ABSTRACT
Understanding the normal physiology of the body is the key to study the changes that occur due to any infection. It is known that enteric infections play a considerable role in affecting normal body status. Thus, this study was designed for investigating the enteric infections in Arabian camels in Al-Muthanna Province. In this investigation, 588 fecal and blood serum samples (for diarrheic camels only) were collected from the camels in different areas of Al-Muthanna Province, Iraq from both sexes of different ages during the period from October 2020 up to the end of August 2021. The samples were examined using routine microscopic examination techniques, hematological techniques, and ELISA for parasitic and viral identification. Eimeria rajasthani, Isospora orlovi were recorded for the first time in Iraqi camels with clinical signs of diarrhea, dehydration, and emaciation. The study recorded four types of protozoa: Eimeria spp., Isospora, Cryptosporidium and Balantidium coli. The recorded types of Eimeria were E. dromedarii, E. cameli, and E. rajasthani. There was a significant effect of age on infection rates with Eimeria spp. as the highest Eimeria ratio was in ages of less than two years animals. The infection rates were also affected with months which reached the highest ratios of Eimeria in October while the lowest ratio of Eimeria was recorded in July. BVDV infection rate was found in camels that suffered from diarrhea. There is no significant effect of sex on the onset of the viral disease in camels. For hematological parameters, there were significant differences in RBCs, WBCs, Hb, and PCV values in protozoal and BVDV infections. In conclusion, different kinds of protozoal and viral infections were recorded. Some of the recorded infections were associated with acute clinical signs and have zoonotic importance.
Subject(s)
Camelus , Coccidiosis , Diarrhea , Eimeria , Feces , Animals , Camelus/parasitology , Feces/parasitology , Feces/virology , Iraq/epidemiology , Male , Female , Diarrhea/veterinary , Diarrhea/epidemiology , Diarrhea/parasitology , Diarrhea/virology , Coccidiosis/veterinary , Coccidiosis/epidemiology , Coccidiosis/parasitology , Eimeria/isolation & purification , Isospora/isolation & purification , Balantidium/isolation & purification , Cryptosporidium/isolation & purification , Isosporiasis/veterinary , Isosporiasis/epidemiology , Isosporiasis/parasitology , Cryptosporidiosis/epidemiologyABSTRACT
Pathogens have traditionally been studied in isolation within host systems; yet in natural settings they frequently coexist. This raises questions about the dynamics of co-infections and how host life-history traits might predict co-infection versus single infection. To address these questions, we investigated the presence of two parasites, a gut parasite (Isospora coccidians) and a blood parasite (Plasmodium spp.), in House Finches (Haemorhous mexicanus), a common passerine bird in North America. We then correlated these parasitic infections with various health and condition metrics, including hematological parameters, plasma carotenoids, lipid-soluble vitamins, blood glucose concentration, body condition, and prior disease history. Our study, based on 48 birds captured in Tempe, Arizona, US, in October 2021, revealed that co-infected birds exhibited elevated circulating lutein levels and a higher heterophil:lymphocyte ratio (H/L ratio) compared to those solely infected with coccidia Isospora spp. This suggests that co-infected birds experience heightened stress and may use lutein to bolster immunity against both pathogens, and that there are potentially toxic effects of lutein in co-infected birds compared to those infected solely with coccidia Isospora sp. Our findings underscore the synergistic impact of coparasitism, emphasizing the need for more co-infection studies to enhance our understanding of disease dynamics in nature, as well as its implications for wildlife health and conservation efforts.
Subject(s)
Bird Diseases , Coccidiosis , Coinfection , Finches , Isospora , Malaria, Avian , Plasmodium , Animals , Finches/parasitology , Coinfection/veterinary , Coinfection/parasitology , Coinfection/epidemiology , Malaria, Avian/epidemiology , Malaria, Avian/parasitology , Malaria, Avian/blood , Bird Diseases/parasitology , Bird Diseases/epidemiology , Bird Diseases/blood , Isospora/isolation & purification , Coccidiosis/veterinary , Coccidiosis/epidemiology , Coccidiosis/parasitology , Plasmodium/isolation & purification , Isosporiasis/veterinary , Isosporiasis/epidemiology , Isosporiasis/parasitology , Arizona/epidemiology , Male , FemaleABSTRACT
Systemic isosporosis, previously atoxoplasmosis, is a significant cause of mortality in juvenile passerine birds. Recommended treatment regimens are empiric and vary in efficacy. The goal of this study was to determine the pharmacokinetics and pharmacodynamics of ponazuril for treatment of systemic isosporosis. Ponazuril, diluted with water to create an oral suspension (50 mg/ml), was administered (100 mg/kg) to 72 European starlings (Sturnus vulgaris) by a single dose via direct oral gavage (n = 24), a single dose injected into superworm larvae (Zophobas morio; n = 24), or a daily dose mixed with commercial dog food to top-dress feed for 5 d (n = 24). Peak plasma concentrations were 5.84, 2.46, and 9.13 µg/ml for the direct gavage, injected larvae, and top-dressed feed groups, respectively. With repeated dosing, mean plasma concentrations from the top-dressed feed group were maintained between 8.12 to 13.11 µg/ml. Results suggested ponazuril at a dosage of 100 mg/kg administered via direct gavage or top-dressed feed, but not via injected larvae, would exceed the concentrations needed to inhibit merogony of other apicomplexan parasites in cell culture (5 µg/ml). To assess the pharmacodynamics of this dose, seven passerine birds, red-vented bulbuls (Pycnonotus cafer; n = 2), blue-grey tanager (Thraupis episcopus; n = 1), and red-capped cardinals (Paroaria gularis; n = 4), were identified as shedders of systemic Isospora spp. via fecal qPCR. Birds were then treated with ponazuril (100 mg/kg) daily on top-dressed feed for 14 d. Fecal shedding was assessed via qPCR for 6 wk from the initiation of treatment. Treatment was associated with reduction in proportions of fecal shedding during the treatment period and the week following treatment, but shedding resumed in all birds by the end of sampling. Results support that treatment of breeding birds with 100 mg/kg ponazuril could reduce the shedding of active oocysts and decrease risk of clinical infection in susceptible juveniles.
Subject(s)
Dog Diseases , Isospora , Isosporiasis , Passeriformes , Animals , Dogs , Isosporiasis/parasitology , Isosporiasis/veterinary , TriazinesABSTRACT
Twenty-one white-rumped shamas (19 necropsied, 2 biopsied) (Copsychus malabaricus) housed at the San Diego Zoo between 1992 and 2020 were diagnosed with Isospora infection based on evaluation of histologic sections. Review of these cases revealed a consistent histologic lesion characterized by nodular aggregates of atypical epithelioid macrophages containing few intracytoplasmic protozoa, with or without lymphocytic infiltrates. Of the 19 necropsied cases, 16 (84%) had systemic lesions variably affecting the liver, spleen, gastrointestinal tract, lung, pancreas, connective tissues, or bone marrow, while all 21 diagnosed cases had skin involvement. The findings suggest that white-rumped shamas have a unique inflammatory response to isosporosis with a predilection for the skin. Skin may be a diagnostically sensitive sampling site for histologic diagnosis of Isospora in this species.
Subject(s)
Bird Diseases , Isospora , Isosporiasis , Passeriformes , Animals , Bird Diseases/pathology , Isosporiasis/parasitology , Isosporiasis/pathology , Isosporiasis/veterinary , Passeriformes/parasitology , Spleen/pathologyABSTRACT
PURPOSE: Members of the genus Isospora commonly infect a wide variety of wild birds. By combining morphometric and genetic data, we are able to differentiate and describe a new apicomplexan parasite, Isospora picoflavae n. sp., from the Northern Yellow-shafted Flicker (Colaptes auratus luteus) in Ontario, Canada. METHODS: Unsporulated oocysts were observed in intestinal contents obtained during necropsy; these oocysts completed exogenous sporulation within 7 days at room temperature. Complete nuclear 18S rDNA and complete mitochondrial genome sequences were obtained from this previously undescribed Isospora sp. to compare with related coccidia. RESULTS: Sporulated oocysts were subspherical in shape measuring an average of 22.7 × 21.7 µm (n = 53; mean shape index 1.05) containing a near-spherical polar granule. Sporocysts were ovoidal to ellipsoidal in shape, measuring an average size of 17.0 × 10.5 µm (n = 9; mean shape index 1.62). Sporocyst residuum was concentrated in an irregular, spherical mass in the middle of each sporocyst. The isolated oocysts differed morphologically from other Isospora species reported to infect members of the family Picidae. Based on phylogenetic analyses using either combined nuclear 18S rDNA and mitochondrial cytochrome c oxidase I (COI) sequences or complete mitochondrial genome sequences, this Isospora sp. n. isolated from the Northern Flicker grouped within a clade containing Isospora species described from various passeriform hosts. CONCLUSION: Based on combined morphological and molecular data, the oocysts found in the gastrointestinal contents of Colaptes auratus luteus represent a new species of Isospora named herein as Isospora picoflavae n. sp.
Subject(s)
Bird Diseases , Isospora , Isosporiasis , Passeriformes , Animals , Bird Diseases/parasitology , DNA, Ribosomal/genetics , Electron Transport Complex IV/genetics , Feces/parasitology , Isosporiasis/parasitology , Ontario , Oocysts , Passeriformes/parasitology , Phylogeny , RNA, Ribosomal, 18S/genetics , RNA, Ribosomal, 28S/geneticsABSTRACT
Cystoisospora belli (C. belli) is an opportunistic coccidian parasite. This case is the first reported C. belli infection associated with AIDS in China. C. belli infection of this case was diagnosed with the presence of oocysts using direct wet mount and Ziehl-Neelsen acid-fast stain method, and confirmed by polymerase chain reaction (PCR) and Sanger sequencing, ruling out the result of metagenomic next-generation sequencing (mNGS). This case demonstrates that C. belli infection in AIDS could be a potential risk factor for persistent diarrhea, and should not be neglected in non-endemic area and emphaise the necessity of accurate mNGS databases.
Subject(s)
Acquired Immunodeficiency Syndrome , Isosporiasis , Acquired Immunodeficiency Syndrome/complications , High-Throughput Nucleotide Sequencing , Humans , Isosporiasis/complications , Isosporiasis/diagnosis , Isosporiasis/parasitology , Metagenomics , Polymerase Chain ReactionABSTRACT
Diarrhea in an immunocompromised patient has a broad infectious differential. Diagnosis is difficult despite advances in diagnostic modalities. We report a case of a 45-year-old Nigerian woman who immigrated to the United States 2 years ago. She presented to the hospital with gastrointestinal bleeding, newly diagnosed HIV, and disseminated Kaposi sarcoma. During hospitalization, the patient had an onset of watery diarrhea and high eosinophilia. Subsequent stool analysis using multi-parallel real-time quantitative polymerase chain reaction for 13 parasites was positive for Cystoisospora belli. The patient was treated with trimethoprim-sulfamethoxazole, but had relapsed disease when her antibiotics were stopped prematurely. After restarting trimethoprim-sulfamethoxazole, her diarrhea and eosinophilia improved, and she had undetectable Cystoisospora belli DNA on repeat stool quantitative polymerase chain reaction. This case highlights the importance of a thorough workup for diarrhea, including parasites, especially for immunocompromised patients. Antibiotic prophylaxis is recommended in patients with Cystoisospora belli and HIV/AIDS.
Subject(s)
Diarrhea/diagnosis , Eosinophilia/diagnosis , Gastrointestinal Hemorrhage/diagnosis , HIV Infections/diagnosis , Immunocompromised Host , Isosporiasis/diagnosis , Sarcoma, Kaposi/diagnosis , Anti-Infective Agents/therapeutic use , Diarrhea/drug therapy , Diarrhea/immunology , Diarrhea/parasitology , Eosinophilia/drug therapy , Eosinophilia/immunology , Eosinophilia/parasitology , Female , Gastrointestinal Hemorrhage/drug therapy , Gastrointestinal Hemorrhage/immunology , Gastrointestinal Hemorrhage/parasitology , HIV Infections/drug therapy , HIV Infections/immunology , HIV Infections/parasitology , Humans , Isospora/immunology , Isosporiasis/drug therapy , Isosporiasis/immunology , Isosporiasis/parasitology , Middle Aged , Sarcoma, Kaposi/drug therapy , Sarcoma, Kaposi/immunology , Sarcoma, Kaposi/parasitology , Treatment Outcome , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic useABSTRACT
An Isospora species, Isospora amphiboluri, originally described by Canon in 1967 and later by McAllister et al. (1995), was isolated from a central netted dragon (Ctenophorus nuchalis) housed at a wildlife rehabilitation centre in Perth, Western Australia. Sporulated oocysts of Isospora amphiboluri (n = 30) are spherical, 24.2 (26.5-23.0) µm in length and 23.9 (22.4-25.9) µm in width, with a shape index of 1.01. The bilayered oocyst wall is smooth and light-yellow in color. Polar granule, oocyst residuum and micropyle are absent. The sporocysts are lemon-shaped, 15.7 (15.2-18.0) × 10.2 (8.9-11.2) µm, with a shape index (length/width) of 1.53. Stieda and substieda bodies are present, the Stieda body being small and hemidome-shaped and the substieda half-moon-shaped. Each sporocyst contains four vermiform sporozoites arranged head to tail. The sporozoites are 11.7 (9.9-16.2) × 3.0 (2.4-3.5) µm, with a shape index (length/width) of 3.87. A sporocyst residuum is present. Sporozoites contain a central nucleus with a finely distributed granular residuum. Comparison of oocyst measurements and their features with other valid Isospora species from hosts in the Agamid family confirmed that this Isospora species is Isospora amphiboluri. Molecular characterization of I. amphiboluri at the 18S rRNA and MTCOI loci showed the highest similarity with I. amphiboluri from the central bearded dragon, 99.8% and 99.7% respectively. This is the first report of I. amphiboluri from a central netted dragon in Australia.
Subject(s)
Host-Parasite Interactions , Isospora/isolation & purification , Isosporiasis/veterinary , Lizards , Animals , Animals, Zoo , Electron Transport Complex IV/analysis , Isospora/classification , Isospora/cytology , Isospora/genetics , Isosporiasis/parasitology , Male , Mitochondrial Proteins/analysis , Oocysts/classification , Oocysts/cytology , Oocysts/isolation & purification , Phylogeny , Protozoan Proteins/analysis , RNA, Protozoan/analysis , RNA, Ribosomal, 18S/analysis , Sporozoites/classification , Sporozoites/cytology , Sporozoites/isolation & purification , Western AustraliaABSTRACT
A new Isospora species is described from New Holland honeyeaters (Phylidonyris novaehollandiae). Sporulated oocysts (n = 25) were characterised as subspheroidal, 29-32 × 28-31 (29.8 × 29.4); length/width (L/W) ratio 1.01-1.02 (1.01). Wall bi-layered, 1.3-1.6 (1.5) thick, outer layer smooth, c.2/3 of total thickness. Micropyle and oocyst residuum absent, but usually two polar granules are present. Sporocysts (n = 25) ovoidal, 18-19 × 12-14 (18.4 × 12.3); L/W ratio 1.42-1.53 (1.50). Stieda body present, flattened, c.0.5 deep × 2.5 wide; sub-Stieda present, rounded, c.2.5 deep × 3.5 wide; para-Stieda body absent; sporocyst residuum present, usually a distinctly irregular body consisting of numerous small granules that appear to be membrane-bound. Sporozoites vermiform, with robust anterior and posterior refractile bodies. Molecular characterization was conducted at the 18S and 28S ribosomal RNA and the mitochondrial (mt) cytochrome oxidase (COI) loci. Phylogenetic analysis of genomic 18S and mt COI sequences indicated that Isospora phylidonyrisae n. sp. was genetically similar to Isospora coronoideae, isolated from an Australian raven (Corvus coronoides) in Western Australia, with a 99.3% and 98.4% homology, respectively. The 28S rRNA sequence was most similar to Isospora anthochaerae (KF766053) and Isospora manorinae (KT224381), both with a 98.2% genetic similarity. Based on morphological and genetic data, this isolate is a new species of Isospora, which is named Isospora phylidonyrisae n. sp. after its host.
Subject(s)
Bird Diseases/epidemiology , Isospora/classification , Isosporiasis/veterinary , Songbirds , Animals , Bird Diseases/parasitology , Isospora/cytology , Isospora/genetics , Isosporiasis/epidemiology , Isosporiasis/parasitology , Phylogeny , Prevalence , Protozoan Proteins/analysis , Western Australia/epidemiologyABSTRACT
Woodcreepers are passerines of the family Dendrocolaptidae, which have a high forest dependency. The current work aimed to redescribe Isospora striata McQuistion et al. 1997, from two new hosts in protected areas in Brazil, revealing new localities of parasitism, in addition to providing preliminary genotypic identifications via sequencing of the mitochondrial cytochrome c oxidase subunit 1 (COI) gene from both host species. Isospora striata has oocysts that are subspheroidal to ovoidal, 19.4 × 16.8 µm with smooth wall. Oocyst residuum is absent, but micropyle and polar granules are present. Sporocysts are ovoidal, 13.6 × 8.3 µm, with both Stieda and sub-Stieda bodies. Sporocyst residuum is present and sporozoites with refractile body, nucleus, and striations. The morphological study and the 100% similarity in sequencing of the COI gene between samples of different dendrocolaptid species confirmed the identification of a single species, supporting the identification of I. striata in the Brazilian Atlantic forest and consequently the wide distribution of this coccidian species in the Neotropical Region.
Subject(s)
Bird Diseases/parasitology , Isospora/physiology , Isosporiasis/veterinary , Passeriformes/parasitology , Animals , Bird Diseases/epidemiology , Brazil/epidemiology , DNA, Protozoan/chemistry , Isospora/classification , Isospora/genetics , Isospora/ultrastructure , Isosporiasis/epidemiology , Isosporiasis/parasitology , Oocysts/cytology , Phylogeny , Prevalence , Sequence Analysis, DNA/veterinary , Sporozoites/cytologyABSTRACT
The summer tanager, Piranga rubra (L., 1758) is a medium-sized songbird formerly belonging to the tanager family Thraupidae but now has been placed within the family Cardinalidae. Nothing is known about the coccidian parasites of this stunningly colorful bird. Feces from 2 P. rubra found dead in McCurtain County, Oklahoma were collected and examined for coccidia; 1 was found to be passing a new species of Isospora. Oocysts of Isospora mccurtainensis n. sp. are subspheroidal to ovoidal with a smooth bilayered wall, measure (length × width [L × W]) 21.7 × 19.5 µm, and have a L/W ratio of 1.1; a micropyle and oocyst residuum were absent but a bilobed and refractile polar granule is present. Sporocysts are ellipsoidal and measure 13.9 × 8.6 µm, L/W 1.6; a knoblike Stieda body is present as well as a distinct sub-Stieda body. The sporocyst residuum is composed of a granular compact cluster with a dense, irregular mass of granules lying between and dispersed among the sporozoites. This is the first coccidian reported from P. rubra and, most important, only the first known from the Cardinalidae in the mainland of the United States.
Subject(s)
Bird Diseases/parasitology , Isospora/classification , Isosporiasis/veterinary , Songbirds/parasitology , Animals , Feces/parasitology , Female , Isospora/isolation & purification , Isosporiasis/parasitology , Male , Microscopy, Interference/veterinary , Oklahoma , Oocysts/isolation & purification , Oocysts/ultrastructureABSTRACT
A new coccidian species, Isospora lugensae n. sp., was described from a single Kerguelen petrel (Lugensa brevirostris). Sporulated oocysts (n = 25) were characterized as subspheroidal to ellipsoidal measuring 24-25 µm × 21-23 µm (24.8 × 22.2 µm) in length/width (L/W), respectively, with a ratio of 1.07-1.14 µm (1.12). They contained a bi-layered wall with a thickness of 0.8-1.2 µm (1.0) and the outer layer smooth, with c.2/3 of total thickness. The oocyst contained two polar granules with both micropyle and oocyst residuum absent. Ovoidal sporocysts (n = 25) measured 15-16 µm × 10-11 µm (15.7 × 10.8 µm) in L/W, with a ratio of 1.41-1.49 µm (1.46). A flattened to knob-like Stieda body was present (c.0.5 µm deep × 2.5 µm wide) as well as a rounded to trapezoidal sub-Stieda (c.1.5 µm deep × 3.0 µm wide); however, no para-Stieda body was detected. The sporocyst residuum was composed of scattered spherules of different sizes, while vermiform sporozoites contained a refractile body, nucleus and visible striations. Analysis of the full-length mitochrondrial (mtDNA) genome revealed 3 protein-coding genes, (CytB, COI and COIII), 18 LSU and 14 small subunit (SSU) rDNA fragments, without transfer RNA genes with a total length of 6257 bp. Phylogenetic analysis of genomic SSU ribosomal sequences indicated that Isospora lugensae n. sp. is genetically similar to Eimeria reichenowi, isolated from a red-crowned crane (Grus japonensis) from Japan, with a 96.6% homology. The mtDNA sequence is most similar to Isospora serinuse with a 95.8% genetic similarity. Based on morphological and molecular data, this isolate is a new species of coccidian parasite that to date has only been found in a Kerguelen petrel.
Subject(s)
Bird Diseases/parasitology , Isospora/classification , Isosporiasis/veterinary , Animals , Birds , DNA, Mitochondrial/chemistry , DNA, Protozoan/chemistry , Eimeria/classification , Feces/parasitology , Gastrointestinal Tract/parasitology , Isospora/genetics , Isospora/ultrastructure , Isosporiasis/parasitology , Japan , Oocysts/ultrastructure , Phylogeny , Sporozoites , Western AustraliaABSTRACT
From a longitudinal survey conducted on 30 Danish mink farms in 2016, 11.0% of faecal samples (456/4140) were positive for Cystoisospora laidlawi oocysts by microscopy, with 60% (189/315) of mink being positive at least once during the study period. Morphological analysis of sporulated oocysts identified Cystoisospora oocysts measuring 34.3 × 29.5 µm with an oocyst length/width (L/W) ratio of 1.2. The morphological features of the oocysts were identical to Isospora laidlawi previously morphological identified in farmed mink from Denmark and elsewhere. Phylogenetic analysis of 18S rDNA sequences (1221 bp) from three positive mink indicated that Cystoisospora from mink shared the highest genetic similarity to C. canis from a Canadian dog (99.6%). The phylogenetic analysis placed Cystoisospora from mink in a clade with other Cystoisospora isolates.
Subject(s)
Isospora/isolation & purification , Isosporiasis/veterinary , Mink/parasitology , Protozoan Infections, Animal/parasitology , Animals , DNA, Protozoan/genetics , Denmark/epidemiology , Farms , Feces/parasitology , Isospora/classification , Isospora/cytology , Isospora/genetics , Isosporiasis/parasitology , Oocysts/classification , Oocysts/cytology , Oocysts/genetics , Oocysts/isolation & purification , Phylogeny , RNA, Ribosomal, 18S/geneticsABSTRACT
Systemic isosporosis (formerly atoxoplasmosis), is a protozoal infection that causes death in nestling and fledgling passerine birds impacting ex situ breeding and reintroduction programs. Because current antemortem diagnostic tests lack sensitivity, a qPCR was developed for detection of Isospora spp. using primers and a fluorescent-tagged MGB probe targeting the large subunit (28s) ribosomal RNA gene (assay efficiency = >100%; sensitivity = <1 dsDNA copy). The assay was used to screen postmortem frozen or formalin-fixed paraffin-embedded tissue samples from passerine birds (n = 24; 12 with confirmed systemic isosporosis), whole blood and feces (n = 38) from live passerines, and other tissues infected with phylogenetically similar protozoa. The qPCR identified Isospora sp. DNA in tissues from 21/24 birds including 12/12 birds with cytologically-histologically confirmed infection (100% sensitivity) and 9/12 birds lacking microscopic organisms. The assay also amplified Eimeria sp. DNA; however, sequence analysis ruled out infection in the passerine cases. Blood and/or feces were positive in 30/38 birds, and in only 7/38 birds, blood and feces both contained Isospora sp. DNA. Finally, the qPCR was utilized to screen 30 consecutive daily fecal samples from live passerines (n = 20) to determine optimal sampling protocols. One or more of the daily fecal samples were positive in all 20 birds. In individual birds, the interval between positive qPCR amplification results ranged from 0 to 23 days, with an average of 5.85 days. Simulated application of 13 potential sample collection schedules was used to identify the sensitivity of repeated testing for identification of infected birds. Increased sampling days resulted in higher sensitivity but increased both cost and animal handling requirements. Based on statistical analysis and clinical considerations, the testing recommendation for detection of fecal shedding was collection and assay of five consecutive daily fecal samples, which had an average diagnostic sensitivity of 0.86.
Subject(s)
Bird Diseases/diagnosis , Isospora/isolation & purification , Isosporiasis/veterinary , Molecular Diagnostic Techniques/veterinary , Real-Time Polymerase Chain Reaction/veterinary , Songbirds , Animals , Bird Diseases/parasitology , Blood/parasitology , Feces/parasitology , Isosporiasis/diagnosis , Isosporiasis/parasitology , Molecular Diagnostic Techniques/methods , Molecular Diagnostic Techniques/standards , Real-Time Polymerase Chain Reaction/methods , Real-Time Polymerase Chain Reaction/standardsABSTRACT
The wood thrush, Hylocichla mustelina, is a North American passerine bird closely related to other thrushes and is widely distributed across North America. Nothing is known of the coccidian parasites of this bird. Feces from a single H. mustelina found dead in McCurtain County, Oklahoma were collected and examined for coccidia; it was found to be passing a new species of Isospora. Oocysts of Isospora gmelini n. sp. are subspheroidal to ellipsoidal with a smooth bilayered wall, measure (length [L] × width [W]) 19.5 × 16.5 µm, and have a L/W ratio of 1.2; a micropyle and oocyst residuum were absent but polar granule(s) are present. Sporocysts are ellipsoidal to elongate and measure 13.4 × 8.9 µm, L/W 1.5; a buttonlike Stieda body is present, but sub-Stieda and para-Stieda bodies are absent. The sporocyst residuum is composed of a compact spheroid with a dense, irregular mass of finer granules lying between and dispersed among the sporozoites. Although several isosporans have been reported from other turdid birds, mainly from Brazil and Costa Rica, this is the initial coccidian reported from H. mustelina and only the second known from the Turdidae in the mainland of the United States.
Subject(s)
Bird Diseases/parasitology , Isospora/isolation & purification , Isosporiasis/veterinary , Songbirds/parasitology , Animals , Feces/parasitology , Isospora/classification , Isospora/ultrastructure , Isosporiasis/parasitology , Male , Microscopy, Interference/veterinary , Oklahoma , Oocysts/ultrastructureSubject(s)
Ileal Diseases/diagnosis , Ileum/pathology , Intestinal Mucosa/pathology , Isospora/isolation & purification , Isosporiasis/diagnosis , Adult , Biopsy , Colonoscopy , Female , Humans , Ileal Diseases/drug therapy , Ileal Diseases/parasitology , Ileal Diseases/pathology , Ileum/diagnostic imaging , Intestinal Mucosa/parasitology , Isosporiasis/drug therapy , Isosporiasis/parasitology , Isosporiasis/pathology , Life Cycle Stages , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic useABSTRACT
In the current work, Isospora massardi Lopes, Berto, Luz, Galvão, Ferreira & Lopes, [10] is identified from white-necked thrushes Turdus albicollis Vieillot, 1818, rufous-bellied thrushes Turdus rufiventris Vieillot, 1818 and from a new host, the yellow-legged thrush Turdus flavipes (Vieillot, 1818) in a new locality, the Itatiaia National Park, in Southeastern Brazil, providing a preliminary genotypic characterization via sequencing of the mitochondrial cytochrome c oxidase subunit 1 (COI) and 18S small subunit ribosomal RNA genes. The oocysts and sporocysts of I. massardi of the current study are morphologically similar to the original description and are uniform in the proportionality of width on length, but exhibited different patterns of size associated with each host species. Furthermore, a genotypic difference of 3% was found in the COI sequences from T. flavipes and T. albicollis. Therefore, an ecological discussion is introduced aimed at associating these morphometric and genotypic differences with an ongoing speciation process.
Subject(s)
Bird Diseases/epidemiology , Isospora/isolation & purification , Isosporiasis/veterinary , Animals , Bird Diseases/parasitology , Brazil/epidemiology , Isospora/cytology , Isospora/genetics , Isosporiasis/epidemiology , Isosporiasis/parasitology , Oocysts/cytology , Oocysts/genetics , Oocysts/isolation & purification , Prevalence , SongbirdsABSTRACT
Using a combination of morphological and molecular data, we describe a new apicomplexan parasite, Isospora svecica sp. n., from the white-spotted bluethroat, Luscinia svecica cyanecula, from the Czech Republic. Oocysts were found in its intestinal tract. Sporulation was exogenous and took 1-3 days. The oocysts were slightly ellipsoidal, of average size 26.17 × 20.33 µm, with a smooth bilayered wall. Micropyle, oocyst residuum, and polar granules were absent. Sporocysts were bottle-shaped, of an average size of 18.82 × 8.82 µm, with a thin, colourless wall. A conspicuous knob-like Stieda body was present. Substieda body was barely visible. Sporocyst residuum was present in the form of granules of various sizes. Sporozoites were banana-shaped and contained large anterior and small posterior refractile bodies. Partial DNA sequences of three genes were obtained from oocysts of Isospora svecica sp. n., being most closely related to other isosporans described from passerines. Little is known about the parasites of the avian family Muscicapidae, including coccidia, a highly prevalent parasitic protist group in all vertebrate classes. Only six species of the genus Isospora have so far been described in Muscicapidae, together with several "Isospora sp." that in fact most likely represent Isospora lacazei. The newly described Isospora svecica sp. n. differs morphologically from other coccidia reported from muscicapid birds, and represents the first coccidian species described from Luscinia svecica.
Subject(s)
Isospora/classification , Isosporiasis/veterinary , Passeriformes/parasitology , Animals , Czech Republic , Genes, Protozoan/genetics , Intestines/parasitology , Isospora/cytology , Isospora/genetics , Isospora/growth & development , Isosporiasis/parasitology , Oocysts/classification , Oocysts/cytology , Oocysts/genetics , Oocysts/growth & development , Sporozoites/classification , Sporozoites/cytology , Sporozoites/genetics , Sporozoites/growth & developmentABSTRACT
A new Isospora (Apicomplexa: Eimeriidae) species is described from an Australian raven (Corvus coronoides) in Western Australia. Sporulated oocysts (n = 21) are ovoid, 21.2 (18.4-23.9) µm in length and 18.8 (16.9-20.6) µm in width, with a shape index of 1.13. The bi-layered oocyst wall is smooth and colourless, 1.2 µm thick. A polar granule and oocyst residuum is present, but the micropyle is absent. The sporocysts are ovoid-shaped, 16.3 (13.7-18.9) × 10.7 (8.4-12.9) µm, with a shape index (length/width) of 1.52. Stieda and substieda bodies are present, the Stieda body being small and hemidome-shaped and the substieda being indistinct. Each sporocyst with four vermiform sporozoites arranged head to tail. The sporozoites are crescent-shaped, 9.0 (8.9-9.2) × 2.7 (2.3-3.0) µm, with a shape index (length/width) of 3.33. The sporocyst residuum is present. The isolated oocysts had different morphological characteristics when compared with all known Isospora spp. The coccidian parasite was analysed at the 18S and 28S ribosomal RNA and the mitochondrial cytochrome oxidase (COI) loci. At the 18S locus, I. coronoideae n. sp. exhibited 98.9% similarity to I. neochmiae from a captive-bred red-browed finch (KT224380) and Isospora sp. from domestic pigeons (Columba livia domestica) (AB757860), 98.5% similarity to I. gryphoni (AF080613) from an American goldfinch and 98.3% similarity to I. manorinae (KT224379) from a yellow-throated miner. At the 28S locus, it exhibited 95.4% and 94.8% similarity to I. manorinae (KT224381) and I. anthochaerae (KF766053), respectively. At the COI locus, it exhibited 99.8% and 99.7% similarity to I. butcherae (KY801687) and I. neochmiae (KT224378), respectively. Based on morphological and molecular data, this isolate is a new species of Isospora, which is named Isospora coronoideae n. sp. after its host, the Australian raven (Corvus coronoides) (Passeriformes: Corvidae) (Linnaeus, 1758).
Subject(s)
Bird Diseases/parasitology , Crows/parasitology , Isospora/isolation & purification , Isosporiasis/veterinary , Animals , Australia , Columbidae/parasitology , Electron Transport Complex IV/genetics , Isospora/classification , Isospora/genetics , Isosporiasis/parasitology , Oocysts/classification , Oocysts/genetics , Oocysts/isolation & purification , Phylogeny , Protozoan Proteins/genetics , RNA, Ribosomal, 18S/genetics , RNA, Ribosomal, 28S/genetics , Western AustraliaABSTRACT
BACKGROUND: The gnateaters Conopophaga spp. are insectivorous passerines commonly observed in high and humid forests, where they remain lodged in thin branches and, sometimes, they fly to the ground to catch insects. The insectivorous feeding habit is related to low prevalence and density of coccidians in passerines; however, several coccidian species are recorded for families of insectivorous passerines. PURPOSE: This study aimed to examine the feces from gnateaters Conopophaga spp. captured in the municipality of Barra Mansa and in the Itatiaia National Park, State of Rio de Janeiro, Southeastern Brazil, to determine what coccidian parasites were present. METHODS: Nine gnateaters were captured with mist nets. Coccidian oocysts were recovered from the fecal samples by flotation in Sheather's saturated solution. Morphological observations, line drawings, photomicrographs and measurements were made in optical microscopy and digitally edited. The molecular analysis included the study of the sequence of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene, with phylogenetic reconstructions based on the neighbor-joining and maximum likelihood analysis. RESULTS: Four Conopophaga spp. were positive for oocysts. An Isospora sp. considered as new to science is described and identified from Conopophaga melanops (Vieillot, 1818) and Conopophaga lineata (Wied, 1831). Isospora borbai n. sp. has oocysts that are subspheroidal, 17-22 × 15-22 (20.2 × 19.1) µm, with rough, bilayered wall, c.1.7 µm thick. Micropyle present, but without micropyle cap. Oocyst residuum absent, but one or two polar granules are present. Sporocysts are ellipsoidal, 12-15 × 8-11 (14.1 × 9.1) µm. The Stieda body is knob-like to half-moon-shaped and sub-Stieda body is rounded. Sporocyst residuum is present, composed of scattered spherules of different sizes. Sporozoites are vermiform with refractile body and nucleus. Molecular analysis at the cox1 gene exhibited similarity greater than 99% with Isospora spp. isolates from other Neotropical passerine birds. CONCLUSION: Based on the morphological and molecular features, I. borbai is considered as new to science and the first coccidian species recorded from Conopophagidae.