Detection of Giardia duodenalis assemblages A and B in human feces by simple, assemblage-specific PCR assays

• Published in: PLoS neglected tropical diseases 2012-08, Vol.6 (8), p.e1776-e1776
• Main Authors: Vanni, Ilaria, Cacciò, Simone Mario, van Lith, Lindy, Lebbad, Marianne, Svärd, Staffan G, Pozio, Edoardo, Tosini, Fabio
• Format: Article
• Language: English
• Subjects: Animals; Biology; Child; Child, Preschool; Cysts; Deoxyribonucleic acid; Developing countries; Diarrhea; DNA; DNA Primers - genetics; DNA sequencing; DNA, Protozoan - chemistry; DNA, Protozoan - genetics; Feces; Feces - parasitology; Genetic aspects; Genomes; Giardia; Giardia lamblia; Giardia lamblia - genetics; Giardia lamblia - isolation & purification; Giardiasis - diagnosis; Giardiasis - parasitology; Humans; Infections; Laboratories; LDCs; Mammals; Medicine; Methods; Microbiological assay; Molecular Diagnostic Techniques - methods; Molecular Sequence Data; Nucleotide sequencing; Parasites; Parasitology - methods; Polymerase Chain Reaction - methods; Primers (Molecular genetics); Properties; Sensitivity and Specificity; Sequence Analysis, DNA; Tropical diseases; Virulence
• ISSN: 1935-2735; 1935-2727; 1935-2735
• DOI: 10.1371/journal.pntd.0001776

The flagellated protozoan Giardia duodenalis is a common gastrointestinal parasite of mammals, including humans. Molecular characterizations have shown the existence of eight genetic groups (or assemblages) in the G. duodenalis species complex. Human infections are caused by assemblages A and B, which infect other mammals as well. Whether transmission routes, animal reservoirs and associations with specific symptoms differ for assemblage A and assemblage B is not clear. Furthermore, the occurrence and clinical significance of mixed (A+B) infections is also poorly understood. To date, the majority of PCR assays has been developed to identify all G. duodenalis assemblages based on the use of primers that bind to conserved regions, yet a reliable identification of specific assemblages is better achieved by ad hoc methods. The aim of this work was to design simple PCR assays that, based on the use of assemblage-specific primers, produce diagnostic bands of different lengths for assemblage A and B. We first generated novel sequence information from assemblage B, identified homologous sequences in the assemblage A genome, and designed primers at six independent loci. Experiments performed on DNA extracted from axenic cultures showed that two of the six assays can detect the equivalent of a single cyst and are not negatively influenced by disproportions between DNA of each assemblage, at least up to a 9:1 ratio. Further experiments on DNAs extracted from feces showed that the two assays can detect both assemblages in single tube reactions with excellent reliability. Finally, the robustness of these assays was demonstrated by testing a large collection of human isolates previously typed by multi-locus genotyping.