Association of Blastocystis ST6 with higher protease activity among symptomatic subjects

• Published in: BMC microbiology 2021-10, Vol.21 (1), p.285-285, Article 285
• Main Authors: Karamati, Seyed Ahmad, Mirjalali, Hamed, Niyyati, Maryam, Yadegar, Abbas, Asadzadeh Aghdaei, Hamid, Haghighi, Ali, Seyyed Tabaei, Seyyed Javad
• Format: Article
• Language: English
• Subjects: Antibiotics; Antigens, Protozoan - metabolism; Asymptomatic; Bacteria; Biomarkers; Blastocystis; Blastocystis - classification; Blastocystis - enzymology; Blastocystis - immunology; Blastocystis - isolation & purification; Blastocystis Infections - parasitology; Blastocystis sp; Cell culture; Clinical symptoms; Cysteine Proteases - metabolism; Cysteine proteinase; Cytokines; Cytokines - genetics; Cytokines - metabolism; Development and progression; Diagnosis; DNA, Protozoan - genetics; Ethics; Feces - parasitology; Freeze-thaw; Freeze-thawing; Gastroenterology; Gene expression; Genetic Variation; Health aspects; HT29 Cells; Humans; Inflammation; Liver diseases; Measurement; Parasites; Pathogenesis; Pro-inflammatory biomarker; Protease; Protease activity; Proteases; Protozoa; Protozoan diseases; Protozoan Proteins - metabolism; Research centers; Subtypes; Virulence
• ISSN: 1471-2180; 1471-2180
• DOI: 10.1186/s12866-021-02341-9

Blastocystis sp. is an anaerobic intestinal protozoan parasite of humans and a wide range of animals worldwide. In the current study the correlation between the cysteine protease activity of clinical samples of Blastocystis sp. ST1-3 and 6 with the levels of pro-inflammatory cytokines was evaluated. Stool samples were collected from subjects with or without clinical symptoms. All samples were cultivated in DMEM medium. The bacteria were eliminated or reduced in Blastocystis sp. positive samples subtypes 1-3 and 6 by a variety of antibiotics and consecutive sub-cultures. To prepare parasite lysate, 1 × 10 Blastocystis sp. from each isolate were harvested and lysed using freeze-thaw. Protease activity of each isolate was measured and the gene expression of pro-inflammatory biomarkers in HT-29 cell line sensed by isolates was investigated using quantitative Real-time PCR. Protease activity assay showed inter- and intra-subtype variations among subtypes regarding the presence of symptoms, while the protease activity of symptomatic isolates was higher than asymptomatic isolates. The highest and lowest levels of protease activity were seen in ST6 and ST2, respectively. However, patterns of the expression of pro-inflammatory biomarkers in HT-29 cell line was different regarding the presence of symptoms and time points. There was no significant correlation between protease activity of different subtypes with the expression levels of pro-inflammatory biomarkers. Our study indicated a higher protease activity among isolates from symptomatic compared to asymptomatic subjects, suggesting functional role for proteases in clinical symptoms due to Blastocystis sp. The lack of correlation between the levels of expression of pro-inflammatory biomarkers with subtypes regarding the presence of clinical symptoms proposes the importance of host-related factors in presentation of clinical symptoms.