BioMed Research International

BioMed Research International / 2013 / Article

Research Article | Open Access

Volume 2013 |Article ID 875048 |

Natália M. N. Fava, Rodrigo M. Soares, Luana A. M. Scalia, Evanguedes Kalapothakis, Isabella F. Pena, Carlos U. Vieira, Elaine S. M. Faria, Maria J. Cunha, Talles R. Couto, Márcia Cristina Cury, "Performance of Glutamate Dehydrogenase and Triose Phosphate Isomerase Genes in the Analysis of Genotypic Variability of Isolates of Giardia duodenalis from Livestocks", BioMed Research International, vol. 2013, Article ID 875048, 9 pages, 2013.

Performance of Glutamate Dehydrogenase and Triose Phosphate Isomerase Genes in the Analysis of Genotypic Variability of Isolates of Giardia duodenalis from Livestocks

Academic Editor: Jacques Cabaret
Received16 Apr 2013
Revised13 Aug 2013
Accepted31 Aug 2013
Published06 Nov 2013


Giardia duodenalis is a small intestinal protozoan parasite of several terrestrial vertebrates. This work aims to assess the genotypic variability of Giardia duodenalis isolates from cattle, sheep and pigs in the Southeast of Brazil, by comparing the standard characterization between glutamate dehydrogenase (gdh) and triose phosphate isomerase (tpi) primers. Fecal samples from the three groups of animals were analyzed using the zinc sulphate centrifugal flotation technique. Out of 59 positive samples, 30 were from cattle, 26 from sheep and 3 from pigs. Cyst pellets were stored and submitted to PCR and nested-PCR reactions with gdh and tpi primers. Fragment amplification of gdh and tpi genes was observed in 25 (42.4%) and 36 (61.0%) samples, respectively. Regarding the sequencing, 24 sequences were obtained with gdh and 20 with tpi. For both genes, there was a prevalence of E specific species assemblage, although some isolates have been identified as A and B, by the tpi sequencing. This has also shown a larger number of heterogeneous sequences, which have been attribute to mixed infections between assemblages B and E. The largest variability of inter-assemblage associated to the frequency of heterogeneity provided by tpi sequencing reinforces the polymorphic nature of this gene and makes it an excellent target for studies on molecular epidemiology.

1. Introduction

Giardia duodenalis (Giardia lamblia, Giardia intestinalis) is a small intestinal parasitic protozoan of several terrestrial vertebrates and has been described throughout the world in livestock, regardless of their capability, sex, and age. Prevalence rates, in humans and in animals, may vary among countries, probably due to differences in the management, weather, and type of study conducted to diagnose the infections [1].

The protozoan is currently considered as a complex of species, due to the existing genetic differences among isolates infecting different hosts [2]. Eight different assemblages have been attributed to this complex but with similar morphologies. Isolates recovered from human feces and feces from other mammal species belong to two genetic groups, called Polish and Belgian in Europe and assemblages A and B in Australia [3, 4]. Six other assemblages have been considered as species-specific (C to H) [5], with C and D prevailing in dogs, E in ungulates, F in cats, G in rats, and assemblage H in marine vertebrates [6].

Substantial differences found in glutamate dehydrogenase (gdh), β-giardin, triose phosphate isomerase (tpi), and SSUr-RNA genes were crucial for the recognition of intraspecific variations, which were called assemblages. These genes have a discriminatory ability, which is enough to identify intra-assemblage variations, used for genotyping, but, mainly, for subgenotyping of isolates [7, 8].

Cattle, pigs, and sheep are susceptible to infections with species-specific assemblage E and also with zoonotic infections of Giardia duodenalis assemblages A and B [913].

For some time, most studies on genotypic characterization were only conducted with a single gene locus; however, studies have shown inconsistent results when distinct loci are sequenced. Thus, the genotyping of more than one gene may improve the attribution of the assemblage to its respective isolate, helping in the understanding of the epidemiology of giardiasis [8].

This work has the purpose of assessing the genotypic variability among isolates of Giardia duodenalis from cattle, pigs, and sheep from the southeastern region of Brazil, when comparing the pattern of characterization between primers targeting glutamate dehydrogenase (gdh) and triose phosphate isomerase (tpi) genes.

2. Materials and Methods

2.1. Population of Study

This work has been approved by “Comitê de Ética na Utilização de Animais da Universidade Federal de Uberlândia” (CEUA-UFU) (Ethics Committee on Animal Use of the Federal University of Uberlândia), protocol 003/12.

Cattle, pigs, and sheep, with an age range of 0 to 10 months, both males and females, and with different breeds from the microregion of Uberlândia, Minas Gerais state, southeastern region of Brazil have been included in the study.

Cattle were distributed in 17 farms; 5 of them were Holstein cattle (PO) (for milk production) and 12 with Girolando cattle, were milk and beef production. Sheep came from a single farm with Corriedale breed with meat and wool production, and pigs came from 10 commercial farms, with Landrace breed.

2.2. Fecal Samples
2.2.1. Sample Collection

Feces were collected individually straight from the rectal ampulla of cattle and sheep. Regarding pigs, samples were collected in pools, straight from the floor of the stalls, as they were grouped in lots of 30 to 40 animals, according to their age. Each pool was considered as a sample.

Due to the intermittent pattern of elimination of Giardia duodenalis cysts, three fecal samples from each cow and sheep were collected every other day in order to increase the reliability of the study. In pigs, samples were collected once due to the sanitary management of the farm.

Feces were collected and stored in plastic bags identified with the number of each animal or lot, the name of the farm, and the date of collection and were sent to Laboratório de Parasitologia (laboratory of parasitology) of Universidade Federal de Uberlândia (UFU) for processing.

2.2.2. Sample Processing

Samples were considered positive for Giardia duodenalis cysts using the zinc sulphate centrifugal flotation technique [14]. Slides and coverslips with positive samples were washed with sodium phosphate buffered saline (PBS), pH 7.2, and then transferred to polystyrene microtubes. These were submitted to three centrifugations at 10,000 xg for ten minutes each. In each centrifugation, the supernatant was discarded, and a new PBS was added. Cyst pellets were stored at −20°C for later use.

2.3. DNA Extraction

After resuspension in 500 μL of lysis buffer (10 mM Tris-HCl, pH 8.0; 25 mM EDTA, pH 8.0; 100 mM NaCl; 1% SDS), cyst pellets were submitted to three cycles of freezing/thawing. Ten mg/mL of proteinase K was added to the liquid product, and then it was incubated at 37°C for 12 hours. DNA was extracted following the phenol-chloroform protocol for DNA extraction described by Sambrook et al., 1989 [15]. Negative controls were used in each extraction group.

2.4. Polymerase Chain Reaction (PCR)

In order to amplify the fragments of glutamate dehydrogenase (gdh) and triose phosphate isomerase (tpi) genes, primers developed by Cacciò et al. [8] and Sulaiman et al. [7] were used.

The fragment of 530 base pairs of gdh gene was obtained using both external (Gdh 1 and Gdh 2) and internal primers (Gdh 3 and Gdh 4).

In order to amplify the fragment of tpi gene (530 pb), external primers (AL3543 and AL3546) and internal primers (AL3544 and AL3545) were used.

PCR and nested-PCR reactions were performed in Mastercycler pro thermocycler (Eppendorf, Brazil) according to the protocols described by Cacciò et al. [8] and Sulaiman et al. [7].

Bands of interest were visualized through the agarose gel electrophoresis technique at 2% (P/V), and stained with ethidium bromide at 0.5 μg/mL with further observation using an ultraviolet transilluminator. Aliquots of 8 μL of the amplified sample were analyzed.

2.5. Sequencing and Alignment of DNA

Positive nested-PCR products were purified with Sephacryl 400 resin (Ilustra-MicroSpin S400 HR Columns) and sequenced in a single direction. Reactions were performed in a Mastercycler pro thermocycler (Eppendorf, Brazil) using Big Dye terminator V.3.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, CA, USA). Products were read using the automatic sequencer ABI 3130 Genetic Analyzer (Applied Biosystems, Foster City, CA, USA).

The quality of the partial sequences and the clustering of the fragments were obtained with the use of Sequence Scanner version 1.0 (Copyright Applied Biosystems, Foster City, CA, USA). Nucleotide alignment was performed manually using BioEdit Sequence Alignment Editor (Hall, 1999) and using as a base the homologous sequences available on GenBank: M84604 (assemblage A), AY826193 (assemblage B), U60982 (assemblage C), U60986 (assemblage D), AY178741 (assemblage E), and AF069057 (assemblage F) for gdh gene and AY655704 (assemblage A, sub-assemblage AI), U57897 (assemblage A, sub-assemblage AII), AF069561 (assemblage B, sub-assemblage BIII), AF069560 (assemblage B, sub-assemblage BIV), AY228641 (assemblage C), DQ246216 (assemblage D), AY228645 (assemblage E), and AF069558 (assemblage F) for tpi gene.

In order to determine the phylogenetic relationship among assemblages, phylograms were constructed using Mega v.5.1 Beta, with the neighbor-joining method, with bootstrap values established in 1000 replicates.

3. Results

3.1. Positivity

Two hundred and fifty-six fecal samples from cattle, 105 from sheep, and 90 from pigs were collected. Due to the fecal collection in triplicate, 768 and 315 fecal examinations were performed in cattle and sheep, respectively.

Positivity for Giardia duodenalis cysts was detected in 30 (11.7%) cattle samples, in 26 (24.8%) sheep samples, and in 3 (3.4%) pools of pig samples with a total of 59 positive samples.

3.2. Molecular Characterization

Out of all positive samples ( ) in three animal species, the amplification of gdh and tpi gene fragments was observed in 25 (42.4%) and 36 (61.0%) samples, respectively.

Out of 25 samples with amplified fragments of gdh gene, 14 were from sheep, 9 from cattle, and 2 from pigs. Out of 36 samples with amplified fragments of tpi gene, 15 were from sheep, 18 from cattle, and 3 from pigs.

In this study, 44 sequences were obtained and analyzed, 24 from gdh gene and 20 from tpi gene. For both genes, isolates were sequenced from the three animal species.

3.2.1. gdh

Fourteen isolates from sheep and nine from cattle, in which gdh gene was sequenced, were identified as assemblage E.

When analyzing each sequence individually and comparing them to their respective base sequence, an intra-assemblage variation was seen in three isolates of sheep identified as E by the gdh gene. These differ from the base sequence AY178741, but they were similar among each other. Positions of nucleotide substitution were the same for the three sequences, and the nucleotides substituted at those positions were also the same (Table 1). The 11 remaining isolates of sheep were not homologous to any sequence but were identical among each other. New sequences of sheep isolates were inserted into the GenBank under the numbers KC816543 and KC816544, respectively. Regarding isolates of cattle, all of them had the same nucleotide variation (T, position 654), when compared to the reference sequence number AY178741. However, this variation made them identical to the sequence number EF07645.1 stored in the GenBank.



*Base sequence of assemblage E stored at GenBank.

The two isolates of pigs differed by genotyping; one was identified as assemblage E and the other as D. The isolate identified as assemblage D was heterogeneous, with double peaks throughout the gene (Figure 1); as it was not homologous with any sequence described, it was deposited in the GenBank under the number KC816545. The isolate identified as E was identical to the reference sequence used in this study (AY178741).

The phylogenetic relationship among isolates genotyped by sequencing gdh gene is shown in the phylogram (Figure 2).

3.2.2. tpi

Genotyping of tpi gene has shown variations in assemblages of 10 isolates from sheep, six identified as assemblage E, two as B, subassemblage BIII, and two as A, subassemblage AII. For cattle, eight out of nine isolates were assemblage E and one was assemblage B, subassemblage BIII. The isolate of pig was identified as a species-specific assemblage E.

Two isolates of sheep and three of cattle had polymorphic sites along the gene sequence between assemblages BIII and E, where the colocalization of conserved nucleotides was observed (Table 2).


Nucleotides positions and replacements

*AF069561: assemblage BIII; *AY228645: assemblage E; **isolates identified as assemblage BIII, ***isolates identified as assemblage E; dots indicate identity to the reference sequences.

When comparing sequences from sheep obtained in this study to those used as reference, four out of ten isolates were homologous to the reference sequence, with one being homologous to the sequence number JQ837919.1 and the others being homologous to the sequence number JQ837808.1, both stored in the Genbank. Out of the six remaining isolates of sheep, each one was different, with no homology to any sequence described, being considered new, and inserted into the Genbank under the numbers KC85814 to KC858149.

Among the sequences from cattle, one isolate was homologous to the other, present in the Genbank (JQ837925.1). The other isolates from cattle differed among each other and are present in the GenBank under the numbers KC858151 to KC858157.

The isolate from pigs was not identical to any other described ones, thus being considered new and inserted into the Genbank under the number KC858150.

While constructing a phylogenetic tree (Figure 3), heterogeneous samples were not removed as they did not interfere with the final arrangement of the phylogram.

3.3. Relationship between gdh and tpi Markers When Genotyping Isolates

Out of all the samples ( ), those with amplified fragments of gdh and tpi genes, 13 (21.3%), had both genes sequenced. Among these, eight (61.5%) were in accordance with the identification of assemblage E. The other four were not in accordance with the interassemblage (Table 3).

Samples gdh tpi
Assemblage AssemblageSubassemblage


La: lambs, Ca: cattle, Pi: pig.

4. Discussion

The region studied is very important in the livestock production in Brazil, with 3% of the total amount of heads of cattle in the country. Nevertheless, there are no studies published on the presence and epidemiological characteristics of Giardia duodenalis in livestock in this region.

PCR for both genes has failed to amplify some positive samples with the microscopic technique in this study. The failure may be attributed to the following: the presence of PCR inhibitors in the feces, the small amount of cysts, the small amount of target DNA present in the samples, and the association of these factors with the low efficiency of the DNA extraction process [1618]. In addition, the small sample volume used and/or the loss of parasites during wash may impair the amplification [16, 19]. The choice of a target gene is also fundamentally important to the success of the amplification [20]. These genes (gdh and tpi) are less conserved and have a greater variability than other genes, which may lead to excessive imbalances in the binding sites of the nucleotide primers, resulting in a low sensitivity of the PCR [21].

Although authors such as Leonhard et al. [22], and Lebbad et al. [23] attribute a greater success of the amplification to the gdh, there is no consensus among researchers regarding which of these two genes is more effective to be the target of this reaction. In this study, tpi gene was more successful, being amplified in a larger number of samples when compared to gdh. In the present study, for three animal species, regardless of the target gene, species-specific assemblage E prevailed, which is in accordance with O’Handley et al. [9], Huetink et al. [24], Trout et al. [25], Castro-Hermida et al. [16], Souza et al. [26], Feng et al. [27]; Santín et al. [28], and Gómez-Muñoz et al. [18].

According to Read et al. [29], Wielinga and Thompson [30], and Cacciò and Ryan [21], among several genes used in the genotyping of Giardia duodenalis isolates, tpi and gdh provided more detailed information on Giardia duodenalis assemblages, as they have polymorphic sequences, which enable us to clearly distinguish genotypes.

In the present study, it was observed that when using gdh gene, PiNUdi001 isolate was identified as D, which is a dog-specific assemblage. With the chromatogram of this sample, in strategic sites along the gene, double peaks were seen, which characterizes a possible mixed infection. Overlapped nucleotides are located on the same positions of assemblages D and E, which suggests the concomitant presence of both assemblages in the isolate. Although rare, these findings were also observed by Langkjær et al. [31] and Sprong et al. [32].

The sequencing of the gdh gene has also shown differences between the reference sequence (assemblage E) and three isolates from sheep, identified as E. The pattern of nucleotide substitution, associated with the analysis of the phylogenetic tree, suggests that these isolates are subassemblages of assemblage E. The position of isolates on the tree is the basis of this hypothesis, as they are grouped in a branch of the tree that is different from the one which gathers other isolates from the same assemblage. Some studies postulate the existence of subassemblages E [33, 34], although there are no factual data supporting this. According to Yang et al. [35], when the result is obtained by a single gene locus, data are not conclusive, as this pattern was observed only when genotyping gdh. Thus, further studies are needed for confirmation.

When genotyping tpi, this gene was seen to have a greater variability of interassemblage when compared to gdh. This result is in agreement with findings of Wielinga and Thompson [30], Cacciò and Ryan [21], and Gómez-Muñoz et al. [18]. In this study, in addition to assemblage E, tpi has also identified zoonotic assemblages BIII in cattle and sheep and AII in sheep. Sulaiman et al. [7] identified tpi gene as the most informative to genotype isolates of Giardia duodenalis. This characteristic becomes evident over the entire gene, both regarding interspecies (Giardia spp.) and intraspecies (Giardia duodenalis), which may be seen in the number of new sequences identified. In this study, tpi has shown 15 new sequences and just two for gdh, reinforcing the comments made by Wielinga and Thompson [30], Cacciò and Ryan [21], and Gómez-Muñoz et al. [18] who highlighted that tpi is an important target of research in order to identify isolates and to study outbreaks [18].

Heterogeneous sequences have been observed when genotyping tpi and a larger number of double peaks were observed over the entire gene when compared to gdh, which is in accordance with the results obtained by Lebbad et al. [23]. Overlapped nucleotides were observed in isolates identified as BIII and E, which suggest a possible mixed infection, BIII/E and E/BIII. Nevertheless, the presence of double peaks in the chromatogram may not always be described as a mixed infection; thus, hypotheses such as the one of meiotic recombination and that of allelic heterozygosity [21] should also be considered. For more consistent results, Levecke et al. [36], Lebbad et al. [23], and Almeida et al. [37] suggest the use of assemblage-specific primers, which are able to distinguish more precisely intra-assemblage infections. Double peaks have been frequently reported in isolates of assemblages B, C, D, and E but never in isolates of assemblages A, F, and G. Cacciò and Ryan [21] and Lalle et al. [38] reported that double peaks are more common in subassemblages B, due to the high level of allelic divergence of the sequence. In the present study, more isolates of assemblage E have been observed with double peaks, which is in agreement with the findings of Lebbad et al. [23]. There are no reports in the literature regarding the simultaneous presence of assemblages B and E in the same isolate, but Yang et al. [35], Feng et al. [27], and Santín et al. [28] reported the existence of mixed infections between assemblages A and E in livestock. Gelanew et al. [17] mentioned the existence of mechanisms such as introgression, which is likely to bring about changes of assemblages when different genes are used. Smith et al. [39] suggest that the occurrence of mixed infections in several assemblages and subassemblages of G. duodenalis reflects the complex behavior of the parasite in the environment and the exposure of humans and animals to multiple sources.

Studies have reported that 15% of isolates genotyped have genotypic inconsistencies between two markers [7]. In the present study, the inconsistency rate was 38.5%. Samples with a complete interassemblage concordance for both genes were identified as E, confirming the predominance of species-specific assemblage in livestock. In most conflicting cases, the presence of subassemblages AII and BIII was seen at the same proportions. According to Read et al. [29] and Leonhard et al. [22], this phenomenon has been found in human and animal isolates, and it seems to be frequent in the combination of different marker genes, when an isolate may be genotyped as zoonotic by a primer and species-specific by another. For molecular epidemiological studies, there are major implications on the inferences from the conclusions depending on the interpretations of the data obtained.

Genetics of the Giardia duodenalis complex has not yet been fully elucidated. Understanding the microepidemiology of giardiasis requires characterizing the sources of contamination and understanding the role of anthroponotic, zoonotic, and environmental transmissions. The choice of the primer may directly influence the results; thus, assemblage-specific primers should be included, mainly when analyzing mixed infections and data should be carefully interpreted.


The authors would like to thank the farm owners who authorized them to collect fecal material and “Fundação de Amparo à Pesquisa do Estado de Minas Gerais” (FAPEMIG) for the financial support.


  1. F. Veronesi, F. Passamonti, S. Cacciò, M. Diaferia, and D. Piergili Fioretti, “Epidemiological survey on equine Cryptosporidium and Giardia infections in Italy and molecular characterization of isolates,” Zoonoses and Public Health, vol. 57, no. 7-8, pp. 510–517, 2010. View at: Publisher Site | Google Scholar
  2. P. T. Monis and R. C. A. Thompson, “Cryptosporidium and Giardia-zoonoses: fact or fiction?” Infection Genetics and Evolution, vol. 3, pp. 233–244, 2003. View at: Publisher Site | Google Scholar
  3. W. L. Homan, F. H. J. van Enckevort, L. Limper et al., “Comparison of Giardia isolates from different laboratories by isoenzyme analysis and recombinant DNA probes,” Parasitology Research, vol. 78, no. 4, pp. 316–323, 1992. View at: Google Scholar
  4. P. Ey, M. Mansouri, J. Kulda et al., “Genetic analysis of Giardia from hoofed farm animals reveals artiodactyl-specific and potentially zoonotic genotypes,” Journal of Eukaryotic Microbiology, vol. 44, no. 6, pp. 626–635, 1997. View at: Google Scholar
  5. E. Lasek-Nesselquist, D. M. Welch, and M. L. Sogin, “The identification of a new Giardia duodenalis assemblage in marine vertebrates and a preliminary analysis of G. duodenalis population biology in marine systems,” International Journal for Parasitology, vol. 40, no. 9, pp. 1063–1074, 2010. View at: Publisher Site | Google Scholar
  6. F. Yaoyu and L. Xiao, “Zoonotic potential and molecular epidemiology of Giardia species and giardiasis,” Clinical Microbiology Reviews, vol. 24, no. 1, pp. 110–140, 2011. View at: Publisher Site | Google Scholar
  7. I. M. Sulaiman, R. Fayer, C. Bern et al., “Triosephosphate isomerase gene characterization and potential zoonotic transmission of Giardia duodenalis,” Emerging Infectious Diseases, vol. 9, no. 11, pp. 1444–1452, 2003. View at: Google Scholar
  8. S. M. Cacciò, R. Beck, M. Lalle, A. Marinculic, and E. Pozio, “Multilocus genotyping of Giardia duodenalis reveals striking differences between assemblages A and B,” International Journal for Parasitology, vol. 38, no. 13, pp. 1523–1531, 2008. View at: Publisher Site | Google Scholar
  9. R. M. O'Handley, M. E. Olson, D. Fraser, P. Adams, and R. C. A. Thompson, “Prevalence and genotypic characterisation of Giardia in dairy calves from Western Australia and Western Canada,” Veterinary Parasitology, vol. 90, no. 3, pp. 193–200, 2000. View at: Publisher Site | Google Scholar
  10. H. van Keulen, P. T. Macechko, S. Wade, S. Schaaf, P. M. Wallis, and S. L. Erlandsen, “Presence of human Giardia in domestic, farm and wild animals, and environmental samples suggests a zoonotic potential for Giardiasis,” Veterinary Parasitology, vol. 108, no. 2, pp. 97–107, 2002. View at: Publisher Site | Google Scholar
  11. A. J. Appelbee, L. M. Frederick, T. L. Heitman, and M. E. Olson, “Prevalence and genotyping of Giardia duodenalis from beef calves in Alberta, Canada,” Veterinary Parasitology, vol. 112, no. 4, pp. 289–294, 2003. View at: Publisher Site | Google Scholar
  12. A. Giangaspero, B. Paoletti, R. Iorio, and D. Traversa, “Prevalence and molecular characterization of Giardia duodenalis from sheep in central Italy,” Parasitology Research, vol. 96, no. 1, pp. 32–37, 2005. View at: Publisher Site | Google Scholar
  13. F. Aloisio, G. Filippini, P. Antenucci et al., “Severe weight loss in lambs infected with Giardia duodenalis assemblage B,” Veterinary Parasitology, vol. 142, no. 1-2, pp. 154–158, 2006. View at: Publisher Site | Google Scholar
  14. E. C. Faust, W. Sawitz, J. Tobie et al., “Comparative efficiency of various technics for the diagnosis of protozoan and helminthes in feces,” Journal of Parasitology, vol. 25, pp. 241–262, 1938. View at: Google Scholar
  15. J. Sambrook, E. F. Fritsch, and T. Maniatis, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, New York, NY, USA, 2nd edition, 1989.
  16. J. A. Castro-Hermida, A. Almeid, M. González-Warleta, J. M. Correia Da Costa, and M. Mezo, “Prevalence and preliminary genetic analysis of Giardia isolated from adult sheep in Galicia (Northwest Spain),” Journal of Eukaryotic Microbiology, vol. 53, no. 1, pp. 172–173, 2006. View at: Publisher Site | Google Scholar
  17. T. Gelanew, M. Lalle, A. Hailu, E. Pozio, and S. M. Cacciò, “Molecular characterization of human isolates of Giardia duodenalis from Ethiopia,” Acta Tropica, vol. 102, no. 2, pp. 92–99, 2007. View at: Publisher Site | Google Scholar
  18. M. T. Gómez-Muñoz, C. Cámara-Badenes, M. C. Martínez-Herrero et al., “Multilocus genotyping of Giardia duodenalis in lambs from Spain reveals a high heterogeneity,” Research in Veterinary Science, vol. 93, no. 2, pp. 836–842, 2012. View at: Publisher Site | Google Scholar
  19. C. S. Palmer, R. J. Traub, I. D. Robertson, G. Devlin, R. Rees, and R. C. A. Thompson, “Determining the zoonotic significance of Giardia and Cryptosporidium in Australian dogs and cats,” Veterinary Parasitology, vol. 154, no. 1-2, pp. 142–147, 2008. View at: Publisher Site | Google Scholar
  20. J. Thompson, R. Yang, M. Power et al., “Identification of zoonotic Giardia genotypes in marsupials in Australia,” Experimental Parasitology, vol. 120, no. 1, pp. 88–93, 2008. View at: Publisher Site | Google Scholar
  21. S. M. Cacciò and U. Ryan, “Molecular epidemiology of giardiasis,” Molecular & Biochemical Parasitology, vol. 160, no. 2, pp. 75–80, 2008. View at: Publisher Site | Google Scholar
  22. S. Leonhard, K. Pfister, P. Beelitz, C. Wielinga, and R. C. A. Thompson, “The molecular characterisation of Giardia from dogs in Southern Germany,” Veterinary Parasitology, vol. 150, no. 1-2, pp. 33–38, 2007. View at: Publisher Site | Google Scholar
  23. M. Lebbad, I. Petersson, L. Karlsson et al., “Multilocus genotyping of human giardia isolates suggests limited zoonotic transmission and association between assemblage B and flatulence in children,” PLoS Neglected Tropical Diseases, vol. 5, no. 8, article e1262, 2011. View at: Publisher Site | Google Scholar
  24. R. E. Huetink, J. W. van der Giessen, J. P. Noordhuizen, and H. W. Ploeger, “Epidemiology of Cryptosporidium spp. and Giardia duodenalis on a dairy farm,” Veterinary Parasitology, vol. 102, no. 1-2, pp. 53–67, 2001. View at: Publisher Site | Google Scholar
  25. J. M. Trout, M. Santín, E. Greiner, and R. Fayer, “Prevalence of Giardia duodenalis genotypes in pre-weaned dairy calves,” Veterinary Parasitology, vol. 124, no. 3-4, pp. 179–186, 2004. View at: Publisher Site | Google Scholar
  26. S. L. P. Souza, S. M. Gennari, L. J. Richtzenhain et al., “Molecular identification of Giardia duodenalis isolates from humans, dogs, cats and cattle from the state of São Paulo, Brazil, by sequence analysis of fragments of glutamate dehydrogenase (gdh) coding gene,” Veterinary Parasitology, vol. 149, no. 3-4, pp. 258–264, 2007. View at: Publisher Site | Google Scholar
  27. Y. Feng, Y. Ortega, V. Cama, J. Terrell, and L. Xiao, “High intragenotypic diversity of Giardia duodenalis in dairy cattle on three farms,” Parasitology Research, vol. 103, no. 1, pp. 87–92, 2008. View at: Publisher Site | Google Scholar
  28. M. Santín, J. M. Trout, and R. Fayer, “A longitudinal study of Giardia duodenalis genotypes in dairy cows from birth to 2 years of age,” Veterinary Parasitology, vol. 162, no. 1-2, pp. 40–45, 2009. View at: Publisher Site | Google Scholar
  29. C. M. Read, P. T. Monis, and R. C. Thompson, “Discrimination of all genotypes of Giardia duodenalis at the glutamate dehydrogenase locus using PCR-RFLP,” Infection, Genetics and Evolution, vol. 4, no. 2, pp. 125–130, 2004. View at: Publisher Site | Google Scholar
  30. C. M. Wielinga and R. C. A. Thompson, “Comparative evaluation of Giardia duodenalis sequence data,” Parasitology, vol. 134, no. 12, pp. 1795–1821, 2007. View at: Publisher Site | Google Scholar
  31. R. B. Langkjær, H. Vigre, H. L. Enemark, and C. Maddox-Hyttel, “Molecular and phylogenetic characterization of Cryptosporidium and Giardia from pigs and cattle in Denmark,” Parasitology, vol. 134, no. 3, pp. 339–350, 2007. View at: Publisher Site | Google Scholar
  32. H. Sprong, S. M. Cacciò, and J. W. B. van der Giessen, “Identification of zoonotic genotypes of Giardia duodenalis,” PLoS Neglected Tropical Diseases, vol. 3, no. 12, article e558, 2009. View at: Publisher Site | Google Scholar
  33. U. M. Ryan, C. Bath, I. Robertson et al., “Sheep may not be an important zoonotic reservoir for Cryptosporidium and Giardia parasites,” Applied and Environmental Microbiology, vol. 71, no. 9, pp. 4992–4997, 2005. View at: Publisher Site | Google Scholar
  34. A. Ruiz, P. Foronda, J. F. González et al., “Occurrence and genotype characterization of Giardia duodenalis in goat kids from the Canary Islands, Spain,” Veterinary Parasitology, vol. 154, no. 1-2, pp. 137–141, 2008. View at: Publisher Site | Google Scholar
  35. R. Yang, C. Jacobson, C. Gordon, and U. Ryan, “Prevalence and molecular characterisation of Cryptosporidium and Giardia species in pre-weaned sheep in Australia,” Veterinary Parasitology, vol. 161, no. 1-2, pp. 19–24, 2009. View at: Publisher Site | Google Scholar
  36. B. Levecke, P. Geldhof, E. Claerebout et al., “Molecular characterisation of Giardia duodenalis in captive non-human primates reveals mixed assemblage A and B infections and novel polymorphisms,” International Journal for Parasitology, vol. 39, no. 14, pp. 1595–1601, 2009. View at: Publisher Site | Google Scholar
  37. A. Almeida, E. Pozio, and S. M. Cacciò, “Genotyping of Giardia duodenalis cysts by new real-time PCR assays for detection of mixed infections in human samples,” Applied and Environmental Microbiology, vol. 76, no. 6, pp. 1895–1901, 2010. View at: Publisher Site | Google Scholar
  38. M. Lalle, F. Bruschi, B. Castagna, M. Campa, E. Pozio, and S. M. Cacciò, “High genetic polymorphism among Giardia duodenalis isolates from Sahrawi children,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 103, no. 8, pp. 834–838, 2009. View at: Publisher Site | Google Scholar
  39. A. Smith, M. Reacher, W. Smerdon, G. K. Adak, G. Nichols, and R. M. Chalmers, “Outbreaks of waterborne infectious intestinal disease in England and Wales, 1992–2003,” Epidemiology and Infection, vol. 134, no. 6, pp. 1141–1149, 2006. View at: Publisher Site | Google Scholar

Copyright © 2013 Natália M. N. Fava et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

1226 Views | 633 Downloads | 13 Citations
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly as possible. We will be providing unlimited waivers of publication charges for accepted research articles as well as case reports and case series related to COVID-19. Review articles are excluded from this waiver policy. Sign up here as a reviewer to help fast-track new submissions.