Correction: Anthelmintic and therapeutic effects of the biogenic zinc oxide nanoparticles against acute kidney injury induced by Parascaris equorum Infection in rats.

[This corrects the article DOI: 10.1007/s12639-023-01637-z.].

Anthelmintic and therapeutic effects of the biogenic zinc oxide nanoparticles against acute kidney injury induced by Parascaris equorum Infection in rats.

Complications of parasite infections, especially kidney disease, have been linked to poorer outcomes. Acute kidney damage, glomerulonephritis, and tubular dysfunction are the most prevalent renal consequences of Parascaris equorum infection. The purpose of this study was to determine the pharmacological effects of green-produced zinc oxide nanoparticles (ZnO NPs) on P. equorum infection in male Wistar rats. Thirty-six male rats were divided into two groups of 18 each: infected and non-infected. Both groups were separated into three subgroups, each of which received distilled water, 30 mg/kg ZnO NPs, and 60 mg/kg ZnO NPs. After 10 days of ZnO NPs administration, four larvae per gram of kidney tissue were present in the untreated infected group. While, no larvae were present in ZnO NPs (30 mg/kg) treated group, and one larva/g.tissue was present in ZnO NPs (60 mg/kg) treated group compared to untreated infected animals. P. equorum infected rats had increased kidney biomarkers (creatinine, urea, uric acid), malondialdehyde, and nitric oxide, with a significant decrease in their antioxidant systems. On the other hand, infected treated rats with green-produced zinc oxide nanoparticles had a substantial drop in creatinine, urea, uric acid, malondialdehyde, and nitric oxide, as well as a significant rise in their antioxidant systems. P. equorum infection in rats caused severe degenerative and necrotic renal tissues. On the other hand, there were no detectable histopathological alterations in rats treated with ZnO NPs (30, 60 mg/kg) as compared to the infected untreated animals. When compared to infected untreated mice, immunohistochemical examination of nuclear factor-kappa B showed a significant decrease during treatment with ZnO NPs (30, 60 mg/kg). Green-produced zinc oxide nanoparticles are a viable therapeutic strategy for Parascaris equorum infection due to their potent anthelmintic activity, including a significant decrease in larval burden in infected treated rats.

Anthelmintic and Hepatoprotective Activities of the Green-Synthesized Zinc Oxide Nanoparticles Against Parascaris equorum Infection in Rats.

MAIN CONCLUSIONS: Green-synthesized zinc oxide nanoparticle is a promising treatment modality against parasitic infection through its powerful anthelmintic, antioxidant, healing promotion, and anti-inflammation effects. BACKGROUND: Nanoparticles have many properties, depending on their size, shape, and morphology, allowing them to interact with microorganisms, plants, and animals. OBJECTIVES: Investigation of the therapeutic effects of green-synthesized zinc oxide nanoparticles (ZnO NPs) on Parascaris equorum infection in rats. METHODS: Thirty-six rats were divided into two divisions: the first division is noninfected groups were allocated into three groups. Group 1: Control, group 2: ZnO NPs (30 mg/kg), and group 3: ZnO NPs (60 mg/kg). The second division is infected groups were allocated into three groups. Group 1: vehicle, group 2: ZnO NPs (30 mg/kg), and group 3: ZnO NPs (60 mg/kg). FINDINGS: Ten days post-infection, two larvae per gram of liver tissue were present in the vehicle group compared to the control group. No larvae were recovered from ZnO NPs (30 mg/kg), and one larva/g.tissue from ZnO NPs (60 mg/kg)-treated groups compared to untreated infected animals. Green-synthesized ZnO NPs caused a significant decrease in liver functions, low-density lipoprotein (LDL), cholesterol, triglycerides, malondialdehyde (MDA), and nitric oxide (NO). While it caused a significant increase in hemoglobin (HB), high-density lipoprotein (HDL), butyrylcholinesterase (BCHE), glutathione (GSH), catalase (CAT), and glutathione S-transferase (GST) in infected treated rats. The histological inflammation and fibroplasia scores showed a significant enhancement during the treatment with ZnO NPs (30, 60 mg/kg) compared to the infected untreated animals that scored the highest pathological destruction score. Immunohistochemical markers of NF-κB showed a significant decrease during the treatment with ZnO NPs (30, 60 mg/kg) compared to the infected untreated animals.

In vitro anti-Toxocara vitulorum effect of silver nanoparticles.

Toxocara vitulorum is a common gastrointestinal nematode of buffaloes and cattle, primarily young calves. This parasitic infection is distributed worldwide, causing a huge economic loss due to reduced meat and milk production and animal mortality. Several studies have indicated that silver nanoparticles have an effective anthelmintic activity. Thus, this study aimed to evaluate the anthelmintic effects of different concentrations of silver nanoparticles on adult Toxocara vitulorum in vitro. Male and female adult worms were incubated for 48 h in 50, 100, and 200 mg/L silver nanoparticles synthesized using lemon juice. Oxidative stress markers, in addition to light and scanning electron microscopic studies of treated worms, were assessed following 48 h incubation in 200 mg/L silver nanoparticles. Light and scanning electron micrographs of treated worms revealed damage in the muscular layer, destruction of the cuticle, distortion in lips structure, and deformed excretory pore and sensory papillae. Also, oxidative stress markers recorded an increase in malondialdehyde and nitric oxide and decreased levels of glutathione reduced, glutathione S-transferase, and catalase after exposure to silver nanoparticles. In Conclusion, the current study demonstrated a substantial destructive effect of silver nanoparticles on adult Toxocara vitulorum, indicating its potential as an anthelmintic alternative to the more expensive drugs.

Optimizing and Evaluating the Antihelminthic Activity of the Biocompatible Zinc Oxide Nanoparticles Against the Ascaridid Nematode, Parascaris equorum In Vitro.

PURPOSE: In the present study, the effect of different biocompatible concentrations from ZnO nanoparticles (ZnO NPs) on the physiological state and surface topography of the nematode P. equorum was determined in vitro. METHODS: Different concentrations of ZnO NPs (100, 200, 300 and 400 mg/l) synthesized using the egg white were prepared followed by the incubation of parasitic worms with these concentrations in vitro. The physiological state of treated worms such as oxidative stress markers, enzymatic activities and biochemical parameters in addition to the surface topography was determined and compared with control untreated worms. RESULTS: In comparison to control worms, it was observed that at high concentrations of ZnO NPs, most of the treated worms showed an increase in the levels of ALT, AST and ALP (worm muscle damage, and gonad injury); enhancement of the total protein content (worm cellular dysfunction); significant increase in MDA level (free radical-mediated worm cell membrane damage); depletion in GST and GSH activities (reduced ability to clear toxic compounds like lipid peroxides); CAT depletion (superoxide dismutase and hydrogen peroxide toxicity) and NO increase (detoxification activity and stressful conditions on worms). SEM showed that there was a modified morphological appearance in the surface of treated worms; lips were wrinkled with irregularly arranged denticles, weathering of cuticle, bursts of cuticle layers, disruption of surface annulations and erosion of surface papillae of male around the cloacal opening. CONCLUSION: ZnO NPs at environmentally relevant concentrations achieved a significant antihelminthic activity against P. equorum which represents a successful model used in parasite control experiments.

Ultrastructural characterization of Pleistophora macrozoarcidis Nigerelli 1946 (Microsporidia) infecting the ocean pout Macrozoarces americanus (Perciformes, Zoarcidae) from the gulf of Maine, MA, USA.

Pleistophora macrozoarcidis a microsporidian parasite infecting the muscle tissue of the ocean pout Macrozoarces americanus collected from the Gulf of Maine of the Atlantic Ocean, MA, USA, was morphologically described on the basis of ultrastructural features. Infection was detected as opaque white or rusty brown lesions scattered throughout the musculature of the fish mainly in the region anterior to anus. Transmission electron microscopy showed that in individual parasitized muscle cells, the infection progresses within parasite formed vesicles which are in direct contact with muscle cell elements. The earliest observed parasitic stages are the globular multinucleated proliferative cells or plasmodia limited by a highly tortuous plasmalemma with intervesicular finger-like digitations projecting into the parasite cytoplasm. These cells divided through the invagination of the plasmalemma and the amorphous coat producing daughter-cells. Fine electron-dense secretion is deposited on the plasmalemma that causes its thickening which is a sign of commencement of the sporogonic phase. This phase is carried out by cytokinesis of the sporonts and results in the formation of sporoblasts and finally spores. Mature spore has a thin electron-dense exospore, a thick electron-lucent endospore, and the plasma membrane which encloses the spore contents. A single nucleus is centrally located with the posterior region containing a posterior vacuole. The majority of spores have 7-13 coils in 1-2 rows, and a small group of spores had about 23 coils forming two rows. Events of polar filament extrusion for penetration of uninfected cells were studied. The polaroplast membranes were expanded and occupy most of the length of the spore. The coils are dislocated from the sides of the spore to throughout the entire sporoplasm. The polar filament everts and extrudes through the polar cap with a sufficient force to pierce adjacent sporophorous vesicle walls. After eversion, the polar filament is referred to as a polar tubule, as it forms a tube through which the sporoplasm travels. It pierces anything in its path and deposits the sporoplasm at a new location to begin another infective cycle.

A new species of Oochoristica (Eucestoda: Cyclophyllidea) parasite of Agama mutabilis (Reptilia: Agamidae) from Egypt.

The morphological and morphometric characterization of Oochoristica mutabili, an anoplocephalid cestode infecting the small intestine of the Egyptian changeable lizard, Agama mutabilis (F: Agamidae) in South Sinai were described by light and scanning electron microscopy as a first description from this host in Egypt. Ten out of fifty six (17.9%) of the examined specimens were infected with Oochoristica. Strobila was 14.6 (11.5-22.3) mm long; composed of 34 (30-45) proglottids; 7 (6-11) undifferentiated, 8 (6-10) contained sexual primordia, 14 (13-20) mature and 5 (3-9) gravid. Scolex 324 (300-360) microm wide with four circular suckers measuring 100 (97-124) microm in diameter; neck region is evident. Genital pores irregularly alternating, situated in the anterior quarter of proglottid; testes in median mass situated in the posterior half of proglottid extending laterally to vitellarium; ovary bilobed and situated in the centre of proglottid, vitellaria entire, slightly wider than one lobe of the ovary. Gravid proglottids contained in a uterine capsule containing numerous oncospheres. The described parasite is compared with different species of the same genus from different hosts, it was found that morphometrically the present species was more or less different from the comparable species and the only morphologically similar species was O. parvovaria. Both species were similar in the presence of the cirrus sac, which lied anterior to the ovary, and the bilobed ovary situated in the center of proglottids. However, it can be differentiated by possessing more proglottids, fewer testes, and the lack of primordial development in immature proglottids of the comparable species.

WITHDRAWN: Comparative study of the karyotypes and electrophoretic patterns of Biomphalaria alexandrina and Bulinus truncatus and the ova of their corresponding trematode hosts.

The Publisher regrets that this article is an accidental duplication of an article that has already been published, doi:10.1016/j.parint.2011.05.006. The duplicate article has therefore been withdrawn.

Incidence and prevalence of Eimeria infection among the hedgehog, Hemiechinus auritus in Yemen.

Fecal samples of ten hedgehogs, Hemiechinus auritus from Taiz Governorate, Yemen were examined for coccidian parasites. Four (40%) were infected with Eimeria spp. Comparison of oocyst's criteria with other species of Eimeria indicated a new eimerian, E. yeminii n.sp. besides the previously described species, E. auriti Mirza, 1970 reported in Iraq. Oocysts of E. yeminii n.sp. are ovoidal to ellipsoidal, measuring 30 x 24.5 microm (27-36 x 20-28). The outer boundary is bilayered with a light reddish colour and perforated by a micropyle. Oocyst residuum and polar granules are present. Sporocysts are spherical in shape 10 x 7.5 microm (11-12.2 x 10-11.2) with granular residuum and Stieda body. Sporozoites are elongate, lying length-wise to the sporocyst long axis. Sporulation takes place within 3-4 days at approximately 26 degrees C. E. auriti Mirza, 1970 is characterized by subspherical oocysts measuring 20 x 17 (22-26 x 16-19.5) microm, a micropyle and oocyst residuum. The oocyst wall is bilayered, smooth and greenish in colour. Sporocysts are subspherical, measuring 9.0 x 8.3 (8.5-1 x 7.5-8) microm with granular residuum and Stieda body. Fully sporulated oocysts are observed within 48 h at approximately 26 degrees C.

Studies on the genus Stylocephalus ellis, 1912 (Apicomplexa: Eugregarinida: Stylocephalidae) in beetles (Coleoptera: Tenebrionidae) from El Fayoum Governorate, Egypt.

Four species of the genus Stylocephalus Ellis, 1912 were recorded and described from beetles in El Fayoum Governorate; S. longicollis, S. phalloides, S. variabilis and S. eastoni. Both S. phalloides and S. variabilis were recorded in Zophosis sp. and Pimelia angulata, respectively for the first time in Egypt. Out of 105 Blaps polychresta, 18 (17.14%) were infected with S. longicollis and 57 (54.29%) with S. eastoni. Out of 30 Pimelia angulata, 17 (56.76%) were infected with S. variabilis and all examined Zophosis sp. (n = 67) were infected with S. phalloides. Scanning electron microscopy on S. longicollis revealed morphological features not reported before; three pairs of longitudinal ribs extending from the second fifth till the posterior extremity of old sporont and a minute pore on the anterior tip of epimerite. In S. eastoni, the epimerite-host epithelium relationship revealed that the parasite invades host's gut with the distal part of epimerite. Regarding the gross pathological symptoms, heavily infected hosts showed a sluggish motility, short antennae, swollen abdomen, lack of fat accumulation, and putrid smell in dead beetles.

Molecular polymorphisms associated with Egyptian, European, Chinese and North American Fasciola hepatica.

A new PCR based system was used that had a broad detection capabilty among parasites based on a conserved region of the 18s of the 18s ribosomal DNA genes. Five samples each of Egyptian, European and Chinese F. hepatica of bovine origin were obtained and DNA was isolated. The PCR primers recognized a fragment of approxiniately 700 nucleotides in length. Sequences were compaici over a 107 base pair region that identified polymorphisms between the strains. All the sequences from Egyptian isolates were identical, similarly so with all European and Chinese isolates. However, there were polymorphisms between these isolates and the isolates from North America. All isolates have a single base additional in target region and there was a single base substitution in Egyptian isolates when compared to others.

Inference of molecular phylogeny of Sarcocystis felis (Sarcocystidae) from cats based on nuclear-encoded ribosomal gene sequences.

The phylogenetic position of four clinical isolates of Sarcocystis felis was assessed using ssurRNA and ITS1 gene sequences in the context of a wide array of other Sarcocystis sp. Phylogenetic reconstructions using neighbour-joining and maximum parsimony methods generated identical tree topologies with strong support values at each node. High ssurRNA sequence similarity (> or =99%) and the resulting phylogeny demonstrated that S. felis and S. neurona are significantly closely related to each other. The two Sarcocystis formed a monophyletic group distinct from the other Sarcocystis sp., irrespective of the alignment algorithms or tree-building method used. The absolute (100%) identity of ssurRNA sequences of sarcocysts and sporocysts obtained from one cat raised the question regarding the cat's role as a potential intermediate host besides its known role as a definitive host of S. felis. On the other hand, S. felis sarcocyst DNA sequence was found to be quite dissimilar over the ITS1 region when compared to S. neurona. These findings indicated that using sequences from two different genetic loci provided a stronger comparative basis than would have been possible using either one.

Molecular and microscopic techniques for detection of Sarcocystis neurona sporocysts in fecal samples.

Diagnosis of Sarcocystis sp. in the definitive host is generally by microscopic detection of the sporocysts in feces. This method is insensitive and cannot differentiate between species because sporocysts lack specific staining criteria. The hypothesis suggested that molecular techniques provide better alternatives to classical detection of Sarcocystis sporocysts. The sensitivity of two PCR assays was compared to one another and to microscopic examination by conventional fecal flotation and Diamant-Fuchsin staining procedures for detection of sporocysts spiked into mice feces. PCR1 assay using LSM1 & LSM2 primers that amplified 496 bp of the ssurRNA gene was more sensitive than the PCR2 method using JNB25 and JD396 primers that amplified 334 bp of a RAPD-derived marker. PCRI gave positive results with 200 microl of fecal suspension spiked with as little as 5 sporocysts compared to 75 sporocysts detected by JNB25 & JD396 primers. PCRI was more sensitive than conventional microscopy. PCR1 or PCR2 followed by sequencing or RFLP analysis not only detected Sarcocystis sporocysts in feces but also enabled to ascertain the genotype of the species as S. neurona.

Spot light survey on fresh-water snails of medical importance in Al Fayoum Governorate, Egypt.

In a survey carried out during Summer and Autumn of 2004, for snails of medical importance, nine species were recovered. These were Biomphalaria alexandrina, B. glabrata, B. pfeifferi, Bulinus truncatus, B. forskalii, Lymnaea natalensis, Bellamya (=Vivipara) unicolor, Physa acuta and Hydrobia musaensis. Parasitological examination revealed that B. alexandrina, B. glabrata and L. natalensis harboured immature stages of their concerned trematode parasites. Moreover, P. acuta harboured the immature stage of the nematode parasite Parastrongylus cantonensis.

Molecular characterization of Cryptosporidium parvum isolates obtained from humans.

Fifty stool specimens collected from severe diarrheic patients attending Misr University Hospital, were examined microscopically for protozoan parasites mainly, Cryptosporidium parvum. Stool examination revealed 22 cases with C. parvum, 8 with E. histolytica, 14 with G. intestinalis and six were parasite-free. The results were compared with the established nested PCR assay to detect DNA directly from stool specimens. After the extraction of DNA from stool, a 402-bp fragment of C. parvum DNA was amplified with two 26-mer outer primers. The amplified products, 194-bp DNA fragment, were used for a second run. This study indicated that the used primers are specific for DNA of C. parvum. The PCR detected a total of 28 positives; six of these cases were negative by AF stool examination, which eventually confirmed to be positive by several successive examinations of the stool and/or duodenal aspiration. Microscopy exhibited 78.5% sensitivity and 100% specificity compared to 100% specificity and sensitivity with PCR. Consequently, PCR is more sensitive and easier to interpret but required more hands-on time to perform and is more expensive than microscopy. However, PCR batch analysis reduces the cost considerably.

Laboratory and field studies on oribatid mites as intermediate host of Moniezia expansa infecting Egytptian sheep.

Three species of oribatid mites, Scheloribates zaherii, Zygoribatula tadrosi and Z. sayedi from pure colonies were experimentally exposed to infection by allowing them to feed on stool sheep infected with Moniezia expansa. The mites were followed up to the development of the infective cysticercoids. M. expansa was able to achieve sucessfully its larval development in the three species of oribatid mites under laboratory conditions. These were demonstrated after 84, 73 & 69 days post infection, respectively. Z. tadrosi is recorded as inter-mediate host for the first time in Egypt. Six species of oribatid mites, Oppiella nova, S. laevigatus, S. zaherii, Xylobates souchiensis, Epilohmannia pallida aegyptiaca and Z. sayedi, recovered from the sheep infested farm soil, were found naturally infected with different developmental stages of M. expansa.

Efficacy of Mirazid (Commiphora molmol) against fascioliasis in Egyptian sheep.

The efficacy of Mirazid (Commiphora molmol or Myrrh) was evaluated in sheep naturally infected with fascioliasis. Total doses of one or two capsules (300 mg each) were given for one, two or three successive days on an empty stomach an hour before breakfast. A total dose of 600 mg gave a cure rate of 83.3%, while a total dose of 900 to 1200 mg gave a complete cure rate (100%), with no clinical side effect. The cure rate was achieved by stool examination and/or macroscopically on slaughtering the sheep. Mirazid proved to be safe and very effective in sheep fascioliasis in Gharbia Governorate.

Mice immunzation using crude Trichinella spiralis antigen.

Four hundred laboratory bred male Swiss strain albino mice, seven to ten weeks old, were experimentally used to determine the effective mode of immunization against T. spiralis infection. In this regard, active immunization using repeated injection of T. spiralis muscle larval antigen was used in comparison with three, commonly used immunosuppressive drugs (Kenacort, Endoxan and Cyclosporin). Also, the minimal oral dose of T. spiralis larvae that can cause the infection was estimated. The use of T. spiralis muscle larval antigen was found promising for vaccination against the spiralis infection. Although Cyclosporin has an immunosuppressive effect, yet it has a direct lethal effect on both adult and larvae of T. spiralis, and being recommended for treatment of trichinosis. The minimal oral dose of T. spiralis larvae that lead to formation of adult worms in the intestine and larvae in muscles was 20 larvae/mouse. Meanwhile, neither adults nor larvae were formed below this dose.

Comparative study between elisa IgG, IgM and PCR in diagnosing and studying toxoplasmosis in Qualyobia Governorate, Egypt.

ELISA IgG, IgM antibodies and PCR for toxoplasmosis were performed on 55 women with complicated gestation and their babies. Besides, ELISA IgG and IgM were applied on 27 uncomplicated gestation (mothers & babies) and 152 randomly selected individuals. Seropositivity to specific IgG antibodies was 36.4%, 59.2% and 57.9% and for IgM was 27.3%, 7.4% and 10.5% in complicated gestation. uncomplicated gestation and random population respectively. PCR was positive in 20%, 50% and 60% of mothers with abortion, premature deliveries and deliveries of babies with congenital anomalies respectively. 55.5% and 40% were found seropositive for IgG from normal full term babies and abnormal babies. 13% of abnormal babies were IgM positive and 46.6% were PCR positive from the same group.