Scientia Agricultura Sinica ›› 2015, Vol. 48 ›› Issue (14): 2839-2847.doi: 10.3864/j.issn.0578-1752.2015.14.015

• ANIMAL SCIENCE·VETERINARY SCIENCERE·SOURCE INSECT • Previous Articles     Next Articles

Difference in Susceptibility to Mycoplasma Pneumonia Among Various Pig Breeds and Its Molecular Genetic Basis

FANG Xiao-min, ZHAO Wei-min, FU Yan-feng, TU Feng, LI Bi-xia, WANG Xue-min, ZHAO Fang, REN Shou-wen   

  1. Institute of Livestock Science, Jiangsu Academy of Agricultural Sciences, Nanjing 210014
  • Received:2014-09-18 Online:2015-07-16 Published:2015-07-16

Abstract: 【Objective】The objective of study is to detect susceptibility differences to M. hyopneumoniae among Chinese native pigs, western pigs and their crossbreed pigs, screen differentially expressed genes and explore the molecular genetic basis of M. hyopneumoniae infection in swine. It wouldThe results of the study will provide a basis and possibility for researchers to investigate the molecular mechanisms of M. hyopneumoniae infection in swine. 【Method】 In this study, Meishan pigs (sensitive to M. hyopneumonia, n=20 ), Landrace (excellent tolerance to M. hyopneumonia, n=20) and Suzhong pigs (cultivated breed derived from crossbred progeny of Meishan and Landrace pigs, n=20) were selected for artificial infection with M. hyopneumoniae. And the pigs were allocated randomly into the treatment group (15 pigs of each breed) or control group (5 pigs of each breed). The pigs of treatment group were administered with M. hyopneumoniae strain JS. Meanwhile, the control pigs were injected with physiological saline solution. The treatment and control groups were isolated and fed an antibiotic-free diet throughout the experimental period. And then, clinical symptoms were observed daily, and average daily weight gain, antibodies level, X-ray transmission and M. hyopneumoniae pathogen were detected at 18 and 28 days post M. hyopneumoniae challenge, respectively. Twenty-eight days post challenge, the pigs were sacrificed and inspected for hepatization of the lung lobes as an indicator of Mycoplasma pneumonia. Then, 2 infected individuals and 2 non-infected individuals of each breed pigs by M. hyopneumoniae were selected to perform Agilent Pig 4x44K Gene Expression Microarray analysis, and the double comparison method of inter- and intra-breed was used to investigate differential expression genes. Furthermore, Gene Ontology (http://www. geneont ology. org) and KEGG pathway (http://www. genome.jp/kegg/) were applied to analyze the roles of these differentially expressed genes involved in signaling pathway and regulatory network to discuss the molecular genetic basis in the process of M. hyopneumoniae infection in swine.【Result】 The results showed that, from day 1 to day 18 of experiment period, the average daily weight gain of the treated pigs was significantly lower than that of the control pigs (0.01≤P<0.05), especially for Meishan pigs. From day 19 to day 28, negative growth (an average daily weight gain of less than 0.00 kg) and a drop in average daily weight gain were recorded for pigs in the treatment group. And the average daily weight gain of treated pigs was significantly lower than that of the control pigs (P<0.01). Eighteen days post M. hyopneumoniae challenge, the antibody level of Landrace pigs and Suzhong pigs had little change and were low with the negative s/p ratio. But the s/p ratios of Meishan pigs were rapidly up to positive level, and were significantly higher than that of Landrace and Suzhong pigs (0.01≤P<0.05), respectively. Twenty-eight days after treatment, the antibody level of Meishan pigs was up to 0.97±0.26, which was significantly higher than those of Landrace (0.15±0.10) and Suzhong pigs (0.46±0.20) (P<0.01, respectively). At 18 days after treatment, clinical symptoms of mycoplasma pneumonia appeared in 11 Meishan pigs in the treatment group. Only two Landrace pigs showed signs of a slight cough. Five Suzhong pigs had early symptoms of mycoplasma pneumonia, such as coughing and lethargy. Twenty-three days into the experiment, one Meishan pig from the treatment group died after infection of M. hyopneumoniae. At the end of study, day 28, all Meishan pigs in the treatment group showed typical clinical symptoms and signs of mycoplasma pneumonia. Seven Landrace pigs from the treatment group had intermittent cough, lethargy and decreased appetite. Five Suzhong pigs had typical clinical symptoms of mycoplasma pneumonia, and further more six pigs had a slight cough. The results of M. hyopneumoniae pathogen detection were generally in accordance with description above. Moreover, on day 18 after treatment administration, the results of X-ray transmission detection revealed that 15 Meishan pigs in the treatment group had cloudy flocculent shadow, and amongst them, six animals had typical clinical symptoms and signs of mycoplasma pneumonia. While, only one of the Landrace pigs had a cloudy flocculent shadow and showed increased lung markings in the lung field, and four pigs had a small cloudy flocculent shadow. The number and degree of M. hyopneumoniae infection of Suzhong pigs appeared to be between that of Meishan and Landrace pigs. On day 28, all Meishan pigs in the treatment group had typical clinical symptoms and signs of mycoplasma pneumonia. Seven Landrace pigs and thirteen Suzhong pigs had clinical pathological evidence of mycoplasma pneumonia. At the end of experiment period, pathological examination of infected pigs indicated that the lung lesion scores of Meishan pigs (mean 23.20±2.54) were significantly higher than that of Landrace pigs  (mean 10.27±8.18) (P<0.01) and Suzhong pigs (mean 18.71±4.78) (0.01≤P<0.05). Profile microarray results showed that 119 differential genes were identified in Mycoplasma pneumonia pigs, including 49 up-regulated and 70 down-regulated genes, compared with the control group. These genes were involved in 18 signal pathways, such as B cell receptor signaling pathway, complement and coagulation cascades, steroid hormone biosynthesis and so on.【Conclusion】The obvious sensitivity differences do exist in the occurrence of swine mycoplasma pneumonia among various pig breeds. The primary immunodeficiency, Toll-like receptor signaling, and steroid metabolism pathways play important roles in the regulation of inflammatory response to M. hyopneumoniae infection in swine.

Key words: pig, mycoplasma pneumonia, susceptibility difference, molecular genetic basis

[1]    辛九庆, 王亮, 李媛. 猪支原体肺炎的研究进展. 猪业科学, 2006, 23(11): 19-22.
Xin J Q, Wang L, Li Y. Research progress on swine mycoplasma opneumoniae. Swine Industry Science, 2006, 23(11): 19-22. (in Chinese)
[2]    邵国青, 华利忠. 混合感染背景下猪呼吸道病的免疫与控制. 中国兽药杂志, 2012, 46(S): 97-99.
Shao G Q, Hua L Z. Immunity and control of swine respiratory tract disease in mixture infection. Chinese Journal of Veterinary Drug, 2012, 46(S): 97-99. (in Chinese)
[3]    Geary S J, Walczak E M. Cytopathic effect of whole cells and purified membranes of Mycoplasma hyopneumoniae. Infection and Immunity, 1983, 41(1): 132-136.
[4]    Geary S J, Walczak E M. Isolation of a cytopathic factor from Mycoplasma hyopneumoniae. Infection and Immunity, 1985, 48(2): 576-578.
[5]    Barate A K, Cho Y, Truong Q L, Hahn T W. Immunogenicity of IMS 1113 plus soluble subunit and chimeric proteins containing Mycoplasma hyopneumoniae P97 C-terminal repeat regions. Fems Microbiology Letters, 2014, 352(2): 213-220.
[6]    Liu W, Xiao S, Li M, Guo S, Li S, Luo R, Feng Z, Li B, Zhou Z, Shao G, Chen H, Fang L. Comparative genomic analyses of Mycoplasma hyopneumoniae pathogenic 168 strain and its high-passaged attenuated strain. BMC Genomics, 2013, 14: 80.
[7]    Okamba F R, Arella M, Music N, Jia J J, Gottschalk M, Gagnon CA.Potential use of a recombinant replication-defective adenovirus vector carrying the C-terminal portion of the P97 adhesin protein as a vaccine against Mycoplasma hyopneumoniae in swine. Vaccine, 2010, 28(30): 4802-4809.
[8]    Cheikh Saad Bouh K, Shareck F, Dea S. Monoclonal antibodies to Escherichia coli-expressed P46 and P65 membranous proteins for specific immunodetection of Mycoplasma hyopneumoniae in lungs of infected pigs. Clinical and Diagnostic Laboratory Immunology,2003, 10(3): 459-468.
[9]    胡茂志,焦新安,潘志明,邵国青,刘秀梵. 抗猪肺炎支原体特异性P36蛋白单克隆抗体的制备与鉴定. 中国兽医学报, 2006, 26(6): 619-921.
Hu M Z, Jiao X A, Pan Z M, Shao G Q, Liu X F. Development of monoclonal antibody against P36 protein of Mycoplasma hyopneumoniae. Chinese Journal Veterinary Science, 2006, 26(6): 619-921. (in Chinese)
[10]   Simionatto S, Marchioro S B, Galli V, Brum C B, Klein C S, Rebelatto R, Silva E F, Borsuk S, Conceição F R, Dellagostin O A. Immunological characterization of Mycoplasma hyopneumoniae recombinant proteins. Comparative Immunology Microbiology and Infectious Diseases,2012, 35(2): 209-216.
[11]   Feng Z X, Shao G Q, Liu M J. Immune responses to the attenuated mycoplasma hyopneumoniae 168 strain vaccine by intrapulmonic immunization in piglets.Agricultural Sciences in China, 2010, 9: 423-431.
[12]   Tassis P D, Papatsiros V G, Nell T, Maes D, Alexopoulos C, Kyriakis S C, Tzika E D. Clinical evaluation of intradermal vaccination against porcine enzootic pneumonia (Mycoplasma hyopneumoniae). Veterinary Record, 2012, 170(10): 261.
[13]   Hillen S, von Berg S, Köhler K, Reinacher M, Willems H, Reiner G. Occurrence and severity of lung lesions in slaughter pigs vaccinated against Mycoplasma hyopneumoniae with different strategies. Preventive Veterinary Medicine, 2014, 113(4): 580-588.
[14] Caron J, Ouardani M, Dea S. Diagnosis and differentiation of Mycoplasma hyopneumoniae and Mycoplasma hyorhinis infections in pigs by PCR amplification of the p36 and p46 genes. Journal of Clinical Microbiology, 2000, 38(4): 1390-1396.
[15]   邵国青. 猪气喘病防制的药物与疫苗. 中国动物保健, 2003, 8: 21-23.
Shao G Q. Drugs and vaccines for prevention of swine mycoplasma opneumoniae. China Animal Health, 2003, 8: 21-23. (in Chinese)
[16]   刘磊, 马松涛. 猪气喘病流行特点及防治措施. 畜牧兽医科技信息, 2007(9): 64-65.
Liu L, Ma S T. Epidemiological characteristics and its prevention of swine enzootic pneumonia. Chinese Journal of Animal Husbandry and Veterinary Medicine, 2007(9): 64-65. (in Chinese)
[17]   邵国青, 刘茂军, 孙佩元, 王继春, 杜改梅, 周勇岐, 刘冬霞. 猪气喘病实验猪模型的建立. 微生物与感染, 2007, 2(4): 215-218.
Shao G Q, Liu M J, Sun P Y, Wang J C, Du G M., Zhou Y Q, Liu D X. The establishment of an experimental swine model of swine mycoplasma pneumonia. Journal of Microbes and Infection, 2007, 2(4): 215-218. (in Chinese)
[18]   Ostanello F, Dottori M, Gusmara C, Leotti G, Sala V, Pneumonia disease assessment using a slaughterhouse lung-scoring method. Journal of veterinary medicine. Journal of Veterinary Medicine Series A-physiology Pathology Clinical Medicine, 2007, 54(2):70-75.
[19]   刘茂军, 张映, 邵国青, 姜俊兵, 冯志新, 王海燕, 孙佩元, 甘源. 猪支原体肺炎可疑肺组织PCR检测方法的建立. 山西农业大学学报: 自然科学版, 2009, 29(5): 444-447.
Liu M J, Zhang Y, Shao G Q, Jiang J B, Feng Z X, Wang H Y, Sun P Y, Gan Y. Establishment of PCR method for detecting the suspicious sample of Mycoplasma hyopneumoniae. Journal of Shanxi Agriculture University: Natural Science Edition, 2009, 29(5): 444-447. (in Chinese)
[20]   刁有祥, 丁家波, 姜世金, 崔治中, 陈本龙. 猪传染性胸膜肺炎病料中PCV-2PRRSVPCR检测. 微生物学报, 2005, 45(3): 397-400.
Diao Y X, Ding J B, Jiang S J, Cui Z Z, Chen B L. PCR detection of PCV-2 and PRRSV in porcine pleuropneumonia samples. Acta Microbiologica Sinica, 2005, 45(3): 397-400. (in Chinese)
[21]   曹正, 季伟. 江苏省规模化猪场猪圆环病毒2型感染的流行病学调查. 畜牧与兽医, 2011,43(3): 85-88.
Cao Z, Ji W. Epidemiological investigation on infection of PCV2 in intensive swine farms of jiangsu province. Animal Husbandry Veterinary Medicine, 2011,43(3): 85-88. (in Chinese)
[22]   Rudd B D, Burstein E, Duckett C S, Li X, Lukacs N W. Differential role for TLR3 in respiratory syncytial virus-induced chemokine expression. Journal of Virology, 2005, 79(6):3350-3357.
[23]   Schulz O, Diebold S S, Chen M, Näslund T I, Nolte M A, Alexopoulou L, Azuma Y T, Flavell R A, Liljeström P, Reis e Sousa C. Toll-like receptor 3 promotes cross-priming to virus-infected cells. Nature, 2005, 433(7028):887-892.
[24]   Kirischian N L, Wilson J Y. Phylogenetic and functional analyses of the cytochrome P450 family. Molecular Phylogenetics and Evolution,2012, 62(1):458-471.
[25]   Messina A, Puccinelli E, Gervasi P G, Longo V. Expression and inducibility of CYP1A1, 1A2, 1B1 by β-naphthoflavone and CYP2B22, CYP3As by rifampicin in heart regions and coronary arteries of pig. Research in Veterinary Science, 2013, 94(1):77-83.
[1] TAN XianMing,ZHANG JiaWei,WANG ZhongLin,CHEN JunXu,YANG Feng,YANG WenYu. Prediction of Maize Yield in Relay Strip Intercropping Under Different Water and Nitrogen Conditions Based on PLS [J]. Scientia Agricultura Sinica, 2022, 55(6): 1127-1138.
[2] CHEN XueSen, YIN HuaLin, WANG Nan, ZHANG Min, JIANG ShengHui, XU Juan, MAO ZhiQuan, ZHANG ZongYing, WANG ZhiGang, JIANG ZhaoTao, XU YueHua, LI JianMing. Interpretation of the Case of Bud Sports Selection to Promote the High-Quality and Efficient Development of the World’s Apple and Citrus Industry [J]. Scientia Agricultura Sinica, 2022, 55(4): 755-768.
[3] MingJie XING,XianHong GU,XiaoHong WANG,Yue HAO. Effects of IL-15 Overexpression on Myoblast Differentiation of Porcine Skeletal Muscle Cells [J]. Scientia Agricultura Sinica, 2022, 55(18): 3652-3663.
[4] YANG ChangPei,WANG NaiXiu,WANG Kai,HUANG ZiQing,LIN HaiLan,ZHANG Li,ZHANG Chen,FENG LuQiu,GAN Ling. Effects and Mechanisms of Exogenous GABA Against Oxidative Stress in Piglets [J]. Scientia Agricultura Sinica, 2022, 55(17): 3437-3449.
[5] DENG FuLi,SHEN Dan,ZHONG RuQing,ZHANG ShunFen,LI Tao,SUN ShuDong,CHEN Liang,ZHANG HongFu. Non-Starch Polysaccharide Enzymes Cocktail of Corn-Miscellaneous Meal-Based Diet Optimization by In Vitro Method and Its Effects on Intestinal Microbiome in Finishing Pigs [J]. Scientia Agricultura Sinica, 2022, 55(16): 3242-3255.
[6] JIN MengJiao,LIU Bo,WANG KangKang,ZHANG GuangZhong,QIAN WanQiang,WAN FangHao. Light Energy Utilization and Response of Chlorophyll Synthesis Under Different Light Intensities in Mikania micrantha [J]. Scientia Agricultura Sinica, 2022, 55(12): 2347-2359.
[7] HU RongRong,DING ShiJie,GUO Yun,ZHU HaoZhe,CHEN YiChun,LIU Zheng,DING Xi,TANG ChangBo,ZHOU GuangHong. Effects of Trolox on Proliferation and Differentiation of Pig Muscle Stem Cells [J]. Scientia Agricultura Sinica, 2021, 54(24): 5290-5301.
[8] TANG ZhenShuang,YIN Dong,YIN LiLin,MA YunLong,XIANG Tao,ZHU MengJin,YU Mei,LIU XiaoLei,LI XinYun,QIU XiaoTian,ZHAO ShuHong. To Evaluate the “Two-Step” Genomic Selection Strategy in Pig by Simulation [J]. Scientia Agricultura Sinica, 2021, 54(21): 4677-4684.
[9] ZHANG DanDan,XU TengTeng,GAO Di,QI Xin,NING Wei,RU ZhenYuan,ZHANG XiangDong,GUO TengLong,SHENTU LuYan,YU Tong,MA YangYang,LI YunSheng,ZHANG YunHai,CAO ZuBing. Transcription Factor TEAD4 Regulates Early Embryonic Development in Pigs [J]. Scientia Agricultura Sinica, 2021, 54(20): 4456-4465.
[10] SHI Jiang,WANG JiaTong,PENG QunHua,LÜ Haipeng,BALDERMANN Susanne,LIN Zhi. Changes in Lipid-Soluble Pigments in Fresh Tea Leaves Treated by Methyl Jasmonate and During Postharvest Oolong Tea Manufacturing [J]. Scientia Agricultura Sinica, 2021, 54(18): 3984-3997.
[11] DU Xing,ZENG Qiang,LIU Lu,LI QiQi,YANG Liu,PAN ZengXiang,LI QiFa. Identification of the Core Promoter of Linc-NORFA and Its Transcriptional Regulation in Erhualian Pig [J]. Scientia Agricultura Sinica, 2021, 54(15): 3331-3342.
[12] YU ZhengWang,ZHOU ZhongXin. Functions of Antibacterial and Inducing Defense Peptide Expression of Medium-Chain Fatty Acid and Its Application in Piglet Feeds [J]. Scientia Agricultura Sinica, 2021, 54(13): 2895-2905.
[13] QIN BenYuan,YANG Yang,ZHANG YanWei,LIU Min,ZHANG WanFeng,WANG HaiZhen,WU YiQi,ZHANG XueLian,CAI ChunBo,GAO PengFei,GUO XiaoHong,LI BuGao,CAO GuoQing. Isolation, Culture, Identification and Biological Characteristics of Pig Skeletal Muscle Satellite Cells [J]. Scientia Agricultura Sinica, 2020, 53(8): 1664-1676.
[14] YaoQun WU,ShaoKang CHEN,XiHui SHENG,XiaoLong QI,XiangGuo WANG,HeMin NI,Yong GUO,ChuDuan WANG,Kai XING. Differential Expression of mRNA and lncRNA in Longissimus Dorsi Muscle of Songliao Black Pig and Landrace Pig Based on High-Throughput Sequencing Technique [J]. Scientia Agricultura Sinica, 2020, 53(4): 836-847.
[15] ZHANG TieYing,ZHANG LiYang,LIU JunLi,LIAO ChaoYong,LÜ Lin,LIAO XiuDong,LUO XuGang. A Survey on Distribution of Arsenic Contents in Feedstuffs for Livestock and Poultry in China [J]. Scientia Agricultura Sinica, 2020, 53(21): 4507-4515.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!