- Short report
- Open Access
First report of Cryptosporidium spp. in white yaks in China
- Si-Yuan Qin†1, 2,
- Xiao-Xuan Zhang†1, 2,
- Guang-Hui Zhao3,
- Dong-Hui Zhou1Email author,
- Ming-Yang Yin1,
- Quan Zhao2 and
- Xing-Quan Zhu1, 2Email author
© Qin et al.; licensee BioMed Central Ltd. 2014
- Received: 29 March 2014
- Accepted: 11 May 2014
- Published: 19 May 2014
Cryptosporidium is an enteric apicomplexan parasite, which can infect yaks, leading to reduction of milk production and poor weight gain. White yak (Bos grunniens) is a unique yak breed inhabiting only in Tianzhu Tibetan Autonomous County, Gansu province, northwestern China. The objective of the present study was to molecularly determine Cryptosporidium infection and species in white yaks.
Seventy-six fecal samples from white yaks in Tianzhu Tibetan Autonomous County, Gansu province were collected. The small subunit ribosomal RNA (SSU rRNA) gene of each sample was amplified using nested PCR and sequenced. The Cryptosporidium species was determined by comparison of the obtained sequences with that of corresponding Cryptosporidium sequences available in GenBank by BLAST (http://www.ncbi.nlm.nih.gov/BLAST/) and phylogenetic analysis with maximum likelihood (ML) using PAUP*. The overall prevalence of Cryptosporidium infection in white yak was 5.26% (4/76). Species identification showed C. andersoni in one sample (collected in September), and C. bovis in three samples (one collected in November and two collected in September).
The present investigation revealed the existence of Cryptosporidium infection in white yaks in China, for the first time, and two Cryptosporidium species, namely C. andersoni and C. bovis, were identified. These findings extend the host range for Cryptosporidium spp., and also provide base-line information for further studies of molecular epidemiology and control of Cryptosporidium infection in the unique white yaks.
- Cryptosporidium spp
- Genetic characterization
- White Yak
Cryptosporidium is an apicomplexan, enteric parasite pathogen, which may lead to diarrheal illness and other severe diseases of animals and humans [1, 2]. Human infection with Cryptosporidium is usually through close contact with infected animals or consuming contaminated water or food . Many animals can be infected with Cryptosporidium spp. including livestock and wild animals [4–8]. Four Cryptosporidium species have been identified in black yaks in previous studies [5, 7].
White yak (Bos grunniens) is a unique yak breed living only in Tianzhu Tibetan Autonomous County, Gansu province, northwestern China, where the air pressure is high and the temperature and oxygen content are low. White yak is known as the pearl of the plateau, and it is a rare and precious semi-wild animal of China and the world. Only approximately 49,400 white yaks were available in Tianzhu Tibetan Autonomous County . Milk and meat of white yaks are the sought-after delicacy for local Tibetan people and other residents in Gansu Province. Previous studies have indicated that Cryptosporidium could infect black yaks, but it is yet to know whether white yaks are infected with Cryptosporidium spp.. The objective of the present study was to determine Cryptosporidium infection and species in white yaks in Tianzhu Tibetan Autonomous County, Gansu Province, China.
This study was approved by the Animal Ethics Committee of Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences (Approval No. LVRIAEC2013-010). The white yaks from which the feces were collected, were handled in accordance with good animal practices required by the Animal Ethics Procedures and Guidelines of the People’s Republic of China.
The study site
The fecal samples used in the present study were collected from white yaks in Tianzhu Tibetan Autonomous County, Gansu Province, northwestern China. The sampling site is between the eastern longitudes of 102°07′-103°46′ and northern latitudes of 36°31′-37°55′. The altitude of Tianzhu Tibetan Autonomous County ranges from 2,040 m to 4,878 m, and the average annual temperature are from -8°C to 4°C, respectively.
A total of 76 white yak fecal samples were randomly collected from two farms between September and November 2013 in Tianzhu Tibetan Autonomous County, Gansu Province, northwestern China. Information about the examined white yaks was obtained from the herdsmen at the time of sample collection. Fecal samples were collected with sterile gloves and transported to the laboratory in Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu Province, China, and stored at 4°C within one week before being tested.
DNA extraction and PCR amplification
Genomic DNA was extracted from each fecal sample using the Stool DNA kit (OMEGA, USA) according to the manufacturer’s instructions, and stored at -20°C until PCR amplification. The small subunit ribosomal RNA (SSU rRNA) gene was amplified using nested PCR to determine species/genotypes of Cryptosporidium spp. . Positive and negative controls were included in each amplification. Amplification products were examined using 1.5% agarose gel containing GoldView (Solarbio, China) and were observed under UV light.
Sequencing and phylogenetic analyses
All positive secondary PCR products were directly sequenced by Sangon Biotech Company (Shanghai, China). The obtained sequences were aligned with Cryptosporidium sequences available in GenBank database using the BLAST (http://www.ncbi.nlm.nih.gov/BLAST/) and Multiple Sequence Alignment Program, Clustal X 1.83 . Phylogenetic relationships of Cryptosporidium spp. were re-constructed using Maximum Likelihood (ML) method, which were performed using a Fitch criterion within PAUP* (version 4.0b4a) and 1000 non-parametric bootstrap replicates. Plasmodium cathemerium (GenBank accession number: AY625607) was used as the out-group. The sequences obtained in the present study were deposited in GenBank with accession numbers of KJ094571 and KJ094572.
The overall Cryptosporidium prevalence in Tianzhu white yaks was 5.26% (4/76) using a molecular approach, which was lower than that in yaks investigated by microscopy (10.4%) , serological test (33.64%)  and PCR (24.2%)  in Shanghai city and Qinghai province of China. The lower prevalence of Cryptosporidium infection in Tianzhu white yaks determined in the present investigation is likely due to the cold sampling seasons (September to November are becoming cold in Tianzhu Tibetan Autonomous County) and the small sample size.
Five Cryptosporidium species/genotypes, namely C. parvum, C. ryanae, Cryptosporidium sp. z13 , C. bovis and deer-like genotype , have been detected in yaks in China. The present study revealed the presence of C. andersoni and C. bovis in white yaks. Of the four Cryptosporidium-positive samples, three represented C. bovis, indicating that C. bovis is the more prevalent Cryptosporidium species in white yaks, which is similar to previous studies that C. bovis is more prevalent in water buffaloes and beef calves [13, 14].
However, C. parvum, C. ryanae, Cryptosporidium sp. z13  and deer-like genotype  were not detected in white yaks in the present study, which may due to the small number of samples examined. C. parvum is one of the most important Cryptosporidium species, which has public health concerns , and it is a common species found in pre-weaned cattle in China and other countries [16–19]. Further studies will sample more white yaks in different seasons of the year to determine the dynamics and full profiles of Cryptosporidium infection in white yaks, to examine the infection status of the local Tibetans with Cryptosporidium, and to assess the zoonotic potential of Cryptosporidium from white yaks.
The present investigation revealed the existence of C. andersoni and C. bovis in Tianzhu white yaks, which is the first report of Cryptosporidium infection in Tianzhu white yaks. These results not only extend the host range for Cryptosporidium spp., but also provide base-line information for further studies of the molecular epidemiology and control of Cryptosporidium infection in Tianzhu white yaks.
This work was supported in part by the “Special Fund for Agro-scientific Research in the Public Interest” (Grant No. 201303037), the Science Fund for Creative Research Groups of Gansu Province (Grant No. 1210RJIA006), the Program for New Century Excellent Talents in University (Grant No. NCET-13-0489) and the Open Funds of the State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences (Grant No. SKLVEB2013KFKT007).
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