Blastocystis spp. has been reported in wildlife, domestic animals and animals housed in ZOO. To-date, 17 genetically diverse lines have been reported in mammals and birds (designated ST) based on differences in the SSU rRNA. In this study, faeces samples were collected from 24 ZOO animals with...

The aim of this study was to draw attention to the risk of transmission of Encephalitozoon, Cryptosporidium and Blastocystis infection due to high animal migration and to point out that even wild animals can be a source of many zoonotic diseases. Encephalitozoon cuniculi, Cryptosporidium spp. and Blastocystis spp. are frequent microscopic organisms that parasitise humans, domestic and wild animals. Two hundred and fifty-five faecal specimens were collected from wild boars, badgers, wolves, bears, foxes and deer from 15 locations in Slovakia. Sequencing of positive PCR products and subsequent sequence comparison with GenBank sequences identified Blastocystis spp. in five wild boars. The ST 5 (n = 4) and ST 10 (n = 1) subtypes were determined by genotyping. We identified Encephalitozoon cuniculi in five wild boars, and genotype II (n = 5) was determined on the basis of ITS repeat sequences. Cryptosporidium scrofarum was sequenced in wolves (n = 4) and wild boars (n = 1), while Cryptosporidium suis only in wild boars (n = 2). None of the wild boars had a mixed infection.

Microsporidia are unicellular obligate intracellular parasitic fungi that infect a wide range of vertebrates and invertebrates. There are two known species of microsporidia infecting honey bees in Slovakia- first Nosema apis and also Nosema ceranae. Our aim was to examine samples of honey bees collected from bee queen breeders in three ecoregions of the Slovak Republic in 2021 and 2022. First, microscopic diagnostics were used, and then randomly selected samples were examined using molecular methods. There were 4018 samples examined using microscopic diagnostics and the positivity was demonstrated in 922 samples. From the microscopically diagnosed positive samples, 507 samples were randomly selected, and using molecular methods, the positivity was proved in 488 samples. After sequencing the positive PCR products and comparing the sequences (BLAST) with the sequences stored in the gene bank, the Nosema ceranae species was detected in all positive samples.

Nosemosis is a disease caused by microsporidia, which are strictly intracellular pathogens, currently considered to be most closely related to fungi. These microscopic parasites infect a variety of hosts, significantly affecting honeybees (Apis mellifera). Nosemosis is one of the most serious diseases of bees and is caused primarily by two species: Nosema apis and Nosema ceranae. This infection adversely affects the digestive tract of the bees, causes a reduction in their vitality, and can lead to the death of entire colonies. The diagnosis of nosemosis has undergone extensive development. Traditionally, the identification of microsporidia was performed by examination of bee digestive tract (macerated) by light microscopy. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) are expensive methods that require skilled personnel and were used only when high resolution was necessary. Modern methods, such as polymerase chain reaction (PCR), allow detection of infection at species and genotype levels, thereby increasing the accuracy of diagnosis. Despite advances in molecular techniques, research into nosemosis still faces challenges. This review focuses on a comparison of different diagnostic techniques and their pitfalls that can be integrated into strategies to combat nosemosis and protect the health of honeybee colonies.

In recent decades, the keeping of exotic animals has gained popularity among enthusiasts worldwide. However, alongside the development of exotic animal husbandry, issues related to health status and adequate veterinary care are coming to the forefront. The introduction of new snakes into a collection and shared enclosures should always be preceded by an assessment of their parasitic status. In our study, we present an overview of the screening for the presence of Cryptosporidium spp. in individuals captured in regions of Indonesia and Suriname, intended for further trade. Out of 40 tested fecal samples, the presence of cryptosporidial oocysts was confirmed in 6 samples. Detection was performed by molecular methods, namely Nested PCR targeting the GP60 gene region (60 kDa glycoprotein). By sequencing, we confirmed the presence of C. parvum in Oligodon octolineatus (n = 1) and Trimeresurus insularis (n = 1), C. tyzzeri in Corallus spp. (n = 2), and C. hominis in Boiga dendrophila spp. gemmicincta (n = 2), which is the very first time that this species has been detected in snakes in captivity. Although the presence of Cryptosporidium species, typical for snakes, was not detected, the identified species may pose a health risk to humans, especially workers who come into direct contact with animals.

The number of outbreaks of water-borne diseases caused by parasites seems to have increased in recent years. Nevertheless, the occurrence of these pathogens in water generally pays little attention. Waterborne transmission is a major route in the epidemiology of the parasite and therefore poses a serious public health problem. Cryptosporidium spp., Encephalitozoon spp. and Enterocytozoon spp. parasites are recognised worldwide as a common cause of diarrhoea. In most cases, it is a dilapidated or poorly maintained standard sanitation and water supply. It is important to perform periodic tests on protozoa, which are often lacking in small laboratories. Since it is necessary to filter large volumes of water for reliable diagnostics and consequently, it is difficult to concentrate them in a large volume of filtrate, it is not easy to detect their presence in the water. Various filtration methods are used to filter these pathogens from water, but cryptosporidial oocysts and microsporidia spores still occur in most of the world’s and Slovak recreational waters. Therefore, it would be appropriate to use the abilities of gill-breathing aquatic animals that filter cryptosporidial oocysts and microsporidia spores from the water by absorbing them with food. Zeolite can also purify water by capturing high concentrations of contaminants, including cryptosporidial oocysts and microsporidial spores.