Development of a new quantification method of Sarcocystis cruzi through detection of the acetyl-CoA synthetase gene

• Published in: Journal of Veterinary Medical Science Vol. 85; no. 1; pp. 105 - 110
• Main Authors: DOI, Rie, OBA, Mami, FURUYA, Tetsuya, MIZUTANI, Tetsuya, TAKEMAE, Hitoshi
• Format: Journal Article
• Language: English
• Published: Japan JAPANESE SOCIETY OF VETERINARY SCIENCE 01.01.2023; Japan Science and Technology Agency; The Japanese Society of Veterinary Science
• Subjects: Abattoirs; Acetate-CoA Ligase - genetics; acetyl-CoA synthetase; Animals; Body weight loss; bradyzoite; Bradyzoites; Cardiac muscle; Cattle; Food poisoning; Genes, Protozoan; Genomes; Humans; Milk production; Next-generation sequencing; Nucleotide sequence; Parasitology; Polymerase Chain Reaction - methods; Polymerase Chain Reaction - veterinary; Protozoa; Protozoan Proteins - genetics; Public health; quantitative real-time PCR; Sarcocystis; Sarcocystis - genetics; Sarcocystis - isolation & purification; Sarcocystis cruzi; Sarcocystosis - diagnosis; Sarcocystosis - veterinary; Sarcocysts; Sarcosporidiosis; Transcriptomes; bradyzoite; acetyl-CoA synthetase; quantitative real-time PCR; Sarcocystis cruzi
• ISSN: 0916-7250; 1347-7439; 1347-7439
• DOI: 10.1292/jvms.22-0481

Sarcocystis cruzi is a member of the genus Sarcocystis, infecting bovine animals such as cattle and bison as intermediate hosts, and canids such as dogs and raccoon dogs as definitive hosts. Acute sarcocystosis of S. cruzi causes occasional symptoms in cattle, including weight loss, reduced milk production, abortions, and death, and similar to other Sarcocystis species can potentially cause food poisoning in humans when raw or undercooked infected cattle meat is consumed. Despite these issues, genetic information on S. cruzi is scarce, and there is no specific quantitative method for the detection and quantification of the parasite in infected cattle. In this study, we aimed to develop a method based on high-throughput sequencing of S. cruzi genome and transcriptome that specifically and quantitatively detects the S. cruzi acetyl-CoA synthetase gene (ScACS). Cardiac muscles were collected from slaughterhouses in Saitama Prefecture to obtain sarcocysts from which DNA and RNA were extracted for the high-throughput sequencing. Using the sequences, we developed a specific quantitative PCR assay which could distinguish S. cruzi ACS from that of Toxoplasma gondii by taking advantage of the differences in their exon/intron organizations and validated the assay with the microscopic counting of the S. cruzi bradyzoites. Thus, this assay will be useful for future studies of S. cruzi pathogenesis in cattle and for the surveillance of infected animals, thereby easing public health concerns.