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Giardia duodenalis and Cryptosporidium spp. are two of the most prominent aetiological agents of waterborne diseases. Therefore, efficient and affordable methodologies for identifying and quantifying these parasites in water are increasingly necessary. USEPA Method 1623.1 is a widely used and validated protocol for detecting these parasites in water samples. It consists of a concentration step, followed by parasite purification and visualization by immunofluorescence microscopy. Although efficient, this method has a high cost particularly due to the immunomagnetic separation (IMS) step, which is most needed with complex and highly contaminated samples. Based on this, the present study aimed to determine whether it is possible to maintain the efficiency of Method 1623.1 while reducing the amount of beads per reaction, using as a matrix the challenge water recommended by the World Health Organization. As for Giardia cysts, a satisfactory recovery efficiency (RE) was obtained using 50% less IMS beads. This was evaluated both with a commercial cyst suspension (56.1% recovery) and an analytical quality assessment (47.5% recovery). Although RE rates obtained for Cryptosporidium parvum did not meet Method 1623.1 criteria in any of the experimental conditions tested, results presented in this paper indicated the relevance of the described adaptations, even in challenge water. HIGHLIGHTS The high cost of current protozoa detection methods limits their widespread use in limited settings.; Immunomagnetic separation improves detection by cleaning the sample.; Recovery efficiency is maintained for Giardia duodenalis with 50% less beads.; Organisms adhering to beads after dissociation may impact recovery levels.;

Giardia duodenalis and Cryptosporidium spp. are two of the most prominent aetiological agents of waterborne diseases. Therefore, efficient and affordable methodologies for identifying and quantifying these parasites in water are increasingly necessary. USEPA Method 1623.1 is a widely used and validated protocol for detecting these parasites in water samples. It consists of a concentration step, followed by parasite purification and visualization by immunofluorescence microscopy. Although efficient, this method has a high cost particularly due to the immunomagnetic separation (IMS) step, which is most needed with complex and highly contaminated samples. Based on this, the present study aimed to determine whether it is possible to maintain the efficiency of Method 1623.1 while reducing the amount of beads per reaction, using as a matrix the challenge water recommended by the World Health Organization. As for Giardia cysts, a satisfactory recovery efficiency (RE) was obtained using 50% less IMS beads. This was evaluated both with a commercial cyst suspension (56.1% recovery) and an analytical quality assessment (47.5% recovery). Although RE rates obtained for Cryptosporidium parvum did not meet Method 1623.1 criteria in any of the experimental conditions tested, results presented in this paper indicated the relevance of the described adaptations, even in challenge water. [ABSTRACT FROM AUTHOR]

Cats (Felis catus) have the potential to spread and infect humans and other animals with a variety of endoparasites. This study was conducted to investigate the prevalence of parasites in community, outdoor, and strictly indoor domestic cats in Rockland County, New York. Between November 2020 and June 2021, fecal samples were collected from 3 populations (community = 65, outdoor domestic = 28, strictly indoor domestic = 35). A minimum of 2 g of feces were collected per sample and examined with centrifugal fecal floatation tests with 33% zinc sulfate solution and microscopy. Overall, community cats had a significantly higher prevalence of parasites compared to outdoor and strictly indoor cats (chi-square test, X2 = 24.943, df = 2, P = 3.835 × 10-6). The most prevalent endoparasite in all 3 populations was Toxocara cati. There was a significant difference between the 3 populations and parasite richness (chi-square test, X2 = 25.452, df = 4, P = 4.081 × 10-5). Polyparasitism was frequently observed in the community population, followed by the outdoor population. This study demonstrates that because community cats spend their entire lives outdoors, they are more at risk of being exposed to parasites and contribute to the contamination of the environment with these parasites., (© American Society of Parasitologists 2022.)