Abstract
The seroprevalence of Chlamydiaceae infection in Tibetan pigs in Tibet, China, was examined by indirect hemagglutination assay (IHA), between April, 2010, and December, 2010. A total of 71 of 427 serum samples (16.63%, 95% confidence interval [CI] 15.31–17.95] were positive for Chlamydiaceae antibodies. Forty Chlamydiaceae seropositives from 232 samples were recorded in sera from Nyingchi (17.24%, 95% CI 15.40–19.08) and 31 positives were recorded in 195 serum samples from Mainling (15.90%, 95% CI 14.02–17.78). The investigation showed that the prevalence in female animals was 17.61% (95% CI 15.22–20.00), and in male animals it was 12.72% (95% CI 11.07–14.37). The prevalence ranged from 0% to 20.61% (95% CI 17.81–23.48) among different age groups, with a higher prevalence in growing pigs (p<0.01). The results indicated that Chlamydiaceae infection was widespread in Tibetan pigs in Tibet, China, which is of public health concern in this region of the world. To our knowledge, this is the first report of Chlamydiaceae seroprevalence in Tibetan pigs in Tibet, China.
Introduction
Chlamydiaceae infections in pigs have been reported worldwide (Eggemann et al. 2000, Vanrompay et al. 2004, Wang et al. 2006, Zhou et al. 2008, Pantchev et al. 2010, Xu et al. 2010); however, little is known about Chlamydiaceae prevalence in Tibetan pigs in Tibet, China. The Tibetan pig is a Chinese native pig breed distributed in the southeastern Tibet Plateau and the surrounding areas. During long-term free-range production, Tibetan pigs have evolved adaptions to low temperature and poor food quality (Xin et al. 2011) and, physically possess powerful musculature, with coarse black hair covering the whole body (Zheng 1998). The animal's meat is a sought-after delicacy with a tender texture and high nutritional value. Thus, Tibetan pigs have become an important source of income for Tibetans. Tibetan pigs may also act as a potential risk in the spread of infectious disease. In this context, the objective of the present study was to investigate using a serological approach whether Chlamydiaceae are prevalent in Tibetan pigs in Tibet, China.
Materials and Methods
Investigation sites
The present study was carried out in Nyingchi and Mainling counties of the Nyingchi Prefecture, southeastern Tibet. As described by Wu et al. (2012), the average elevation of the surveyed area is more than 3000 meters above sea level, covering about 120,000 km2. This region is influenced by the warm current from the Pacific and Indian Ocean, and has a humid tropical climate.
Serum samples
A total of 427 Tibetan pig blood samples including 232 from Nyingchi county and 195 from Mainling county were collected by veterinary practitioners between April, 2010, and December, 2010. The samples were centrifuged at 3000×g for 5 min. Then, the serum was removed and stored at −20°C until further analysis.
Serological tests
The commercially available indirect hemagglutination assay (IHA) kit (Lanzhou Veterinary Research Institute, Chinese Academy of Agriculture Sciences) was used to examine antibodies to Chlamydiaceae. The detection procedures were carried out as previously reported (Xu et al. 2010). Samples that reacted at dilutions of 1:16 or higher were considered positive for Chlamydiaceae antibodies. Positive results from dilutions of between 1:4 and 1:16 were considered “suspect” and were retested.
Statistical analysis
Differences in the prevalence of Chlamydiaceae in Tibetan pigs from different geographical locations and age groups were analyzed with a chi-squared test using SPSS for Windows (release 18.0 standard version, SPSS Inc., Chicago, IL). All tests were 2-sided, and values of p<0.05 were considered as statistically significant.
Results and Discussion
Seventy-one out of 427 serum samples (16.63%, 95% confidence interval [CI] 15.31–17.95) were seropositive for Chlamydiaceae by IHA. Antibody titers were 1:256 in 2, 1:128 in 2, 1:64 in 5, 1:32 in 10, and 1:16 in 52 in the seropositive Tibetan pigs. Of the total of 71 seropositive results, 40 (of 232) samples came from Nyingchi (17.24%, 95% CI 15.40–19.08) and 31 (of 195) originated from Mainling (15.90%, 95% CI 14.02–17.78) (Table 1), although the difference in seroprevalnce between the 2 counties was not statistically significant (p>0.05). As shown in Table 1, the investigation revealed that the prevalences in female and male animals were 17.61% (95% CI 15.22–20.00) and 12.72% (95% CI 11.07–14.37), respectively. Among these positive Tibetan pigs, seroprevalence varied in different age groups, ranging from 0 to 20.61% (95% CI 17.81–23.48) (Table 2).
IHA, indirect hemagglutination assay; CI, confidence interval.
Surveys of Chlamydiaceae infections in pigs have been performed in many countries (Eggemann et al. 2000, Vanrompay et al. 2004, Pantchev et al. 2010) and some provinces in China (Suo et al. 2005, Luo et al. 2006, Wang et al. 2006, Xian et al. 2007, Zhou et al. 2008, Xu et al. 2010), but little is known about infection with Chlamydiaceae in Tibetan pigs, which are one of the main sources of food and economic activity in Tibet. In this study, the overall seropositivity for Chlamydiaceae exposure was 16.63% (95% CI 15.31–17.95) in Tibetan pigs, which was lower than that of the intensively raised pigs in other provinces of China (Jin et al. 2005, Li 2005, Suo et al. 2005, Luo et al. 2006, Wang et al. 2006, Xian et al. 2007, Zhou et al. 2008, Xu et al. 2010), but higher than that observed in Yunnan province (10.5%) in China (Cao and Zhang 2007). The low seropositivity of Chlamydiaceae in Tibetan pigs may be attributed to higher resistance of Tibetan pigs to the disease compared with pigs from intensive farming systems and inbreeding of Tibetan pigs that could decrease the opportunity of transmission through mating with other populations of pigs.
Among different age groups of Tibetan pigs, a higher prevalence (20.61%, 95% CI 17.81–23.48) was detected in growing pigs (p<0.01), whereas no seroprevalence was detected in breeding boars and sows, possibly due to the limited number of samples. In other reports in China, the seropositivity of Chlamydiaceae in breeding boars and sows from intensive farms was usually more than 30% (Jin et al. 2005, Li 2005, Suo et al. 2005, Luo et al. 2006, Wang et al. 2006, Xian et al. 2007, Zhou et al. 2008, Xu et al. 2010). Further studies of Chlamydiaceae infection in Tibetan pigs should focus on breeding boars and sows.
No statistically significant difference in Chlamydiaceae seroprevalence was observed between female and male Tibetan pigs (p>0.05). However, a tendency for higher prevalence among females was observed. This tendency was also observed in the previous surveys of wild boars in Italy (females, 45.95%; males, 38.8%) (Antonietta et al. 2011) and Germany (females, 83.3%; males, 42.9%) (Helmut et al. 2004) by microimmunofluorescence (MIF) and PCR. Therefore, further studies should be performed to ascertain whether gender is a crucial factor for Chlamydiaceae infection. In this present study, the Chlamydiaceae seropositivity in the 2 counties did not differ significantly (p>0.05), probably because of the use of similar environmental and free-range systems.
Many wild birds (Kaleta and Taday 2003) and ruminants (Cubero-Pablo et al. 2000) can also carry some species of Chlamydiaceae. Cross-species transmission is widespread in chlamydial circulation (Lemus et al. 2010). Whether Tibetan pigs acquired Chlamydiaceae through wild animals interacting with domestic animal husbandry practices in this region could not be assessed based on the present data. Further investigations should study the transmission of Chlamydiaceae in Tibetan pigs, other animals, and humans in Tibet.
In conclusion, the present study demonstrated that there was a 16.63% (95% CI 15.31–17.95) seroprevalence of Chlamydiaceae infection in Tibetan pigs in Tibet, China, which provided baseline data for the effective prevention and control of chlamydiosis in Tibetan pigs in this unique region of the world. To our knowledge, the present report is the first to document the seroprevalence of Chlamydiaceae infection in Tibetan pigs in China.
Footnotes
Acknowledgments
Project support was provided, in part, by the Science Fund for Creative Research Groups of Gansu Province (Grant No. 1210RJIA006), the Open Funds of the State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences (grant nos. SKLVEB2011KFKT004, SKLVEB2011KFKT011, SKLVEB2010KFKT009, and SKLVEB2011KFKT010), and the Yunnan Provincial Program for Introducing High-level Scientists (grant no. 2009CI125).
Author Disclosure Statement
No completing financial interests exist. The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the funding agencies.
