology , Computer Simulation , Reproduction/physiology , Sexual Behavior, Animal/physiology , Probability , Ovum/physiology , Humans
2.
Commun Biol ; 7(1): 1175, 2024 Sep 19.
Article in English | MEDLINE | ID: mdl-39294220

ABSTRACT

Biological studies of the determinants of Cryptosporidium infectivity are lacking despite the fact that cryptosporidiosis is a major public health problem. Recently, the 60-kDa glycoprotein (GP60) has received attention because of its high sequence polymorphism and association with host infectivity of isolates and protection against reinfection. However, studies of GP60 function have been hampered by its heavy O-linked glycosylation. Here, we used advanced genetic tools to investigate the processing, fate, and function of GP60. Endogenous gene tagging showed that the GP60 cleavage products, GP40 and GP15, are both highly expressed on the surface of sporozoites, merozoites and male gametes. During invasion, GP40 translocates to the apical end of the zoites and remains detectable at the parasite-host interface. Deletion of the signal peptide, GPI anchor, and GP15 sequences affects the membrane localization of GP40. Deletion of the GP60 gene significantly reduces parasite growth and severity of infection, and replacement of the GP60 gene with sequence from an avirulent isolate reduces the pathogenicity of a highly infective isolate. These results have revealed dynamic changes in GP60 expression during parasite development. They further suggest that GP60 is a key protein mediating host infectivity and pathogenicity.


Subject(s)
Cryptosporidiosis , Cryptosporidium parvum , Protozoan Proteins , Cryptosporidium parvum/genetics , Cryptosporidium parvum/pathogenicity , Cryptosporidium parvum/metabolism , Animals , Protozoan Proteins/genetics , Protozoan Proteins/metabolism , Cryptosporidiosis/parasitology , Host-Parasite Interactions , Mice , Humans , Sporozoites/metabolism , Sporozoites/genetics , Membrane Glycoproteins/genetics , Membrane Glycoproteins/metabolism
3.
Parasitol Res ; 123(9): 329, 2024 Sep 24.
Article in English | MEDLINE | ID: mdl-39316149

ABSTRACT

Aggregation is a fundamental feature of parasite distribution in the host population, but the biological implications of the aggregation indices used to describe the relationships between the populations of parasites and hosts are not evident. It is speculated that the form of distribution in each case is predicated on the host's varying resistance to the infection, which is hard to control, making it difficult to adequately interpret the index values. This paper examines several cases from trout farms in Russian Karelia to explore the monogenean Gyrodactylus spp. infection in rainbow trout of varying ages. The genetic homogeneity of cage-reared fish and the direct life cycle of the helminths make the relationship between the species more lucid than in natural host-parasite systems. The results give no ground to speak of any specific patterns: as well as in the natural systems, the infection rates in trout vary widely, i.e., the helminth distribution has not become more uniform; the observed distributions in all cases are adequately approximated by the negative binomial model; the positive abundance-occupancy relationships (AORs) and abundance-variance relationships (AVRs) common for parasitic systems apply to the basic infection parameters. The form of the negative binomial distribution is shaped by two parameters-k and θ, the former being a metric of the infection variability, which depends on the host's individual resistance, and the latter representing the parasites' reproduction and establishment success rates. A rise in the parameter k indicates increased aggregation and a higher parameter θ points to a more uniform frequency distribution. These parameters can be used as a representative tool for monitoring the parasite communities in salmonid fishes, including in aquaculture.


Subject(s)
Fish Diseases , Host-Parasite Interactions , Oncorhynchus mykiss , Trematoda , Trematode Infections , Animals , Oncorhynchus mykiss/parasitology , Fish Diseases/parasitology , Trematode Infections/veterinary , Trematode Infections/parasitology , Trematoda/physiology , Trematoda/genetics , Trematoda/classification , Trematoda/isolation & purification , Russia , Platyhelminths/physiology , Platyhelminths/genetics , Platyhelminths/classification
4.
Parasite ; 31: 58, 2024.
Article in English | MEDLINE | ID: mdl-39331805

ABSTRACT

This study was conducted to clarify the host specificity and the geographical distribution of Gasterophilus species (Diptera, Oestridae) in the Serengeti ecosystem. A total of 317 larvae were recovered from two common zebras (Equus quagga, formerly Equus burchellii) in Maswa Game Reserve, and 58 larvae were recovered from an African lion (Panthera leo) in the Serengeti National Park. The study emphasizes the rare occurrence of Gasterophilus sp. in lions, shedding light on the broader life cycle and physiological implications for hosts. Genetic analysis of cox2 genes from Gasterophilus species, sourced from a single geographic location, reveals significant genetic distinctions and host specificity. This study reports the first case of G. intestinalis infestation in an African lion in the Serengeti ecosystem, extending its known range from zebras and other equids, and highlighting ecological and veterinary implications. This unusual prey-predator transmission highlights the value of molecular taxonomic tools in clarifying host-parasite dynamics and guiding targeted conservation strategies.


Title: Infestation par Gasterophilus intestinalis chez le lion (Panthera leo) et le zèbre des plaines (Equus quagga) dans l'écosystème du Serengeti : profilage morphologique et moléculaire. Abstract: Cette étude a été menée pour clarifier la spécificité de l'hôte et la répartition géographique des espèces de Gasterophilus (Diptera, Oestridae) dans l'écosystème du Serengeti. Au total, 317 larves ont été récoltées chez deux zèbres communs (Equus quagga, anciennement Equus burchellii) dans la réserve de gibier de Maswa, et 58 larves ont été récoltées chez un lion d'Afrique (Panthera leo) dans le parc national du Serengeti. L'étude souligne la rareté de l'occurrence de Gasterophilus sp. chez les lions, mettant en lumière le cycle biologique plus large et les implications physiologiques pour les hôtes. L'analyse génétique des gènes cox2 des espèces de Gasterophilus, provenant d'un seul lieu géographique, révèle des distinctions génétiques et une spécificité d'hôte significatives. Cette étude rapporte le premier cas d'infestation par G. intestinalis chez un lion africain dans l'écosystème du Serengeti, étendant son aire de répartition déjà connue chez les zèbres et autres équidés, et mettant en évidence des implications écologiques et vétérinaires. Cette transmission inhabituelle de proie à prédateur souligne l'intérêt des outils de taxonomie moléculaire pour clarifier la dynamique hôte-parasite et guider les stratégies de conservation ciblées.


Subject(s)
Ecosystem , Equidae , Host Specificity , Larva , Lions , Myiasis , Animals , Lions/parasitology , Equidae/parasitology , Larva/genetics , Larva/classification , Myiasis/parasitology , Myiasis/veterinary , Myiasis/epidemiology , Diptera/genetics , Diptera/classification , Diptera/physiology , Tanzania , Male , Female , Cyclooxygenase 2/genetics , Host-Parasite Interactions , Phylogeny
5.
Nature ; 633(8031): 840-847, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39261731

ABSTRACT

Parasitoid wasps are exceptionally diverse and use specialized adaptations capable of manipulating the physiology and behaviour of host organisms1. In more than two centuries since the first records of Drosophila-parasitizing wasps, nearly 200 described and provisional parasitoid species of drosophilids have been identified2. These include endoparasitoids and ectoparasitoids, as well as species attacking larval and pupal hosts3. Despite a deep history of research attention and remarkable biodiversity, a wasp species that attacks and develops inside the adult stage of a fly host has not been described previously. Here we report the discovery of a wasp species that infects the adult stage of fruit flies in the genus Drosophila, including one of the most deeply studied model organisms in biology, Drosophila melanogaster. Notably, this wasp can be easily collected from backyard fly baits and has a broad geographic distribution throughout the eastern USA. We document its life history and unique host interactions, including egg-laying into and larval emergence from adult flies, and provide protocols to raise wasps from wild-caught host flies. Our results emphasize the need for ongoing research investment in insect biodiversity and systematics. As parasitoid research continues to uncover unusual biology and supports fundamental mechanistic insights into immunity4, metabolism5, ecology6, evolution7-9 and behaviour10-12, we anticipate that this wasp's association with the laboratory model organism, D. melanogaster, will provide new research opportunities across the life sciences.


Subject(s)
Drosophila melanogaster , Host-Parasite Interactions , Larva , Oviposition , Wasps , Animals , Wasps/physiology , Drosophila melanogaster/parasitology , Female , Larva/parasitology , Male , Drosophila/parasitology
6.
Commun Biol ; 7(1): 1226, 2024 Sep 30.
Article in English | MEDLINE | ID: mdl-39349621

ABSTRACT

Copper plays a key role in host-pathogen interaction. We find that during Leishmania major infection, the parasite-harboring macrophage regulates its copper homeostasis pathway in a way to facilitate copper-mediated neutralization of the pathogen. Copper-ATPase ATP7A transports copper to amastigote-harboring phagolysosomes to induce stress on parasites. Leishmania in order to evade the copper stress, utilizes a variety of manipulative measures to lower the host-induced copper stress. It induces deglycosylation and degradation of host-ATP7A and downregulation of copper importer, CTR1 by cysteine oxidation. Additionally, Leishmania induces CTR1 endocytosis that arrests copper uptake. In mouse model of infection, we report an increase in systemic bioavailable copper in infected animals. Heart acts as the major organ for diverting its copper reserves to systemic circulation to fight-off infection by downregulating its CTR1. Our study explores reciprocal mechanism of manipulation of host copper homeostasis pathway by macrophage and Leishmania to gain respective advantages in host-pathogen interaction.


Subject(s)
Copper-Transporting ATPases , Copper , Homeostasis , Leishmania major , Leishmaniasis, Cutaneous , Macrophages , Animals , Copper/metabolism , Leishmania major/physiology , Mice , Leishmaniasis, Cutaneous/parasitology , Leishmaniasis, Cutaneous/metabolism , Copper-Transporting ATPases/metabolism , Copper-Transporting ATPases/genetics , Macrophages/parasitology , Macrophages/metabolism , Copper Transporter 1/metabolism , Female , Host-Pathogen Interactions , Host-Parasite Interactions
7.
Ecology ; 105(10): e4397, 2024 Oct.
Article in English | MEDLINE | ID: mdl-39223438

ABSTRACT

Most organisms are at risk of being consumed by a predator or getting infected by a parasite at some point in their life. Theoretical constructs such as the landscape of fear (perception of risk) and nonconsumptive effects (NCEs, costly responses sans predation or infection) have been proposed to describe and quantify antipredator and antiparasite responses. How prey/host species identify and respond to these risks determines their survival, reproductive success and, ultimately, fitness. Most studies to date have focused on either predator-prey or parasite-host interactions, yet habitats and ecosystems contain both parasitic and/or predatory species that represent a complex and heterogenous mosaic of risk factors. Here, we experimentally investigated the behavioral responses of a cactophilic fruit fly, Drosophila nigrospiracula, exposed to a range of species that include parasites (ectoparasitic mite), predators (jumping spiders), as well as harmless heterospecifics (nonparasitic mites, ants, and weevils). We demonstrate that D. nigrospiracula can differentiate between threat and non-threat species, increase erratic movements and decrease velocity in the presence of parasites, but decrease erratic movements and time spent grooming in the presence of predators. Of particular importance, flies could distinguish between parasitic female mites and nonparasitic male mites of the same species, and respond accordingly. We also show that the direction of these NCEs differs when exposed to parasitic mites (i.e., risk of infection) versus spiders (i.e., risk of predation). Given the opposing effects of predation versus infection risk on fly behavior, we discuss potential trade-offs between parasite and predator avoidance behaviors. Our findings illustrate the complexity of risk assessment in a landscape of fear and the fine-tuned NCEs that arise in response. Moreover, this study is the first to examine these behavioral NCEs in a terrestrial system.


Subject(s)
Drosophila , Fear , Host-Parasite Interactions , Animals , Female , Male , Fear/physiology , Drosophila/physiology , Drosophila/parasitology , Predatory Behavior/physiology , Spiders/physiology , Mites/physiology , Behavior, Animal/physiology , Ants/physiology
8.
Ecology ; 105(10): e4394, 2024 Oct.
Article in English | MEDLINE | ID: mdl-39234933

ABSTRACT

Parasite-host systems are a good study model for answering ecological and evolutionary questions. In this regard, mistletoes have been increasingly studied in recent decades in both temperate and tropical zones. The genus Phoradendron is a group of American mistletoes that has been studied from different evolutionary and ecological approaches as a model of parasite-host systems. Currently, however, no systematic compilation of the plant species parasitized by these mistletoes is available. To address this issue, we conducted a thorough search and compilation of interactions between mistletoe species of the genus Phoradendron and their hosts. This involved consulting multiple sources, including monographs, digitized herbaria material, and scientific publications. Additionally, we incorporated information regarding the presence records of Phoradendron from the most authoritative databases at the national, continental, and global levels. This process yielded a comprehensive dataset consisting of two independent tables, offering information on the interactions and occurrences of Phoradendron throughout its distribution range in the Americas. The dataset includes the interactions between 159 mistletoe species and 118 hosts at the family level, 379 hosts at the genus level, and 544 hosts at the species level, totaling 2929 interactions between species of the genus Phoradendron and their hosts. This data paper represents an updated compilation of a genus of parasitic plants, with the purpose of making this database of interactions accessible for researchers to address questions at multiple scales and from disciplines as varied as biogeography, ecology, evolution, and epidemiology. We plan to use and expand this database with subsequent studies from the authors. There are no copyright restrictions on the dataset; please cite this data paper when using data from this publication. We also encourage you to contact the authors if you are interested in contributing to this database.


Subject(s)
Host-Parasite Interactions , Animals , Plant Dispersal
9.
Bull Entomol Res ; 114(4): 534-542, 2024 Aug.
Article in English | MEDLINE | ID: mdl-39263761

ABSTRACT

Many parasitoids alter their reproductive behaviour in response to the quality of encountered hosts. They make adaptive decisions concerning whether to parasitise a potential host, the number of eggs laid on an accepted host, and the allocation of sex to their offspring. Here we present evidence that Goniozus jacintae Farrugia (Hymenoptera: Bethylidae), a gregarious ectoparasitoid of larval tortricids, adjusts its reproductive response to the size and developmental stage of larvae of the light brown apple moth (LBAM), Epiphyas postvittana (Walker) (Lepidoptera: Tortricidae). Goniozus jacintae parasitises instars 3-6 of LBAM, but most readily parasitises the later, larger, instars. Brood sizes were bigger on larger hosts and brood sex ratios were female biased (proportion of males = 0.23) with extremely low variance (never >1 male in a brood at emergence), perhaps the most precise of all studied bethylids. Host size did not influence brood development time, which averaged 19.64 days, or the body size of male offspring. However, the size of females was positively correlated with host size and negatively correlated with brood size. The sizes of individual males and females were positively related to the average amount of host resource available to individuals within each brood, suggesting that adult body size is affected by scramble competition among feeding larvae. Average brood sizes were: 3rd instar host, 1.3 (SE ± 0.075); 4th instar, 2.8 (SE ± 0.18); 5th instar, 4.7 (SE ± 0.23); 6th instar, 5.4 (SE ± 0.28). The largest brood size observed was 8 individuals (7 females, 1 male) on the 6th instar of LBAM. These results suggest that later instars would give the highest yield to optimise mass-rearing of G. jacintae if used for augmentative biological pest control.


Subject(s)
Host-Parasite Interactions , Larva , Moths , Reproduction , Wasps , Animals , Male , Female , Moths/parasitology , Moths/growth & development , Larva/growth & development , Larva/physiology , Larva/parasitology , Wasps/physiology , Wasps/growth & development , Sex Ratio , Body Size
10.
Microb Ecol ; 87(1): 119, 2024 Sep 28.
Article in English | MEDLINE | ID: mdl-39340548

ABSTRACT

Microbiota associated with host-parasite relationships offer an opportunity to explore interactions among plants, parasites, and microbes, thereby contributing to the overall complexity of community structures. The dynamics of ecological interactions between parasitic plants and their hosts in arid environments remain largely understudied, especially in Africa. This study aimed to examine the bacterial communities of Cuscuta epithymum L. (clover dodder), an epiphytic parasitic plant, and its host, Ziziphus lotus L. (jujuba), in an arid environment. Our goal was to uncover the ecological complexities of microbial communities within the framework of plant-plant interactions. We conducted a comprehensive analysis of the bacterial composition and diversity within populations of the C. epithymum parasite, the infected- and non-infected jujuba host, and their interface at the shoots of the host. This involved amplicon sequencing, targeting the V5-V6 regions of the 16S rRNA gene. A total of 5680 amplicon sequence variants (ASVs) were identified, with Pseudomonadota, Bacillota, and Actinobacteriota being prevalent phyla. Among the bacterial communities, three genera were dominant: Cutibacterium, Staphylococcus, and Acinetobacter. Interestingly, analyses of alpha-diversity (p = 0.3 for Shannon index and p = 0.5 for Simplon index) and beta-diversity (PERMANOVA, with p-values of 0.6 and 0.3) revealed no significant differences between Cuscuta-infected and non-infected jujube shrubs, suggesting a shared shoot endophytic bacteriome. This finding advances our comprehension of microbial communities linked to plant-parasite interactions in the arid environments of Africa. Further research on various hosts is required to confirm plant-to-plant bacterial transmission through Cuscuta infection. Additionally, studies on functional diversity, cytology, ecophysiology and the mechanisms by which bacterial communities transferred between host and parasite are necessary.


Subject(s)
Bacteria , Cuscuta , Endophytes , Microbiota , RNA, Ribosomal, 16S , Ziziphus , Cuscuta/physiology , Cuscuta/microbiology , Cuscuta/genetics , Ziziphus/microbiology , RNA, Ribosomal, 16S/genetics , Endophytes/genetics , Endophytes/physiology , Endophytes/classification , Endophytes/isolation & purification , Bacteria/genetics , Bacteria/classification , Bacteria/isolation & purification , Host-Parasite Interactions , DNA, Bacterial/genetics
11.
Parasitol Res ; 123(10): 336, 2024 Sep 30.
Article in English | MEDLINE | ID: mdl-39347812

ABSTRACT

Echinococcosis is a zoonotic disease, which seriously endangers human health. The immune game between parasite and host is not fully understood. Exosomes are thought to be one of the ways of information communication between parasite and host. In this study, we attempted to explore the communication between Echinococcus granulosus and its host through the medium of exosomes. We collected plasma from E. granulosus patients (CE-EXO) and healthy donors (HD-EXO) and extracted exosomes from the plasma. The expression profile of miRNA in plasma was determined by second generation sequencing. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to annotate the function of target genes of differential miRNAs. Meanwhile, we co-cultured plasma exosomes from healthy donors and plasma exosomes from E. granulosus patients with Jurkat T cells with or without phytohaemagglutinin (PHA) stimulation. The expression of CD69 on Jurkat T cells was detected by flow cytometry. The results showed that the miRNA of exosomes between healthy donors and E. granulosus patients was significantly different. GO and KEGG were used to annotate the function of target genes of differential miRNAs. The results indicate that many important pathways are involved in inflammation, metabolism, and immune response after parasite infection, such as p53 signaling pathway, PI3K-Akt signaling pathway, and glycolysis/gluconeogenesis. Flow cytometry showed that CE-EXO reduced the expression of CD69 + on Jurkat T cells. Our present results suggest that these differentially expressed miRNAs may be important regulators of parasite-host interactions. Meanwhile, functional prediction of its target genes provides valuable information for understanding the mechanism of host-parasite interactions. These results provide clues for future studies on E. granulosus escape from host immune attack, which could help control E. granulosus infection.


Subject(s)
Echinococcosis , Echinococcus granulosus , MicroRNAs , Humans , Echinococcosis/immunology , Echinococcosis/blood , Echinococcosis/parasitology , Echinococcosis/genetics , MicroRNAs/blood , MicroRNAs/genetics , Pilot Projects , Echinococcus granulosus/genetics , Echinococcus granulosus/immunology , Animals , Exosomes/genetics , Exosomes/immunology , Exosomes/metabolism , Immunomodulation , Jurkat Cells , Gene Expression Profiling , Host-Parasite Interactions/immunology
12.
Dis Aquat Organ ; 159: 209-214, 2024 Sep 26.
Article in English | MEDLINE | ID: mdl-39324593

ABSTRACT

Marteilia pararefringens is a protistan parasite that mainly infects the digestive gland of mussels Mytilus spp. Despite observations of marteiliosis in mussels since the 1970s, the reported host species has generally not been verified by molecular methods. The 3 closely related mussels Mytilus edulis, M. galloprovincialis, and M. trossulus cannot be distinguished morphologically and hybridise in regions where they overlap. Norway is the only country where both M. pararefringens and M. trossulus are known to occur. Here, we report the first detection of marteiliosis, caused by M. pararefringens, in M. trossulus and an M. edulis-M. trossulus hybrid in a heliothermic oyster pond-a poll-in Hardangerfjorden, Norway. The observed infections were severe, containing early, intermediate, and advanced (sporulating) stages present in the digestive epithelium. There was no host reaction associated with the infections. This finding confirms that all known Mytilus species present in Europe are susceptible to M. pararefringens.


Subject(s)
Mytilus , Animals , Mytilus/parasitology , Norway , Host-Parasite Interactions
13.
Proc Biol Sci ; 291(2031): 20240991, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39317313

ABSTRACT

Pairwise host-parasite relationships are typically embedded in broader networks of ecological interactions, which have the potential to shape parasite evolutionary trajectories. Understanding this 'community context' of pathogen evolution is vital for wildlife, agricultural and human systems alike, as pathogens typically infect more than one host-and these hosts may have independent ecological relationships. Here, we introduce an eco-evolutionary model examining ecological feedback across a range of host-host interactions. Specifically, we analyse a model of the evolution of virulence of a parasite infecting two hosts exhibiting competitive, mutualistic or exploitative relationships. We first find that parasite specialism is necessary for inter-host interactions to impact parasite evolution. Furthermore, we find generally that increasing competition between hosts leads to higher shared parasite virulence while increasing mutualism leads to lower virulence. In exploitative host-host interactions, the particular form of parasite specialization is critical-for instance, specialization in terms of onward transmission, host tolerance or intra-host pathogen growth rate lead to distinct evolutionary outcomes under the same host-host interactions. Our work provides testable hypotheses for multi-host disease systems, predicts how changing interaction networks may impact virulence evolution and broadly demonstrates the importance of looking beyond pairwise relationships to understand evolution in realistic community contexts.


Subject(s)
Biological Evolution , Host-Parasite Interactions , Virulence , Animals , Symbiosis , Parasites/pathogenicity , Models, Biological
14.
Proc Biol Sci ; 291(2031): 20240934, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39317318

ABSTRACT

Infection duration affects individual host fitness and between-host transmission. Whether an infection is cleared or becomes chronic depends on the complex interaction between host immune responses and parasite growth. Empirical and theoretical studies have suggested that there are critical thresholds of parasite dose that can determine clearance versus chronicity, driven by the ability of the parasite to manipulate host immunity. However, the mammalian immune response is characterized by strong positive and negative feedback loops that could generate duration thresholds even in the absence of direct immunomodulation. Here, we derive and analyse a simple model for the interaction between T-cell subpopulations and parasite growth. We show that whether an infection is cleared or not is very sensitive to the initial immune state, parasite dose and strength of immunological feedbacks. In particular, chronic infections are possible even when parasites provoke a strong and effective immune response and lack any ability to immunomodulate. Our findings indicate that the initial immune state, which often goes unmeasured in empirical studies, is a critical determinant of infection duration. This work also has implications for epidemiological models, as it implies that infection duration will be highly variable among individuals, and dependent on each individual's infection history.


Subject(s)
Host-Parasite Interactions , Animals , Models, Immunological , Feedback, Physiological , T-Lymphocytes/immunology
15.
Biol Lett ; 20(9): 20240411, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39317329

ABSTRACT

As the avian embryo grows and develops within the egg, its metabolic rate gradually increases. Obligate avian brood-parasitic birds lay their eggs in the nests of other species to avoid the costs of parental care, and all but one of these brood-parasitic species are altricial at hatching. Yet the chicks of some altricial brood-parasitic species perform the physically demanding task of evicting, stabbing or otherwise killing host progeny within days of hatching. This implies a need for high metabolic rates in the embryo, just as precocial species require. Using flow-through respirometry in situ, we investigated embryonic metabolic rates in diverse avian brood parasite lineages which either kill host offspring (high virulence) or share the nest with host young (low virulence). High-virulence brood parasite embryos exhibited higher overall metabolic rates than both non-parasitic (parental) species and low-virulence parasites. This was driven by significantly elevated metabolic rates around the halfway point of incubation. Additionally, a fine-scale analysis of the embryos of a host-parasitic pair showed faster increases in metabolic rates in the parasite. Together these results suggest that the metabolic patterns of the embryos of high-virulence parasites facilitate their early-life demands.


Subject(s)
Birds , Host-Parasite Interactions , Animals , Birds/parasitology , Birds/embryology , Embryo, Nonmammalian/metabolism , Virulence , Nesting Behavior , Energy Metabolism
16.
Mem Inst Oswaldo Cruz ; 119: e240073, 2024.
Article in English | MEDLINE | ID: mdl-39319874

ABSTRACT

Extracellular vesicles (EVs) are lipid-bilayered membrane-delimited particles secreted by almost any cell type, involved in different functions according to the cell of origin and its state. From these, cell to cell communication, pathogen-host interactions and modulation of the immune response have been widely studied. Moreover, these vesicles could be employed for diagnostic and therapeutic purposes, including infections produced by pathogens of diverse types; regarding parasites, the secretion, characterisation, and roles of EVs have been studied in particular cases. Moreover, the heterogeneity of EVs presents challenges at every stage of studies, which motivates research in this area. In this review, we summarise some aspects related to the secretion and roles of EVs from several groups of pathogens, with special focus on the most recent research regarding EVs secreted by extracellular protozoan parasites.


Subject(s)
Extracellular Vesicles , Extracellular Vesicles/metabolism , Humans , Host-Parasite Interactions , Protozoan Infections/parasitology , Animals , Host-Pathogen Interactions
17.
Parasit Vectors ; 17(1): 381, 2024 Sep 06.
Article in English | MEDLINE | ID: mdl-39242536

ABSTRACT

BACKGROUND: Trypanosoma cruzi is transmitted to humans by hematophagous bugs belonging to the Triatominae subfamily. Its intra-vectorial cycle is complex and occurs exclusively in the insect's midgut. Dissecting the elements involved in the cross-talk between the parasite and its vector within the digestive tract should provide novel targets for interrupting the parasitic life cycle and affecting vectorial competence. These interactions are shaped by the strategies that parasites use to infect and exploit their hosts, and the host's responses that are designed to detect and eliminate parasites. The objective of the current study is to characterize the impact of T. cruzi establishment within its vector on the dynamics of its midgut. METHODS: In this study, we evaluated the impact of T. cruzi infection on protein expression within the anterior midgut of the model insect Rhodnius prolixus at 6 and 24 h post-infection (hpi) using high-throughput quantitative proteomics. RESULTS: Shortly after its ingestion, the parasite modulates the proteome of the digestive epithelium by upregulating 218 proteins and negatively affecting the expression of 11 proteins involved in a wide array of cellular functions, many of which are pivotal due to their instrumental roles in cellular metabolism and homeostasis. This swift response underscores the intricate manipulation of the vector's cellular machinery by the parasite. Moreover, a more in-depth analysis of proteins immediately induced by the parasite reveals a pronounced predominance of mitochondrial proteins, thereby altering the sub-proteomic landscape of this organelle. This includes various complexes of the respiratory chain involved in ATP generation. In addition to mitochondrial metabolic dysregulation, a significant number of detoxifying proteins, such as antioxidant enzymes and P450 cytochromes, were immediately induced by the parasite, highlighting a stress response. CONCLUSIONS: This study is the first to illustrate the response of the digestive epithelium upon contact with T. cruzi, as well as the alteration of mitochondrial sub-proteome by the parasite. This manipulation of the vector's physiology is attributable to the cascade activation of a signaling pathway by the parasite. Understanding the elements of this response, as well as its triggers, could be the foundation for innovative strategies to control the transmission of American trypanosomiasis, such as the development of targeted interventions aimed at disrupting parasite proliferation and transmission within the triatomine vector.


Subject(s)
Chagas Disease , Insect Vectors , Mitochondria , Rhodnius , Trypanosoma cruzi , Animals , Rhodnius/parasitology , Rhodnius/metabolism , Trypanosoma cruzi/physiology , Trypanosoma cruzi/metabolism , Insect Vectors/parasitology , Mitochondria/metabolism , Chagas Disease/transmission , Chagas Disease/parasitology , Gastrointestinal Tract/parasitology , Proteomics , Host-Parasite Interactions , Proteome
18.
Sci Rep ; 14(1): 20785, 2024 09 06.
Article in English | MEDLINE | ID: mdl-39242861

ABSTRACT

Most host-parasite associations are explained by phylogenetically conservative capabilities for host utilization, and therefore parasite switches between distantly related hosts are rare. Here we report the first evidence of a parasitic spillover of the burrowing sea anemone Edwardsiella carnea from the invasive ctenophore Mnemiopsis leidyi to two scyphozoan hosts: the native Mediterranean barrel jellyfish Rhizostoma pulmo and the invasive Indo-Pacific nomad jellyfish Rhopilema nomadica, collected from the Eastern Mediterranean Sea. Edwardsiella carnea planulae found in these jellyfish were identified using molecular analyses of the mitochondrial 16S and nuclear 18S rRNA genes. Overall, 93 planulae were found on tentacles, oral arms, and inside of the gastrovascular canals of the scyphomedusae, whereas no infection was observed in co-occurring ctenophores. DNA metabarcoding approach indicated seasonal presence of Edwardsiella sp. in the Eastern Mediterranean mesozooplankton, coinciding with jellyfish blooms in the region. Our findings suggest a non-specific parasitic relationship between Edwardsiella carnea and various gelatinous hosts based on shared functionality rather than evolutionary history, potentially driven by shifts in host availability due to jellyfish blooms. This spillover raises questions about the ecological impacts of parasitism on native and invasive scyphozoan hosts and the potential role of Edwardsiella in controlling their populations.


Subject(s)
Ctenophora , Phylogeny , Scyphozoa , Sea Anemones , Animals , Ctenophora/genetics , Scyphozoa/microbiology , Scyphozoa/parasitology , Sea Anemones/parasitology , Host-Parasite Interactions , RNA, Ribosomal, 18S/genetics , Mediterranean Sea , RNA, Ribosomal, 16S/genetics
19.
J Insect Sci ; 24(4)2024 Jul 01.
Article in English | MEDLINE | ID: mdl-39243220

ABSTRACT

Ascogaster mimetica Viereck is an egg-larval parasitoid that targets Sparganothis sulfureana Clemens, a major cranberry pest in North America. While previous studies have shown that other Ascogaster species respond to cues from their hosts' eggs, it remains unknown whether A. mimetica utilizes these cues to recognize S. sulfureana. We hypothesized that female A. mimetica recognizes S. sulfureana from another cranberry pest, Choristoneura parallela Robinson, based on the presence of surface cues on eggs. To test this, we observed female A. mimetica behavior when exposed to eggs from its host, S. sulfureana; a nonhost, C. parallela; and eggs of S. sulfureana that were washed clean with hexane. Additionally, we tracked parasitism rates in each group. Our results revealed that A. mimetica spent 9.5 times longer walking when exposed to C. parallela eggs and 6 times longer when exposed to hexane-washed S. sulfureana eggs compared to unwashed S. sulfureana eggs. Also, A. mimetica spent 3 times longer grooming when exposed to hexane-washed than unwashed S. sulfureana eggs. In contrast, females spent 6 and 18 times longer drumming and probing/ovipositing on unwashed S. sulfureana eggs than on C. parallela eggs and 5 times longer probing/ovipositing on unwashed S. sulfureana eggs than on hexane-washed S. sulfureana eggs. Higher parasitism rates were observed from unwashed S. sulfureana eggs compared to those from C. parallela eggs and hexane-washed S. sulfureana eggs. Our findings suggest that the presence of egg surface cues, like scales, of S. sulfureana likely plays a crucial role in host acceptance and parasitism success for A. mimetica.


Subject(s)
Moths , Ovum , Wasps , Animals , Ovum/parasitology , Wasps/physiology , Female , Moths/parasitology , Moths/physiology , Host-Parasite Interactions
20.
J Exp Biol ; 227(17)2024 Sep 01.
Article in English | MEDLINE | ID: mdl-39253831

ABSTRACT

The ability of parasitic wasps to manipulate a host's metabolism is under active investigation. Components of venom play a major role in this process. In the present work, we studied the effect of the venom of the ectoparasitic wasp Habrobracon hebetor on the metabolism of the greater wax moth host (Galleria mellonella). We identified and quantified 45 metabolites in the lymph (cell-free hemolymph) of wax moth larvae on the second day after H. hebetor venom injection, using NMR spectroscopy and liquid chromatography coupled with mass spectrometry. These metabolites included 22 amino acids, nine products of lipid metabolism (sugars, amines and alcohols) and four metabolic intermediates related to nitrogenous bases, nucleotides and nucleosides. An analysis of the larvae metabolome suggested that the venom causes suppression of the tricarboxylic acid cycle, an increase in the number of free amino acids in the lymph, an increase in the concentration of trehalose in the lymph simultaneously with a decrease in the amount of glucose, and destructive processes in the fat body tissue. Thus, this parasitoid venom not only immobilizes the prey but also modulates its metabolism, thereby providing optimal conditions for the development of larvae.


Subject(s)
Hemolymph , Larva , Moths , Wasp Venoms , Wasps , Animals , Wasps/physiology , Wasp Venoms/metabolism , Wasp Venoms/chemistry , Moths/parasitology , Moths/growth & development , Moths/metabolism , Larva/growth & development , Larva/metabolism , Hemolymph/metabolism , Hemolymph/chemistry , Metabolome/drug effects , Magnetic Resonance Spectroscopy , Host-Parasite Interactions/drug effects
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