Abstract

Among helminth parasites, Paragonimus (zoonotic lung fluke) gains considerable importance from veterinary and medical points of view because of its diversified effect on its host. Nearly fifty species of Paragonimus have been described across the globe. It is estimated that more than 20 million people are infected worldwide and the best known species is Paragonimus westermani, whose type locality is probably India and which infects millions of people in Asia causing disease symptoms that mimic tuberculosis. Human infections occur through eating raw crustaceans containing metacercarie or ingestion of uncooked meat of paratenic hosts such as pigs. Though the fluke is known to parasitize a wide range of mammalian hosts representing as many as eleven families, the status of its prevalence, host range, pathogenic manifestations and its possible survivors in nature from where the human beings contract the infection is not well documented in India. We took advantage of the whole genome sequence data for P. westermani, generated by Next Generation Sequencing, and its comparison with the existing data for the P. westermani for comparative mt DNA phylogenomic analyses. Specific primers were designed for the 12 protein coding genes with the aid of existing P. westermani mtDNA as the reference. The Ion torrent next generation sequencing platform was harnessed to completely sequence the mitochondrial genome, and applied innovative approaches to bioinformatically assemble and annotate it. A strategic PCR primer design utilizing the whole genome sequence data from P. westermani enabled us to design specific primers capable of amplifying all regions of the mitochondrial genome from P. westermani. Assembly of NGS data from libraries enriched in mtDNA sequence by PCR gave rise to a total of 11 contigs spanning the entire 14.7 kb mt DNA sequence of P. westermani available at NCBI. We conducted gap-filling by traditional Sanger sequencing to fill in the gaps. Annotation of non-protein coding genes successfully identified tRNA regions for the 24 tRNAs coded in mtDNA and 12 protein coding genes. Bayesian phylogenetic analyses of the concatenated protein coding genes placed P. westermani within the family Opisthorchida. The complete mtDNA sequence of P. westermani is 15,004 base pairs long; the lung fluke is the major etiological agent of paragonimiasis and the first Indian representative for the family Paragonimidae to be fully sequenced that provides important genetic markers for ecological, population and biogeographical studies and molecular diagnostic of digeneans that cause trematodiases.

Highlights

  • Among about 50 known species of the genus Paragonimus, Paragonimus westermani, one of the causative agents of paragonimiasis, was first described as early as 1878 and is the most well-known species within the genus Paragonimus because of its wide geographical distribution and medical importance (Blair, Xu & Agatsuma, 1999)

  • The mapped reads were extracted in fastq format using custom perl script

  • We took advantage of the whole genome sequence data generated by next generation sequencing (NGS) technology for P. westermani Indian isolate and its comparison to existing data for the P. westermani (Korean isolate) mitochondrial genome for the purpose of comparative analysis between the mt genomes of the two isolates

Read more

Summary

Introduction

Among about 50 known species of the genus Paragonimus, Paragonimus westermani, one of the causative agents of paragonimiasis, was first described as early as 1878 and is the most well-known species within the genus Paragonimus because of its wide geographical distribution and medical importance (Blair, Xu & Agatsuma, 1999). As per the recent estimates, about 293 million people are at risk, while several millions are infected worldwide (Keiser & Utzinger, 2009) This may be an underestimate as there are still many places where the disease burden has yet to be assessed. The state-of-the-art molecular biology techniques, generation sequencing (NGS) technology and their rapid development in contemporary times may provide additional tools for the differential identification of digenean trematode infections to overcome limitations of current morphology-based diagnostic methods. Owing to their high nucleotide substitution rates, parasitic flatworm mitochondrial (mt) genomes have become very popular markers for diagnostic purposes and for resolving their phylogenetic relationships at different taxonomic ranks. Comparative mitochondrial genomics can provide more reliable results and reveal important informations of mtDNA architectural features such as gene order and structure of non-coding regions

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call