A novel high-resolution multilocus sequence typing of Giardia intestinalis Assemblage A isolates reveals zoonotic transmission, clonal outbreaks and recombination

被引:37
作者
Ankarklev, Johan [1 ]
Lebbad, Marianne [2 ]
Einarsson, Elin [2 ]
Franzen, Oscar [3 ]
Ahola, Harri [4 ]
Troell, Karin [4 ]
Svard, Staffan G. [2 ]
机构
[1] Stockholm Univ, Dept Mol Biosci, SE-10691 Stockholm, Sweden
[2] Uppsala Univ, Dept Cell & Mol Biol, BMC, Box 596, SE-75124 Uppsala, Sweden
[3] Karolinska Inst, Integrated Cardio Metab Ctr, Novum, Box 285, SE-14157 Stockholm, Sweden
[4] Natl Vet Inst, Dept Microbiol, SE-75189 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
Parasite; Diarrhea; Recombination; Zoonosis; Transmission; DUODENALIS; LAMBLIA; IDENTIFICATION; INFECTION; LOCUS; GENOTYPES; CHILDREN; EXCHANGE; HUMANS; GENES;
D O I
10.1016/j.meegid.2018.02.012
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Molecular epidemiology and genotyping studies of the parasitic protozoan Giardia intestinalis have proven difficult due to multiple factors, such as low discriminatory power in the commonly used genotyping loci, which has hampered molecular analyses of outbreak sources, zoonotic transmission and virulence types. Here we have focused on assemblage A Giardia and developed a high-resolution assemblage-specific multilocus sequence typing (MLST) method. Analyses of sequenced G. intestinalis assemblage A genomes from different sub-assemblages identified a set of six genetic loci with high genetic variability. DNA samples from both humans (n = 44) and animals (n = 18) that harbored Giardia assemblage A infections, were PCR amplified (557-700 bp products) and sequenced at the six novel genetic loci. Bioinformatic analyses showed five to ten-fold higher levels of polymorphic sites than what was previously found among assemblage A samples using the classic genotyping loci. Phylogenetically, a division of two major clusters in assemblage A became apparent, separating samples of human and animal origin. A subset of human samples (n = 9) from a documented Giardia outbreak in a Swedish day-care center, showed full complementarity at nine genetic loci (the six new and the standard BG, TPI and GDH loci), strongly suggesting one source of infection. Furthermore, three samples of human origin displayed MLST profiles that were phylogenetically more closely related to MLST profiles from animal derived samples, suggesting zoonotic transmission. These new genotyping loci enabled us to detect events of recombination between different assemblage A isolates but also between assemblage A and E isolates. In summary, we present a novel and expanded MLST strategy with significantly improved sensitivity for molecular analyses of virulence types, zoonotic potential and source tracking for assemblage A Giardia.
引用
收藏
页码:7 / 16
页数:10
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