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Giardia duodenalis genetic assemblages and hosts
by
Heyworth, Martin F.
in
Animals
/ Assemblage
/ Chromosomes
/ Contamination
/ Cysts
/ Disease Outbreaks
/ Electrophoretic mobility
/ Environmental Pollution
/ Enzymes
/ Feces - parasitology
/ Gene sequencing
/ Genotype
/ Genotyping
/ Giardia
/ Giardia duodenalis
/ Giardia infections
/ Giardia lamblia - classification
/ Giardia lamblia - genetics
/ Giardia lamblia - growth & development
/ Giardia lamblia - isolation & purification
/ Giardia lamblia - physiology
/ Giardiasis
/ Giardiasis - epidemiology
/ Giardiasis - parasitology
/ Giardiasis - transmission
/ Giardiasis - veterinary
/ Glutamate dehydrogenase
/ Host Specificity
/ Host-Parasite Interactions
/ Humans
/ Infections
/ Oocysts
/ Review
/ Ribonucleic acid
/ RNA
/ Rodent Diseases - parasitology
/ Rodentia - parasitology
/ rRNA
/ Species Specificity
/ Trophozoites
/ Vertebrates - parasitology
/ Water Pollution
/ Zoonoses
2016
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Giardia duodenalis genetic assemblages and hosts
by
Heyworth, Martin F.
in
Animals
/ Assemblage
/ Chromosomes
/ Contamination
/ Cysts
/ Disease Outbreaks
/ Electrophoretic mobility
/ Environmental Pollution
/ Enzymes
/ Feces - parasitology
/ Gene sequencing
/ Genotype
/ Genotyping
/ Giardia
/ Giardia duodenalis
/ Giardia infections
/ Giardia lamblia - classification
/ Giardia lamblia - genetics
/ Giardia lamblia - growth & development
/ Giardia lamblia - isolation & purification
/ Giardia lamblia - physiology
/ Giardiasis
/ Giardiasis - epidemiology
/ Giardiasis - parasitology
/ Giardiasis - transmission
/ Giardiasis - veterinary
/ Glutamate dehydrogenase
/ Host Specificity
/ Host-Parasite Interactions
/ Humans
/ Infections
/ Oocysts
/ Review
/ Ribonucleic acid
/ RNA
/ Rodent Diseases - parasitology
/ Rodentia - parasitology
/ rRNA
/ Species Specificity
/ Trophozoites
/ Vertebrates - parasitology
/ Water Pollution
/ Zoonoses
2016
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Giardia duodenalis genetic assemblages and hosts
by
Heyworth, Martin F.
in
Animals
/ Assemblage
/ Chromosomes
/ Contamination
/ Cysts
/ Disease Outbreaks
/ Electrophoretic mobility
/ Environmental Pollution
/ Enzymes
/ Feces - parasitology
/ Gene sequencing
/ Genotype
/ Genotyping
/ Giardia
/ Giardia duodenalis
/ Giardia infections
/ Giardia lamblia - classification
/ Giardia lamblia - genetics
/ Giardia lamblia - growth & development
/ Giardia lamblia - isolation & purification
/ Giardia lamblia - physiology
/ Giardiasis
/ Giardiasis - epidemiology
/ Giardiasis - parasitology
/ Giardiasis - transmission
/ Giardiasis - veterinary
/ Glutamate dehydrogenase
/ Host Specificity
/ Host-Parasite Interactions
/ Humans
/ Infections
/ Oocysts
/ Review
/ Ribonucleic acid
/ RNA
/ Rodent Diseases - parasitology
/ Rodentia - parasitology
/ rRNA
/ Species Specificity
/ Trophozoites
/ Vertebrates - parasitology
/ Water Pollution
/ Zoonoses
2016
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Journal Article
Giardia duodenalis genetic assemblages and hosts
2016
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Overview
Techniques for sub-classifying morphologically identical Giardia duodenalis trophozoites have included comparisons of the electrophoretic mobility of enzymes and of chromosomes, and sequencing of genes encoding β-giardin, triose phosphate isomerase, the small subunit of ribosomal RNA and glutamate dehydrogenase. To date, G. duodenalis organisms have been sub-classified into eight genetic assemblages (designated A–H). Genotyping of G. duodenalis organisms isolated from various hosts has shown that assemblages A and B infect the largest range of host species, and appear to be the main (or possibly only) G. duodenalis assemblages that undeniably infect human subjects. In at least some cases of assemblage A or B infection in wild mammals, there is suggestive evidence that the infection had resulted from environmental contamination by G. duodenalis cysts of human origin.
Les techniques pour sous-classer morphologiquement des trophozoïtes identiques de Giardia duodenalis ont inclus des comparaisons de la mobilité électrophorétique des enzymes et des chromosomes et le séquençage des gènes codant pour la β-giardine, la triose-phosphate isomérase, la petite sous-unité ribosomique de l’ARN et la glutamate déshydrogénase. À ce jour, G. duodenalis a été sous-classé en 8 assemblages génétiques (désignés par A-H). Le génotypage de G. duodenalis isolés à partir de divers hôtes a montré que les assemblages A et B infectent le grand plus grand nombre d’espèces d’hôtes, et semblent être les assemblages principaux (ou peut-être uniques) qui infectent les sujets humains de manière indéniable. Dans au moins certains cas d’infection chez les mammifères sauvages par les assemblages A ou B, des éléments indiquent que l’infection était due à la contamination de l’environnement par des kystes de G. duodenalis d’origine humaine.
Publisher
EDP Sciences
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