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Cryptosporidium is a genus of apicomplexan parasites that infect the gastrointestinal tract of a wide range of vertebrate hosts, including humans. These enteropathogens are commonly detected in surface waters and Cryptosporidium is responsible of numerous waterborne outbreaks in industrialised countries. Filters of granular activated carbon (GAC) are mainly used to eliminate emerging micropollutants or control unpleasant odour and taste in drinking water. Recently, GAC has been also employed for removal of microorganisms from different types of water. This work evaluates the capability of GAC in the elimination of the infective forms of Cryptosporidium parvum (oocysts) from drinking water. For this, well water was spiked with oocysts of C. parvum and passed through a chromatographic column filled with fresh GAC at different bed heights (5–50 cm) and a filtration rate of 100 mL/min, approximately. By immunofluorescence microscopy, the number of oocysts in the water samples was determined. The logarithmic reduction (LR) was calculated by comparing the number of oocysts quantified in the filtered samples and the corresponding influent samples. High efficiencies of GAC in removing C. parvum oocysts from water were obtained. Thus, with a bed height of 35 cm, removal efficiencies > 2 LR were achieved. The highest LR (3.47 ± 0.31) was observed when a GAC bed height of 50 cm was used. Taking into account the results obtained, C. parvum oocysts were eliminated remarkably and, therefore, GAC adsorption filters may be considered additional barriers against this waterborne enteropathogen in drinking water at the household level in developing countries.

Specimens of Salmo trutta (n = 613) captured by local anglers in different rivers in Galicia (NW Spain) during the 2015 fishing season (15 March–15 August) were examined. In total 1479 adult helminths were recovered from the gastrointestinal tracts of 221 fish. Moreover, the microscopic observation of the sediments obtained, previous diphasic concentration, revealed the presence of helminth eggs in 485 trout specimens. The following species were identified by morphological and molecular analysis: Crepidostomum metoecus (8.97%) (Trematoda); Salmonema ephemeridarum (16.97%), Raphidascaris acus (9.46%) and Pseudocapillaria sp. (2.12%) (Nematoda); and Echinorhynchus truttae (8.48%) (Acanthocephala). The prevalence, mean intensity and mean abundance of each helminth species were determined in relation to size/age of the fish. The helminth infracommunity comprised a maximum of four species and the species richness was S = 5. The biological cycles of most of the helminth species recovered are dependent on benthic macroinvertebrate fauna, which, in turn, is influenced by the water quality. Therefore, any changes that take place in the aquatic ecosystem (due to anthropogenic activities or climate change) may be reflected in the helminth composition

Tritrichomonas foetus isolates from feline and bovine origin has been previously shown to carry a certain degree of genetic heterogeneity. Here, novel candidate molecular markers were developed by means of multilocus sequence typing of the gap2 gene (encoding for T. foetus glyceraldehyde-3-phosphate dehydrogenase), ITS region, the TR7/TR8 variable-length repeat and microsatellite genotyping. These markers were used to characterize T. foetus field isolates from bulls and domestic cats and to compare phylogenetically with the following ATCC isolates: T. foetus isolated from cattle and pig (syn. Tritrichomonas suis), Tritrichomonas mobilensis, Tetratrichomonas gallinarum and Pentatrichomonas hominis. Among them, TFMS10 and TFMS7 were found to be the most polymorphic markers. Moreover, an 809 bp fragment of the gap2 gene was successfully amplified from all the trichomonads included in this study and the sequence analysis revealed differences between T. foetus porcine and feline genotypes and T. mobilensis in comparison to the bovine T. foetus ATCC isolate. The TR7/TR8 repeat pattern was not reproducible, being only consistent the fragments of approximately 110 and 217 bp. Sequence analysis of the latter revealed the existence of 3 SNPs resulting in 98.6 % homology between bovine and feline isolates. A search for similar sequences was carried out to develop a Restriction Length Fragment Polymorphism analysis. A 503 bp region, named TF1, revealed the existence of two BbvI restriction enzyme sites that were able to generate different length fragments for T. foetus feline and bovine isolates. Finally, the neighbour-joining analyses showed that T. foetus porcine genotype clusters together with bovine genotype, whereas T. mobilensis and the feline genotype form a separate cluster., Depto. de Sanidad Animal, Fac. de Veterinaria, TRUE, pub

Cryptosporidium and Giardia are two important genera of intestinal protozoan parasites that infect a wide range of vertebrate hosts, including humans. The route of transmission for these enteropathogens is the faecal-oral route, directly from person to person or animal to person, or indirectly via contaminated food and water, being the latter the most common route. They cause the self-limited illnesses cryptosporidiosis and giardiosis, which symptoms depend on the immunity status of the host, varying from asymptomatic to diarrhoea, malaise or fatigue, abdominal pain, anorexia and weight loss. The infective forms, oocysts and cysts (oo/cysts), are highly resistant to environmental conditions and to the conventional disinfection treatments of water. Thus, oo/cysts have been reported to occur in different types of water (surface water, drinking water, wastewater) being identified in waterborne outbreaks worldwide. Therefore, new technologies that enhance or optimize conventional methods are needed. This chapter reviews the current knowledge about the efficacy of different technologies that can be applied in the removal of Cryptosporidium and Giardia from water such as photochemical advanced oxidation processes (AOPs), ultrasound (a non-photochemical AOPs) and granular activated carbon adsorption

This is the first study reporting the detection and molecular characterization of Eimeria in bats in Spain, specifically in 12 of 32 chiropteran species described in the Iberian Peninsula. A total of 76 faecal samples were collected from different bat roosting sites across Spanish territory. The DNA was extracted from the samples and sequenced by targeting the Eimeria SSU-rRNA gene. Two Eimeria species were detected in 29 of the 76 faecal samples (38%), and the bat-specific Eimeria rioarribaensis and rodent-specific Eimeria jerfinica were detected in 4 (5%) and 25 (33%) of the samples, respectively. This is the first report of E. rioarribaensis in the bats Rhinolophus euryale, Myotis myotis and Nyctalus lasiopterus, extending the host and geographical ranges for this bat coccidian parasite. The identification of the rodent-specific parasite species E. jerfinica in bats indicates the occurrence of this species in Spain, although its presence has not previously been reported in wild rodents in this country. Considering that most of the Eimeria spp. reported in bats were described only on the basis of morphometric data, molecular studies are required to determined which Eimeria species occur in bats, to complete the identification of these species and to clarify the phylogeny

Species of the genus Cryptosporidium (phylum Apicomplexa) infect the epithelium of the gastrointestinal tract of several vertebrate hosts, including humans and domestic and wild animals. In the past 20 years, several studies have focused on Cryptosporidium in fish. To date, a total of four piscine-host-specific species (Cryptosporidium molnari, Cryptosporidium huwi, Cryptosporidium bollandi and Cryptosporidium abrahamseni), nine piscine genotypes and more than 29 unnamed genotypes have been described in fish hosts. In addition, Cryptosporidium species and genotypes typical of other groups of vertebrates have also been identified. This review summarizes the history, biology, pathology and clinical manifestations, as well as the transmission, prevalence and molecular epidemiology of Cryptosporidium in wild, cultured and ornamental fish from both marine and freshwater environments. Finally, the potential role of piscine hosts as a reservoir of zoonotic Cryptosporidium species is also discussed

Water contamination with the enteroprotozoan parasite Cryptosporidium is a current challenge worldwide. Solar water disinfection (SODIS) has been proved as a potential alternative for its inactivation, especially at household level in low-income environments. This work presents the first comprehensive kinetic model for the inactivation of Cryptosporidium parvum oocysts by sunlight that, based on the mechanism of the process, is able to describe not only the individual thermal and spectral actions but also their synergy. Model predictions are capable of estimating the required solar exposure to achieve the desired level of disinfection under variable solar spectral irradiance and environmental temperature conditions for different locations worldwide. The thermal contribution can be successfully described by a modified Arrhenius equation while photoinactivation is based on a series-event mechanistic model. The wavelength-dependent spectral effect is modeled by means of the estimation of the C. parvum extinction coefficients and the determination of the quantum yield of the inactivation process. Model predictions show a 3.7% error with respect to experimental results carried out under a wide range of temperature (30 to 45 °C) and UV irradiance (0 to 50 W·m−2). Furthermore, the model was validated in three scenarios in which the spectral distribution radiation was modified using different plastic materials common in SODIS devices, ensuring accurate forecasting of inactivation rates for real conditions

Water reclamation is considered as one of the most important priorities worldwide. However, the reuse of treated wastewater involves health risk related with the transmission of certain pathogens. This Doctoral Thesis evaluates the efficacy of new technologies based on advanced oxidation processes against Cryptosporidium, which infectious forms have a robust nature, and they are often detected in wastewater treatment plant effluents, indicating that conventional sewage treatments do not remove this waterborne enteroparasite. The results obtained suggest that these methods are promising alternatives for improving the microbiological quality of reclaimed water, reducing the risk of transmission of infectious diseases.

Cryptosporidiumis an important genus of emerging enteropathogens responsible for waterborne outbreaksworldwide. This parasite has a robust infective form (oocyst), which is highly resistant to the environmentalconditions and to the conventional disinfection treatments of water. This work evaluates for thefirst time thephoto-Fenton process againstCryptosporidium parvum.For that, a factorial design was used to study the com-bined effects of the Fe2+/H2O2concentration (5/10, 10/20 and 20/50 mg L−1), pH (3, 5.5 and 8) and exposuretime (2, 4 and 6 h) on the oocyst survival in distilled water under natural sunlight. The oocyst viability wasdetermined by inclusion/exclusion of thefluorogenic vital dye propidium iodide. The variables Fe2+/H2O2concentration and exposure time showed statistically significant effects on the oocyst viability, as did the in-teraction of pH with Fe2+/H2O2concentration. The maximum oocyst inactivation rates corresponded to thecombination of the highest concentration of Fe2+/H2O2(20/50 mg L−1), the lowest pH value (3) and longestexposure times (4 and 6 h) (3.68 ± 1.38% and 6.39 ± 2.65%, respectively,vs91.67 ± 3.63%, initial oocystviability). Although further studies are needed to evaluate the influence of the water matrix and optimize thephoto-Fenton process, the results obtained demonstrate the efficacy of this advanced oxidation process againstC.parvumoocysts. The inactivation of this enteropathogen would probably ensure elimination of other less re-sistant infectious agents, providing an appropriate protection for the environment and, consequently, for humanand animal health

Cryptosporidium es un género de protozoos parásitos que incluye especies con importancia en salud pública y sanidad animal. Sin embargo, a pesar de su amplia dispersión en ambientes acuáticos, la información existente en organismos de agua dulce es escasa. La presente memoria aborda el estudio de este enteropatógeno de transmisión hídrica en dos especies de salmónidos de interés socioeconómico: la trucha común (Salmo trutta) y la trucha arcoíris (Oncorhynchus mykiss). Además, contribuye al conocimiento de otros protozoos, mixozoos y helmintos que forman parte de la parasitofauna gastrointestinal de la trucha de los ríos gallegos.

Background: Solar water disinfection (SODIS) is an appropriate technology for household treatment of drinking water in low-to-middle-income communities, as it is effective, low cost and easy to use. Nevertheless, uptake is low due partially to the burden of using small volume polyethylene terephthalate bottles (1.5–2 L). A major challenge is to develop a low-cost transparent container for disinfecting larger volumes of water. (2) Methods: This study examines the capability of transparent polypropylene (PP) buckets of 5 L- and 20 L- volume as SODIS containers using three waterborne pathogen indicators: Escherichia coli, MS2-phage and Cryptosporidium parvum. (3) Results: Similar inactivation kinetics were observed under natural sunlight for the inactivation of all three organisms in well water using 5 L- and 20 L-buckets compared to 1.5 L-polyethylene-terephthalate (PET) bottles. The PP materials were exposed to natural and accelerated solar ageing (ISO-16474). UV transmission of the 20 L-buckets remained stable and with physical integrity even after the longest ageing periods (9 months or 900 h of natural or artificial solar UV exposure, respectively). The 5 L-buckets were physically degraded and lost significant UV-transmission, due to the thinner wall compared to the 20 L-bucket. (4) Conclusion: This work demonstrates that the 20 L SODIS bucket technology produces excellent bacterial, viral and protozoan inactivation and is obtained using a simple transparent polypropylene bucket fabricated locally at very low cost ($2.90 USD per unit). The increased bucket volume of 20 L allows for a ten-fold increase in treatment batch volume and can thus more easily provide for the drinking water requirements of most households. The use of buckets in households across low to middle income countries is an already accepted practice.

Giardia duodenalis is a zoonotic parasite that infects the gut of a wide range of vertebrates, including numerous wildlife species. However, little is known about this protozoan parasite in reptiles. Fecal samples from 31 wild lizards were collected in Galicia (northwest Spain) and screened for the presence of Giardia by PCR amplification and sequencing of the ITS1-5.8S-ITS2 region in the ribosomal unit. This allowed detection of the parasite in 5 samples (16.1%), and enabled identification of G. duodenalis assemblage A2 in two samples of Iberian rock lizard (Iberolacerta monticola), G. duodenalis assemblage B in other two samples of I. monticola, and G. duodenalis assemblage E in one sample of Bocage’s wall lizard (Podarcis bocagei). The results obtained after PCR amplification and sequencing of the SSU-rDNA gene confirmed the presence of G. duodenalis assemblage A in two samples of I. monticola. This is the first report of G. duodenalis in free-living lizards, although further studies are needed to distinguish between actual infection and mechanical dissemination of cysts. The detection of zoonotic and livestock-specific assemblages of G. duodenalis demonstrates the wide environmental contamination by this parasite, possibly due to human activities, Giardia duodenalis é um parasito zoonótico que infecta o intestino delgado de uma ampla gama de vertebrados, sendo detectado em numerosas espécies selvagens. No entanto, pouco se conhece sobre a presença deste parasito protozoário em répteis. Para estudar a presença de Giardia, foram obtidas amostras fecais provenientes de 31 lagartos e coletadas em diferentes localizações de Galicia (Noroeste da Espanha). Mediante a aplicação da técnica de PCR e posterior sequenciamento da região ITS1-5.8S-ITS2 da unidade ribossômica, detectou-se Giardia em 5 amostras (16,1%), identificando-se o genótipo A2 de G. duodenalis em 2 amostras de lagartos da montanha (Iberolacerta monticola), G. duodenalis genótipo B em outras 2 amostras de I. monticola e G. duodenalis genótipo E em outra amostra de lagarto de Bocage (Podarcis bocagei). Os resultados obtidos, após amplificação e sequenciamento de um fragmento do gene SSU-rDNA, confirmam a presença de G. duodenalis genótipo A em 2 amostras de I. monticola. Esta é a primeira vez que se descreve G. duodenalis em lagartos selvagens, embora sejam necessários outros estudos complementares para confirmar se estes animais sofrem uma infecção real ou se apenas atuam como disseminadores mecânicos da contaminação ambiental. Além disso, a detecção de genótipos zoonóticos e específicos de ruminantes domésticos demonstra a contaminação do ambiente selvagem por G. duodenalis, possivelmente devido à atividade humana

El objetivo del presente trabajo de investigación es contribuir al establecimiento de las bases científico-técnicas que permitan garantizar la calidad y la seguridad de los moluscos bivalvos destinados al consumo humano, determinando para ello el papel que desempeñan estos organismos en la transmisión de la cryptosporidiosis.