Abstract

BackgroundThe protozoan Giardia duodenalis is a common but highly diverse human parasite that comprises a complex of seven morphologically identical genetic assemblages, further divided into sub-assemblages. There is very little information available on the diversity of Giardia sub-assemblages and multi-locus genotypes infecting people in the United Kingdom. In this study we studied the molecular epidemiology of Giardia in symptomatic patients from North West England.MethodsWhole faecal DNA was extracted from the faecal samples of 406 Giardia cases and the parasites assemblage, sub-assemblage and multi-locus genotype were determined using PCR amplification, DNA sequencing and phylogenetic analysis of the beta-giardin, glutamate dehydrogenase, triose-phosphate isomerase and small-subunit ribosomal RNA genes. Information about age, gender and self-reported clinical outcomes was also collected from the patients to check for differences associated with the infecting Giardia assemblage.ResultsOur results showed a difference in the age prevalence of the two assemblages, with assemblage A being more common in older cases. Cases infected with assemblage B more often reported vomiting and a longer illness than cases infected with assemblage A. The majority of infections (64 %) were caused by assemblage B followed by assemblage A (33 %), while mixed-assemblage infections were rare (3 %). Assemblage A isolates mostly belonged to the sub-assemblage AII and showed completed identity with previously described isolates. The level of genetic sub-structuring was significantly higher in assemblage B isolates, since a higher proportion of novel assemblage B sequences was detected compared to assemblage A. A high number of assemblage B sequences showed heterogeneous nucleotide positions that prevented the unambiguous assignment to a specific sub-assemblage. Both previously described and novel multi-locus genotypes were described in both assemblages, and up to 17 different assemblage B multi-locus genotypes were found.ConclusionsWe have produced the first data on the parasite multi-locus genotypes in the UK and have demonstrated that the molecular diversity of Giardia is similar to other developed countries. Furthermore, we showed that the parasite assemblages infecting humans may be associated with patients of different ages and with different clinical outcomes.Electronic supplementary materialThe online version of this article (doi:10.1186/s13071-015-1059-z) contains supplementary material, which is available to authorized users.

Highlights

  • The protozoan Giardia duodenalis is a common but highly diverse human parasite that comprises a complex of seven morphologically identical genetic assemblages, further divided into sub-assemblages

  • As reported in the aforementioned studies, we observed multi-locus genotypes (MLGs) showing different combinations of bg, gdh and tpi subtypes that have never been reported before. These results suggest that humans can be infected with an array of very diverse assemblage A genotypes, and that the multi-locus sequence typing (MLST) approach should be consistently used in all future molecular epidemiological studies in other geographical regions

  • This study has shown that the molecular diversity of Giardia in symptomatic patients from North West England is largely similar to other areas of Europe, and that the two assemblages may differ in their distribution amongst people of different ages and in the illness they cause

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Summary

Introduction

The protozoan Giardia duodenalis is a common but highly diverse human parasite that comprises a complex of seven morphologically identical genetic assemblages, further divided into sub-assemblages. Giardiasis is one of the most common parasitic gastrointestinal diseases in humans worldwide, and it is considered a neglected tropical disease [1] It is caused by the parasitic protozoan Giardia duodenalis, which is transmitted either through contaminated water and food or from person to person. This parasite is a highly diverse organism and a complex of at least seven morphologically identical genetic assemblages (named A to G) that can infect a variety of mammalian hosts [2]. Humans are infected by parasites belonging to assemblage A (G. duodenalis) and B (G. enterica), and the latter is usually the most prevalent in human populations [4]

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