z-logo
open-access-imgOpen Access
Molecular detection and genotyping of intestinal protozoa from different biogeographical regions of Colombia
Author(s) -
Adriana Higuera,
Ximena Villamizar,
Giovanny Herrera,
Julio César Giraldo Forero,
Luis Reinel Vásquez Arteaga,
Plutarco Urbano,
Oswaldo Alberto Romero Villalobos,
Catalina Tovar,
Juan David Ramírez
Publication year - 2020
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.8554
Subject(s) - blastocystis , biology , entamoeba , cryptosporidium , entamoeba histolytica , genotyping , protozoa , enterocytozoon bieneusi , microbiology and biotechnology , giardia , genotype , feces , microsporidiosis , genetics , microsporidia , gene , spore
Background Intestinal parasitic protozoa represent a serious problem of public health particularly in developing countries. Protozoa such as Blastocystis, Giardia intestinalis , Entamoeba histolytica and Cryptosporidium spp. are associated with diarrheal symptoms. In Colombia, there is little region-specific data on the frequency and circulating genotypes/species of these microorganisms. Therefore, the main objective of our study was to employ molecular detection and genotyping of G. intestinalis and Blastocystis , Cryptosporidium and Entamoeba spp. in samples from different biogeographical regions of Colombia. Methods We collected 649 human fecal samples from five biogeographical regions of Colombia: the Amazon, Andean, Caribbean, Orinoco and Pacific regions. Blastocystis, G. intestinalis, Cryptosporidium spp. and Entamoeba complex were detected by microscopy and conventional PCR. Molecular genotyping was conducted to identify Blastocystis subtypes (STs) (18s), G. intestinalis assemblages (triose phosphate isomerase and glutamate dehydrogenase) and Cryptosporidium species (18s). Genetic diversity indices were determined using dnasp.5. Results We detected G. intestinalis in 45.4% ( n = 280) of samples, Blastocystis in 54.5% ( n = 336) of samples, Cryptosporidium spp. in 7.3% ( n = 45) of samples, Entamoeba dispar in 1.5% ( n = 9) of samples, and Entamoeba moshkovskii in 0.32% ( n = 2) of samples. Blastocystis STs 1–4, 8 and 9 and G. intestinalis assemblages AII, BIII, BIV, D and G were identified. The following Cryptosporidium species were identified: C. hominis , C. parvum , C. bovis , C. andersoni , C. muris , C. ubiquitum and C. felis . The Caribbean region had the highest frequency for each of the microorganisms evaluated (91.9% for G. duodenalis , 97.3% for Blastocystis , 10.8% for Cryptosporidium spp., 13.5% for E. dispar and 2.7% for E. moshkovskii ). The Orinoco region had a high frequency of Blastocystis (97.2%) and the Andean region had a high frequency of G. intestinalis (69.4%). High and active transmission was apparent in several regions of the country, implying that mechanisms for prevention and control of intestinal parasitosis in different parts of the country must be improved.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom