Skip to main content

Advertisement

Log in

Escherichia coli aggravates endoplasmic reticulum stress and triggers CHOP-dependent apoptosis in weaned pigs

  • Original Article
  • Published:
Amino Acids Aims and scope Submit manuscript

Abstract

Intestinal cells can sense the presence of pathogens and trigger many important signaling pathways to maintain tissue homeostasis and normal function. Escherichia coli and lipopolysaccharides (LPS) are the main pathogenic factors of intestinal disease in pigs. However, the roles of endoplasmic reticulum stress (ERS) and its mediated apoptosis in intestinal malfunction induced by E. coli or LPS remain unclear. In the present study, we aimed to evaluate whether ERS could be activated by E. coli fed to piglets and whether the underlying mechanisms of this disease process could be exploited. Eighteen weaned pigs (21 days old) were randomly assigned to one of two treatment groups (n = 9 per group). After pre-feeding for 1 week, the diets of the piglets in one group were supplemented with E. coli (W25 K, 109 cells kg−1 diet) for 7 days. At the end of the experiment, all piglets were slaughtered to collect jejunum and ileum samples. Western blotting and immunofluorescence experiments were used to determine the expression levels and histological locations of ERS and its downstream signaling proteins. The intestinal porcine epithelial cell line J2 (IPEC-J2) was used as in vitro model to investigate the possible mechanism. The results showed that E. coli supplementation in the diet increased the GRP78 expression in the jejunum and ileum, especially in the jejunal epithelium and ileac germinal center, and elevated the expression levels of CHOP (in both the jejunum and ileum) and caspase-11 (in the ileum), indicating that ERS and CHOP–caspase-11 dependent apoptosis were activated in the porcine small intestine. Moreover, as demonstrated by in vitro experiments, the CHOP inhibitor 4-phenylbutyrate alleviated the damage to IPEC-J2 cells induced by LPS derived from E. coli. Taken together, these data strongly suggest that ERS can be triggered in the small intestine by dietary supplementation with E. coli and that CHOP–caspase-11 dependent apoptosis may play a key role in maintaining normal homeostasis of the intestine in response to pathogenic factors.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Abbreviations

LPS:

Lipopolysaccharide

ERS:

Endoplasmic reticulum stress

CHOP:

C/EBP homologous protein

GRP78:

Glucose-regulated protein78

E. coli :

Escherichia coli

IPEC-J2:

Intestinal porcine epithelial cell line J2

4-PBA:

4-phenylbutyrate

References

  • Ajakaiye A, Fan MZ, Forsberg CW, Phillips JP, Golovan S, Meidinger RG, Archbold T, Hacker RR (2004) Digestion and absorption of calcium in soybean meal is completed by the end of the small intestine in the transgenic phytase Enviropig (TM). Faseb J 18(4):A526–A526

    Google Scholar 

  • Bloemendaal ALA, Buchs NC, George BD, Guy RJ (2016) Intestinal stem cells and intestinal homeostasis in health and in inflammation: a review. Surgery 159(5):1237–1248. doi:10.1016/j.surg.2016.01.014

    Article  PubMed  Google Scholar 

  • Broz P, Ruby T, Belhocine K, Bouley DM, Kayagaki N, Dixit VM, Monack DM (2012) Caspase-11 increases susceptibility to Salmonella infection in the absence of caspase-1. Nature 490(7419):288–291. doi:10.1038/nature11419

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bucker R, Schulz E, Wiegand S, Siegmund B, Troeger H, Schulzke JD (2014) E. Coli alpha-hemolysin (HlyA) mediates colonic inflammation. Gastroenterology 146(5):S697–S697

    Article  Google Scholar 

  • D’Alessio S, Tacconi C, Correale C, Gandelli A, Genua M, Vetrano S, Danese S (2014) Conditional deletion of Prep1 in the intestinal epithelium alters epithelial homeostasis, intestinal development, and controls colitis susceptibility. Gastroenterology 146(5):S38–S38

    Article  Google Scholar 

  • Deitmer R, Parra A (2017) Efficacy of passive immunisation of piglets against E. coli- and C. perfringens-diarrhoea from the newborn to the weaning period. Tieraerztliche Umschau 72(4):114–122

    Google Scholar 

  • Endo M, Mori M, Akira S, Gotoh T (2006) C/EBP homologous protein (CHOP) is crucial for the induction of caspase-11 and the pathogenesis of lipopolysaccharide-induced inflammation. J Immunol 176(10):6245–6253

    Article  CAS  PubMed  Google Scholar 

  • Fernandez A, Ordonez R, Reiter RJ, Gonzalez-Gallego J, Mauriz JL (2015) Melatonin and endoplasmic reticulum stress: relation to autophagy and apoptosis. J Pineal Res 59(3):292–307. doi:10.1111/jpi.12264

    Article  CAS  PubMed  Google Scholar 

  • Fradejas N, Pastor MD, Burgos M, Tranque P, Calvo S (2009) Caspase-11 mediates ischemia-induced astrocyte death: involvement of er stress and chop. Glia 57(13):S56–S56

    Google Scholar 

  • Fryer LGD, Jones B, Duncan EJ, Hutchison CE, Ozkan T, Williams PA, Alder O, Nieuwdorp M, Townley AK, Mensenkamp AR, Stephens DJ, Dallinga-Thie GM, Shoulders CC (2014) The endoplasmic reticulum coat Protein II transport machinery coordinates cellular lipid secretion and cholesterol biosynthesis. J Biol Chem 289(7):4244–4261. doi:10.1074/jbc.M113.479980

    Article  CAS  PubMed  Google Scholar 

  • Gitlin AD, Shulman Z, Nussenzweig MC (2014) Clonal selection in the germinal centre by regulated proliferation and hypermutation. Nature 509(7502):637–640. doi:10.1038/nature13300

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Guo GK, Meng Y, Tan W, Xia YF, Cheng C, Chen XL, Gu ZF (2015) Induction of apoptosis coupled to endoplasmic reticulum stress through regulation of CHOP and JNK in bone marrow mesenchymal stem cells from patients with systemic lupus erythematosus. J Immunol Res. doi:10.1155/2015/183738

    Google Scholar 

  • He HL, Lam M, McCormick TS, Distelhorst CW (1997) Maintenance of calcium homeostasis in the endoplasmic reticulum by bcl-2. J Cell Biol 138(6):1219–1228. doi:10.1083/jcb.138.6.1219

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • He LQ, Yang HS, Hou YQ, Li TJ, Fang J, Zhou XH, Yin YL, Wu L, Nyachoti M, Wu GY (2013) Effects of dietary l-lysine intake on the intestinal mucosa and expression of CAT genes in weaned piglets. Amino Acids 45(2):383–391. doi:10.1007/s00726-013-1514-0

    Article  CAS  PubMed  Google Scholar 

  • Jiang Q, He LQ, Hou YQ, Chen JS, Duan YH, Deng D, Wu GY, Yin YL (2016) Alpha-ketoglutarate enhances milk protein synthesis by porcine mammary epithelial cells. Amino acids. doi:10.1007/s00726-016-2249-5 AMAC-D-16-00132.3

  • Jin SQ, Sun Q, Liao H, Deng MH, Li Q, Billiar TR (2017) Mechanical ventilation augments poly(I:C) induced lung inflammation and pyroptosis: roles of caspase-1 and caspase-11. Shock 47(6):101–102

    Google Scholar 

  • Kaira K, Toyoda M, Shimizu A, Shino M, Sakakura K, Takayasu Y, Takahashi K, Asao T, Chikamatsu K (2016) Expression of ER stress markers (GRP78/BiP and PERK) in adenoid cystic carcinoma. Acta Otolaryngol 136(1):1–7. doi:10.3109/00016489.2015.1083120

    Article  CAS  PubMed  Google Scholar 

  • Kaser A, Lee AH, Franke A, Glickman JN, Zeissig S, Tilg H, Nieuwenhuis EES, Higgins DE, Schreiber S, Glimcher LH, Blumberg RS (2008) XBP1 links ER stress to intestinal inflammation and confers genetic risk for human inflammatory bowel disease. Cell 134(5):743–756. doi:10.1016/j.cell.2008.07.021

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kim JG, Lee SJ, Kagnoff MF (2003) Nod1 has a key functional role in the activation of NF-kB and NF-kB target genes in human intestinal epithelial cells infected with enteroinvasive E. coli. Gastroenterology 124(4):A44–A44. doi:10.1016/S0016-5085(03)80218-4

    Article  Google Scholar 

  • Kondo T, Handa K, Genda T, Hino S, Hamaguchi N, Morita T (2017) Digestion-resistant dextrin derivatives are moderately digested in the small intestine and contribute more to energy production than predicted from large-bowel fermentation in rats. J Nutr 147(3):330–336. doi:10.3945/jn.116.239855

    CAS  PubMed  Google Scholar 

  • Li KF, Xiao YP, Chen JC, Chen JG, He XX, Yang H (2017) Microbial composition in different gut locations of weaning piglets receiving antibiotics. Asian-Australas J Anim Sci 30(1):78–84. doi:10.5713/ajas.16.0285

    Article  PubMed  Google Scholar 

  • Ling SCW, Lau EKK, Al-Shabeeb A, Nikolic A, Catalano A, Iland H, Horvath N, Ho PJ, Harrison S, Fleming S, Joshua DE, Allen JD (2012) Response of myeloma to the proteasome inhibitor bortezomib is correlated with the unfolded protein response regulator XBP-1. Haematologica J 97(1):64–72. doi:10.3324/haematol.2011.043331

    Article  CAS  Google Scholar 

  • Liu J, Wang P, Xue YX, Li Z, Qu CB, Liu YH (2015) Enhanced antitumor effect of shikonin by inhibiting endoplasmic reticulum stress via JNK/c-Jun pathway in human glioblastoma stem cells. Biochem Biophys Res Commun 466(1):103–110. doi:10.1016/j.bbrc.2015.08.115

    Article  CAS  PubMed  Google Scholar 

  • Liu G, Chen S, Guan G, Tan J, Al-Dhabi NA, Wang H, Duraipandiyan V, Fang J (2016) Chitosan modulates inflammatory Responses in rats infected with enterotoxigenic Escherichia coli. Mediators Inflamm 2016:7432845. doi:10.1155/2016/7432845

    PubMed  PubMed Central  Google Scholar 

  • Ma A (2008) Unresolved ER stress inflames the intestine. Cell 134(5):724–725. doi:10.1016/j.cell.2008.08.023

    Article  CAS  PubMed  Google Scholar 

  • Man SM, Karki R, Kanneganti TD (2017) Molecular mechanisms and functions of pyroptosis, inflammatory caspases and inflammasomes in infectious diseases. Immunol Rev 277(1):61–75. doi:10.1111/imr.12534

    Article  CAS  PubMed  Google Scholar 

  • McGuckin MA, Eri RD, Das I, Lourie R, Florin TH (2010) ER stress and the unfolded protein response in intestinal inflammation. Am J Physiol Am J Physiol Gastrointest Liver Physiol 298(6):G820–G832. doi:10.1152/ajpgi.00063.2010

    Article  CAS  Google Scholar 

  • Mroz Z (2001) Some developments on Dutch nutritional approaches to protect piglets against post-weaning gastrointestinal disorders in the absence of in-feed antibiotics. J Agric Food Chem 10:153–167

    Google Scholar 

  • Pietzak MM, Chakraborty E (2004) Induction of intestinal epithelial cell apoptosis by E. coli K1 strain RS218. Gastroenterology 126(4):A562–A562

    Google Scholar 

  • Pluske JR (2013) Feed- and feed additives-related aspects of gut health and development in weanling pigs. J Anim Sci Biotechnol. doi:10.1186/2049-1891-4-1

    PubMed  PubMed Central  Google Scholar 

  • Prapasarakul N, Tummaruk P, Niyomtum W, Tripipat T, Serichantalergs O (2010) Virulence genes and antimicrobial susceptibilities of hemolytic and nonhemolytic Escherichia coli isolated from post-weaning piglets in central thailand. J Vet Med Sci 72(12):1603–1608. doi:10.1292/jvms.10-0124

    Article  CAS  PubMed  Google Scholar 

  • Ren W, Liu G, Yin J, Chen S, Li T, Kong X, Peng Y, Yin Y, Hardwidge PR (2014a) Draft genome sequence of enterotoxigenic Escherichia coli strain W25K. Genome Announc. doi:10.1128/genomeA.00593-14

    PubMed  PubMed Central  Google Scholar 

  • Ren WK, Duan JL, Yin J, Liu G, Cao Z, Xiong X, Chen S, Li TJ, Yin YL, Hou YQ, Wu GY (2014b) Dietary l-glutamine supplementation modulates microbial community and activates innate immunity in the mouse intestine. Amino Acids 46(10):2403–2413. doi:10.1007/s00726-014-1793-0

    Article  CAS  PubMed  Google Scholar 

  • Ringseis R, Kynast AM, Couturier A, Most E, Eder K (2016) Ingestion of frying fat leads to activation of the endoplasmic reticulum stress-induced unfolded protein response in the duodenal mucosa of pigs. Mol Nutr Food Res 60(4):957–963. doi:10.1002/mnfr.201500687

    Article  CAS  PubMed  Google Scholar 

  • Ron D, Hubbard SR (2008) How IRe1 reacts to ER stress. Cell 132(1):24–26. doi:10.1016/j.cell.2007.12.017

    Article  CAS  PubMed  Google Scholar 

  • Senft D, Ronai ZA (2015) UPR, autophagy, and mitochondria crosstalk underlies the ER stress response. Trends Biochem Sci 40(3):141–148. doi:10.1016/j.tibs.2015.01.002

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sovolyova N, Healy S, Samali A, Logue SE (2014) Stressed to death—mechanisms of ER stress-induced cell death. Biol Chem 395(1):1–13. doi:10.1515/hsz-2013-0174

    Article  CAS  PubMed  Google Scholar 

  • Sriburi R, Jackowski S, Mori K, Brewer JW (2004) XBP1: a link between the unfolded protein response, lipid biosynthesis, and biogenesis of the endoplasmic reticulum. J Cell Biol 167(1):35–41. doi:10.1083/jcb.200406136

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Verfaillie T, Garg AD, Agostinis P (2013) Targeting ER stress induced apoptosis and inflammation in cancer. Cancer Lett 332(2):249–264. doi:10.1016/j.canlet.2010.07.016

    Article  CAS  PubMed  Google Scholar 

  • Wali V, Bachawal S, Sylvester P (2009) Tocotrienol-induced apoptosis in neoplastic plus SA mammary epithelial cells is mediated through PERK/eIF2α/CHOP endoplasmic reticulum stress pathway. Cancer Res 69

  • Wu ZC, Liu Y, Dong WH, Zhu GQ, Wu SL, Bao WB (2016) CD14 in the TLRs signaling pathway is associated with the resistance to E. coli F18 in Chinese domestic weaned piglets. Sci Rep. doi:10.1038/srep24611

    Google Scholar 

  • Yang CW, Zhu X, Liu N, Chen Y, Gan HX, Troy FA, Wang B (2014a) Lactoferrin up-regulates intestinal gene expression of brain-derived neurotrophic factors BDNF, UCHL1 and alkaline phosphatase activity to alleviate early weaning diarrhea in postnatal piglets. J Nutr Biochem 25(8):834–842. doi:10.1016/j.jnutbio.2014.03.015

    Article  CAS  PubMed  Google Scholar 

  • Yang JR, Yao FH, Zhang JG, Ji ZY, Li KL, Zhan J, Tong YN, Lin LR, He YN (2014b) Ischemia-reperfusion induces renal tubule pyroptosis via the CHOP-caspase-11 pathway. Am J Physiol Renal Physiol 306(1):F75–F84. doi:10.1152/ajprenal.00117.2013

    Article  CAS  PubMed  Google Scholar 

  • Yoda K, Miyazawa K, Hosoda M, Hiramatsu M, Yan F, He F (2014) Lactobacillus GG-fermented milk prevents DSS-induced colitis and regulates intestinal epithelial homeostasis through activation of epidermal growth factor receptor. Eur J Nutr 53(1):105–115. doi:10.1007/s00394-013-0506-x

    Article  CAS  PubMed  Google Scholar 

  • Zhang BL, Yu CN, Lin M, Fu YN, Zhang L, Meng MJ, Xing S, Li JL, Sun H, Gao F, Zhou GH (2015) Regulation of skeletal muscle protein synthetic and degradative signaling by alanyl-glutamine in piglets challenged with Escherichia coli lipopolysaccharide. Nutrition 31(5):749–756. doi:10.1016/j.nut.2014.11.010

    Article  CAS  PubMed  Google Scholar 

  • Zhong JT, Yu J, Wang HJ, Shi Y, Zhao TS, He BX, Qiao B, Feng ZW (2017) Effects of endoplasmic reticulum stress on the autophagy, apoptosis, and chemotherapy resistance of human breast cancer cells by regulating the PI3 K/AKT/mTOR signaling pathway. Tumour Biol. doi:10.1177/1010428317697562

    Google Scholar 

  • Zou P, Chen M, Ji J, Chen W, Chen X, Ying S, Zhang J, Zhang Z, Liu Z, Yang S, Liang G (2015) Auranofin induces apoptosis by ROS-mediated ER stress and mitochondrial dysfunction and displayed synergistic lethality with piperlongumine in gastric cancer. Oncotarget 6(34):36505–36521. doi:10.18632/oncotarget.5364

    PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

Q.J. G.L. and K.Y. conceived the experiment(s), Q.J. S.C. W.R. and G.L. conducted the experiments, Q.J. G.W. and Y.Y. analyzed the results. Q.J. G.L. and K.Y. prepared the manuscript. All authors reviewed the manuscript.

Corresponding authors

Correspondence to Gang Liu or Kang Yao.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical standards

The protocol for this study was approved by the Committee on the Ethics of Animal Experiments of Institute of Subtropical Agriculture, Chinese Academy of Sciences (Permit Number: 201509-03) and it was conducted out in accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of Institute of Subtropical Agriculture, Chinese Academy of Sciences.

Funding

This study was jointly supported by the National Science Foundation for Distinguished Young Scholars of Hunan Province (2016JJ1015), Key Programs of frontier scientific research of the Chinese Academy of Sciences, the National Basic Research Program of China (2013CB127306), the Open Foundation of Key Laboratory of Agro-ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Sciences (ISA2016101), the Chinese Academy of Sciences “Hundred Talent” award (Y451022111) and the National Natural Science Foundation Project (31772642, 31472107).

Additional information

Handling Editors: C.-A.A. Hu, Y. Yin, Y. Hou, G. Wu, Y. Teng.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jiang, Q., Chen, S., Ren, W. et al. Escherichia coli aggravates endoplasmic reticulum stress and triggers CHOP-dependent apoptosis in weaned pigs. Amino Acids 49, 2073–2082 (2017). https://doi.org/10.1007/s00726-017-2492-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00726-017-2492-4

Keywords

Navigation