Endogenous Stages Research Articles

The endogenous development and pathogenicity of Eimeria anseris (Kotlan, 1932) in domestic goslings.

Twenty-one, 25-day-old, artificially reared, coccidia-free goslings (Anser cygnoides var. domestica) were inoculated orally with 0.5 × 104, 1 × 104, or 100 × 104 sporulated oocysts of Eimeria anseris and sacrificed at intervals from 24 to 216h post-inoculation (HPI). Nine uninfected goslings served as negative controls. Parts of the visceral organs from goslings, including the intestines, kidneys, and liver, were fixed, sectioned, and observed microscopically. The results revealed that two generations of meronts occurred in the life cycle of E. anseris. The first generation of meronts developed at 24-96 HPI and the second generation at 90-128 HPI. Each meront contained 4-10 merozoites. Development of gamonts began at 128 HPI and mature oocysts appeared at 168 HPI. Developmental stages presented mainly in the epithelial cells of crypts and lamina propria in the posterior parts of the jejunum and ileum. Parasites localized mostly in the cytoplasm and occasionally in the nuclei of host cells. Histological lesions were pronounced in the jejunum and ileum. Desquamation and necrosis of the epithelium of intestine and crypts, infiltration of inflammatory cells, and hemorrhage and mucosal edema were associated with aggregates of endogenous stages. The infected goslings mainly showed severe diarrhea, depression, anorexia, and emaciation, suggesting that E. anseris is highly pathogenic in goslings.

Redescription and new locality record of Choleoeimeria turcicus from the gallbladder of Hemidactylus turcicus in Egypt, with notes on its endogenous development.

Upton et al. J Protozool 35:24-25, 1988 originally described Eimeria turcicus from the gallbladder of the Mediterranean gecko, Hemidactylus turcicus, in the USA. Shortly after establishing the genus Choleoeimeria, Paperna and Landsberg S Afr J Zool 24:345-355, 1989 transferred E. turcicus to this genus, renaming it as Choleoeimeria turcicus. This paper reports the findings of a survey of coccidian parasites of lizards in Egypt, during which tetrasporocystic oocysts were reported from the gallbladder of H. turcicus. Based on the oocysts' morphological and morphometric characteristics and the same host, it can be deduced for the first time that the present species is conspecific with E. turcicus. In the present study, the gallbladder was the sole site for the endogenous development and no endogenous stages were noticed in the intestine. The endogenous stages induce hypertrophy and displacement of the infected cells from the original biliary epithelium to form a prolonged and branching outgrowth. We therefore followed Paperna and Landsberg S Afr J Zool 24:345-355, 1989 and considered the biliary coccidium recorded in this study to be a member of the genus Choleoeimeria. This represents a new locality record for C. turcicus, which was previously known in the USA and Israel.

A new species of Eimeria Schneider, 1875 (Apicomplexa: Eimeriidae) from Alectoris barbara (Aves: Phasianidae) from the Canary Islands (Spain).

The present study was conducted with the objective of identifying the species of Eimeria present in a cynegetic farm. A new coccidian (Apicomplexa: Eimeriidae) species is described from Barbary partridge, Alectoris barbara, from the Canary Islands. Experimental infections were carried out in order to determine the prepatent period, sporulation time, site of infection, and morphology of endogenous stages. One species is described as new. Eimeria barbarae n. sp. has ellipsoidal oocysts, 20.0 × 14.4 (16-23 × 13-16) μm, with a shape-index (SI) of 1.39. Sporocysts are almond-shaped, 9.0 × 5.4 (6.5-11 × 4.5-6) μm, SI = 1.56. The endogenous development takes place along the intestine. The present study showed that E. barbarae causes severe pathologies in A. barbara chickens, with impact on their health condition. Control strategies needs to be implemented to reduce the loss due to coccidiosis at studied farm.

Ultrastructural effects of acetamizuril on endogenous phases of Eimeria tenella.

To explore the primary stage or site of action of acetamizuril (AZL), a novel triazine anticoccidial compound, the ultrastructural development of Eimeria tenella at different endogenous stages was studied in experimentally infected chickens treated with a single oral dose of 15 mg/kg AZL. As a result of drug action, the differentiations of second-generation schizonts and microgamonts were largely inhibited and merozoites became irregular in shape. Meanwhile, the outer membrane blistering and perinuclear space enlargement were obvious in the second-generation schizonts and microgamonts, which were never observed in the classic triazine anticoccidiosis drug diclazuril-treated E. tenella. The chromatin aggregation, anachromasis, and marginalization were visible in merozoites and microgamonts. Furthermore, the abnormal evagination of microgametes finally resulted in the degeneration of microgamonts and the failure of subsequent fertilization. The most marked micromorphological alteration occurring in the macrogamonts was the WFB2. Even if the fertilization occurred, the formation of oocyst wall became malformed and the zygote proceeded to the obvious degeneration. In addition, mitochondria swelling and cytoplasm vacuolization were discerned in respective intracellular stages, while endoplasmic reticulum and Golgi body swelling was less seen. These alterations may be the causes leading to the final death of E. tenella and also provide some information for further exploring the mechanism of action of AZL at the molecular level.

Reclassification of Eimeria pogonae Walden (2009) as Choleoeimeria pogonae comb. nov. (Apicomplexa: Eimeriidae).

The presented paper provides a reclassification of Eimeria pogonae from Pogona vitticeps into the correct genus Choleoeimeria. A description of exogenous and endogenous stages of biliary coccidium is given. Sporulation of the oocysts was endogenous. The mature oocysts contained four sporocysts each with two sporozoites. Oocysts were ellipsoidal in shape, with average length/width ratio 1.7 and measured 28.4 (SD1.5) × 16.8 (SD 1.5). The micropyle, residuum, and polar granules were absent from the sporulated oocysts. Ovoidal in shape, sporosysts without Steida bodies contained residuum and two elongated and boat-shaped sporozoites. The endogenous stages of the coccidia were located mainly in the epithelium of bile ducts; however, single-epithelium cells of the gallbladder were also infected.

Life cycle of Eimeria rhinopomi sp. nov. (Apicomplexa Eimeriidae) infecting lesser mouse-tailed bat, Rhinopoma hardwickii Gray, 1831 (Chiroptera Rhinopomatidae) in Egypt.

Developmental stages of the life cycle of E. rhinopomi sp. nov. were described for the first time from the lesser mouse-tailed bat, Rhinopoma hardwickii in Egypt. 152 bats were collected from October 2012 to December 2014 and examined for the presence of coccidian parasites. The infection rate was 26.32%. The collected unsporulated oocysts from the naturally infected bats were allowed to sporulate in 2.5% potassium dichromate solution. Events of sporulation and sporulation time were described. The sporulated oocysts were subspherical to ovoid measuring 29.1-36.2 x 27.3-30.2 μm and limited by a smooth double-layered wall; no micropyle but a polar granule and oocyst residuum were observed. The sporocyst measured 8.6-9.1 x 6.4-7.3 μm with a sporocyst residuum; Stieda and substieda bodies were also observed. Experimental inoculation of sporulated oocysts was carried out and the developmental endogenous stages (merogony and gamogony) were followed up and described. The prepatent period was 4 days while the patent period was 10-12 days. Endogenous stages took place in the lamina propria and epithelial cells of the upper third of the small intestine of the experimentally infected bats. Merogony occurred at 25-60 h p.i. and only one generation was observed. The mature meronts measured 10.3 x 6.2μm and yielded up to 50 merozoites. Gamogony occurred at 72-96 h p.i. The mature microgamonts measured 8.2 x 6 μm and contained up to 30 small nuclei while the mature macrogamonts measured 11.3 x 10.2 μm and contained 2 types of wall-forming bodies (types I&II). At 90-96 h p.i., newly-formed zygotes or young oocysts were observed

LIFE CYCLE OF ISOSPORA PARDALI SP. NOV. (APICOMPLEXA: EIMERIIDAE) INFECTING THE LEOPARD FRINGE-FINGERED LIZARD, ACANTHODACTYLUS PARDALIS LICHTENSTEIN, 1823 (REPTILIA: LACERTIDAE) IN EGYPT

In the present study, the developmental stages of the life cycle of Isospora pardali sp. nov. were described for the first time from the leopard fringe-fingered lizard, Acanthodactylus pardalis in Egypt. Exactly 135 lizards were collected from South Sinai from October 2012 to December 2014 and examined for the presence of coccidian parasites. Oocysts were shed unsporulated, in early stages of sporulation and rarely sporulated. Events of sporulation and sporulation time were described for unsporulated oocysts. The infection rate was 37%. The sporulated oocysts were subspherical to ovoid measuring 22.6-26.8 x 22.3-24.6 μm and limited by a smooth double-layered wall; no micropyle, polar granule or oocyst residuum was observed. The sporocyst measured 10.6-14.4 x 8.6-9.6 μm with a sporocyst residuum; stieda and substieda bodies were observed. Experimental inoculation of sporulated oocysts was carried out and the developmental endogenous stages (merogony and gamogony) were followed up and described. The prepatent period was 4 days, while the patent period was 8-10 days. Endogenous stages took place in the lamina propria, enterocytes of small intestine and the liver of the experimentally infected lizards. Merogony occurred at 25-60 hours post inoculation and two generations were observed. The mature meronts measured 5.9-12.8x 3.8-12 μm and yielded up to 30 merozoites. Gamogony occurred at 72-96 hours post inoculation. The mature microgamonts measured 7.1-10.1 x 6.3-6.5 μm and contained up to 30 small nuclei, while the mature macrogamonts measured 12.2-18.8 x 12-12.6 μm and contained the two types of wall-forming bodies. At 90-96 hours post inoculation, newly-formed zygotes or young oocysts were observed.

Coccidia of gallinaceous meat birds in Brazil.

Coccidiosis is a disease that limits the production and marketing of gallinaceous birds in North America, especially quails, pheasants and chukar partridges. Virtually no research has been conducted in South America on the causative agents of diseases among these birds, including coccidia. The aim of this work was to make first observations on Eimeria spp. in the chukar partridge Alectoris chukar and the grey quail Coturnix coturnix, which are reared for meat in Brazil. Fecal and tissue samples were collected from commercial farms and were examined for oocysts, gross and microscopic lesions or endogenous stages. From this examination, it was found that partridges raised in Brazil did not have any visible infection. However, grey quails presented mild infection and two Eimeria species that had previously been described in other birds were identified.

A new species of Eimeria Schneider, 1875 (Apicomplexa: Eimeriidae) from the brown anole Anolis sagrei Duméril & Bibron (Sauria: Dactyloidae) in Florida, USA

During July 2014, 14 brown anoles, Anolis sagrei Duméril & Bibron were collected from Orange County, Florida, USA, and their faeces examined for coccidian parasites. One (7%) lizard harboured an eimerian that we describe here as new. Oöcysts of Eimeria garmani n. sp. were ellipsoidal with a uni-layered wall and measured 19.3×12.5µm, with a length/width ratio of 1.5. A micropyle and oöcyst residuum were absent but 1-2 polar granule(s) were present. Sporocysts were subspheroidal, 6.8×6.3µm, with a length/width ratio of 1.1. Stieda, sub-Stieda and para-Stieda bodies were absent. A sporocyst residuum was present as dispersed granules. Endogenous stages were observed within the small intestine. This is the first coccidian reported from the brown anole and the third eimerian reported from anoles in the United States.

Experimental transmission of Cystoisospora felis-like coccidium from bobcat (Lynx rufus) to the domestic cat (Felis catus)

Cystoisospora felis is an ubiquitous coccidian of cats. The domestic cat (Felis catus) is its definitive host and several mammalian and avian species are its optional intermediate/transport hosts. Nothing is known if it is transmissible to wild felids. In the present study C. felis-like oocysts were found in two naturally infected bobcats (Lynx rufus) from Pennsylvania. To study transmission of C. felis-like parasite from bobcats to domestic cats, sporulated oocysts of C. felis-like from one bobcat were orally inoculated into interferon gamma gene knockout (KO) mice, and 56 days later tissues of KO mice were fed to two coccidian-free cats; two littermate cats were uninoculated controls. The inoculated cats and controls were euthanized five and seven days later, and their small intestines were studied histologically. One inoculated cat excreted C. felis-like oocysts seven days post inoculation (p.i.) and was immediately euthanized. Mature schizonts, mature male and female gamonts, and unsporulated oocysts were found in the lamina propria of small intestine; these stages were morphologically similar to C. felis of domestic cats. No parasites were seen in histological sections of small intestines of the remaining three cats. The experiment was terminated at seven days p.i. (minimum prepatent period for C. felis) to minimize spread of this highly infectious parasite to other cats. Although oocysts of the parasite in bobcats were morphologically similar to C. felis of domestic cats, the endogenous stages differed in their location of development. The bobcat derived parasite was located in the lamina propria of ileum whereas all endogenous stages of C. felis of domestic cats are always located in enterocytes of intestinal epithelium. Characterization of DNA isolated from C. felis-like oocysts from the donor bobcat revealed that sequences of the ITS1 region was only 87% similar to the ITS1 region of C. felis from domestic cats. These results indicate that the parasite in bobcat is likely different than C. felis of cats.

Endogenous Life Cycle of Eimeria marmosopos (Apicomplexa: Eimeriidae) from the Opossum, Didelphis marsupialis (Didelphimorphia: Didelphidae) in Costa Rica.

The endogenous life cycle of Eimeria marmosopos was studied in experimentally infected young opossums, Didelphis marsupialis . All the endogenous stages were located in the epithelial cells of villi in the small intestine. Giemsa-stained mucosal scrapings and histological sections were studied for the diagnosis of all the life cycle stages. Eimeria marmosopos has 3 generations of meronts (M) that differ by size, shape, and number of merozoites (m), which also differ in their size, shape, and location of their nuclei within the cytoplasm of the meronts. The 3 meront types, M(1)-M(3), respectively, had 8-15 (m(1)), 4-9 (m(2)), and 22-30 (m(3)) merozoites. Macrogametocytes and microgametocytes, as well as macrogametes and microgametes, completed the sexual cycle, finishing with the formation of unsporulated oocysts. This parasite's endogenous development produced severe intestinal lesions in experimentally infected opossums. There are 56 Eimeria species known from all marsupials worldwide, but this is the first complete life cycle in which both the asexual and sexual stages have been documented.

A new species of Isospora Schneider, 1881 (Apicomplexa: Eimeriidae) infecting the intestine of the Mediterranean house gecko Hemidactylus turcicus Linnaeus (Reptilia: Gekkonidae).

A new species of Isospora Schneider, 1881 was discovered in the Mediterranean house gecko, Hemidactylus turcicus (Linnaeus) in Saudi Arabia. Both exogenous (sporulated oöcysts) and endogenous developmental stages (meronts, gamonts) were studied and measured. Sporulated oöcysts are spheroidal to slightly subspheroidal, 17-22 (18)µm wide, with a smooth, bi-layered oöcyst wall; micropyle, polar granule and oöcyst residuum are all absent. Sporocysts are ovoidal, 9-11×6-8 (10×7)µm, with both Stieda and sub-Stieda bodies, a dispersed granular sporocyst residuum, and four sporozoites. Endogenous stages develop extranuclearly in the cytoplasm of epithelial cells of the small intestine. Early uninucleate meronts are spheroidal, c.3-5 (4)µm wide. Multinucleated meronts are subspheroidal, 11-15×9-12 (13×10)µm, but mature meront and merozoites were not seen. Mature microgamonts, with up to 60 microgametes, are spheroidal, 11-15 (13)µm; macrogamonts are subspheroidal, with a prominent central nucleus, and measured 11-14×7-10 (12×8)µm.

Electron microscopic study of the developmental stages of Eimeria intestinalis cheissin, 1948 in domestic rabbit. (Oryctolagus Cuniculus) with reference to endodyogeny.

The endogenous stages in Eimeria intestinalis were studied in experimentally infected coccidia-free rabbits by transmission electron microscopy. Four asexual generations were ob- served.Two types of merozoites were reported. Binucleated merozoites possess all the characteristics of apical complex indicating asexual reproduction by endodyogeny. While the second type, the mononuclear merozoites have one central nucleus. Gamonts were developed mainly from the third generation merozoites where the mature gamonts were recorded together with the fourth generation schizonts. Macro- and microgametogenesis were clearly observed. Development of microgametes and its fine structural characteristics were detected. Mature macrogametes with central large nucleus and the appearance of two types of wall forming body (I, II) were observed. Many reserve food materials including amylopectin granules and lipids droplets were very characteristic. Control experimentally infected rabbits shed unsporulated oocysts on the day eight p.i.

Identification and characterization of a cathepsin-L-like peptidase in Eimeria tenella.

Avian coccidiosis, caused by Eimeria spp., is one of the major parasitic diseases in birds. Cysteine protease is a major virulence factor in parasitic protozoa, and it may be a suitable chemotherapeutic target and vaccine candidate molecule. A 100 amino acid (aa.) partial sequence of cathepsin L, which is a cysteine protease, was reported by Katrib et al. (Ac. No. CDJ41293) (2012). A 219 aa. sequence was reported by Reid et al. (Ac. No. AFV92863) (2013). However, the open reading frame (ORF) was not reported. In this study, a full sequence of a cathepsin-L-like peptidase in Eimeria tenella (EtcatL) was obtained and its biochemical characterizations and expression profiles were analyzed across different stages of the parasite's life cycle. Results showed that the EtcatL gene encodes a protein 470 aa. in length, with 47 and 49% identity to Toxoplasma gondii and Eimeria acervulina. Considering the close phylogenetic relationship, TgcatL (PDB. ID 3F75) was selected for use as a template for homology modeling with quality factors of 90.9. Gelatin SDS-PAGE showed it to exert protease activity at ≈38 and ≈26 kDa. Further analysis showed the kinetic parameters of the recombinant peptidase to be K m = 8.9 μM and V max = 5.7 RFU/s μM at pH 5.5 containing 10 mM dithiothreitol (DTT) in the reaction matrix, and the IC50 value of E64 was 65.32 ± 3.02 nM. The recombinant protein was active from 25 to 50 °C, with optimal activity at 42 °C. The RT-PCR and Western blot results showed it to be expressed mainly at the endogenous stages and the initial phase of the sporulation. The protective experiment showed that chickens immunized with 100 and 200 μg rEtcatL had reduction of weight loss values 48.7 and 57.9% those of infected controls, respectively. Their reduction of lesion scores (RLS) were 25.0 and 47.2% that of control chickens, and relative oocyst production (ROP) was 39.6 and 15.5% that of control chickens. These results indicate that the EtcatL can be used as an effective immunogen, and further studies are needed to enhance its potential as a vaccine candidate molecule.

Effects of different inoculation routes on the parasitic sites of Cryptosporidium baileyi infection in chickens

Cryptosporidiosis is prevalent in domesticated, caged, and wild birds. Cryptosporidium baileyi, an ascendant species of avian Cryptosporidium, is an important pathogen. It causes respiratory disease in chickens, especially chickens younger than 50days. In this study, SEM, histological, semi-quantitative PCR, and nested PCR techniques were used to explore the impact of different inoculation routes on sites of C. baileyi infection in chickens. Results showed that inoculation with sporozoites or oocysts via the rectum was an effective means of causing infection. This may provide an important reference for the development of the transfection system of C. baileyi in chickens. Numerous endogenous stages of C. baileyi were observed in the bursas of Fabricius (BF) and cloacas of chickens inoculated with sporozoites or oocysts via the rectum, but no parasite was seen in the tracheas of any of these chickens. In chickens infected with oocysts via the crop, the number of parasites in the BF was approximately 23-fold more than in the trachea. All blood samples collected after inoculation were negative for C. baileyi. These data show that C. baileyi was not transferred by blood circulation between the BF and respiratory tract. Different routes of inoculation were here found to distinctly affect sites of parasitism in chickens. These findings may facilitate further understanding of the biology of C. baileyi and efforts to control avian cryptosporidiosis.

Ultrastructural aspects of Cystoisospora belli (syn. Isospora belli) in continuous cell lines.

Cystoisospora belli is an opportunistic protozoan that causes human cystoisosporiasis, an infection characterized by diarrhea, steatorrhea, abdominal pain, fever, and weight loss. The lack of animal models susceptible to C. belli, and the difficulty in obtaining clinical samples with fair amounts of oocysts have limited the research pertaining to the basic biology of this parasite. This study aimed to describe the ultrastructure of endogenous stages of C. belli in Monkey Rhesus Kidney Cells (MK2) and Human Ileocecal Adenocarcinoma cells (HCT-8). Zoites of C. belli exhibited typical morphological features of coccidia, which included a trilaminar pellicle, an apical complex formed by a conoid, polar rings, rhoptries, and micronemes, in addition to dense granules and the endoplasmic reticulum. No crystalloid body was observed but various lipid and amylopectin granules were usually present in the cytoplasm of zoites. We observed a tendency of the endoplasmic reticulum of the host cell to be located near the parasitophorous vacuole membrane. Merozoites were formed by endodyogeny and during replication, the apical complex of the mother cell remained intact. The formation of gametes or oocysts was not observed. The ultrastructural findings of C. belli are further evidence of its proximity to Sarcocystidae family members and corroborate their reclassification as Cystoisospora spp.

Eimeria arloingi: Further studies on the development of some endogenous stages

The present study investigated the ultrastructural characteristics of gamogony and oocyst wall formation of Eimeria arloingi in experimentally infected kids. The 18 newborn animals allocated to 3 equal groups. Two of groups, A, B were inoculated with a single dose of 1×103 and 1×105 sporulated oocysts of E. arloingi, respectively. At 7, 14, 21, 28, 35, and 42days postinoculation (DPI), 1 kid from each group was necropsied for ultrastructural studies. Transmission electron microscopy was used to screen for the presence of developmental stages of the parasite. All stages of microgametocyte and macrogametocyte developments and also oocyst wall formation were observed from 7 to 42DPI. Different stages of schizigony accompanied by marked proliferation of endoplasmic reticulum, mitochondria and several granular dividing nuclei were diagnosed in the affected epithelial cells. Young microgamonts were recognizable by an electron lucent parasitophorous vacuole and several dividing nuclei with prominent nucleolar and peripheral chromatin in the cytoplasm. At a later stage, the nuclei began to elongate and a single mitochondrion and two basal bodies were observed in close proximity nucleus. These bodies eventually protruded from the surface of the gametocyte and formed two flagellar structures. Up to 80–120 microgametes were produced per microgamont. Macrogamonts were recognized by the presence of wall-forming bodies of types 1 and 2. Electron lucent WFB2 appeared earlier than the electron denser WFB1 during the process of macrogametogenesis. The outer layer of the oocyst wall was formed by the release of the contents of WFB1 at the surface to form an electron dense layer. The WFB2 appeared, subsequently, to give rise to the electron lucent inner layer. WFB1 plays a major role in oocyst wall formation.

Histopathological and histochemical studies on naturally occurring coccidial infections in caprines of Marathwada region

The histopathological and histochemical studies of intestines of goats affected with various species of Eimeria were conducted. Goats revealed acute to chronic enteritis evidenced by minimal to mild desquamation, disruption and exfoliation of glandular epithelial cells with bluntness of villi, exudation at the tip of villus, mild to moderate infiltration of polymorphonuclear cells, plasma cells, eosinophills and macrophages. In addition, there was hypertrophy and hyperplasia of epithelium of villi with goblet cell hyperplasia. The mature macrogamete contained a large number of eosinophilic granules, whereas, the microgametes showed presence of whorls formed by granules within them. The tissue sections stained with PAS revealed moderate positivity for presence of glycogen specially within the epithelial cells of villi wherein the schizont lodgement was marked. The tissue sections exposed to PAS Alcian blue staining revealed mild to intense positive reaction for mucin specially at the places in villus having the lodgment of gametocytes, whereas, the reaction at other portion of small intestines without invasion of endogenous stages, appeared to be comparatively less positive.

A New Species ofIsospora(Apicomplexa: Eimeriidae) Infecting the Baiuch Rock Gecko,Bunopus tuberculatus, in Saudi Arabia

Isospora bors n. sp. (Apicomplexa: Eimeriidae) is described from 6 of 30 (20%) Baiuch rock gecko Bunopus tuberculatus Blanford in Saudi Arabia. Sporulated oocysts are subspheroidal to spheroidal, 18 × 16 (17-20 × 15-17) μm, with a bilayered, smooth, yellow-orange wall, without striae or micropyle. Polar body and oocyst residuum, both absent. Sporocysts are ovoidal, 10 × 7 (9-11 × 6-9) μm, with a Stieda body and sporocyst residuum. Endogenous stages developed in the cytoplasm of epithelial cells of the small intestine and above the host cell nucleus.

Evolutionary Plasticity in Coccidia – Striking Morphological Similarity of Unrelated Coccidia (Apicomplexa) from Related Hosts: Eimeria spp. from African and Asian Pangolins (Mammalia: Pholidota)

Two morphologically similar, but phylogenetically unrelated Eimeria species from ancient mammals, African Tree Pangolin Phataginus tricuspis and Sunda Pangolin Manis javanica (Pholidota: Manidae), from two distant biogeographic realms (Afrotropical and Oriental), are characterized and compared morphologically and molecularly. Phylogenetic analyses produced an unstable topology. However, while precise position of the two Eimeria species from pangolins could not be firmly established due to the lack of related taxa, it is evident that they are not closely related and do not fall into any of the so far recognized eimerian lineages. Moreover, an eimerian found in P. tricuspis is described as a new species Eimeria nkaka n. sp., based on morphology of oocysts, endogenous developmental stages and sequence data.