The presence of Giardia intestinalis in donkeys, Equus asinus, in China

Background Giardia intestinalis is one of the most important zoonotic enteric parasites. As no information regarding prevalence and genotype of G. intestinalis in donkeys (Equus asinus) in China is available, 181 faecal samples from 48 donkeys from Jilin Province, from 104 from Shandong Province and from 29 from Liaoning Province were examined between May and December 2015. Findings Twenty-eight (15.47%) out of 181 donkey samples were tested G. intestinalis-positive by nested amplification of the triosephosphate isomerase (tpi) gene. The prevalence in different regional groups varied from 10.42 to 18.27%. The prevalence in adult and young donkeys was 14.29 and 22.92%, respectively. Otherwise, the prevalence was 11.69% in summer and 18.27% in winter. However, no statistically significant differences were found in relation to region or age group. Sequence analysis of the tpi, glutamate dehydrogenase (gdh) and beta giardin (bg) loci identified 4, 1 and 3 subtypes of assemblage B, respectively. Moreover, four novel multilocus genotypes (MLGs novel-1 to novel-4) were identified in assemblage B. Conclusions This first report of G. intestinalis in donkeys in China indicates that further studies of nation-wide molecular epidemiology and geographical distribution of Giardia in donkeys are warranted. Effective strategies should be implemented to control G. intestinalis infection in donkeys, other animals and humans. Electronic supplementary material The online version of this article (doi:10.1186/s13071-016-1936-0) contains supplementary material, which is available to authorized users.


Background
Giardia intestinalis is the only species of Giardia which is found in human beings [1][2][3][4]. It is not only distributed worldwide, but also can infect many vertebrates [5,6]. Eight assemblages (A-H) have been identified within G. intestinalis [6][7][8]. Of these, assemblages C-H seem to be animal-specific [9], but assemblages A and B can infect humans and a wide range of non-human hosts [6,10]. Diarrhea is the main symptom of giardiasis [11] and transmission is mainly through ingestion of Giardia cysts in contaminated food or water [12]; approximately 2.8 × 10 8 cases of human giardiasis are reported world-wide per year, and the majority of them are reported in developing countries [6]. In view of such a serious situation, giardiasis has attracted considerable attention around the world. Although G. intestinalis infections have been reported in humans and a variety of animal species [13][14][15][16], there is little information in donkeys (Equus asinus).
Giardia intestinalis infection in horses has been reported in many countries around the world including China [17][18][19][20][21]. The donkey belongs to the genus Equus. It is an important edible animal species and used in Chinese traditional medicine, and is closely related to horses. Because they are maintained in a close association with their owners and veterinary personnel, donkeys are the important reservoirs for transmission of pathogens (such as Cryptosporidium hominis and Toxoplasma gondii) to humans and other animals [22,23]. To determine whether donkeys are hosts of G. intestinalis, we conducted a study on the prevalence and genotypes of G. intestinalis in donkeys in Jilin, Liaoning and Shandong Provinces, China.

Collection and preparation of faecal samples
A total of 181 donkey faecal samples (48 from Jilin, 27 from Liaoning and 104 from Shandong) were collected from three provinces, in northeastern and eastern China, between March and December 2015. Each of the fresh faecal samples was collected into sterile gloves separately after its defecation onto the ground, placed into box with ice and transported to the laboratory immediately. Genomic DNA was extracted directly from each faecal sample using the Stool DNA kit (OMEGA, Norcross, Georgia, USA) according to the manufacturer's instructions. Genomic DNA was stored at -20°C until PCR amplification.

PCR amplification
The prevalence and genotypes of G. intestinalis were determined by the nested PCR amplification of the triosephosphate isomerase (tpi) gene, beta giardin (bg) gene and glutamate dehydrogenase (gdh) genes as described by Zhao et al. [24]. The primers and their annealing temperatures are listed in Table 1. Positive and negative controls were included in each amplification. Amplification products were observed under UV light after electrophoresis in 1.5% agarose gels containing GoldView™ (Solarbio, Beijing, China).

Sequence and phylogenetic analyses
Positive secondary PCR products were sequenced by Genscript Company (Nanjing, China). Bidirectional sequencing was used to confirm the accuracy of the sequences. Sequences with mutations were considered as novel genotypes when confirmed from independent two PCR reactions on the same sample. To identify the assemblages and subtypes, nucleotide sequences were aligned with known reference tpi, gdh and bg gene sequences of G. intestinalis available in GenBank using the BLAST (http://www.ncbi.nlm.nih.gov/ BLAST/) and computer program Clustal X 1.83.

Statistical analysis
The relationship between prevalence of G. intestinalis-infected donkeys and different variables including age, geographic origin and seasons were analyzed by Chi-square test using SPSS version 17.0 (SPSS Inc., Chicago, IL, USA) [25]. The results were considered significant statistically if P < 0.05. Odds ratios (ORs) and their 95% confidence intervals (CI) are also given.
The overall prevalence of G. intestinalis infection in donkeys was 15.47% (28/181, 95% CI: 10.20-20.74), which was higher than that in horses in Xinjiang (1.5%) [17], Brazil (0.5%) [26], foals in Belgium (14.2%) [20], Germany (10%) [20], Greece (11.6%) [20], the Netherlands (11.4%) [20] and Italy (8.6%) [18], but lower than that in horses in Colombia (17.4%) [19]. Previous studies demonstrated that survival of G. intestinalis is more likely to be affected  [6,27], so the difference in G. intestinalis prevalence in different regions may be due to different local climatic conditions, as well as the detection methods, sampling time and sample sizes. Moreover, probably because of the smaller sample sizes, seasonal and age-related correlates previously found in cattle [6] and horses [20] were not found in this study. Assemblages A and B, responsible for the vast majority of human giardiasis [6,28], and assemblage E, a common assemblage of G. intestinalis in cattle [9], have also been reported in horses [20]. However, perhaps due to the smaller sample sizes, only assemblage B was identified in donkeys in the present study. Assemblage B has a broad host range worldwide [20,28]. In China, isolates of assemblage B have also been found in non-human primates [2], rabbits [3], horses [17], cattle [29], golden takins (Budorcas taxicolor bedfordi) [24], pet chinchillas (Chinchilla lanigera) [30], captive wildlife [13], sheep [31] and goats [31], suggesting interspecies transmission of G. intestinalis may be commonly occurring in China, and we should pay enough attention to. More importantly, assemblage B was also identified in raw urban wastewater in northern China [32]. Therefore, our results also suggest that donkeys could be a source of giardiasis outbreaks.
Mixed infections of G. intestinalis genotypes have been recorded from a wide range of hosts worldwide [29,33]. In cases of co-infections, some assemblages may be detected preferentially using a single locus primers [34]; thus PCR amplification of a single locus may not reflect the accurate information to G. intestinalis infection [34,35]. A multilocus genotype (MLG) method (tpi, gdh and bg loci) has been developed and widely used for detection of G. intestinalis infection [6,33,34]. In the present study, 28 G. intestinalis-positive samples were also genotyped based on bg and gdh loci. A total of 28 tpi, 22 bg and 16 gdh gene sequences were obtained, and analysis of these genes revealed only one assemblage (B); however, high genetic polymorphism was observed at these loci within this assemblage (Table 4), implying high genetic diversity of G. intestinalis in donkeys in the investigation regions. At the tpi locus, seven polymorphic sites were found compared with the GenBank reference sequence AY368169 (Table 4), and four different assemblage B subtypes were identified (Table 4, Additional file 1: Figure S1c). These sequences all represented new subtypes (KU892519-KU892522), and showed a 99% similarity with the reference sequence (accession no. AY368169, from wastewater in USA [36]). Only one subtype was found at the gdh locus (Additional file 1: Figure S1b), and the sequence (KU892523) had 99% similarity with the reference sequence available in GenBank with accession number of KR048463 (from a takin in China [24]). Moreover, a total of five SNPs were observed at the bg locus (Table 4), and these sequences (KU892516-KU892518) represented three subtypes (Additional file 1: Figure S1a). Moreover, these subtypes were closely clustered with sub-assemblage BIV (Additional file 1: Figure S1), suggesting that subassemblage BIV was the most common subtype in donkeys   in the investigated regions. Furthermore, phylogenetic analysis of these isolates showed that these isolates exhibit close relationship with isolates from horses, humans and chinchillas, suggesting that transmission of G. intestinalis may be occurring among these hosts. Furthermore, 10 out of 28 positive isolates were successfully amplified at all three loci. These samples provided four novel MLGs in the assemblage B, namely MLGs novel-1 to novel-4 ( Table 5, Fig. 1). Of these, MLG novel-1 (n = 5) was the most prevalent MLG, and responsible for 50% of all MLGs in the present study. These findings suggest a high genetic diversity of this prevalent genotype in donkeys in China, in agreement with previous conclusions that G. intestinalis isolates of the same assemblage may be grouped into distinct MLGs [6,24].

Conclusions
The present study demonstrated the occurrence of G. intestinalis infection in donkeys in China. Sequences analysis suggested that all the G. intestinalis isolates represented assemblage B, with four, one and three subtypes of assemblage B at the tpi gdh and bg loci, respectively. Moreover, four novel MLGs (MLGs novel-1 to novel-4) were identified within assemblage B. The results of the present study not only improve the information of the distribution of G. intestinalis genotypes in China, but also provide the foundation data for preventing and controlling G. intestinalis infection in donkeys, other animals and humans.
gdh 219 Reference sequence G KR048463   1 Phylogenetic relationships of Giardia intestinalis inferred by the neighbour-joining analysis of concatenated β-giardin, gdh and tpi gene sequences. Multi-locus genotypes from a previous study (Lebbad et al. [38]) are indicated. The bootstrapping was performed using 1000 replicates. Isolates identified in this study are indicated by solid circles