Infections with endoparasites in dogs and cats have been determined by analysing the results of faecal examinations (Flotation, MIFC, sedimentation, Baermann, smear, ProSpecT Giardia Microplate Assay). Samples of 8438 dogs and 3167 cats from the years 1999 until 2002 have been included in the investigation. 2717 dogs (32.2%) and 771 cats (24.3%) have been infected with endoparasites. In the infected dogs the following parasites have been identified: Class Nematodea: Toxocara canis: 22.4%, Toxascaris leonina: 1.8%, Ancylostomatidae: 8.6%, Trichuris vulpis: 4.0%, Capillaria spp.: 2.3%, Crenosoma vulpis: 0.9%, Angiostrongylus vasorum: 0.3%; Class Cestodea: Taeniidae: 1.2%, Dipylidium caninum: 0.4%, Diplopylidium/Joyeuxiella: 0.1%, Mesocestoides: 0.2%, Diphyllobothrium latum: < 0.1%; Class Sporozoea: Sarcocystis spp.: 9.0%, Cystoisospora spp.: 22.3%, C. canis: 8.0%, C. ohioensis: 17.0%, Hammondia/Neospora: 1.7%; Class Zoomastigophorea: Giardia spp.: 51.6%. In the 771 infected cats the following prevalences of parasites have been found: Class Nematodea: Toxocara mystax: 26.2%, Ancylostoma tubaeforme: 0.3%, Capillaria spp.: 7.0%, Aelurostrongylus abstrusus: 2.7%; Class Cestodea: Taeniidae: 2.6%, Dipylidium caninum: 0.1%; Class Sporozoea: Sarcocystis spp.: 2.2%, Cystoisospora spp.: 21.9%, C. felis: 15.3%, C. rivolta: 7.9%, Toxoplasma/Hammondia: 4.5%; Class Zoomastigophorea: Giardia spp.: 51.6%.
In a retrospective study, the results of parasitological examinations of faecal samples from 8,560 cats and 24,677 dogs between January 2003 and December 2010 in Germany were analysed. 30.4 % of the examined dogs and 22.8 % of the cats were infected with endoparasites. The examination of the faecal samples from dogs revealed stages of Giardia spp. (18.6 %), Toxocara canis (6.1 %), Toxascaris leonina (0.6 %), Ancylostomatidae (2.2 %), Trichuris vulpis (1.2 %), Capillaria spp. (1.3 %), Crenosoma vulpis (0.4 %), Angiostrongylus vasorum (0.5 %), Taeniidae (0.4 %), Dipylidiidae (< 0.1 %), Mesocestoides spp. (< 0.1 %), Isospora spp. (5.6 %), I. ohioensis-complex (3.9 %), I. canis (2.4 %), Sarcocystis spp. (2.2 %) and Hammondia heydorni/Neospora caninum (0.3 %). Dogs in the age groups up to 3 months and > 3 up to 6 months of age showed significantly higher infection rates with Giardia spp. (37.5 % and 38.2 %, respectively), Toxocara canis (12.0 % and 12.4 %, respectively), Toxascaris leonina (1.1 % and 1.6 %, respectively), Isospora spp. (23.4 % and 11.8 %, respectively), I. ohioensis-complex (15.6 % and 7.2 %, respectively) and I. canis (11.8 % and 5.2 %, respectively) compared to older dogs. In faecal samples from cats, stages of Giardia spp. (12.6 %), Toxocara cati (4.7 %), Toxascaris leonina (0.1 %), Ancylostoma tubaeforme (0.2 %), Aelurostrongylus abstrusus (0.5 %), Capillaria spp. (1.0 %), Taeniidae (0.6 %), Dipylidium caninum (< 0.1 %) Mesocestoides spp. (< 0.1 %), Isospora spp. (6.0 %), I. felis (4.4 %), I. rivolta (2.2 %), Toxoplasma gondii/Hammondia hammondi (0.8 %) and Sarcocystis spp. (0.3 %) were detected. Cats in the age groups up to 3 months and > 3 up to 6 months of age showed significantly higher infection rates with Giardia spp. (19.5 % and 24.0 %, respectively), T. cati (8.1 % and 6.9 %, respectively), Isospora spp. (12.8 % and 8.6 %, respectively), I. felis (10.0 % and 5.9%, respectively) and I. rivolta (4.6 % and 2.9%, respectively) compared to older cats.
Capillaria aerophila is a trichuroid nematode affecting the respiratory system of dogs, cats, wild carnivores and, occasionally, humans. Animals become infected by ingesting larvated eggs or earthworms, which act as facultative intermediate hosts. The aim of this work is to present new insights into morphological and biological features of this neglected lungworm. Typical features of C. aerophila eggs, differentiating them from those of most known trichuroid whipworms (i.e. size, asymmetry of bipolar plugs and a wall with a network of anastomosing ridges), were detected upon light and scanning electron microscopy. Eggs of C. aerophila were used for in vitro development. Light microscopy showed typical features of C. aerophila eggs: size, asymmetry of bipolar plugs and a wall with a network of anastomosing ridges. All these features were confirmed upon SEM, in that C. aerophila eggs showed an outer densely striated and net-like shell. Eggs of T. vulpis, used for a comparative analysis, were bigger than those of C. aerophila and showed a thick and smooth wall at both light and scanning electron microscopy. Eggs started to develop after 35 days from shedding and mobile larvae were observed in the eggs after two months. The results of this study provide key information on the biological cycle of C. aerophila and present key morphological characters for the identification of eggs in faeces.
SUMMARYDogs infected with Angiostrongylus vasorum, a potentially lethal parasite parasitizing the heart and pulmonary arteries, may present severe respiratory, haematological and neurological signs. In this first large-scale seroepidemiological survey, 4003 sera originating from Germany and 4030 from the UK were tested by an ELISA for the detection of circulating antigen of A. vasorum, and by a separate ELISA detecting specific antibodies. In Germany, where mainly western federal states were sampled, 0·3% (n = 13, CI: 0·2–0·6%) of dogs were positive in both ELISAs, whereas in total 0·5% (n = 20, CI: 0·3–0·8%) were antigen-positive and 2·25% (n = 90, CI: 1·8–2·8%) were positive for specific antibodies. Regions with antigen- and antibody-positive animals were overlapping. In the UK, where mainly the south of the country was sampled, 0·97% (n = 39, CI: 0·7–1·3%) of dogs were antigen- and antibody positive. In total, 1·32% (n = 53, CI: 1·0–1·7%) were antigen-positive, and 3·2% (n = 129, CI: 2·7–3·8%) were positive for specific antibodies, again in overlapping regions. These results confirm the occurrence of A. vasorum in a random dog population originating from large parts of the countries investigated. The use of the tests alone or in combination was considered as a function of their sensitivities and specificities, in order to guide efficient clinical and epidemiological application.
In order to assess the occurrence and regional geographical distribution of Angiostrongylus vasorum and Crenosoma vulpis in Germany, faecal samples of 810 dogs with clinical symptoms of respiratory and circulatory disease, bleeding disorder and/or neurological signs were collected from September 2007 to March 2009. The zinc chloride/sodium chloride flotation and Baermann funnel technique were used to examine the samples for presence of lungworm larvae. Infections with lungworms were diagnosed in 105 (13.0%) of the examined dogs. A. vasorum and C. vulpis were found in 60 (7.4%) and 49 (6.0%) faecal samples, respectively. 33 A. vasorum- and 12 C. vulpis-positive dogs were located in Baden-Württemberg, 13 and 12 in North Rhine-Westphalia, 3 and 4 in Bavaria, 1 and 7 in Rhineland-Palatinate, 7 and 4 in Saarland, 1 and 2 in Saxony, respectively. In Brandenburg only 2 dogs with A. vasorum and in Hesse a total of 5 dogs with C. vulpis were detected. In Mecklenburg-Western Pomerania, Lower Saxony and Thuringia only 1 dog with C. vulpis was detected at a time. 4 dogs were coinfected with A. vasorum and C. vulpis. These surprisingly high prevalence rates indicate that both parasites are endemic in Germany.
BackgroundPhagocyte-derived extracellular traps (ETs) were recently demonstrated mainly in vertebrate hosts as an important effector mechanism against invading parasites. In the present study we aimed to characterize gastropod-derived invertebrate extracellular phagocyte trap (InEPT) formation in response to larval stages of important canine and feline metastrongyloid lungworms. Gastropod haemocytes were isolated from the slug species Arion lusitanicus and Limax maximus, and the snail Achatina fulica, and exposed to larval stages of Angiostrongylus vasorum, Aelurostrongylus abstrusus and Troglostrongylus brevior and investigated for gastropod-derived InEPT formation.ResultsPhase contrast as well as scanning electron microscopy (SEM) analyses of lungworm larvae-exposed haemocytes revealed ET-like structures to be extruded by haemocytes thereby contacting and ensnaring the parasites. Co-localization studies of haemocyte-derived extracellular DNA with histones and myeloperoxidase in larvae-entrapping structures confirmed classical characteristics of ETs. In vivo exposure of slugs to A. vasorum larvae resulted in InEPTs being extruded from haemocytes in the slug mucous extrapallial space emphasizing the pivotal role of this effector mechanism against invasive larvae. Functional larval entrapment assays demonstrated that almost half of the haemocyte-exposed larvae were contacted or even immobilized by released InEPTs. Overall, as reported for mammalian-derived ETs, different types of InEPTs were here observed, i.e. aggregated, spread and diffused InEPTs.ConclusionsTo our knowledge, this study represents the first report on metastrongyloid lungworm-triggered ETosis in gastropods thereby providing evidence of early mollusc host innate immune reactions against invading larvae. These findings will contribute to the better understanding on complex parasite-intermediate host interactions since different gastropod species bear different transmitting capacities for metastrongyloid infections.Electronic supplementary materialThe online version of this article (doi:10.1186/s13071-016-1961-z) contains supplementary material, which is available to authorized users.
BackgroundCutaneous dirofilariosis is a canine mosquito-borne zoonosis that can cause larva migrans disease in humans. Dirofilaria repens is considered an emerging pathogen occurring with high prevalence in Mediterranean areas and many parts of tropical Asia. In Hong Kong, a second species, Candidatus Dirofilaria hongkongensis, has been reported. The present study aimed to compare mitochondrial genomes from these parasites and to obtain population genetic information.Methods and FindingsComplete mitochondrial genomes were obtained by PCR and Sanger sequencing or ILLUMINA sequencing for four worms. Cytochrome oxidase subunit 1 sequences identified three as D. repens (all from Europe) and one as C. D. hongkongensis (from India). Mitochondrial genomes have the same organization as in other spirurid nematodes but a higher preference for thymine in the coding strand. Phylogenetic analysis was in contradiction to current taxonomy of the Onchocercidae but in agreement with a recent multi-locus phylogenetic analysis using both mitochondrial and nuclear markers. D. repens and C. D. hongkongensis sequences clustered together and were the common sister group to Dirofilaria immitis. Analysis of a 2.5 kb mitochondrial genome fragment from macrofilaria or canine blood samples from Europe (42), Thailand (2), India (1) and Vietnam (1) revealed only small genetic differences in the D. repens samples including all European and the Vietnam sample. The Indian C. D. hongkongensis and the two Thai samples formed separate clusters and differences were comparatively large.ConclusionGenetic differences between Dirofilaria spp. causing cutaneous disease can be considerable whereas D. repens itself was genetically quite homogenous. C. D. hongkongensis was identified for the first time from the Indian subcontinent. The full mitochondrial genome sequence strengthens the hypothesis that it represents an independent species and the Thai samples might represent another cryptic species, Candidatus Dirofilaria sp. ‘Thailand II’, or a quite divergent population of C. D. hongkongensis.
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