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. 2021 Jun 1;65(11):1895–1903. doi: 10.1007/s00484-021-02146-5

Heat stress inhibits TLR4-NF-κB and TLR4-TBK1 signaling pathways in broilers infected with Salmonella Typhimurium

Wei-Hao Li 1, Yi-Lei Liu 1, Jian-Chi Lun 1, Yong-Ming He 1, Lu-Ping Tang 1,✉
PMCID: PMC8536552  PMID: 34061266

Abstract

With the global warming, the harm of heat stress (HS) to the breeding industry has become more common, which causes the decline of animal production performance and low immunity. This study aimed to analyze the effect of HS on the intestinal immune function of Salmonella-infected chickens. Fourteen-day-old broilers were divided into the following four groups of eight replicates: control (Control), heat stress (HS), Salmonella Typhimurium (ST), and heat stress + Salmonella Typhimurium (HS+ST). The broilers were subjected to a heat stress of 35 °C from 15 to 28 days of age. Salmonella Typhimurium (ST, 14028, 109 cfu/mL) was inoculated, via oral administration at 29 days of age, into ST and HS+ST group birds. On the 4th day after Salmonella Typhimurium administration, an increase in jejunum IgA levels was observed in chickens infected with Salmonella Typhimurium. Mechanistic regulation of TLR4-NFκB-NLRP3 and TLR4-TBK1 signaling by heat stress was evaluated in Salmonella Typhimurium–infected broilers. Heat stress markedly inhibited the expression of cytokines including TNF-α, IL-6, IL-1β, NLRP3, caspase-1, NF-κB-p65, and p-NF-κB-p65, and the TLR4-TBK1 cytokines IFN-α, IFN-γ, p-IRF3, and p-TBK1 in jejunum of broilers infected with Salmonella Typhimurium. Collectively, our results demonstrate that heat stress can inhibit intestinal immune response by downregulating the expression of TLR4-NFκB-NLRP3 and TLR4-TBK1 signaling pathways in broilers infected with Salmonella Typhimurium.

Keywords: Broiler, Caspase-1, Intestinal immunity, Inflammation, NLRP3

Introduction

Heat stress (HS) is a reality in the poultry industry in tropical countries for a long time. Other factors in the animal facilities, or animal density and others, could also induce increase of temperature of the production system can increase or cause HS in poultry production. The global warming will boost the issue. Broilers lack sweat glands on the skin, and genetic selection also decreases their heat tolerance to enable rapid growth rates, thereby rendering broilers particularly susceptible to high ambient temperatures (Varasteh et al., 2015). Extensive research has shown that heat stress affects broiler physiology, resulting in the occurrence of various physiological disorders such as slow growth and accelerated death rate (Quinteiro-Filho et al., 2012). Additionally, it has been previously observed that HS disrupts intestinal integrity in response to injury (Garriga et al., 2006), particularly affecting the integrity of the intestinal epithelium and triggering immunosuppression (Abdelqader et al., 2017; Pearce et al., 2013) and inflammation (Burkholder et al., 2008).

Studies show that environmental stress may induce colonization and shedding of intestinal pathogens and promote the transmission of pathogens between animals (Rychlik & Barrow, 2005). Furthermore, acute heat stress can transform the epithelial structure of the normal intestine (Alhenaky et al., 2017), which may lead to increased attachment and colonization of Salmonella Enteritidis (Sellin et al., 2014). In young chickens infected with Salmonella, decreased growth performance and intestinal lesions, as well as inflammation and injury of intestinal permeability, have been observed (Alhenaky et al., 2017). Salmonella Typhimurium, a gram-negative intracellular pathogen, is responsible for 1.3 billion cases of gastroenteritis and 3 million deaths worldwide each year (Dunkley et al., 2009). Salmonella Typhimurium colonizes the small intestine and causes enterotoxins to disrupt the intestinal barrier, triggering inflammation of the intestinal mucosa, and then causes bacteremia which results in the development of severe intestinal inflammation (Broz et al., 2012; Wotzka et al., 2017). A combinatorial effect of HS and Salmonella Enteritidis infection has been reported to damage the intestinal barrier, eventually leading to the development of inflammatory infiltrates in the intestine (Quinteiro-Filho et al., 2012). However, the studies on intestinal immunity in chickens treated with heat stress and pathogenic bacteria are limited.

Upon bacterial entry, it is specifically recognized by TLR4 and induces various proinflammatory cytokines, including TNF-α, IL-8, IL-6, and IL-1β. The expression of pro-inflammatory cytokines is regulated by NF-κB expression. Type I interferon can be induced by TBK1, which inhibits pathogens such as Salmonella, enteropathogenic E. coli to thrive in the host. This study specifically aimed to investigate the effects of heat stress on the immunological response of Salmonella Typhimurium–infected broilers. We will study the protein levels of TLR4, NF-κB, NLRP3, Caspase-1, TNF-α, IL-6, IL-1β, TBK1, IRF3, IFN-α, and IFN-γ in jejunum of broilers to measure the changes of intestinal immune function.

Materials and methods

Broilers

A total of 32 one-day-old male broilers were purchased from a commercial hatchery (Foshan Nanhai Poultry Corporation, Foshan, China). One-day-old broilers were housed in climate-controlled rooms at Foshan University (Guangdong, China). Throughout the experiment, broilers were maintained in isolator chambers with high-efficiency particulate air (HEPA) filters. The broilers were provided with water and feed ad libitum. The humidity was monitored and maintained at 60%.

Ethical considerations

Care and handling of chickens were performed in compliance with the Animal Ethics Committee Guidelines of the Academy of National Food and Strategic Reserves Administration (Beijing, China). Permission to use samples was also granted by the Ethical Clearance Committee of Foshan University.

Group and heat stress

From days 1 to 14 of life (ED1 to ED14), the broilers were maintained at the recommended environmental temperatures (33 °C ± 1 °C from ED1 to ED7 and 28 °C ± 1 °C from ED7 to ED14). At ED15, the broilers were randomly divided into four groups with eight birds in each group.

The treatments were as follows: control group (Control), heat stress group (HS), Salmonella Typhimurium group (ST), and heat stress + Salmonella Typhimurium (HS + ST) group. Broilers in the HS + ST group and HS group were subjected to 35 °C ± 2 °C heat stress for 2 weeks (14–28 days of age); then, the broilers in the ST and HS+ST groups were inoculated with 1-mL suspension of Salmonella Typhimurium (1×109 cfu/mL) by oral administration, and broilers in the control and HS groups were treated with sterile saline only. On the 4th day after Salmonella Typhimurium challenge (ED32), the broilers were euthanized by CO2 inhalation and jejunum samples were collected immediately for histological observation and examination.

Inoculation of the Salmonella Typhimurium strain

The Salmonella Typhimurium strain was originally obtained from the Guangdong Microbial Culture Collection Center (Guangdong, China). The frozen strain was thawed and incubated with 1×109 CFU/mL of the inoculum. On day 29, 1 mL of the inoculum (109 cfu/mL of Salmonella Typhimurium) was orally administered into birds in the ST and the HS + ST group, using a lavage apparatus.

Histochemistry of the jejunum

The jejunum tissues were fixed in 10% buffered formalin, embedded in paraffin, and cut into 5-μm-thick sections. The sections were stained with hematoxylin and eosin (H&E) for analysis by light microscopy (Nikon ECLIPSE E200, Tokyo, Japan).

Western blot analysis

Briefly, the jejunum tissues were homogenized using a protein lysis buffer, separated on a 10% SDS-polyacrylamide gel, and electroblotted onto PVDF membranes. Membrane blots were incubated with antibodies (anti-Hsp70, anti-TLR4, anti-TBK1, anti-p-TBK1, anti-IRF3, anti-p-IRF3, anti-IFN-α, anti-IFN-γ, anti-NLRP3, anti-Caspase-1, anti-pro-IL-1β, anti-IL-1β, anti-NF-κB p65, anti-p-NF-κB p65, anti-IκB α, anti-p-IκB α, anti-IL-6, anti-TNF-α, anti-HMGB1, and anti-β-actin) (Cell Signaling Technology, Boston, USA) for 2 h, at room temperature. The membranes were subjected to washing steps using TBST buffer thrice, followed by 1 h of incubation with HRP-conjugated secondary anti-mouse (or anti-rabbit) IgG from goat. Protein expression was analyzed using the ImageJ software.

Intestinal IgA determination

The birds were euthanized by CO2 inhalation and jejunums were collected. Jejunums were cleaned with PBS, and 0.1-g jejunum samples were removed in 0.9 mL PBS and homogenized. The mixture was centrifuged 3000g for 20 min at 4 °C. Then, the supernatant was collected for further test. Total IgA jejunum levels were detected using an enzyme-linked immunosorbent assay (ELISA) kit purchased from Jiangsu Meimian industrial Co., Ltd. in accordance with the manufacturer’s protocol.

Statistical analyzes

The data are presented as the mean ± standard deviation. Statistical significance among treatment groups was calculated using one-way and two-way ANOVAs (SPSS 17.0). Different letters indicate significant differences between treatments (P <0.05). *P <0.05 indicates the interaction between heat stress and Salmonella infection.

Results

Heat stress induces changes in the intestinal morphology in ST-infected broilers

The villi in the jejunum showed normal arrangement and displayed a regular shape in the control broilers (Fig. 1), while the microvilli were markedly damaged in the HS broilers. Additionally, the villi of the ST group broilers were missing or shortened, and the mucosal villi were edematous and enlarged. The width of lamina propria and epithelial was increased, and there was little inflammatory infiltration in ST group broilers, compared with control broilers. The injury showed worse outcomes in the HS+ST group after subjection to heat stress, expressed more serious inflammatory infiltration, villi shortened, and the mucosal villi edematous.

Fig. 1.

Fig. 1

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Effects of heat stress on jejunum morphology in ST-infected broilers (H&E staining, magnification: ×100)

Heat stress increases the jejunum IgA levels in ST-infected broilers

As shown in Fig. 2, heat stress and ST administration significantly increased the jejunum IgA levels (P<0.05 and P<0.05, respectively). IgA levels were significantly higher in the HS+ST group than those in the ST group (P<0.05).

Fig. 2.

Fig. 2

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Effects of heat stress on the jejunum IgA levels in ST-infected broilers. Extracted intestinal mucus samples were titrated for IgA level determination. Different letters indicate significant differences between treatments (P <0.05). *P <0.05 indicates the interaction between heat stress and Salmonella infection. n = 8/group

Heat stress decreases TBK1-activated interferons in the jejunum of ST-infected broilers.

As shown in Fig. 3A, compared with control group, ST infection decreased the jejunum protein expression of IFN-α (P<0.05). However, a significantly lower protein level of IFN-α and IFN-γ was observed (P<0.05 and P<0.05) in the HS+ST group than that in the ST group. HS and ST infection alone decreased the protein expression of IRF3 (P<0.05 and P<0.05, respectively) in the jejunum of broilers compared with control group broilers. There was no significant difference in p-IRF3 expression levels between the HS and control groups. However, heat-stressed broilers infected with ST showed reduced protein expression of p-IRF3 compared with the ST group (P<0.05). There had been an interaction between heat stress and Salmonella infection in the expressions of IFN-α, IFN-γ, IRF3, and p-IRF3.

Fig. 3.

Fig. 3

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Effects of heat stress on the jejunum TBK1-IRF3 and interferon protein expression levels in ST-infected broilers. (A) IRF3, p-IRF3, and interferon protein expression levels and (B) TBK1 and p-TBK1 protein expression levels in the jejunum of broilers were determined by performing western blot analysis. Different letters indicate significant differences between treatments (P <0.05). *P <0.05 indicates the interaction between heat stress and Salmonella infection

As shown in Fig. 3B, the individually administered HS and ST infections decreased the protein expression of TBK1 in the jejunum of broilers (P<0.05 and P<0.05, respectively). There was no significant difference in p-TBK1 levels between the heat stress and ST group birds. However, in the HS+ ST group, the protein expression of TBK1 was increased (P<0.05) and p-TBK1 was significantly reduced (P<0.05) compared with the ST group.

Heat stress inhibits NLRP3/Caspase-1 and inflammatory cytokines protein expressions in the jejunum of ST-infected broilers

As shown in Fig. 4A, broilers in the ST group exhibited higher TNF-α and IL-1β levels and lower pro-IL-1β protein levels than those in the control group (P < 0.05, P < 0.05, and P < 0.05, respectively). Broilers in the HS+ST group exhibited lower TNF-α, IL-6, and IL-1β protein levels than those in the ST group (P < 0.05, P < 0.05, and P < 0.05, respectively).

Fig. 4.

Fig. 4

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Effects of heat stress on NLRP3 and caspase-1 protein expression levels in ST-infected broilers. (A) TNF-α, IL-6, pro-IL-1β, and IL-1β protein expression levels and (B) NLRP3 and Caspase-1 protein expression levels in the jejunum of broilers were determined by performing western blot analysis. Different letters indicate significant differences between treatments (P <0.05). *P <0.05 indicates the interaction between heat stress and Salmonella infection

As shown in Fig. 4B, broilers infected with ST showed increased NLRP3 expression levels but decreased Caspase-1 protein expression levels compared to those in the control group (P < 0.05 and P < 0.05). Broilers in the HS+ST group exhibited lower NLRP3 and Caspase-1 protein levels than those in the ST group (P < 0.05 and P < 0.05, respectively). There had been an interaction between heat stress and Salmonella infection in the expressions of TNF-α, IL-6, IL-1β, pro-IL-1β, and NLRP3.

Heat stress decreases the phosphorylation of NF-κB p65 and IκB-α in the jejunum of broilers infected with ST

As shown in Fig. 5, broilers in the ST group exhibited higher p-NF-κB p65 and lower IκB-α and p-IκB-α protein levels than those in the control group (P < 0.05, P < 0.05, and P < 0.05, respectively). HS also increased p-NF-κB p65 levels and decreased p-IκB-α protein levels compared with those in the control group (P < 0.05 and P < 0.05, respectively). Broilers in the HS+ST group exhibited lower NF-κB p65, p-NF-κB p65, and p-IκB-α protein levels than those in the ST group (P < 0.05, P < 0.05, and P < 0.05, respectively).

Fig. 5.

Fig. 5

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Effects of heat stress on the NF-κB signaling pathway expression levels in ST-infected broilers. Protein expression levels in the jejunum of broilers were determined by performing western blot analysis. Different letters indicate significant differences between treatments (P <0.05). *P <0.05 indicates the interaction between heat stress and Salmonella infection

Heat stress decreases protein expression of TLR4 and HSP70 in the jejunum of broilers infected with ST

As shown in Fig. 6, HS decreased TLR4 protein expression in the HS+ST group (P < 0.05) compared with the ST group. There were no significant differences in HSP70 protein levels among the groups (P > 0.05).

Fig. 6.

Fig. 6

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Effects of heat stress on TLR4 and Hsp70 protein expression levels in ST-infected broilers. Protein expression levels in the jejunum of broilers were determined by performing western blot analysis. Different letters indicate significant differences between treatments (P <0.05). *P <0.05 indicates the interaction between heat stress and Salmonella infection

Discussion

Immunosuppression is a major challenge in chronic stress, especially when the animals are challenged with Salmonella (Calefi et al., 2016; Quinteiro-Filho et al., 2017; Alhenaky et al., 2017). Heat stress can restrain intestinal barrier function, which may be attributed to the suppression of the mucosal immune system, particularly in animals with intestinal infections (Mestecky, 1987). IgA plays a crucial role against bacterial pathogens and viral and parasitic infections. Mice infected with Salmonella Typhimurium showed increased IgA levels in the intestinal lamina propria (Allen et al., 2000). HS or Salmonella Typhimurium infection alone significantly enhanced the IgA levels, and HS chickens infected with Salmonella Typhimurium showed higher IgA levels than those infected with Salmonella Typhimurium alone. These results suggest that heat stress increases IgA levels, which may result in the elicitation of a strong local immune response to Salmonella Typhimurium invasion.

Upon bacterial entry, Toll like receptor 4 (TLR4) endotoxin lipopolysaccharide (LPS) is specifically recognized by TLR4 and induces macrophages to express various proinflammatory cytokines, including TNF-α, IL-8, IL-6, and IL-1β (Ramachandran, 2014). IL-1β deficiency increases both severity and mortality rate associated with Salmonella infection (Eckmann & Kagnoff, 2001). Evidence suggests that IL-6 secretion is a crucial factor in broiler chickens that confers protection against Salmonella infection (Chappell et al., 2009). In this study, HS significantly inhibited the protein expression of TNF-α, IL-6, and IL-1β in chickens infected with Salmonella Typhimurium, indicating that reduction in cytokines might result in successful Salmonella Typhimurium invasion, which was consistent with the findings reported by Quinteiro-Filho (Quinteiro-Filho et al., 2017). Innate immunity helps to eliminate pathogens and confers cellular protection through the production of pro-inflammatory cytokines, and the downregulation of these cytokines before resolving inflammation stress may tend to favor Salmonella colonization (Malago et al., 2002; Nemeth et al., 2006; Yoo et al., 2000).

The expression of pro-inflammatory cytokines is regulated by nuclear factor kappa-B (NF-κB) expression. TLR4 plays an important role in elicitation of an early host defense against invading pathogens and subsequent occurrence of the inflammatory response (Akira & Takeda, 2004; Newton & Dixit, 2012; Wittebole et al., 2010). Upon LPS stimulation, TLR4 activates the IKK complex to induce the phosphorylation of IκBs, and IκBs translocate into the nucleus to regulate the production of inflammatory cytokines (Akira & Takeda, 2004; Beutler, 2004; Guijarro-Munoz et al., 2014; Newton & Dixit, 2012). Based on our data, the levels of TLR4 were decreased in the heat stress-induced and Salmonella Typhimurium–infected chickens as compared to the Salmonella Typhimurium group birds, which suggested that heat stress might impair early host defense against Salmonella invasion. Heat stress also decreased the protein expression levels of p-NF-κB p65 and p-IκBα in chickens infected with Salmonella Typhimurium, and the levels of TLR4 were also decreased, suggesting that heat stress might regulate TLR4-NF-κB signaling in broiler chickens infected with Salmonella Typhimurium.

Caspase-1, as an intracellular inflammasome, is considered a mechanism of intestinal epithelial cells to resist microbial pathogens (Martinon & Tschopp, 2004). Activated caspase-1 induces the maturation of the proinflammatory cytokines IL-1β and IL-18 (Sansonetti et al., 2000), which play pivotal roles in resisting an invasion from a variety of pathogens (Mariathasan et al., 2005). Studies have shown that Casp1 transcript levels decrease slightly with the progression of Salmonella infection, and the lack of caspase-1 renders the body more susceptible to pathogens (Sellin et al., 2014). The results confirmed that heat stress may render chickens more susceptible to Salmonella by decreasing capase-1 protein levels in heat-stressed and ST-infected chickens. Research has shown that NLRP3 can activate caspase-1 and cleave pro-IL-1β to IL-1β (Bergsbaken et al., 2009). A significant decrease in NLRP3 expression was observed, indicating that it played a mechanistic role in caspase-1-mediated IL-1β inhibition upon occurrence of heat stress in ST-infected chickens. LPS stimulation triggered NF-κB-mediated upregulated expression of NLRP3 and pro-IL-1β (Bauernfeind et al., 2009). These results suggest that heat stress may regulate TLR4-NF-κB-NLRP3 signaling in broiler chickens infected with ST.

Few studies have reported that type I interferon maintains barrier function by regulating tight junction proteins in intestinal epithelial cells infected by enteropathogenic E. coli (Long et al., 2014). In our study, the levels of IFN-γ and IFN-α were decreased in heat-stressed and ST-infected chickens. Following viral infection, a protein named recombinant TANK binding kinase 1 (TBK1) sends a signal that induces a protective program to inhibit viral replication (Yuichiro Tojima et al., 2000). TBK1 deficiency enables pathogens such as Salmonella, enteropathogenic E. coli, and group A Streptococci to thrive easily in the host cytoplasm (Perrin et al., 2004). Salmonella has flagellin and LPS, which stimulate TLR4 expression in the lamina propria (Long et al., 2014). TBK1-IKKε mediates the phosphorylation of IRF3 and induces the expression of type I interferon (Doyle et al., 2002; Eva et al., 2004). Finally, p-TBK1 was decreased in the jejunum of heat-stressed broiler chickens infected with ST. Consistent with the heat stress-mediated suppression of TLR4-induced IFN-α expression, the inhibition of p-IRF3 and p-TBK1 expression in heat stressed chickens infected with ST was also observed, suggesting that heat stress inhibited IFN-α activation by inhibiting TBK1 activation.

Conclusion

Our results indicate that heat stress impairs the intestinal immune function in broilers, resulting in increased susceptibility of the broilers to Salmonella Typhimurium infection. In summary, our study demonstrates altered TLR4-mediated TBK1 and NF-κB signaling in heat stress-induced broilers infected with Salmonella (Fig. 7). These findings may provide a convincing scientific rationale for heat stress-induced lowering of intestinal immunity in poultry.

Fig. 7.

Fig. 7

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Heat stress inhibits the activation of the TLR4-NF-κB/TBK1 signaling pathway in broilers infected with Salmonella Typhimurium

Author contribution

Investigation, writing original draft, and funding acquisition, Lu-Ping Tang; investigation and methodology, Wei-Hao Li and Yi-Lei Liu; conceptualization and funding acquisition, Yong-Ming He; data curation and software, Jian-Chi Lun.

Funding

This project was supported by the Natural Science Foundation of Guangdong Province, China (Grant No. 2017A030310607); Guangdong Science and Technology Department, China (Grant No. 2015A040404048); Guangdong Province Department of Agriculture and Rural Affairs (Grant No. 2019KJ119); and Guangdong Province Department of education (Grant No. 2017GCZX006).

Declarations

Conflict of interest

The authors declare no competing interests.

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