Prevalence and subtype analysis of Blastocystis in healthy Indian individuals

• Published in: Infection, genetics and evolution genetics and evolution, 2015-04, Vol.31, p.296-299
• Main Authors: Pandey, Prashant Kumar, Verma, Pankaj, Marathe, Nachiket, Shetty, Sudarshan, Bavdekar, Ashish, Patole, Milind Shivaji, Stensvold, Christen Rune, Shouche, Yogesh Shreepad
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Blastocystis - classification; Blastocystis - genetics; Blastocystis Infections - epidemiology; Blastocystis Infections - parasitology; DNA; DNA Barcoding, Taxonomic; DNA, Protozoan; DNA, Ribosomal; Epidemiology; Evolution, Molecular; Female; Genetic diversity; Humans; India - epidemiology; Male; Microbiology; Middle Aged; Parasite; Phylogeny; Prevalence; Public Health; Young Adult
• ISSN: 1567-1348; 1567-7257
• DOI: 10.1016/j.meegid.2015.02.012

•First survey on Blastocystis in India.•30 infants included in the study were Blastocystis-negative, while 27 out of 100 adults were positive.•ST3 was seen in all individuals positive for Blastocystis.•ST1 was uncommon and seen only in mixed infection with ST3.•ST3 is common in the background population in Maharashtra, India. There is a growing interest in subtype (ST) analysis of the intestinal parasite Blastocystis due to its extensive genetic diversity that might reflect differences in pathogenicity. Although essential for reference, few studies are available on Blastocystis in healthy individuals. Moreover, molecular epidemiology data on Blastocystis in India still remain to emerge. In the present study we identified the prevalence and ST distribution of Blastocystis in healthy Indian individuals. A total of 220 stool samples were obtained; four of 100 samples from 100 adults were chosen randomly for construction of small subunit (SSU) rRNA gene clone libraries in order to elucidate micro-eukaryotic diversity in the human gut. From the SSU rDNA library, 64 sequences annotated to Blastocystis were used for ST analysis along with sequences obtained by direct sequencing of SSU rDNA PCR products amplified from the remaining samples and generated using primers targeting Blastocystis. Of 220 stool samples collected, 120 samples from 30 infants (aged 1week to 1year) were PCR-negative. Of the remaining 100 samples from 100 adults, 27 resulted in specific amplification. Out of these 27, four samples were suspected of mixed ST infection and so these samples were further analyzed by construction of clone libraries. Analysis of cloned sequences revealed that indeed 2 samples had mixed ST infection (ST1 and ST3) while the remaining two showed infection with two separate ST3 strains. ST3 was the most common ST present in our study group (100%) followed by ST1 (7.4%); ST1 was seen only in mixed infections. SSU rDNA clone library sequences generated by processing of pooled samples were identified as ST3. The majority of ST3 sequences exhibited allele 34 commonly found in the European population.