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Apicomplexa

Apicomplexa is a phylum of single-celled, obligate intracellular eukaryotic parasites within the kingdom Protista, distinguished by the presence of an apical complex—a specialized array of secretory organelles and cytoskeletal elements at the anterior pole that enables active invasion of host cells.^[1] Comprising over 6,000 described species, these protozoans exhibit a highly diverse parasitic lifestyle, infecting a broad range of eukaryotic hosts from invertebrates to vertebrates, including humans and livestock.^[2] Many apicomplexans possess a unique, non-photosynthetic organelle called the apicoplast, derived from a secondary endosymbiosis event involving a red alga, which plays essential roles in fatty acid and isoprenoid biosynthesis.^[3] The life cycles of apicomplexans are complex and typically heteroxenous, involving both asexual and sexual reproduction across intermediate and definitive hosts, with transmission occurring via vectors such as insects, ingestion of oocysts in contaminated food or water, or direct predation.^[1] Infective stages, known as sporozoites, penetrate host cells using the apical complex to form a parasitophorous vacuole, followed by intracellular replication that produces merozoites for further dissemination or gametocytes for sexual stages.^[3] This intricate biology underpins their pathogenicity, as seen in genera like Plasmodium (causing malaria through erythrocyte invasion and rupture), Toxoplasma (forming tissue cysts in warm-blooded hosts), and Cryptosporidium (adhering to intestinal epithelia).^[1] Apicomplexans are of profound medical, veterinary, and economic significance due to the diseases they cause, which collectively affect billions and result in substantial mortality and morbidity.^[3] For instance, Plasmodium species transmit malaria, leading to an estimated 263 million cases and 597,000 deaths globally in 2023, predominantly in sub-Saharan Africa.^[4] Toxoplasma gondii chronically infects approximately one-third of the human population, posing severe risks to immunocompromised individuals and fetuses.^[3] Other notable pathogens include Theileria parva, responsible for East Coast fever in cattle, and Cryptosporidium species, which cause diarrheal disease in humans and animals, particularly affecting young children and those with weakened immunity.^[3] Despite their parasitic nature, some apicomplexans also serve as biological control agents against agricultural pests.^[1]

Morphology and Cell Biology

Apical Complex

The apical complex is the defining ultrastructural feature of the phylum Apicomplexa, located at the anterior end of motile stages and consisting of cytoskeletal elements and secretory organelles that enable host cell invasion. It includes the polar ring complex, which serves as a microtubule-organizing center, and associated secretory vesicles such as rhoptries, micronemes, and dense granules. Electron microscopy reveals the apical complex as a specialized site where the inner membrane complex (IMC) opens to the plasma membrane, facilitating regulated exocytosis.^[5] Key components include the conoid, a dynamic, hollow, tubulin-based structure in many species that extrudes during invasion; the apical polar ring, an unusual ring-shaped microtubule-organizing center marked by proteins like RNG1 and RNG2; rhoptries, club-shaped organelles with necks and bulbs containing invasion proteins; micronemes, elongated vesicles that secrete adhesins; and dense granules, which release factors post-invasion. Transmission electron microscopy shows the conoid as a cone-shaped array of tubulin fibers within the polar ring in species like Toxoplasma gondii, with rhoptries and micronemes converging apically. Molecular components encompass RNG2, which links the polar ring to the conoid and regulates secretion, and TRAP (thrombospondin-related anonymous protein) family adhesins from micronemes, featuring integrin-like and TSR domains for substrate binding.^[5]^[6] The apical complex drives gliding motility and host cell penetration through an actin-myosin motor system, where micronemal adhesins like TRAP link the parasite's exterior to the actin cytoskeleton via aldolase, powering rearward translocation beneath the IMC. This motility reorients the parasite apex toward the host cell, triggering sequential microneme and rhoptry secretion to form a moving junction for penetration. Dense granules then secrete to modify the parasitophorous vacuole. Disruption of components like RNG2 reduces gliding and invasion by up to 66%, highlighting their essential role.^[5]^[6] Apical complex structure varies between Conoidasida (e.g., Toxoplasma, with a prominent, mobile conoid) and Aconoidasida (e.g., Plasmodium, historically considered conoid-lacking). Recent super-resolution microscopy and proteomics reveal a conserved tubulin-based conoid ring in Aconoidasida, such as in Plasmodium sporozoites and ookinetes, where it assembles dynamically during motility and lacks the full fiber array of Conoidasida. Electron tomography confirms this ring's presence, unifying the phylum under a shared apical apparatus despite morphological differences.^[7]

Apicoplast

The apicoplast is a relict, non-photosynthetic plastid organelle unique to apicomplexans, originating from the secondary endosymbiosis of a red alga by an ancestral eukaryote. This event involved the engulfment of a photosynthetic red algal cell, followed by the loss of photosynthetic capabilities while retaining other metabolic functions essential for parasite survival. The organelle's evolutionary history underscores the apicomplexans' algal ancestry, distinguishing them from other protozoans.^[8]^[9] Structurally, the apicoplast is bounded by four membranes, reflecting its secondary endosymbiotic origin, and contains a small, circular genome of approximately 35 kb that encodes about 30 proteins, along with ribosomal and transfer RNAs for organellar translation. It is typically located near the nucleus and often closely associated with the mitochondrion, facilitating coordinated cellular processes. The multi-membranous envelope includes an outermost membrane continuous with the endoplasmic reticulum, an intermembrane space, and inner membranes derived from the original plastid.^[8]^[10] The apicoplast performs critical metabolic roles absent in mammalian cells, including the synthesis of isoprenoid precursors via the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway, which produces isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) for protein prenylation, ubiquinone formation, and membrane stability. It also houses a type II fatty acid synthesis (FAS II) pathway that generates long-chain fatty acids for apicoplast membranes, parasite membranes, and glycosylphosphatidylinositol (GPI) anchors. Additionally, the organelle contributes to heme biosynthesis through the Shemin pathway, where enzymes produce coproporphyrinogen III, a precursor essential particularly during the mosquito stages of Plasmodium. Unlike plant chloroplasts, the apicoplast lacks photosynthetic machinery and relies on host-derived carbon sources.^[8]^[10]^[11] Most apicoplast proteins are nuclear-encoded and imported post-translationally via a bipartite targeting signal: an N-terminal endoplasmic reticulum-type signal peptide followed by a transit peptide resembling those in plants. This sequence directs proteins through the secretory pathway to the outermost membrane, followed by translocation across the inner membranes via a specialized import machinery, ensuring the organelle's functionality despite its reduced genome.^[8]^[12] Due to its prokaryotic-like biochemistry and absence in humans, the apicoplast is a prime target for antimalarial drugs; for instance, fosmidomycin inhibits the MEP pathway enzyme 1-deoxy-D-xylulose 5-phosphate reductoisomerase (IspC), disrupting isoprenoid production and leading to parasite death. Clinical trials of fosmidomycin combined with agents like clindamycin showed initial efficacy but ultimately failed due to recrudescence, with recent studies (as of 2025) identifying host-derived geranylgeraniol as a potential rescue factor.^[10]^[13]^[14]

Other Cellular Features

The pellicle of apicomplexan cells forms a rigid yet flexible outer boundary, consisting of the outer plasma membrane closely apposed to the inner membrane complex (IMC), a series of flattened vesicles underlying the plasma membrane. The IMC provides structural support and is anchored to longitudinal subpellicular microtubules that originate from the apical polar ring and extend posteriorly, typically numbering 20-28 in motile stages such as sporozoites and merozoites. These microtubules maintain the characteristic elongated, crescentic shape of invasive forms and contribute to gliding motility by facilitating actin-myosin interactions at the pellicle's cytoplasmic face.^[15]^[16]^[17] Apicomplexans possess a single, compact mitochondrion with a dense matrix and tubular or bulbous cristae, which houses a reduced electron transport chain adapted for parasitic lifestyles. This organelle supports essential functions beyond canonical ATP production, including the generation of intermediates for pyrimidine biosynthesis and maintenance of redox balance, particularly in intracellular stages where oxygen levels are low. In species like Plasmodium falciparum, the mitochondrion's electron transport chain is active but uncoupled from oxidative phosphorylation during blood-stage replication, emphasizing apicomplexan-specific metabolic adaptations.^[18]^[19]^[20] The nucleus in apicomplexans features a persistent nuclear envelope during closed mitosis, with chromatin organized in a peripheral heterochromatin layer surrounding a more euchromatic core, facilitating rapid replication in asynchronous division cycles. Cytokinesis occurs without centrioles, relying instead on a bipartite centrosomal structure—the outer core for spindle pole organization and the inner core for microtubule nucleation via a nucleus-associated organelle (NAO). This centriole-independent mechanism enables diverse division modes, such as endodyogeny in Toxoplasma gondii, where daughter cells bud internally around segregated nuclei.^[21]^[22]^[23] In intracellular stages, apicomplexans depend heavily on glycolysis for ATP production under anaerobic conditions, with most enzymes localized to the cytosol rather than specialized organelles like glycosomes found in kinetoplastids. Some glycolytic intermediates, such as dihydroxyacetone phosphate, are shuttled to the apicoplast for fatty acid synthesis, highlighting compartmental crosstalk, while cytosolic pyruvate kinase ensures efficient energy yield from host-derived glucose.^[24]^[25]^[26]

Reproduction and Life Cycles

Asexual Reproduction

Asexual reproduction in Apicomplexa primarily occurs through specialized forms of merogony, enabling rapid clonal expansion within host cells to amplify parasite numbers during infection. The two predominant mechanisms are schizogony and endodyogeny, which differ in their division strategies but both produce invasive daughter cells known as merozoites or tachyzoites. These processes are tightly regulated to ensure efficient dissemination and adaptation to intracellular niches.^[27] Schizogony involves multiple rounds of asynchronous nuclear division without intervening cytokinesis, resulting in a multinucleate schizont that subsequently undergoes coordinated cytokinesis to form numerous daughter merozoites. This process is exemplified in the liver stages of Plasmodium species, where up to 30,000 merozoites can be produced from a single sporozoite, facilitating massive amplification before blood-stage infection. The nuclear divisions occur through conventional mitosis, with DNA replication initiating in S-phase and progressing asynchronously across nuclei, leading to a syncytial-like state prior to daughter formation.^[28]^[29] Endodyogeny, in contrast, is a binary fission variant characterized by internal budding, where two daughter cells assemble within the confines of the mother cell's cytoplasm before its lysis. This mechanism is prevalent in the rapidly dividing tachyzoite stage of Toxoplasma gondii, allowing for quick doubling of parasite numbers in host tissues with minimal external reorganization. Daughter formation begins with the de novo synthesis of an inner membrane complex (IMC) scaffold around each daughter nucleus, which elongates and incorporates maternal organelles, ensuring equipartition of cellular components.^[30]^[31] Variants of merogony, such as endopolygeny, introduce further diversity by incorporating multiple DNA replication cycles without corresponding nuclear divisions, yielding polyploid nuclei that resolve during final cytokinesis; this is observed in certain coccidian parasites like Sarcocystis neurona. These modes exhibit plasticity, with the number of daughters and division timing modulated by host environmental cues, including nutrient availability and immune pressure, which trigger switches between binary and multinucleate replication to optimize survival. For instance, environmental stressors can shift Toxoplasma from endodyogeny to schizogony-like modes in vitro.^[32] Genetically, schizogony often involves transient polyploidy, where unreduced genome copies accumulate during early replication phases before karyokinesis distributes chromosomes to daughters, maintaining genetic stability across asynchronous cycles. Daughter cell formation in both schizogony and endodyogeny relies on the IMC, a flattened vesicular sac underlying the plasma membrane, which acts as a cytoskeletal template for budding and apical complex assembly, ensuring motile progeny with invasion capability. This IMC-mediated process coordinates organelle segregation and cytokinesis, preventing aneuploidy in the resulting merozoites.^[27]^[33]

Sexual Reproduction

In Apicomplexa, sexual reproduction is a critical phase that generates genetic diversity through gamete fusion and meiosis, typically occurring within the vector or definitive host. Gametocytes, the precursor cells to gametes, differentiate from earlier asexual stages in response to environmental cues such as a decrease in temperature from 37°C to around 20°C, along with shifts in pH and the presence of mosquito-derived factors like xanthurenic acid, particularly in Plasmodium species ingested during a blood meal.^[34] This differentiation is genetically programmed but environmentally induced, ensuring sexual commitment aligns with transmission opportunities.^[35] Gametocytes develop into two distinct forms: microgametocytes and macrogametocytes. Microgametogenesis in microgametocytes involves three rapid asynchronous rounds of nuclear division in Plasmodium, producing eight flagellated, biflagellate microgametes that resemble sperm cells and enable motility for fertilization; these microgametes are elongated, banana-shaped, and propelled by axonemes derived from basal bodies.^[35] In contrast, macrogametocytes mature into non-motile macrogametes through the synthesis of specialized organelles, including wall-forming bodies and dense granules, which prepare the female gamete for zygote development without locomotion.^[35] This dimorphism ensures efficient gamete interaction in the confined environment of the vector's midgut. Syngamy occurs when a microgamete penetrates and fuses with a macrogamete, forming a diploid zygote that rounds up and initiates further transformation. The zygote differentiates into a motile, elongated ookinete, which traverses the peritrophic matrix and midgut epithelium of the vector before encysting as an oocyst on the basal lamina, where meiosis and sporogony produce infectious sporozoites.^[35] This process facilitates transmission to new hosts via the vector. Meiosis within the oocyst enables genetic recombination, promoting outcrossing in species like Plasmodium falciparum, where natural populations exhibit high rates of novel genotypes from cross-fertilization rather than selfing, enhancing adaptability to host immunity and drugs.^[36]^[37]

General Life Cycle Stages

Apicomplexans typically exhibit a heteroxenous life cycle, alternating between definitive and intermediate hosts to complete their development, with invasive stages such as sporozoites and merozoites facilitating transmission and infection.^[1] This cycle integrates asexual and sexual reproduction, involving distinct proliferative phases that ensure parasite dissemination across hosts via vectors, feces, or predation.^[38] Sporogony represents the post-zygotic phase where oocysts develop in the environment or within vectors, undergoing meiosis to produce infective sporozoites enclosed in sporocysts.^[1] These sporozoites are released upon oocyst rupture and actively invade host cells in the intermediate host, initiating infection.^[38] Following invasion, merogony occurs as an asexual multiplication process within intermediate host tissues, where sporozoites transform into schizonts that divide to yield numerous merozoites, which can reinvade cells or differentiate further.^[21] This stage amplifies parasite numbers and may involve multiple generations, contributing to acute infection.^[1] Gamogony, the sexual phase, typically unfolds in the definitive host or vector, where certain merozoites develop into gametocytes, which produce male microgametes and female macrogametes that fuse into zygotes.^[38] These zygotes then encyst as oocysts, setting the stage for sporogony and transmission.^[1] In some coccidian apicomplexans, encystment leads to the formation of tissue cysts containing bradyzoites, dormant and slowly replicating forms that persist in intermediate hosts, enabling chronic infections and resistance to immune clearance.^[39] This stage underscores the parasite's strategy for long-term survival and reactivation.^[38]

Taxonomy and Phylogeny

Historical Classification

The earliest observations of apicomplexan parasites date back to the mid-19th century, with gregarines being among the first groups recognized. In 1843, David Gruby and Charles Philippe Robin Delafond described gregarines as parasites inhabiting the digestive tracts of insects, marking the initial documentation of these extracellular protozoans.^[40] Subsequent studies by Albert von Kölliker between 1845 and 1848 confirmed their unicellular nature and expanded knowledge of their morphology, distinguishing them from multicellular organisms. These findings laid the groundwork for understanding apicomplexans as a distinct parasitic lineage, primarily based on their spore-forming reproductive stages. Coccidian parasites were described shortly thereafter, with early reports emerging in the 1850s and 1870s. In 1857, Édouard Balbiani identified coccidia-like "psorosperms" in earthworms, though their protozoan identity was not fully appreciated at the time.^[41] By 1878, Achille Rivolta provided the first clear description of a vertebrate coccidian, naming Eimeria stiedae from rabbit livers, which highlighted their intracellular nature and sporulation process.^[41] The haemosporidian Plasmodium, causative agent of malaria, was discovered in 1880 by Alphonse Laveran in the blood of infected humans, with Italian pathologists Ettore Marchiafava and Amico Bignami confirming and elaborating on these observations in the early 1880s through detailed histological studies.^[42] Alfred Kühn's comprehensive work in the early 1900s further systematized coccidian taxonomy, emphasizing their life cycles and distinguishing them from other sporozoans.^[41] The formal taxonomic framework for these parasites began to coalesce in the late 19th century. In 1879, Friedrich Leuckart proposed the class Sporozoa within Protozoa to encompass spore-producing parasites, including gregarines and coccidia, divided into subclasses Gregarinina and Coccidiina based on morphological and habitat differences.^[43] This classification was refined in 1900 by Louis Léger, who introduced orders within the gregarines, such as Eugregarinida and Schizogregarinida, to account for variations in syzygy and sporulation.^[44] By the mid-20th century, Sporozoa encompassed diverse groups like coccidia, gregarines, and piroplasms, though polyphyletic issues persisted due to reliance on light microscopy. The modern phylum Apicomplexa was established in 1970 by Norman D. Levine, who elevated the group from the class Sporozoea within Sporozoa to phylum status, unified by the presence of an apical complex—a set of organelles essential for host cell invasion—in at least one life cycle stage.^[45] This shift addressed the artificial nature of Sporozoa and emphasized ultrastructural features, retaining early divisions into subclasses like Gregarinasida and Coccidiasida while incorporating emerging electron microscopy data.^[46]

Modern Classification

The phylum Apicomplexa is classified within the larger eukaryotic supergroup Alveolata, a diverse clade characterized by cortical alveoli and other shared ultrastructural features.^[47] Approximately 6,000 species of Apicomplexa have been described, though estimates suggest the total diversity could be orders of magnitude higher due to their obligate parasitic lifestyles and under-sampling in many host taxa.^[48] The modern taxonomic framework emphasizes molecular phylogenetics alongside morphological traits, such as the presence or absence of the conoid—a bundle of microtubules at the apical end of motile stages—dividing the phylum into two primary classes: Aconoidasida and Conoidasida.^[47] Aconoidasida comprises parasites lacking a conoid structure, primarily infecting vertebrate blood cells; key orders include Haemosporida (e.g., Plasmodium species causing malaria) and Piroplasmida (e.g., Babesia and Theileria, agents of piroplasmosis).^[47] In contrast, Conoidasida includes taxa with a well-developed conoid and encompasses a broader range of hosts and habitats; representative orders are Gregarinida (extracellular gut parasites in invertebrates) and Eimeriida (intracellular coccidians in vertebrates and invertebrates).^[47] This class-based division, first proposed in the early 2000s, reflects phylogenetic analyses integrating small subunit ribosomal RNA genes and other molecular markers to resolve relationships beyond traditional morphology-driven groupings. Recent molecular discoveries have expanded the phylum's framework, notably with the erection of the class Marosporida in 2021 to accommodate a novel lineage of marine apicomplexans infecting bivalve mollusks, such as Margolisiella islandica and Rhytidocystis rubra.^[49] These post-2010 findings, based on phylogenomic data from hundreds of genes, position Marosporida as sister to the coccidian-hematozoan clade, highlighting the phylum's hidden diversity in non-vertebrate hosts.^[49] Key revisions to apicomplexan taxonomy include the schemes outlined by Perkins et al. (2000), which formalized the Aconoidasida-Conoidasida split using ultrastructural and developmental data, and the comprehensive eukaryotic classification by Adl et al. (2019), which integrated multilocus phylogenies to refine orders and incorporate environmental sequences.^[50]^[47] A significant update in the latter is the firm placement of Cryptosporidiidae (e.g., Cryptosporidium, a major waterborne pathogen) as a relative within Apicomplexa, specifically under Conoidasida in the order Cryptogregarinorida, resolving prior debates about its affinities based on genome-scale analyses.^[47]

Phylogenetic Relationships

Apicomplexa are positioned within the eukaryotic supergroup Alveolata, alongside dinoflagellates and ciliates, based on shared ultrastructural features such as cortical alveoli and molecular phylogenies derived from small subunit ribosomal RNA (SSU rRNA) genes.^[51] Within Alveolata, Apicomplexa form part of the subclade Myzozoa, which also includes dinoflagellates and perkinsids, characterized by predatory or parasitic lifestyles involving a feeding structure like the apical complex or peduncle.^[52] More specifically, phylogenomic analyses using concatenated protein datasets have established chrompodellids—encompassing predatory colpodellids and photosynthetic chromerids—as the closest sister group to Apicomplexa within Myzozoa, supporting a common ancestry for these lineages with non-photosynthetic plastids derived from secondary endosymbiosis of a red alga.^[51] This relationship is robustly recovered in multi-gene trees, with bootstrap support exceeding 90% in maximum-likelihood reconstructions, highlighting the evolutionary transition from free-living predators to obligate parasites in apicomplexans.^[51] Internally, Apicomplexa exhibit a deep bifurcation into two major classes: Aconoidasida (lacking a conoid, including haemosporidians like Plasmodium) and Conoidasida (possessing a conoid, including coccidians like Toxoplasma), a split consistently confirmed by SSU rRNA phylogenies and multi-protein analyses.^[53] For instance, maximum-likelihood trees of RNA-binding domain abundant (RAP) proteins from apicomplexan genomes show Aconoidasida forming a monophyletic clade distinct from Conoidasida, with high posterior probabilities (>0.95) across 175 aligned sequences.^[53] Recent single-cell phylogenomic studies from the 2020s have resolved previously enigmatic marine apicomplexans, such as ichthyocolids infecting fish erythrocytes, as early-diverging lineages within Apicomplexa, branching basal to major parasitic clades like those in Coccidia.^[54] These analyses, employing single-amplified genomes and concatenated markers including 18S rRNA and apicoplast genes, place ichthyocolids as sisters to corallicolids (coral parasites), revealing a diverse basal radiation of aquatic apicomplexans outside terrestrial host-adapted groups.^[54] Evidence of horizontal gene transfer (HGT) is prominent in the apicoplast genome of Apicomplexa, where reductive evolution has led to the relocation of numerous genes to the nuclear genome, alongside acquisitions from bacterial donors.^[55] Systematic phylogenomic surveys identify numerous nuclear genes of probable prokaryotic origin in apicomplexans, many linked to the apicoplast's metabolic pathways, such as isoprenoid biosynthesis, with phylogenetic signals indicating transfers from the original endosymbiont or other bacteria during plastid integration.^[55] This HGT pattern underscores the organelle's role in facilitating parasitism through genome streamlining and functional innovation.^[56]

Diversity of Major Groups

Gregarinasina

Gregarinasina, a major subgroup within the Apicomplexa, encompasses the gregarines, which are predominantly extracellular parasites infecting the intestinal tracts of invertebrate hosts such as insects, annelids, and marine invertebrates. These protists are distinguished by their large, elongated trophozoites that resemble worms, often measuring up to several millimeters in length, and feature a prominent attachment organelle called the mucron or epimerite for adhering to host epithelial cells without penetrating tissues. Unlike many other apicomplexans, gregarines exhibit a simplified apical complex, including a rudimentary conoid, reflecting their basal phylogenetic position as one of the earliest diverging lineages in the phylum.^[57]^[58]^[59] The life cycle of gregarines is typically monoxenous, confined to a single invertebrate host and occurring extracellularly within the gut lumen or attached to the intestinal epithelium, without invading deeper tissues or requiring intermediate hosts. Infection begins when hosts ingest oocysts containing infectious sporozoites, which excyst and develop into trophozoites that feed on host cell contents via osmotrophy. Sexual reproduction involves the pairing of gamonts in a process known as syzygy, where male and female gamonts align end-to-end to form a gametocyst; within this structure, gametes fuse, leading to zygotes that undergo sporogony to produce oocysts filled with sporozoites, which are then released into the environment via host feces to complete the cycle. This lifecycle emphasizes attachment and nutrient absorption over invasive motility, contrasting with the intracellular strategies of other apicomplexans.^[60]^[61]^[62] Gregarinasina exhibits substantial diversity, with approximately 1,600 described species distributed across three main orders: Archigregarinida, primarily marine parasites of polychaetes and other annelids; Eugregarinida, the largest group infecting terrestrial insects and annelids; and Neogregarinida, which includes tissue-migrating forms in insects but retains extracellular gamogony. These parasites are globally widespread, thriving in diverse habitats from terrestrial soils to marine sediments, and infect a broad spectrum of invertebrate phyla, including arthropods, mollusks, and echinoderms. Representative genera include Gregarina in coleopterans and Lecudina in polychaetes, highlighting their host specificity and morphological variations in attachment structures.^[63]^[64] Ecologically, gregarines play a subtle yet significant role as commensal or mildly pathogenic parasites that rarely cause host mortality but can influence invertebrate population dynamics by reducing fecundity, altering gut physiology, or modulating immune responses. In many cases, they are non-pathogenic under normal conditions, serving as indicators of environmental health in invertebrate communities, particularly in aquatic ecosystems where high infection prevalence correlates with host density. Their abundance underscores the evolutionary success of extracellular parasitism in regulating invertebrate populations without driving host extinction.^[65]^[62]^[59]

Coccidiasina

Coccidiasina represents a subclass of obligate intracellular parasites within the phylum Apicomplexa, primarily infecting the tissues of vertebrates and characterized by their invasive sporozoite stages that form cysts or multiply within host cells. These parasites are notable for their role in causing coccidiosis and related diseases, with a focus on epithelial and tissue infections rather than extracellular or blood-stage development. Unlike gregarines, coccidians actively invade host cells using apical complex structures, leading to schizogony as a brief asexual multiplication mechanism before gametogony and oocyst formation.^[66] The diversity of Coccidiasina encompasses approximately 2,000 described species, predominantly within the order Eimeriida, though surveys indicate that only a fraction of potential hosts have been examined, suggesting thousands more undiscovered taxa across vertebrate classes. Key genera include Eimeria, which comprises over 1,800 species highly specific to intestinal epithelia of livestock and wildlife; Toxoplasma, a ubiquitous genus with T. gondii infecting warm-blooded animals worldwide; and Sarcocystis, featuring species that form persistent cysts in muscle tissues. These genera exemplify the subclass's adaptation to monoxenous or heteroxenous strategies, with Eimeria typically monoxenous and the others heteroxenous involving intermediate and definitive hosts.^[66]^[67] Life cycles in Coccidiasina generally begin with the ingestion of sporulated oocysts shed in the feces of infected hosts, followed by excystation in the gastrointestinal tract where enzymes like trypsin facilitate the release of invasive sporozoites. In monoxenous cycles, such as those of Eimeria, sporozoites invade intestinal cells, undergo multiple rounds of asexual schizogony to produce merozoites, then shift to sexual gametogony, culminating in unsporulated oocysts that sporulate externally in favorable environmental conditions before reinfection. Heteroxenous cycles, exemplified by Toxoplasma and Sarcocystis, involve tissue cyst formation in intermediate hosts—bradyzoites in Toxoplasma persist latently in brain or muscle—while definitive hosts (e.g., felids for Toxoplasma) complete sexual reproduction and shed oocysts. Excystation triggers rapid invasion, with sporozoites gliding via microneme secretion to enter host cells.^[66]^[68]^[69] Pathogenesis in Coccidiasina arises from cellular destruction during replication and cyst persistence, leading to conditions like enteritis from Eimeria species, which damage intestinal mucosa causing hemorrhage and malabsorption in poultry and ruminants. Toxoplasma gondii induces encephalitis in immunocompromised hosts through bradyzoite-laden cysts in neural tissue, where slow-growing forms evade immunity and reactivate during stress. Similarly, Sarcocystis species form sarcocysts in skeletal or cardiac muscle of intermediate hosts, potentially causing myositis or chronic inflammation upon ingestion by definitive hosts, though many infections remain subclinical. These mechanisms highlight the subclass's impact on host physiology without direct bloodstream involvement.^[66]^[39]^[67]

Aconoidasida

Aconoidasida is a class of apicomplexan parasites characterized by the absence of a conoid, a defining apical structure present in other apicomplexans that aids in host cell invasion. This class primarily comprises blood-dwelling parasites that infect vertebrates and are transmitted by arthropod vectors, alternating between sexual reproduction in the vector and asexual replication in the vertebrate host's circulatory system. The two main orders within Aconoidasida are Haemosporida, which includes genera such as Plasmodium and Haemoproteus vectored by mosquitoes, and Piroplasmida, encompassing genera like Babesia and Theileria transmitted by ticks. These parasites exhibit heteroxenous life cycles adapted to erythrocytic environments, distinguishing them from tissue-invasive groups in other apicomplexan classes.^[70] In Haemosporida, the life cycle features pre-erythrocytic stages in the vertebrate host, where sporozoites develop into schizonts in tissues such as the liver before invading erythrocytes for schizogony, producing merozoites that continue intraerythrocytic replication. Gametocytes form within infected red blood cells and are taken up by mosquito vectors during feeding, initiating sexual stages. Piroplasmida share erythrocytic schizogony but lack prominent pre-erythrocytic phases; instead, they undergo asexual binary fission or budding within erythrocytes, with gametocytes also circulating in the blood for uptake by ticks. Both orders involve motile kinetes (or ookinetes in Haemosporida) in the vector, which traverse the gut wall to reach salivary glands or other tissues, facilitating transmission. Vector transmission underscores their dependence on hematophagous arthropods for dispersal.^[71]^[72]^[73] Aconoidasida encompasses significant diversity, with over 600 described species in Haemosporida, predominantly avian and reptilian parasites alongside mammalian ones, and approximately 43 valid species in Piroplasmida, mainly affecting livestock and wildlife. This group represents a specialized evolutionary adaptation to blood parasitism, with genomic analyses revealing compact genomes suited to intracellular lifestyles, such as ~23 Mb in Plasmodium species. Recent phylogenomic studies have reinforced the molecular distinction of Aconoidasida from Conoidasida, confirming their monophyly through multi-gene analyses and highlighting ancient divergences within Apicomplexa. These findings support the class's separation based on both ultrastructural and genetic traits.^[74]^[75]^[70]^[49]

Ecology and Distribution

Host Interactions and Transmission

Apicomplexan parasites exhibit diverse transmission strategies that rely heavily on arthropod vectors for certain groups, particularly those within the haemosporidia and piroplasms. For instance, Plasmodium species, responsible for malaria, undergo biological transmission through female Anopheles mosquitoes, where the parasite completes sexual reproduction in the vector's gut before sporozoites are injected into a vertebrate host during a blood meal.^[76] Similarly, Babesia species are transmitted biologically by hard ticks such as Ixodes spp., with sporozoites developing in the tick's salivary glands and infecting mammalian hosts upon feeding; transstadial and transovarial transmission can occur in ticks, enhancing persistence.^[76] In contrast, coccidian apicomplexans like Eimeria and Isospora primarily employ mechanical or fecal-oral transmission without obligatory vectors, where unsporulated oocysts are shed in host feces and sporulate in the environment to become infectious. To persist within hosts, apicomplexans employ sophisticated immune evasion mechanisms that allow chronic infections. Plasmodium falciparum utilizes antigenic variation of the PfEMP1 protein, encoded by var genes, to alter surface antigens on infected erythrocytes, thereby escaping adaptive immunity and sequestering in host tissues to avoid splenic clearance. Toxoplasma gondii forms tissue cysts containing bradyzoites, a latent stage that resides intracellularly in the host's brain and muscles, shielded from immune detection; the cyst wall, composed of proteins like CST1, resists immune-mediated lysis and enables lifelong persistence. These strategies, including modulation of host cytokine responses such as downregulation of IFN-γ, facilitate survival across multiple host cell types.^[76] Host specificity in apicomplexans reflects long-term co-evolution with vertebrates and invertebrates, often driven by host-switching events that shape parasite adaptation. Toxoplasma gondii demonstrates broad host specificity, infecting virtually all warm-blooded animals due to versatile surface adhesins like SAG1 that bind diverse host receptors, contributing to its high zoonotic potential through cross-species transmission. In contrast, Neospora caninum is more host-restricted, primarily affecting cattle and canids, with efficient vertical transmission linked to specific placental interactions; such specificity arises from co-evolutionary pressures favoring vertical over horizontal spread in livestock. Overall, host-switching, rather than strict co-speciation, appears to be the primary driver of diversification, as evidenced by phylogenetic mismatches between apicomplexans and their reptilian or mammalian hosts. Environmental transmission plays a crucial role for coccidian apicomplexans, with oocysts exhibiting remarkable resilience to facilitate indirect spread. Toxoplasma gondii oocysts, shed unsporulated in cat feces, sporulate within 1-5 days and can survive in moist soil or water for up to 18 months at 4°C or tolerate temperatures from -20°C to 35°C, resisting common disinfectants like chlorine.^[77] This durability allows contamination of water sources, produce, and shellfish, leading to ingestion-based transmission in intermediate hosts; similar resilience is observed in Cryptosporidium parvum oocysts, which are highly resistant to chlorine and can persist in soil and water for months to years, underscoring the environmental reservoir's importance for zoonotic cycles.^[77]^[78]

Global Distribution and Environmental Factors

Apicomplexa exhibit a cosmopolitan distribution, with species inhabiting diverse terrestrial, freshwater, and marine environments across all continents. Members of this phylum are particularly prevalent in tropical and subtropical regions, where environmental conditions favor their survival and proliferation. For instance, Plasmodium species, responsible for malaria, are predominantly found in tropical countries, with the highest burden in sub-Saharan Africa, Southeast Asia, and parts of South America.^[79] In contrast, Eimeria species are ubiquitous in livestock populations worldwide, infecting cattle and other ruminants on nearly all farms due to the widespread environmental contamination by oocysts.^[80] Environmental factors play a critical role in shaping the distribution of apicomplexans, with climate variables such as temperature and precipitation exerting strong influences on their global patterns. On a broad scale, apicomplexan distributions correlate positively with warmer temperatures and higher precipitation levels, which enhance oocyst viability and sporulation in soil and water. Soil pH emerges as a key determinant in terrestrial habitats, structuring community composition and abundance, particularly in acidic tropical environments where apicomplexans thrive. Habitat specificity further modulates distribution; for example, gregarines predominate in soil ecosystems, comprising up to 98% of apicomplexan sequences in tropical soil surveys, while reflecting associations with invertebrate hosts in these substrates. In marine settings, the recently identified class Marosporida infects invertebrates such as scallops and squid, highlighting adaptation to oceanic environments.^[81]^[82] Recent environmental changes have contributed to shifts in apicomplexan distributions, including expansions facilitated by climate warming. Rising temperatures and altered precipitation are enabling the northward spread of tick vectors for piroplasms like Babesia and Theileria, potentially invading new regions in temperate zones. Urbanization has also amplified the role of wildlife as reservoirs, with species such as wild carnivores harboring piroplasms and other apicomplexans in peri-urban areas, increasing exposure risks through habitat fragmentation.^[83]^[84] Biodiversity hotspots for apicomplexans are concentrated in tropical soils, where recent studies from the 2020s reveal exceptionally high diversity and prevalence. Apicomplexans are detected in over 83% of tropical soil samples, often accounting for 30% of the protist community, with gregarines dominating and exhibiting strong correlations to local edaphic conditions like pH and moisture. These patterns underscore the phylum's ecological breadth, driven by the abundance of potential invertebrate hosts in biodiverse tropical ecosystems.^[81]

Evolution

Origins and Ancient Traits

The Apicomplexa are estimated to have emerged between 800 and 1000 million years ago from a free-living predatory ancestor within the alveolate lineage, marking a key transition from predation to obligate parasitism.^[85]^[86] This divergence likely occurred after the initial radiation of alveolates around 1 billion years ago, with the apicomplexan lineage specializing in host cell invasion.01330-4) The predatory ancestor resembled modern chrompodellids, such as colpodellids, which use a myzocytotic feeding mechanism to extract cytoplasmic contents from prey cells.^[87]^[86] A pivotal endosymbiotic event in the early evolution of the apicomplexan lineage involved the acquisition of a red algal-derived plastid, known as the apicoplast, approximately 1.3 billion years ago by the common ancestor of chromalveolates.^[88] This secondary endosymbiosis provided metabolic capabilities that were later reduced in parasitic apicomplexans, but the organelle persists as a non-photosynthetic relic essential for isoprenoid biosynthesis and other functions.^[89] The timing aligns with molecular clock analyses calibrated against eukaryotic divergence events, predating the parasitic specialization of Apicomplexa.^[88] Several ancient traits are conserved from this predatory ancestor, notably the apical complex, which is homologous to the myzocytotic apparatus observed in chrompodellids.^[86] In colpodellids, this structure facilitates attachment to prey and direct suction of nutrients via a peduncle-like extension, a process termed myzocytosis or "cellular vampirism."^[86]^[90] In apicomplexans, the apical complex has been co-opted for host cell penetration, retaining components like rhoptries and micronemes that secrete adhesive and invasive molecules, underscoring its evolutionary continuity from predation to parasitism.^[86]^[91] Direct fossil evidence for Apicomplexa is ambiguous and scarce, with no unambiguous records preserved due to their intracellular lifestyle and lack of mineralized structures.^[85] Evolutionary timelines are thus primarily inferred from molecular clock methods applied to ribosomal RNA and protein sequences, which integrate substitution rates with calibration points from broader eukaryotic phylogenies.^[85]^[92] These estimates suggest the crown group radiation occurred in the Neoproterozoic era, consistent with the absence of earlier microfossils attributable to the group.^[85]

Diversification and Adaptations

The diversification of Apicomplexa into major groups began with early radiations that established key lineages, including the split between gregarines (Gregarinasina) and coccidians (Coccidiasina), estimated to have occurred around 800 million years ago during the Precambrian period when multicellular hosts first emerged.^[93] This ancient divergence allowed gregarines to primarily parasitize invertebrates through extracellular lifestyles, while coccidians evolved intracellular parasitism across a broader range of hosts, setting the stage for further branching within the phylum.^[94] Subsequent radiations, such as the evolution of Aconoidasida, enabled adaptation to vertebrate blood niches, where parasites like Plasmodium and Babesia exploit circulatory systems for dissemination via hematophagous vectors.^[95] A hallmark adaptation in Aconoidasida is the loss or reduction of the conoid—a tubulin-based apical structure involved in host cell invasion—facilitating streamlined invasion mechanisms suited to erythrocyte environments and distinguishing them from conoid-bearing groups like coccidians.^[96] This morphological simplification correlates with genome reduction and streamlining across Apicomplexa, where parasite genomes are notably compact (often 10-30 Mb) compared to free-living relatives, reflecting the loss of genes for independent metabolism and nutrient acquisition in favor of host-dependent strategies.^[70] Such reductions enhance replication efficiency within constrained intracellular or intravascular spaces, with examples like Cryptosporidium showing extreme compaction to ~9 Mb while retaining essential invasion machinery.^[97] Co-speciation with hosts and vectors has driven much of apicomplexan diversification, particularly in haemosporidian lineages where phylogenetic congruence between parasites and avian or reptilian hosts indicates long-term parallel evolution, though host switching remains common and promotes speciation across host families.^[98] Recent discoveries underscore ongoing diversification in marine environments; in 2024, ichthyocolids were identified as a novel, widespread clade of apicomplexans infecting teleost fish globally, from tropical to polar waters, expanding known diversity beyond terrestrial and freshwater systems.^[99] These blood parasites, transmitted likely via leeches or other vectors, highlight adaptive radiations into aquatic niches paralleling ancient terrestrial ones.^[100] Genomic analyses reveal expanded gene families as critical for host manipulation, with lineages like coccidians showing proliferation of ApiAP2 transcription factors and rhoptry kinases that reprogram host cell signaling for immune evasion and nutrient provisioning.^[101] These expansions, often species-specific, enable fine-tuned adaptations to diverse hosts, such as altered erythrocyte permeability in Plasmodium, underscoring how genomic plasticity fuels the phylum's success as obligate parasites.^[70]

Medical and Economic Importance

Human Pathogens

Apicomplexan parasites pose significant threats to human health, primarily through species that cause malaria, toxoplasmosis, and cryptosporidiosis. These infections affect millions globally, with Plasmodium species responsible for the highest mortality, while Toxoplasma gondii and Cryptosporidium spp. lead to substantial morbidity, particularly in vulnerable populations such as pregnant women, children, and immunocompromised individuals.^[4]^[102] Plasmodium species, transmitted by Anopheles mosquitoes, cause malaria, a life-threatening disease characterized by fever, chills, and anemia. Among the five Plasmodium species infecting humans—P. falciparum, P. vivax, P. ovale, P. malariae, and P. knowlesi—P. falciparum is the most lethal, accounting for nearly all malaria-related deaths due to its ability to cause severe complications like cerebral malaria and multi-organ failure. In 2023, malaria resulted in an estimated 597,000 deaths worldwide, predominantly among children under five in sub-Saharan Africa. The parasite's life cycle involves asexual reproduction in human erythrocytes and sexual stages in the mosquito vector, enabling rapid transmission in endemic regions.^[103]^[4]^[104] Toxoplasma gondii, an obligate intracellular parasite, causes toxoplasmosis, which is often asymptomatic in healthy adults but can lead to severe outcomes in immunocompromised patients and during congenital infection. In individuals with AIDS, it commonly manifests as encephalitis, while in pregnant women, it can result in fetal abnormalities such as chorioretinitis, hydrocephalus, and intrauterine death. Globally, approximately 30% of the human population is seropositive for T. gondii, with higher prevalence in regions with warm, humid climates and close contact with cats or undercooked meat. Transmission occurs via oocysts in contaminated water or soil and tissue cysts in infected meat.^[105] Cryptosporidium species, particularly C. parvum and C. hominis, cause cryptosporidiosis, a gastrointestinal illness marked by profuse watery diarrhea, abdominal cramps, and dehydration. While self-limiting in immunocompetent hosts, it can be chronic and life-threatening in immunocompromised individuals, such as those with HIV/AIDS, leading to substantial weight loss and malnutrition. The parasite is transmitted through fecally contaminated water, food, or direct contact, with outbreaks often linked to recreational water sources. Globally, cryptosporidiosis contributes to an estimated 7.6% prevalence in human populations, disproportionately affecting children in low-resource settings.^[102]^[106] Treatment of these apicomplexan infections relies on specific antiprotozoal drugs, though challenges like drug resistance and toxicity persist. For malaria, artemisinin-based combination therapies (ACTs) are the first-line treatment for uncomplicated P. falciparum cases, rapidly reducing parasitemia, while atovaquone-proguanil serves as an alternative for prophylaxis and mild infections. However, artemisinin resistance has emerged in Southeast Asia and parts of Africa, complicating control efforts. Toxoplasmosis is typically managed with pyrimethamine combined with sulfadiazine and folinic acid, which targets folate synthesis in the parasite, though alternatives like atovaquone are used in sulfa-intolerant patients. Cryptosporidiosis treatment is limited; nitazoxanide shortens symptoms in immunocompetent children but shows poor efficacy in severely immunocompromised adults, often requiring supportive care like hydration. Ongoing research emphasizes the need for new drugs to address resistance and improve outcomes in high-burden areas.30820-0/fulltext)

Veterinary and Wildlife Impacts

Apicomplexan parasites inflict substantial economic burdens on livestock industries through diseases like babesiosis and theileriosis, primarily affecting cattle via tick vectors. Theileria species cause theileriosis, resulting in global annual losses of approximately US$300 million from cattle mortality, reduced milk production, and treatment costs. Babesia infections, particularly bovine babesiosis, exacerbate these impacts; in enzootic regions like Mexico, vector control measures alone account for US$573.6 million in yearly expenditures. These losses highlight the parasites' role in compromising animal health and farm profitability worldwide. In poultry production, Eimeria species drive coccidiosis, a leading parasitic disease with profound economic consequences in intensive broiler systems. Global estimates place annual losses at over US$13 billion, driven by impaired growth, diminished feed efficiency, higher mortality rates, and the costs of preventive anticoccidials. This disease remains a critical challenge in aquaculture, where uncontrolled outbreaks can reduce flock performance by up to 20-30% in severe cases. Wildlife populations face severe threats from apicomplexans, contributing to conservation concerns for endangered species. Haemoproteus parasites, transmitted by biting midges, cause high mortality in avian hosts; for instance, Haemoproteus minutus has triggered fatal outbreaks in captive parrots from Australasia and South America, affecting 29% of species classified as vulnerable to critically endangered on the IUCN Red List. In marine ecosystems, Sarcocystis neurona leads to protozoal encephalitis and significant die-offs among mammals, including the threatened southern sea otter (Enhydra lutris nereis), where it accounts for a notable portion of strandings and deaths along the northeastern Pacific coast. Mitigation efforts emphasize targeted interventions to curb these impacts. Live attenuated vaccines against Eimeria species, administered to chicks, induce protective immunity by allowing controlled replication of oocysts, reducing clinical coccidiosis severity in poultry flocks. For tick-borne apicomplexans like Babesia and Theileria, vector management relies on acaricides to lower ixodid tick populations, alongside pasture rotation and quarantine to prevent disease spread. Recent advancements in the 2020s include genomic surveillance tools, such as parasite reference genomes, which enhance detection and tracking of veterinary apicomplexans through metagenomic sequencing for early outbreak response.

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Eimeriosis in Cattle: Current Understanding - Daugschies - 2005
Dec 2, 2005 · Eimeria spp. are ubiquitous parasites and are present on all farms (Cornelissen et al., 1995; Wacker et al., 1999). Thus all calves acquire ...<|separator|>
[79]
The Biogeography of Apicomplexan Parasites in Tropical Soils
Jun 2, 2025 · Previous research has shown that, on a global scale, Apicomplexa distributions are linked to precipitation and temperature (Oliverio, Geisen, ...
[80]
Phylogenomics Identifies a New Major Subgroup of Apicomplexans ...
Abstract. The phylum Apicomplexa consists largely of obligate animal parasites that include the causative agents of human diseases such as malaria.Missing: Ichthyocolids | Show results with:Ichthyocolids
[81]
Impact of Climate Trends on Tick-Borne Pathogen Transmission - PMC
Concerns exist about how predicted climate changes may alter tick–host–pathogen relationships and particularly tick potential for invasion of new areas and ...
[82]
Natural history of Zoonotic Babesia: Role of wildlife reservoirs
Babesia are tick-borne parasites in the Phylum Apicomplexa. Two closely related genera, Theileria and Cytauxzoon, are also tick-borne, and collectively these ...
[83]
Evolutionary origin of Plasmodium and other Apicomplexa based
The Apicomplexa is a large and complex protist phylum, consisting of nearly 5000 described species, with as many as. 60,000 yet to be named (ref. 1, pp. 1-6 ...
[84]
The 3D Structure of the Apical Complex and Association with ... - NIH
Jan 2, 2014 · The P. pacifica apical complex is associated with the gullet and consists of the pseudoconoid, micronemes, and electron dense vesicles.
[85]
[PDF] early evolutionary history of dinoflagellates and apicomplexans ...
The phylogeny of colpodellids (Eukaryota, Alveolata) using small subunit rRNA genes suggests they are the free-living ancestors of apicom- plexans. J. Eukaryot.
[86]
Molecular Timeline for the Origin of Photosynthetic Eukaryotes
2001; Yoon et al. 2002; Harper and Keeling 2003); therefore, it is likely that the alveolates diverged sometime after 1,274 MYA, before the split of the ...
[87]
Evolution of the apicoplast and its hosts - ScienceDirect.com
Here we review our knowledge on the evolutionary history of Apicomplexa and particularly their plastids, with a focus on the pathway by which they evolved from ...
[88]
Adaptations and metabolic evolution of myzozoan protists across ...
Oct 10, 2024 · The phylogenetic tree of Myzozoa shows the relationships between major groups including Dinoflagellates and Apicomplexans. Open in a new tab.
[89]
Nutrient Acquisition and Attachment Strategies in Basal Lineages
Jul 2, 2021 · This review summarises the current state of knowledge on the attachment/invasive and nutrient uptake strategies displayed by apicomplexan parasites.
[90]
The timing of eukaryotic evolution: Does a relaxed molecular clock ...
On average, the divergence times among eukaryotes were 1.7 times deeper with a global clock than with a relaxed clock (Table 5, which is published as supporting ...
[91]
Phylogenetic Analysis of Coccidian Parasites from Invertebrates
The time of further radiation of the phylum Apicomplexa is placed in the Precambrian period, ∼800 Mya (Escalante and Ayala 1995), when multicellular organisms ...Missing: early | Show results with:early
[92]
[PDF] Phylogenomic diversity of archigregarine apicomplexans
Sep 26, 2024 · Gregarines are a large and diverse subgroup of Apicomplexa, a lineage of obligate animal symbionts including pathogens such as Plasmodium,.
[93]
SAS6-like protein in Plasmodium indicates that conoid-associated ...
Jun 24, 2016 · Plasmodium has been traditionally considered to lack the conoid (it is classified in the Aconoidasida) based on ultrastructural data, ...
[94]
Molecular characterization of the conoid complex in Toxoplasma ...
We show that the conoid is a conserved apicomplexan element at the heart of the invasion mechanisms of these highly successful and often devastating parasites.Missing: granules | Show results with:granules<|separator|>
[95]
Proteome size reduction in Apicomplexans is linked with loss ... - NIH
Dec 6, 2020 · Life cycle adaptations, hosts and cell specificity might influence genome size in Apicomplexans, with more complex life cycles being linked ...
[96]
Species formation by host shifting in avian malaria parasites - PNAS
We find that host shifting, often across host genera and families, is the rule. Sympatric speciation by host shifting would require local reproductive ...
[97]
A new and widespread group of fish apicomplexan parasites
May 30, 2024 · Ichthyocolids are a new, widespread group of fish-infecting apicomplexan parasites, lacking chlorophyll-biosynthesis genes, and are related to ...
[98]
Previously uncharacterized parasite uncovered in fish worldwide
The Ichthyocolids belong to Apicomplexa, a large group of parasites including the ones that causes malaria and toxoplasmosis.
[99]
Large, rapidly evolving gene families are at the forefront of host ...
In this review I compare and contrast the genomic context, gene structure, gene expression, protein localization and function of these families across different ...
[100]
About Crypto Infections | Cryptosporidium ("Crypto") - CDC
May 27, 2025 · Cryptosporidiosis is a disease that causes watery diarrhea. It is caused by a microscopic germ (parasite) called Cryptosporidium.Missing: 2024 | Show results with:2024
[101]
Plasmodium falciparum Malaria - StatPearls - NCBI Bookshelf - NIH
Severe and fatal malaria is predominantly caused by Plasmodium falciparum. Its management and prognosis depend on the awareness of a possible diagnosis.
[102]
DPDx - Malaria - CDC
The number 1 . Sporozoites infect liver cells The number 2 and mature into schizonts The number 3 , which rupture and release merozoites The number 4 . (Of ...
[103]
[PDF] Global status of Toxoplasma gondii infection - MSPTM
This parasite infects approximately one third of the world's population and is considered one of the most successful human parasites (Peng et al.,. 2011; CDC, ...<|control11|><|separator|>
[104]
Global epidemiology and species/genotype distribution of ...
Non-animal meta-analyses have indicated a global prevalence of Cryptosporidium in humans (Dong et al., 2020) and water reservoirs (Daraei et al., 2021) at 7.6% ...