Multilocus genotyping of Giardia duodenalis in Brazilian children

被引:22
|
作者
Scalia, Luana A. M. [1 ]
Fava, Natalia M. N. [1 ]
Soares, Rodrigo M. [2 ]
Limongi, Jean E. [1 ]
da Cunha, Maria Julia R. [1 ]
Pena, Isabella F. [3 ]
Kalapothakis, Evanguedes [3 ]
Cury, Mrcia C. [1 ]
机构
[1] Univ Fed Uberlandia, Inst Ciencias Biomed, Lab Parasitol, Ave Para 1720,Bl 4C, BR-38400902 Uberlandia, MG, Brazil
[2] Univ Sao Paulo, Dept Med Vet Prevent & Saude Anim, Fac Med Vet & Zootecnia, Ave Prof Dr Orlando Marques de Paiva 87, BR-05508270 Sao Paulo, SP, Brazil
[3] Univ Fed Minas Gerais, Inst Ciencias Biol, Lab Biotecnol & Marcadores Mol, Ave Antonio Carlos 6627, BR-31270010 Belo Horizonte, MG, Brazil
关键词
beta-giardin; Children; Giardia duodenalis; Glutamate dehydrogenase; Heterogeneity; Triose phosphate isomerase; MOLECULAR EPIDEMIOLOGY; LOCUS; CRYPTOSPORIDIUM; IDENTIFICATION; TRANSMISSION; PREVALENCE; ASSEMBLAGE; INFECTION; REGION; STATE;
D O I
10.1093/trstmh/trw036
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Giardia duodenalis is a parasite of several mammalian species, including humans, distributed worldwide. This research aimed to identify the molecular assemblages/sub-assemblages of G. duodenalis and to determine the intra-assemblage genetic variation of the different genes of assemblages A and B in preschool children in the cities of Araguari and UberlIndia, Minas Gerais, Brazil. Methods: The molecular characterization followed beta-giardin (bg), glutamate dehydrogenase (gdh) and triose phosphate isomerase (tpi) protocols. Results: Of 226 stool samples, G. duodenalis cysts were found in 45 (19.9%). The tpi gene was amplified in 34 samples: 16 assemblage A, 14 B and four mixed samples A/B. The gdh gene was amplified in 32 samples, including 14 A, 16 B and two A/B. For the bg gene, 19 samples were sequenced: nine assemblage A, five B, three E, and two mixed, A/E and B/E. Animal-specific assemblage E were identified by bg, but were not confirmed for other genes. Twelve samples were characterized by full agreement of the three genes. Two new multilocus genotyping (MLGs) for assemblage A and two new MLGs for assemblage B were also described. Conclusions: These findings substantiate the importance of using more than one gene protocol since the sensitivity and genetic variability changes with the locus used.
引用
收藏
页码:343 / 349
页数:7
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