Literature DB >> 22154970

Assessment of three methods for multilocus fragment typing of Cryptosporidium parvum from domestic ruminants in north west Spain.

P Díaz1, S J Hadfield, J Quílez, M Soilán, C López, R Panadero, P Díez-Baños, P Morrondo, R M Chalmers.   

Abstract

The performance of three different methods, capillary electrophoresis (CE), high resolution slab-gel electrophoresis and sequencing, for PCR fragment size analysis of two Cryptosporidium parvum microsatellite regions, ML1 and ML2, was investigated by analysing 27 isolates from calves and 14 from lambs. To assess genetic variability of this protozoan in domestic ruminants in north west Spain, results were combined with sequence analysis of the 60 kDa glycoprotein (GP60) gene creating a multilocus type and analysed by farm and host species. CE showed greater overall typability (T), discriminatory power and ease of use than slab-gel electrophoresis and sequencing which were both affected by PCR stutter, especially at ML2. CE fragment sizes were consistently 4 bp longer compared to sequencing which is considered the gold standard for allele sizing but which gave the lowest typability; CE sizes were therefore adjusted. Only three alleles were identified at the ML1 locus (ML1-238, ML1-229 and ML1-226). The ML2 locus was more polymorphic and eight alleles were found (ML2-235, ML2-233, ML2-231, ML2-229, ML2-227, ML2-225, ML2-201 and ML2-176). Adjusted ML1 and ML2 CE fragment sizes were combined with GP60 subtype for 37 of the 41 C. parvum isolates which were typable at all three loci (T=0.90): nine multilocus types (MLTs) were identified. The discriminatory power of the 3-locus typing method was 0.83. Greater genetic variability was observed in calf isolates (7 MLTs) than in those from lambs (4 MLTs) although more calf isolates were studied. The most common MLT in cattle was MLT1 (ML1-238, ML2-231, GP60 subtype IIaA15G2R1), while MLT3 (ML1-238, ML2-227, GP60 IIaA16G3R1) was predominant in lambs. Our findings demonstrate that high discrimination can be achieved by means of multilocus typing. CE appears to be an economic and rapid option for performing microsatellite fragment size analysis offering good typability, discrimination and ease of use but may require calibration to sequenced standards.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 22154970     DOI: 10.1016/j.vetpar.2011.11.039

Source DB:  PubMed          Journal:  Vet Parasitol        ISSN: 0304-4017            Impact factor:   2.738


  9 in total

1.  Validation of fragment analysis by capillary electrophoresis to resolve mixed infections by Cryptosporidium parvum subpopulations.

Authors:  Joaquín Quílez; Stephen J Hadfield; Ana Ramo; Claudia Vergara-Castiblanco; Rachel M Chalmers
Journal:  Parasitol Res       Date:  2014-03-08       Impact factor: 2.289

2.  Emergence of novel subtypes of Cryptosporidium parvum in calves in Poland.

Authors:  Agnieszka Kaupke; Artur Rzeżutka
Journal:  Parasitol Res       Date:  2015-09-11       Impact factor: 2.289

3.  Molecular characterization of Cryptosporidium isolates from high-excreting young dairy calves in dairy cattle herds in Western France.

Authors:  A Rieux; C Chartier; I Pors; A Delafosse; C Paraud
Journal:  Parasitol Res       Date:  2013-07-03       Impact factor: 2.289

4.  Multilocus Sequence Typing helps understand the genetic diversity of Cryptosporidium hominis and Cryptosporidium parvum isolated from Colombian patients.

Authors:  Johanna Uran-Velasquez; Juan F Alzate; Ana E Farfan-Garcia; Oscar G Gomez-Duarte; Larry L Martinez-Rosado; Diego D Dominguez-Hernandez; Winston Rojas; Ana Luz Galvan-Diaz; Gisela M Garcia-Montoya
Journal:  PLoS One       Date:  2022-07-08       Impact factor: 3.752

5.  Host association of Cryptosporidium parvum populations infecting domestic ruminants in Spain.

Authors:  Joaquín Quílez; Claudia Vergara-Castiblanco; Luis Monteagudo; Emilio del Cacho; Caridad Sánchez-Acedo
Journal:  Appl Environ Microbiol       Date:  2013-06-28       Impact factor: 4.792

6.  Epidemiology and molecular relationships of Cryptosporidium spp. in people, primates, and livestock from Western Uganda.

Authors:  Stephanie J Salyer; Thomas R Gillespie; Innocent B Rwego; Colin A Chapman; Tony L Goldberg
Journal:  PLoS Negl Trop Dis       Date:  2012-04-10

7.  Development of a framework for genotyping bovine-derived Cryptosporidium parvum, using a multilocus fragment typing tool.

Authors:  Emily J Hotchkiss; Janice A Gilray; Marnie L Brennan; Robert M Christley; Liam J Morrison; Nicholas N Jonsson; Elizabeth A Innes; Frank Katzer
Journal:  Parasit Vectors       Date:  2015-10-01       Impact factor: 3.876

8.  Genotyping Cryptosporidium andersoni in cattle in Shaanxi Province, Northwestern China.

Authors:  Guang-Hui Zhao; Wan-Xin Ren; Man Gao; Qing-Qing Bian; Bing Hu; Mei-Mei Cong; Qing Lin; Rong-Jun Wang; Meng Qi; Mao-Zhen Qi; Xing-Quan Zhu; Long-Xian Zhang
Journal:  PLoS One       Date:  2013-04-01       Impact factor: 3.240

9.  Intra-Species Diversity and Panmictic Structure of Cryptosporidium parvum Populations in Cattle Farms in Northern Spain.

Authors:  Ana Ramo; Joaquín Quílez; Luis Monteagudo; Emilio Del Cacho; Caridad Sánchez-Acedo
Journal:  PLoS One       Date:  2016-02-05       Impact factor: 3.240

  9 in total

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