Prevalence Of Sarcocystis Research Articles

First Molecular Identification and Prevalence of Sarcocystis spp. in Sheep Intended for Human Consumption in Shanxi Province, China.

Sarcocystis species are intracellular coccidian protozoans that can infect a range of animals and humans and cause public health problems and economically significant losses. Sarcocystosis in sheep (Ovis aries) can cause abortion, neurological symptoms, and even death and results in significant economic losses to the livestock industry. To date, however, it is yet unknown whether sheep in Shanxi Province, north China, are infected with Sarcocystis spp. The purpose of this study was to investigate the prevalence of Sarcocystis spp. in sheep in Shanxi Province. Thus, 582 muscle samples of sheep were purchased from farmers' markets from ten representative counties in Shanxi Province, north China, and examined for the presence and prevalence of Sarcocystis spp. by PCR amplification of the mitochondrial cytochrome c oxidase subunit I (cox1) gene. Of the examined 582 mutton samples, 197 samples (33.85%) were Sarcocystis-positive and were sequenced. Of the obtained 197 cox1 sequences, 196 sequences showed nucleotide similarity of 98.56-99.81% with those of S. tenella, and the remaining one cox1 sequence showed nucleotide similarity of 99.71% with that of S. arieticanis. Two representative cox1 sequences of S. tenella (accession nos. PQ189447 and PQ189448) have 99.52% and 99.61% identity with S. tenalla (KC209725) and S. tenalla (MK419984), respectively. The sequence of S. arieticanis (accession no. PQ165949) obtained in this study has 99.71% identity with S. arieticanis (MK419975). This present study documents the occurrence and prevalence of Sarcocystis spp. in sheep in Shanxi Province for the first time, which enriches the data on the distribution of Sarcocystis spp. in sheep in China and has implications for the control of sheep sarcocystosis.

Macroscopic and Microscopic Survey of Sarcocystis spp. Infection in Slaughtered Cattle and Sheep in Tabriz, Iran

Background & Aims: Sarcocystis infection is one of the most common protozoan infections between humans and animals, which is caused by different species of Sarcocystis. The study aimed to investigate Sarcocystis infection in cattle and sheep slaughtered in Tabriz slaughterhouse by microscopic and macroscopic methods. Materials amd Methods: Diaphragmatic muscles of 500 cattle and 800 sheep were randomly selected for macroscopic and microscopic Sarcocystis cysts. A naked eye examination was done for macroscopic sarcocysts, while peptic digestion and Daub smear method were used for the microscopic cysts. Results: The overall prevalence of Sarcocystis spp. infection was 44.0% and 68.25% in cattle and sheep, respectively. The results showed that rate of infection of cattle with Sarcocystis spp. was 10.4%, 90.0%, and 22.3% by macroscopic, peptic digestion, and Daub smear methods, respectively. Meanwhile, the percentage of infected sheep was determined by macroscopic, peptic digestion, and Daub smear methods as 30.6%, 100.0%, and 44.1%, respectively (P<0.05). Conclusion: It is concluded that digestion is a perfect method for diagnosing sarcocysts in cattle and sheep. As well as, the high prevalence of microscopic Sarcocystis spp. in cattle and sheep of Tabriz, is suggested that meat should be cooked sufficiently, the people to be trained not to feed their dogs and cats with uncooked meat.

Macroscopic sarcocystosis in a pig carcass from an Italian abattoir.

Different food-safety institutions, including the European Food Safety Authority, encourage monitoring and characterising Sarcocystis spp. in animals and foodstuffs; among meat-producing animals, domestic pigs (Sus scrofa domesticus) can host two different Sarcocystis spp., that is Sarcocystis miescheriana and the zoonotic Sarcocystis suihominis. Herein, we report for the first time the presence of macrocysts of Sarcocystis miescheriana in a domestic pig resulting in carcass condemnation. In North-West Italy, in June 2022 the carcass of a clinically healthy sow was condemned due to the detection of multifocal macroscopic whitish fusiform lesions. Affected muscle samples were submitted to histological and molecular analyses targeting the mtDNA cox1 and 18S rRNA genes. At gross examination and histology, well demarcated, oval or elongated macrocysts up to 8mm in length characterized by a calcified central core surrounded by fibrosis were detected. The molecular amplification and sequencing of the cox1 mtDNA and 18S rRNA genes revealed the presence of Sarcocystis miescheriana DNA in all sampled macrocysts. Our study provides the first molecularly confirmed case of Sarcocystis miescheriana infection in a domestic pig in Italy. The present report highlights the need to increase data related to the occurrence and the prevalence of Sarcocystis spp. in meat-producing animals, and in wild and domestic pigs in particular, taking into account the zoonotic potential of Sarcocystis suihominis and the possible financial losses related to carcass discard due to macroscopic Sarcocystis spp. cysts.

Sarcocystis infection in beef and industrial raw beef burgers from butcheries and retail stores: A molecular microscopic study

Sarcocystis is a genus of eucoccidian parasites, which globally infects humans and various animals. In addition to economic losses in livestock industries, the parasite is a zoonosis that infects humans through contaminated beef and pork with the parasite sarcocysts. Therefore, this study was carried out to assess Sarcocystis contamination in beef and industrial raw beef burger samples from butcheries and retail stores in Tehran, Iran. Overall, 180 samples of 90 beefs and 90 raw industrial beef burgers with at least 80% meat were randomly collected in Tehran, Iran. Samples were studied microscopically after peptic digestion. Furthermore, sample genomic DNAs were used in conventional polymerase chain reaction (PCR) to amplify approximately 900-bp fragments from 18S ribosomal DNA. Of 180 samples, 170 samples (94.4%) were microscopically and 161 samples (89.44%) were molecularly positive for Sarcocystis spp. Eucoccidial DNA fragments were detected in 161 samples (89.4%), including 78 (86.6%) beef and 83 (92.2%) beef burger samples. No significant differences were found between the beef and beef burger infestations by Sarcocystis bradyzoites using statistical analysis (P > 0.05). Statistically significant differences were seen between the sample type and the intensity of parasites in samples (P = 0.003). Furthermore, differences between the conventional PCR results (positive/negative) and the intensity of parasites in samples were statistically significant (P < 0.001). The considerable prevalence of Sarcocystis spp. in beef and beef burger samples reflects high transmission of the parasite in meat producing cattle, which is important due to food hygiene. Although the most prevalent bovine species, S. cruzi, is not a zoonosis, it is highly recommended to follow guidelines on the parasite transmission prevention due to the existence of S. hominis as a zoonotic bovine species.

Molecular Evidence of Sarcocystis Species Infecting Reptiles in Peninsular Malaysia

The genus Sarcocystis consists of intracellular coccidian protozoan parasites with the ability to invade muscle tissue and mature into sarcocysts, causing the zoonotic disease sarcocystosis. These parasites have an obligatory two-host life cycle, which correlates with prey-predator relationship. The distribution and prevalence of Sarcocystis in reptiles remains unclear, despite several previous reports. The aim of this study was to identify the genetic assemblage of the species of Sarcocystis infecting Malaysian snakes and lizards by screening stool samples. Overall, 54 fecal samples of various snake species and four fecal samples of several lizard species in Malaysia were taken within the course of August 2015 to January 2016 from Seremban, Melaka, Tioman Island, Pahang, Klang and Langkawi Wildlife Park located in Malaysia. The samples were examined for Sarcocystis through PCR amplification of the 18S rDNA sequence at the Department of Parasitology, University of Malaya. Fourteen snake fecal samples were positive via PCR; however, only eight samples (14%) were found positive for Sarcocystis species, whereas four were positive for other genera and the identity of another three samples was unable to be determined. Further phylogenetic analysis of the 18S rDNA sequences revealed that the snakes were infected with either S. singaporensis, S. lacertae, or undefined Sarcocystis species closely related to either S. singaporensis or S. zuoi. Sarcocystis nesbitti infection was not identified in any of the infected snakes. This is the first report of identification of S. lacertae in the black-headed cat snake.

Prevalence of Sarcocystis in goat carcasses slaughtered at the industrial Abattoir of Urmia, Iran by Digestive method

Prevalence of Sarcocystis in goat carcasses slaughtered at the industrial Abattoir of Urmia, Iran by Digestive method

Prevalence of Sarcocystis spp. and Hammondia spp. microcysts in esophagus tissue of sheep and cattle, emphasized on their morphological differences.

Sarcocystis and Hammondia are two obligatory protozoan parasites. These genera belong to cyst-forming coccidia group of the phylum Apicomplexa. They both need two different hosts to complete their life cycles. Felids and canids can act as definitive hosts, while herbivores, such as sheep and cattle, are the most important intermediate hosts. Reports verify that no important disease has been caused by Hammondia spp.; on the other hand, Sarcocystis spp. can cause some severe infectious disease in livestock industry such as abortion. Economic losses are another concern due to carcass condemnation during meat inspection in abattoirs and decrease in the quality and quantity of milk and wool production. Due to the Sarcocystis and Hammondia tissue cysts being similar, the distinction between these different genera is so important. In this study, the prevalence of Sarcocystis and Hammondia in the esophagus tissue of sheep and cattle slaughtered in one of the industrial abattoir in Iran was reported and an easy and rapid method for accurate diagnosing of Sarcocystis and Hammondia bradyzoites was explained.

Prevalence of Sarcocystis spp. in rodents in Peninsular Malaysia

Prevalence of Sarcocystis spp. in rodents in Peninsular Malaysia

Prevalence of Sarcocystis spp. in Two Subspecies of Caribou (Rangifer tarandus) in Newfoundland and Labrador, and Foxes (Vulpes vulpes), Wolves (Canis lupus), and Husky Dogs (Canis familiaris) as Potential Definitive Hosts

A study was conducted to determine the prevalence and geographical distribution of Sarcocystis spp. infecting 2 subspecies of caribou (Rangifer tarandus) inhabiting Newfoundland and Labrador and its potential definitive hosts. Muscle samples of caribou were obtained, primarily from hunters, and feces of red foxes (Vulpes vulpes) and wolves (Canis lupus), from trappers, and Husky dogs (Canis familiaris), from owners. Histological sections of muscle and flotation methods for feces were used for parasitic detection. Sarcocystis sp. infected more than 50% of barren-ground caribou (R. t. tarandus) from 4 locations in Newfoundland, but it was significantly greater in the north, where 99% of woodland caribou (R. t. caribou) from Labrador harbored the infection. Sporocysts were observed in 27 of 32 red foxes from eastern and northern Newfoundland, whereas 15 of 15 wolves and 22 of the 38 Husky dogs were infected. Wolves and red foxes probably acquired the infection through scavenging, and Husky dogs, from meat they were fed.

Prevalence of Sarcocystis in slaughtered one-humped camels (Camelus dromedarius) in Iran

Prevalence of Sarcocystis in slaughtered one-humped camels (Camelus dromedarius) in Iran

Sarcocystis spp. infection in roe deer (Capreolus capreolus) from the north-west of Spain

Samples of heart, oesophagus and diaphragm muscle from 132 roe deer (Capreolus capreolus) hunted in game reserves from Lugo province (north-western Spain) were examined to determine the prevalence ofSarcocystis infection. Sarcocysts were examined by light (LM) and transmission electron microscopy (TEM). The overall prevalence of infection was 85.6%, with a density of 15±16.8 cysts/g of muscle. The highest prevalence was observed in the large preserve in Ancares (97.3%) compared to that of the smaller reserves (81.1%). Size and shape differences were observed in the sarcocysts from the different muscular organs. The highest density of infection was in the heart, particularly to the inner part of the myocardium. LM distinguished two types of sarcocysts: thin-walled cysts present in all the positive organs and a thick-walled cyst, identified asS. hofmanni, found in the oesophagus of one animal. By TEM only one type of cyst wall, having a thin primary wall that formed folded hairlike protrusions, could be differentiated. Ultrastructural features of the cyst wall demonstrated that this species corresponds with the unnamed speciesSarcocystis sp.

Prevalence of Sarcocystis sp. in stranded Atlantic white-sided dolphins (Lagenorhynchus acutus).

In January 1998 and 1999, two mass strandings of dolphins occurred in Wellfleet, Massachusetts. The strandings were composed of 97 and 53 animals, respectively. Tissues from 35 Atlantic white-sided dolphins (Lagenorhynchus acutus) from the 1998 stranding and 52 from the 1999 stranding were examined histologically. In the 1998 stranding, unidentified protozoal tissue cysts were seen in skeletal muscle from 11 of 28 (39%) dolphins. In addition, two dolphins had a protozoal tissue cyst in cardiac muscle. In the 1999 stranding, nine of 23 (39%) dolphins had the same protozoal tissue cysts in skeletal muscle. The identification of these protozoal tissue cysts as Sarcocystis sp. was confirmed by light and transmission electron microscopy. The high prevalence of sarcocysts in these dolphins suggests that they are likely intermediate hosts for previously undescribed Sarcocystis spp. The ultrastructure of the sarcocyst walls suggests that more than one species of Sarcocystis are present in dolphins.

Prevalence of Sarcocystis spp. in meat-producing animals in Iraq

The prevalence of Sarcocystis spp. infection was investigated in 605 sheep, 826 goats, 1080 cattle, 580 water buffaloes and 36 camels slaughtered from 1992 to1996 in the Baghdad area (Iraq) using naked eye examination for macroscopic sarcocysts, and peptic digestion, muscle squash, squeezing methods and indirect fluorescent antibody test (IFAT) for microscopic types. The intestinal stages of the parasite were also studied in dogs experimentally fed with tissues containing microscopic cysts. The percentage prevalence of macroscopic cysts were 4.1, 33.6, 0.2, 15.6 and 0, and of the microscopic type, 97.0, 97.4, 97.8, 82.9 and 91.6 for the above-mentioned hosts, respectively. Among the different organs examined, macroscopic cysts were found to be highest in the oesophagus and the lowest in the heart. Peptic digestion method gave the highest rate (93.3%) followed by indirect fluorescent antibody test (IFAT) (88.6%), squeezing (81.3%), and muscle squash (81.2%). Each infected dog shed a total of about 150–200 million sporocysts. Histologically, developmental stages of the parasite were detected in the small intestinal mucosa of the dogs on Days 7 and 13 post-infection.

Prevalence of Sarcocystis in camels ( Camelus dromedarius) from Al-Ahsa, Saudi Arabia

The oesophagus, diaphragm and heart of 103 camels slaughtered at Al-Ahsa abattoir were investigated for infection with sarcocysts. Sarcocystis cysts were found in 91 camels (88.35%): in the diaphragm of 79.6%, oesophagus of 72.8% and heart of 71.8%. Two morphologically distinct sarcocysts were found. Thin-walled cysts (141–400 × 70.5–188 μm) were in all the three indicator organs while the thick-walled cysts (170–194 × 117.5–188 μm) were only found in the oesophagus. Experimental feeding of four cats and two dogs with sarcocysts-infected meat showed that cats were refractory to the infection while dogs excreted Sarcocystis sp. sporocysts (10.7–14.3 × 8.3–10.7 μm mean, 13.2 ± 0.32 × 9.4 ± 0.20 μm) after a prepatent period of 9–10 days. It was concluded that dogs may be the final host of both types of sarcocysts or that one of these cysts develops in dogs while the other one uses other carnivores living in the desert as the final host.

Prevalence of Sarcocystis in sows from Iowa

The hearts of 893 sows from Iowa killed for food between January 1990 and February 1992 were examined for Sarcocystis bradyzoites by the digestion technique. Bradyzoites were found in 163 (18.2%) hearts. Sections of formalin-fixed tissues from 28 hearts with demonstrable bradyzoites were examined for sarcocysts. Sarcocystis miescheriana sarcocysts were found in six pigs. The prevalence of Sarcocystis was apparently not affected by season.

Prevalencia de Sarcocystis sp. en vacunos, ovinos y caprinos beneficiados en los camales de Lima

Se ha realizado el presente estudio para determinar la prevalencia de Sarcocystis sp. en vacunos, ovinos y caprinos utilizando el método del tríquinoscopio con muestras de tejido cardíaco y esófago. Los resultados mostraron que de 85 muestras de tejido cardíaco de ganado vacuno, 76 fueron positivas (89.5%); de 134 muestras de ganado ovino 122 fueron positivas (91.04%) mientras que de 63 muestras de ganado capriino solo en 33 (52.4%) se encontró la presencia del parásito. En cuanto a las muestras de esófago los porcentajes de parasitismo fueron los siguientes: 2% para el vacuno; 39.8% para el ovino y 76.2% para el caprino. Estos valores indicaron que el mayor parasitismo en vacunos y ovinos está localizado en el corazón, mientras que en caprinos el órgano más infestado es el esófago. Por lo tanto existe un elevado parasitismo por Sarcocystis sp. en el ganado beneficiado para consumo humano.

Prevalence of Sarcocystis in domestic pigs in India

Muscle samples from 890 slaughtered pigs were examined for the presence of sarcocysts. A high prevalence rate of 67.98% was observed. Two types of microsarcocysts were recorded. The sarcocyst wall of one type had redial striations and the other possessed hair-like villar protrusions. The species were identified as Sarcocystis miescheriana and Sarcocystis suihominis; there was a slightly higher incidence of the latter species (47.11%) than of the former (43.14%). S. suihominis has been identified for the first time from pigs in India.

An investigation of the potential for spread ofSarcocystisspp. and other parasites by feral cats

Abstract The potential for spread by feral cats of parasites infecting sheep and cattle was investigated on 5 km2 of New Zealand farmland. Faeces were collected to study diet and the prevalence of Sarcocystis and other parasites. The diet consisted primarily of rodents (50% by weight) with scavenged sheep (7%) relatively unimportant. Sarcocystis sporocysts were found in 4.8% of the faeces samples; given the predominance of rodents in the diet, it is more likely that these derived from species infecting rodents rather than farm animals. Toxoplasma gondii oocysts were not found. Eggs of the nematodes Toxocara cati and Capillaria spp. occurred in 67 and 52% of the samples, respectively. The home range and movements of feral cats were estimated using radiotelemetry. Female cats using barns and pasture had larger home ranges (1.88-2.79 km2) than those living in willows (0.37-1.09 km2). Adult males and a dispersing subadult male had larger home ranges (2.76-3.00 km2) than females. The density of resident feral cats was maintained at about 3.5/km2 and seasonally supplemented by young and transient cats. The relative importance of feral and farm cats in the distribution of Sarcocystis and Toxoplasma gondii on farmland and the possibilities of controlling these vectors are discussed.

Prevalence, ultrastructure of the cyst wall and infectivity for the dog and cat of Sarcocystis sp. from fallow deer (Cervus dama).

The prevalence of Sarcocystis sp. (Protozoa: Sarcocystidae) in fallow deer (Cervus dama) in Tuscany, Italy was determined by digestion technique and histological examination. Forty-four of 45 fallow deer were infected. Infections occurred in adult deer and in fawns. Samples from the heart were more intensively parasitized than samples from tongue, oesophagus and diaphragm muscle. With transmission electron microscopy, the primary cyst wall was folded and formed narrow, overlapping, sinuous projections which were often parallel to the cyst surface. Dogs fed heart samples from infected fallow deer shed sporocysts after 10-11 days. Cats fed the same samples did not shed any sporocysts.

Prevalence of Sarcocystis in wolves and white-tailed deer in Northeastern Minnesota.

The prevalence of Sarcocystis (Protozoa: Sarcocystidae) in white-tailed deer (Odocoileus virginianus) from northeastern Minnesota was determined by histologic examination of tongue samples. Seventy-nine of 100 deer were infected; infection was higher in yearlings and adults than in fawns. Sporocysts of Sarcocystis were found in 3% of 72 wolf (Canis lupus) scats. Three of four captive wolves fed muscle from a white-tailed deer naturally infected with Sarcocystis shed sporocysts 12-14 days later.