Figures
Abstract
Background
Giardia duodenalis is a common intestinal parasite that infects humans and many other mammals, mainly distributing in some areas with poor sanitation. The proportion of the human giardiasis burden attributable to G. duodenalis of animal origin differs in different geographical areas. In Mainland China, genetic data of the gdh and bg genes of G. duodenalis from animals are only limited in dogs and cats. The aim of the study was to provide information on the genetic characterizations of animal-derived G. duodenalis isolates (from rabbits, sheep and cattle) at both loci in Heilongjiang Province, Northeastern China, and to assess the potential for zoonotic transmission.
Methodology/Principal Findings
61 G. duodenalis isolates from animal feces (dairy and beef cattle, sheep and rabbits) in Heilongjiang Province were characterized at the gdh and bg loci in the present study. The gdh and bg gene sequences of sheep-derived G. duodenalis assemblage AI, and the gdh sequences of rabbit-derived G. duodenalis assemblage B had 100% similarity with those from humans, respectively. Novel subtypes of G. duodenalis were identified, with one and seven subtypes for assemblages A and E at the gdh locus, and two and three subtypes for assemblages B and E at the bg locus, respectively. Three pairs of the same bg sequences of assemblage E were observed in sheep and cattle.
Conclusions/Significance
This is the first description of genetic characterizations of the gdh and bg genes of G. duodenalis from rabbits, sheep and cattle in Mainland China. Homology analysis of assemblages AI and B implied the possibility of zoonotic transmission. The novel subtypes of assemblages of G. duodenalis may represent the endemic genetic characteristics of G. duodenalis in Heilongjiang Province, China.
Citation: Liu A, Yang F, Shen Y, Zhang W, Wang R, Zhao W, et al. (2014) Genetic Analysis of the Gdh and Bg Genes of Animal-Derived Giardia duodenalis Isolates in Northeastern China and Evaluation of Zoonotic Transmission Potential. PLoS ONE 9(4): e95291. https://doi.org/10.1371/journal.pone.0095291
Editor: Ikuo Igarashi, Obihiro University of Agriculture and Veterinary Medicine, Japan
Received: September 29, 2013; Accepted: March 25, 2014; Published: April 18, 2014
Copyright: © 2014 Zhang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The study was supported by grants from the Natural Science Foundation of Heilongjiang Province No. D200628(AL) and the National S & T Major Program for Infectious Disease of China Nos. 2012ZX10004-201 and 2009ZX10004-201(JC). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Giardia duodenalis (syn. G. lamblia, G. intestinalis) is an intestinal, parasitic, flagellate protozoan that infects humans as well as a wide variety of domestic animals and wildlife species. Giardiasis is one of the major neglected tropical diseases occurring in rural areas and poor urban areas. Human giardiasis has complicated clinical manifestations, ranging from the absence of symptoms to acute or chronic diarrhea, abdominal pain, nausea, vomiting and so on, depending on the health status of hosts, and the dose and virulence of the parasites [1]. It has been shown that G. duodenalis is a complex species, with eight genetically distinct assemblages (A-H) having been identified; each of them has significant differences in host range or host specificity [2], [3]. Assemblages A and B have the broadest host specificity, and are found to infect humans and many other mammals. However, the other assemblages are mostly found in non-human mammals, with assemblages C and D in dogs, assemblage E in hoofed livestock, assemblage F in cats, assemblage G in rodents, and assemblage H in marine mammals [3], [4]. In fact, the majority of cases of human giardiasis are caused by assemblages A and B, with assemblages C, D, E and F occasionally isolated from humans [4].
Based on the fact that assemblages A and B in humans have also been found in animals, the role host animals play in the epidemiology of human giardiasis has received increasing attention. The animal-derived sequences of assemblages A and B have been reported to show 100% similarity with those from humans at the triose phosphate isomerase (tpi), glutamate dehydrogenase (gdh) and β-giardin (bg) loci; thus, both assemblages are considered to have the possibility of zoonotic transmission [5]–[7]. PCR-based molecular analysis techniques have been used widely to trace the sources of infection or contamination and to assess the human giardiasis burden attributable to animal origin. Currently, several genetic loci are used to identify Giardia isolates at the genotype and subtype levels, most commonly including the small subunit ribosomal RNA (SSU rRNA), bg, gdh and tpi genes [8]. Tpi, gdh and bg genes are common genotyping and subtyping markers of G. duodenalis, whereas the SSU rRNA gene is commonly used markers for the species and assemblage differentiation of Giardia [9]. Although a single locus has been used in most of epidemiological studies of giardiasis, multilocus genotyping (MLG) tools are used increasingly in characterizing G. duodenalis isolates from humans and animals. The data based on MLG tools can greatly improve our understanding of the relationship between humans and animals as hosts and reservoirs, including elucidation of the transmission routes and dynamics of human giardiasis, and assessment of the burden of human giardiasis of animal origin.
In Mainland China, the majority of genetic data of G. duodenalis from humans and animals are based on the tpi gene and only one report described the genetic characterizations of the gdh and bg gene of animal-derived G. duodenalis conducted in Guangzhou [10]. In the present study, we obtained gdh and bg gene sequences of G. duodenalis isolates from rabbits, sheep and cattle in Heilongjiang Province. The aim of the study was to understand the endemic genetic characterizations of animal-derived isolates of G. duodenalis at both loci and to assess its potential for zoonotic transmission in the investigated areas by aligning the obtained sequences with those from GenBank.
Materials and Methods
Ethics Statement
The study was conducted in accordance with the guidelines of the Regulations for the Administration of Affairs Concerning Experimental Animals and was approved by the Animal Ethical Committee of Harbin Medical University (HMUIRB20130009). No other specific permits were required for the described field studies. The locations where we sampled are not protected in any way. The field studies did not involve endangered or protected animal species. Before beginning work on the study, we contacted the farm owners and obtained their permission. In this study, all the samples were taken immediately from animal fresh feces deposited on the ground after animal defecation instead of operating or experimenting on the animals. During the procedure, the animals were not hurt at all.
Source of isolates
G. duodenalis isolates were all obtained from animal feces (26 from cattle in seven farms, 21 from sheep in four farms and 14 from rabbits in five farms) in Heilongjiang Province, China between October 2008 and November 2011. Genomic DNA was extracted using a QIAamp DNA Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's recommendations and DNA preparations were stored at −20°C before PCR analysis. 61 G. duodenalis isolates, which were identified based on the tpi gene in the previous studies [5], , were randomly chosen as the study subjects of genetic characterizations of the gdh and bg genes of G. duodenalis (Table 1).
PCR amplification of the gdh and bg genes of G. duodenalis
Each DNA preparation of G. duodenalis was characterized using two distinct protocols for nested PCR depending on the target to be amplified. A fragment of approximately 530 bp of the gdh gene was amplified using the external primers Gdh1 and Gdh2, and internal primers Gdh3 and Gdh4 [13]. The amplification of 511 bp of the bg gene was performed using the external primers G7 and G759 [14], and the internal primers GBF and GBR [6]. PCR products were visualized by electrophoresis in 1.5% agarose gel stained with ethidium bromide. DNA preparations of PCR-negative samples at either or both of the two loci were subjected to three repeated PCR amplifications.
DNA sequencing and molecular analysis
All secondary PCR products were sequenced with secondary PCR primers at each locus on an ABI PRISMTM 3730 DNA Analyzer (Applied Biosystems, Carlsbad, CA, USA), using a BigDye Terminator v3.1 Cycle Sequencing kit (Applied Biosystems, USA). Accuracy of the sequencing data was confirmed by sequencing in both directions. Nucleotide sequences obtained in the present study were subjected to BLAST searches (http://www.ncbi.nlm.nih.gov/blast/) and were then aligned with G. duodenalis reference sequences downloaded from GenBank and analyzed using Clustal X 1.83.
Results
PCR amplification of G. duodenalis at the gdh and bg loci
61 Giardia DNA preparations were subjected to nested PCR amplification of the gdh and bg genes. 52 were successfully amplified at the gdh locus, with four assemblage A, 10 assemblage B, and 38 assemblage E being identified. A fragment of the bg gene of the expected size was obtained out of 45 samples, with four assemblage A, 12 assemblage B, and 29 assemblage E being identified. The PCR amplification rates were 85.2% (52/61) at the gdh locus versus 73.8% (45/61) at the bg locus, with 100% (4/4) versus 100% (4/4) for assemblage A, 71.4% (10/14) versus 85.7% (12/14) for assemblage B, and 88.4% (38/43) versus 67.4% (29/43) for assemblage E (Table 1).
Characterization of the gdh and bg gene sequences of assemblage A
Sequence analysis of the gdh gene from four sheep-derived G. duodenalis isolates revealed the presence of two subtypes of assemblage A. One subtype (KC960643) (n = 3) was identified as AI, having 100% homology with the human-derived subtype AI sequences (GQ329674 and GQ329676) [15]; the same sequences have been found in seals and cats [3], [16]. The other subtype (KC960644) was not identical to any reported assemblage A sequences.
However, at the bg locus, four identical sequences (KC960630) were shown to have 100% similarity with those of human-derived (GQ329671, GQ329672) and animal-derived assemblage AI isolates (alpacas, sheep, ferrets and cattle) [15], [17]–[20].
Characterization of the gdh and bg gene sequences of assemblage B
10 out of 14 rabbit-derived G. duodenalis isolates were successfully amplified and sequenced at the gdh locus, with all of them being identified as assemblage B. Nine were identical to each other (KC960645) and had 100% similarity with the human-derived assemblage B sequence from Brazil (EF507682) [16]. The remaining one (KC960646) had 100% homology with the sequences isolated from humans in Australia (EF685680) and Brazil (EF507646, EF507664, EF507668, EF507671, EF507672), and from chinchillas in Brazil (HM134212-HM134214) [16], [21], [22].
12 bg gene sequences of rabbit-derived G. duodenalis isolates were successfully obtained and identified as assemblage B. Two novel subtypes were detected with a single base variation between each other, with one representing 10 sequences (KC960631) and the other representing two sequences (KC960632), and both of them have one or two base differences with the published sequence AB618785, respectively.
Characterization of the gdh and bg gene sequences of assemblage E
16 out of 17 sheep-derived G. duodenalis isolates were successfully amplified and sequenced at the gdh locus, belonging to four novel subtypes of assemblage E (KC960647 to KC960650). Four subtypes of assemblage E were observed from 22 gdh gene sequences obtained successfully from 26 cattle-derived G. duodenalis isolates, with one subtype (KC960651) having the same sequence as those of the cattle-derived isolates (EF507644 and EF507645) [16] and the other three subtypes (KC960652 to KC960654) being novel (Tables 1, 2). Using the sequence EF507645 as a reference sequence, genetic polymorphism was observed with one- to five-base variations at 12 nucleotide sites in the gdh nucleotide sequences (Table 2).
At the bg locus, five subtypes of assemblage E were found among 12 successful sequences obtained from sheep-derived G. duodenalis isolates. Three subtypes (KC960633 to KC960635) have been described previously in sheep, goats and cattle [18], [23]–[26] and the remaining two subtypes (KC960636 and KC960637) were novel. 17 bg sequences of cattle-derived G. duodenalis isolates belonged to five subtypes, with four subtypes (KC960638 to KC960641) having been reported in sheep, goats and cattle [8], [18], [23]–[26] and the remaining one (KC960642) being novel (Tables 1, 3). Using the sequence EU726980 as a reference sequence, genetic polymorphism was observed with one- to three-base variations at seven nucleotide sites in the bg nucleotide sequences (Table 3).
It was also observed that three sheep-derived bg gene sequences of assemblage E (KC960634, KC960633 and KC960635) showed 100% homology with the three from cattle (KC960638, KC960639 and KC960641), respectively (Table 3).
Discussion
PCR-based techniques have been used widely for the identification, population genetics and epidemiology of G. duodenalis in humans, animals and environmental samples. MLG analysis is increasingly used for the characterizations of G. duodenalis isolates and assessment of human disease burden caused by zoonotic transmission. G. duodenalis isolates from different animal origins were characterized at the gdh and bg loci in the present study. The gdh gene sequence (KC960643) representing three sheep-derived assemblage AI isolates has been described in human giardiasis cases in Sweden [15]. Meanwhile, all the four assemblage AI isolates from sheep were identical to each other (KC960630) and had 100% similarity at the bg locus with a human-derived G. duodenalis isolate from Sweden [15]. To date, identification of genetic variations of nucleotide sequences within assemblage A at the gdh, bg and tpi loci has led to the designation of assemblages AI, AII and AIII, which all appear to have host specificity. Assemblage AI is commonly found in animals and is sometimes seen in humans; assemblage AII mainly infects humans and is occasionally detected in animals; assemblage AIII has circulated in wildlife [27]. Recently, assemblage AIV was designated based on the base differences of the tpi gene sequence compared to AI, AII and AIII [5]. In the present study, the assemblage AI sequences at the gdh and bg loci showed 100% homology with those from humans in Sweden [15]. The result above implied that sheep infected with assemblage AI pose a significant threat to local inhabitants and are of public health importance. Unfortunately, no genetic data of human-derived G. duodenalis isolates have been obtained in the investigated areas although human giardiasis cases were reported early in 1990 [28]. Even in China, there are also only a few reports about molecular identification of human-derived G. duodenalis isolates [29]–[32]. Thus, the transmission routes and dynamics of subtype AI and the human giardiasis burden attributable to G. duodenalis of animal origin remain to be clarified by epidemiological data of human and animal giardiasis cases.
Assemblage B is one of the two major assemblages causing human giardiasis with a broad animal host range. It has been isolated from cattle, sheep, pigs, horses, dogs, cats, and rabbits [27]. Two subtypes (KC960645 and KC960646) were identified in the present study by analyzing 10 gdh gene sequences from rabbits and both of them had been reported in human giardiasis cases from Brazil and Australia [16], [21]. The result indicated a high potential for cross-species transmission of assemblage B between rabbits and humans due to the similar genetic backgrounds. So far, the strongest evidence supporting transmission from rabbits to humans was based on the report of a foodborne outbreak of giardiasis associated to a family party, where the food preparer, his child, guests, and a pet rabbit were positive for Giardia cysts [33]. However, these Giardia isolates were not genotyped or subtyped. The outbreak emphasized not only the possibility of domestic-animal-to-person transmission of G. duodenalis but also the importance of good hygienic practices in food preparation to prevent the spread of animal-derived G. duodenalis cysts in humans. In fact, an early case-control study in eastern England showed an association of giardiasis with exposure to farm animals and pets, particularly pigs, dogs, and cats [34]. In southwestern England, a visit to a farm led to a high frequency of giardiasis among case patients, but none of the associations with specified animal exposures (dogs, cats, horses, cows, sheep) was statistically significant [35].
Assemblage E is mainly found in cloven-hoofed domestic mammals (cattle, water buffaloes, sheep, goats, and pigs [27]. In addition, it has been occasionally reported in cats [4], [8], [36]. The prevalence of assemblage E in cattle was reported to be high up to 75.1% (422/562) in a European study of G. duodenalis [4]. High occurrence of G. duodenalis has also been described in goats and sheep in Spain, with a prevalence of 100% (39/39) for goats and 98.7% (74/75) for sheep [18], [23]. By DNA sequence analysis within the partial tpi, gdh and bg genes, the genetic polymorphism of assemblage E has been observed [5], [8], [12], [18], [25], [37], [38]. In the present study, the alignment result of the gdh gene sequences showed the presence of seven novel subtypes of assemblage E, four from sheep (KC960647 to KC960650) and three from cattle (KC960652 to KC960654) (Table 2). At the bg locus, five subtypes were observed among sheep-derived and cattle-derived G. duodenalis assemblage E isolates, respectively, with three novel subtypes (KC960636, KC960637, KC960642) being found in total. The identification of three pairs of the same bg sequences from sheep and cattle (KC960634 versus KC960638, KC960633 versus KC960639 and KC960635 versus KC960641) indicated the possibility of cross-species transmission of G. duodenalis E between cloven-hoofed animals in the investigated areas (Table 3).
In the present study, we observed the phenomenon of “assemblage-swapping” (different assemblages at different loci in the same isolate. Cattle-derived G. duodenalis isolates were identified as assemblage E based on successful PCR and sequencing analysis, respectively at the gdh locus (n = 8) and at the bg locus (n = 4); however, all the DNA preparations used above were previously identified as assemblage B based on the tpi gene (Table 1). Similar findings were reported in an identification study of dog-derived G. duodenalis isolates, where an isolate was typed as assemblage AI based on the tpi gene while it was typed as assemblage D based on the gdh and bg genes [39]. It has also been observed that three out of five human-derived G. duodenalis isolates were identified as assemblage A at the18S rRNA locus and assemblage B at the gdh locus, while the remaining two were identified as assemblage B at the 18S rRNA locus and assemblage A at the gdh locus [40]. A recent multi-locus genotyping identified 41 human-derived G. duodenalis isolates as assemblage B and 13 as assemblage A based on tpi, gdh and bg genes, whereas 14 showed multiple assemblage depending on the marker loci [41]. “Assemblage-swapping” in the diagnosis of G. duodenalis infection may be related to mixed assemblage infections in the fecal samples or recombination between assemblages.
MLG is a powerful tool for tracing the infection or contamination source of G. duodenalis and assessing the zoonotic potential of giardiasis. In the present study, homology analysis showed that two gdh sequences of rabbit-derived assemblage B isolates (KC960645 and KC960646) were identical to those from humans. However, at the bg locus, no sequences had 100% similarity with those from the cases of human giardiasis. The results indicated that single gene nucleotide analysis of G. duodenalis isolates from animals and humans at the genotype and subtype levels are insufficient for assessment of the disease burden of zoonotic transmission.
In the present study, PCR was observed to have higher amplification rate at the gdh locus (85.2%, 52/61) than at the bg locus (73.8%, 45/61), which might be mainly related to the primers and genetic structure of target fragments, for the other factors influencing PCR efficiency were identical such as the same quality and quantity of DNA templates and the quality and characterization of DNA polymerase used. Even though the primers were designed to bind ‘conserved’ regions in the amplified genes, excessive mismatches in the binding regions of primer sequences might result in the failure of PCR amplification for some isolates of G. duodenalis. In fact, numerous molecular data have confirmed both inter- and intra-assemblage genetic variations [27]. Variable base substitution rates of G. duodenalis have been reported at different genetic loci [9]. Such differences in nucleotide sequences, especially base variations in primer binding sites, might lead directly to the failure in the primer-template binding in some G. duodenalis isolates. PCR analysis by Scorza et al showed positive amplification of the gdh, bg, and tpi genes in 91.0% (172/189), 84.8% (145/171) and 19.8% (34/172) of G. duodenalis cyst-positive samples from the mammalian feces, respectively [39]. PCR amplification rates were 100% (63/63), 61.9% (39/63) and 56.0% (14/25), respectively at the gdh, bg and tpi loci in a study of molecular characterization of Giardia isolates from clinical infections following a waterborne outbreak [42]. In another comparative study of the tpi and gdh genes for detection and genotyping of human-derived G. duodenalis isolates, the tpi gene was amplified from 96.2% (25/26) of samples, whereas only 81% (21/26) were positive when the gdh gene was targeted [43]. It was also observed that PCR amplification rates differed between different assemblages. Assemblage A had the highest amplification rate (100%) at either the gdh locus or the bg locus, followed by assemblage E (88.4%) and assemblage B (71.4%) at the gdh locus versus assemblage B (85.7%) and assemblage E (67.4%) at the bg locus (Table 1). In general, no matter which gene was amplified, assemblage A had higher amplification rate than assemblage B. This result might be related to the fact that assemblage B exhibits higher allelic sequence heterogeneity and genetic recombination compared to assemblage A [27], [4], [44], [45]. In a recent study, both intra- and inter-assemblage recombination and meiotic sex were seen from assemblages A to G by analyzing two or more genes of G. duodenalis isolates from humans and other animals [21]. Thus, the reasons for different PCR amplification rates of different assemblages at different loci need to be elucidated by more systematic and more complete genetic data from a large number of G. duodenalis isolates in the future.
The present study is the first report about genetic characterizations of the gdh and bg genes of G. duodenalis isolates from rabbits, sheep and cattle in Mainland China. In conclusion, the obtained data provide useful information for further genotyping or subtyping studies of G. duodenalis. The findings of animal-derived assemblages AI and B having 100% homology with human-derived G. duodenalis isolates at the gdh and bg loci imply the possibility of zoonotic transmission in the investigated areas. The identification of the novel subtypes of assemblages AI, B and E based on the gdh and bg genes might reflect the characteristic geographical distribution of G. duodenalis. To better understand the transmission dynamics of G. duodenalis and assess the burden of human giardiasis caused by animals, molecular epidemiological studies of giardiasis should be conducted in humans and animals living in the same household or localized focus of endemicity.
Author Contributions
Conceived and designed the experiments: W. Zhang JC AL. Performed the experiments: AL FY W. Zhang. Analyzed the data: RW YS W. Zhao. Contributed reagents/materials/analysis tools: LZ HL. Wrote the paper: AL W. Zhang JC.
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