Skip to main content
Iranian Journal of Public Health logoLink to Iranian Journal of Public Health
letter
. 2018 Aug;47(8):1210.

Response Letter to the Editor in Reference to Letter to the Editor about “Molecular Characterization of Animal Fasciola spp. Isolates from Kermanshah, Western Iran”

Arezoo BOZORGOMID 1, Naser NAZARI 2, Eshrat BEIGOM KIA 1, Homa HAJJARAN 1, Mehdi MOHEBALI 1,3, Mojgan ARYAEIPOUR 1, Peyman HEIDARIAN 1, Mohammad Saeid EZATI 4, Mohamad Bagher ROKNI 1,3,*
PMCID: PMC6123579  PMID: 30186795

Dear Editor-in-Chief

We would like to thank Dr Lee for his interest in our paper and for taking time to express their concerns. We agree that chimeric sequences in eukaryotes like other prokaryotic organisms could result in false perceptions novel haplotype or species. Chimeras are artifact sequences formed by two or more biological sequences concatenated into a single one (1). The ability to detect chimeric sequences during PCR amplification of the 18S ribosomal RNA genes is critical to avoid from polluting the public databases (2).

Coding regions of rDNA in the phylogenetic studies of various organisms have been well studied in past decades (3, 4). The primary objective of our study was to identify of Fasciola species in Kermanshah Province, western Iran by PCR-RFLP of 18S, ITS1 and 5.8S rRNA genes. It should be noted, however, sequencing rRNA-ITS1 region was used to confirm the results of PCR-RFLP (5). While efforts to detect chimeric sequences in 16S rRNA have been made in the prokaryotic community, parallel efforts in the eukaryotic community have been underdeveloped (1). However, there are no comprehensive databases for better understanding of chimeras in eukaryotic organisms especially Fasciola parasites.

References

  • 1.Wright Erik S., Safak Yilmaz L., Noguera Daniel R. (2012). DECIPHER, a search-based approach to chimera identification for 16S rRNA sequences. Appl Environ Microbiol, 78(3): 717–725. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Porazinska DL, Giblin-Davis RM, Sung W, Thomas WK. (2012). The Nature and Frequency of Chimeras in Eukaryotic Metagenetic Samples. J Nematol, 44(1):18–25. [PMC free article] [PubMed] [Google Scholar]
  • 3.Rokni MB, Bozorgomid A, Heydarian P, Aryaeipour M. (2018). Molecular evidence of human fasciolosis due to Fasciola gigantica in Iran: a case report. Iran J Public Health, 47(5):750–754. [PMC free article] [PubMed] [Google Scholar]
  • 4.Teofanova D, Hristov P, Yoveva A, Rdoslavov G. (2012). Issues associated with genetic diversity studies of the Liver Fluke, Fasciola hepatica (Platyhelminthes, Digenea, Fasciolidae). In: Genetic Diversity in Microorganisms (ed. Caiskan M.) ISBN: 978-953-51-0064-5, InTech, doi: 10.57772/34038. [Google Scholar]
  • 5.Bozorgomid A, Nazari N, Rahimi H, et al. (2016). Molecular characterization of animal Fasciola spp. isolates from Kermanshah, Western Iran. Iran J Public Health, 45(10):1315–1321. [PMC free article] [PubMed] [Google Scholar]

Articles from Iranian Journal of Public Health are provided here courtesy of Tehran University of Medical Sciences

RESOURCES