key: cord-0798553-nt1jt2ut
authors: Han, Shuaijuan; Wen, Yang; Yang, Fengfan; He, Pingli
title: Chicken Egg Yolk Antibody (IgY) Protects Mice Against Enterotoxigenic Escherichia coli Infection Through Improving Intestinal Health and Immune Response
date: 2021-04-13
journal: Front Cell Infect Microbiol
DOI: 10.3389/fcimb.2021.662710
sha: e2a02ba23290c208cac912e9dfb50533e43e771c
doc_id: 798553
cord_uid: nt1jt2ut

Chicken egg yolk antibody (IgY), considered as a potential substitute for antibiotics, has been used for preventing pathogens infection in food, human and animals. This study investigated effects of IgY on growth, adhesion inhibitory and morphology of enterotoxigenic Escherichia coli (ETEC) K88 in vitro, and evaluated the protective effects of IgY on intestinal health and immune response of mice infected with ETEC in vivo. Sixty pathogen-free C57BL/6J (4-6 weeks of age) mice were divided into six treatments: control (neither IgY nor ETEC infection), ETEC infection, ETEC-infected mice treated with 250 μL of high-dose (32 mg/mL), medium-dose (16 mg/mL) or low-dose (8 mg/mL) anti-ETEC IgY, or ETEC-infected mice treated with 250 μL of non-specific IgY (16 mg/mL). Anti-ETEC IgY inhibited ETEC growth, reduced adherence of ETEC to intestinal epithelial cells J2 and damaged the morphology and integrity of ETEC cell. Oral administration of anti-ETEC IgY effectively ameliorated ETEC-induced clinical signs, reduced ETEC colonization and intestinal permeability, alleviated inflammatory response through reducing the production and expression of proinflammatory cytokines, improved intestinal morphology, and inhibited excessive activation of the mucosal immune response of challenged mice. The overall protective effects of high-dose and medium-dose anti-ETEC IgY against ETEC infection were more effective. These results suggest that anti-ETEC IgY may function as a promising novel prophylactic agent against enteric pathogens infection.

Enterotoxigenic Escherichia coli (ETEC) cause serious health problems for young animals and human infants due to contaminated food or water. ETEC cause diarrhea, intestinal inflammatory diseases and alter intestinal microbial diversity by adhering to intestinal epithelial cells, secreting enterotoxin and releasing lipopolysaccharide (Fleckenstein et al., 2010; Smith et al., 2010) . In practice, antibiotics are currently used to prevent and treat pathogens, but long-term application will cause negative effects such as bacterial resistance, imbalance of intestinal flora in animals and drug residues, which seriously threaten animal and human health (Thacker, 2013) . Hence, finding safe and effective antibiotic alternatives to prevent ETEC infection is an urgent and significant task in animal husbandry.

Chicken IgY, known as the immunoglobulin Y, is an antigenspecific antibody produced by B lymphocytes and accumulated in the yolk of chicken eggs. IgY as a bioactive constituent has been used for preventing pathogens infection in food, human and animals. Compared with other immunoglobulins obtained from mammalian animals, chicken IgY has several advantages, including: (a) IgY production process is hygienic, non-invasive, cost-efficient and convenient; (b) IgY does not cause an adaptive immune response of animals (Nilsson et al., 2007) ; (c) IgY neither activate complement nor recognized by intestinal epithelial Fc-receptors in mammals (Silva and Tambourgi, 2010; Kovacs-Nolan and Mine, 2012) ; (d) IgY shows high avidity and antigen-specificity and is extraordinarily stable (Kovacs-Nolan and Mine, 2012) . Thus, IgY has attracted much attention for passive immunization (Baloch et al., 2015; Li et al., 2015; Abbas et al., 2019) . Numerous studies have shown that specific IgY has positive effects in the prevention and treatment of pathogens including rotaviruses, coronavirus, epidemic diarrhea virus and transmissible gastroenteritis virus (Diraviyam et al., 2014; Lee et al., 2015) . Another study reported that anti-Salmonella IgY significantly reduced the number of Salmonella in feces and cecal contents, and reduce morbidity and mortality of infected chickens (Rahimi et al., 2007) . Several possible mechanisms of action have been proposed, including: (i) IgY causes pathogen agglutination; (ii) inhibition of pathogen adhesion to cells; (iii) neutralization of toxins; (iv) regulation of phagocytosis by phagocytes and modulation of body immunity to provide passive immune protection for young animals (Zhou and Ma, 2018; Xu et al., 2019) . In our previous study, we found that hyperimmunized egg yolk powder could reduce diarrhea incidence and E. coli numbers in feces, ameliorate negative effects of E. coli on intestinal health indices, and enhance immunity of weaned pigs (Han et al., 2019) . However, the exact mechanisms of biological function to affect the health status of humans and animals are still unclear. Furthermore, few studies have determined the intestinal health and immune-modulatory effects of specific IgY on the host.

Given that ETEC cause serious health problems for young animals and human infants and the current use of antibiotics is tightly restricted, new antibacterial strategies are urgently needed. Therefore, the objective was to evaluate whether IgY exerts obvious anti-bacterial activity in vitro. A second objective was to explore potential uses and possible mechanisms of IgY in preventing ETEC infection in a mouse model of intestinal inflammation. This study provides a theoretical reference for IgY in protecting animals from bacterial diseases such as ETEC infection.

ETEC K88 (BNCC 125988) were purchased from Beijing Beina Chuanglian Biotechnology Institute (Beijing, China). Bacterial culture conditions were performed according to our previous study (Han et al., 2019) . The cell suspension (2.5 × 10 9 , 5 × 10 10 colony forming units (CFU)/mL) was used for the immunization of laying hens and mice infection, respectively. Anti-ETEC K88 IgY was obtained according to the method in our previous study (Han et al., 2019) .

The ETEC K88 (1.0 × 10 7 CFU/mL) was grown in Luria-Bertani medium including a range of density (0, 1.25, 2.5 and 5 mg/mL) of sterilized anti-ETEC K88 IgY, which was filtered using a 0.22 mm filter. Non-specific IgY (5 mg/mL) was performed as the negative control. These mixtures were incubated at 37°C with shaking at 200 rpm. Suspensions were collected and measured at OD 600 nm at 2-h intervals with three biological replicates. Then, growth inhibition curves of IgY were measured by plotting the value of OD 600 nm against time.

Intestinal epithelial cells J2 (IPEC-J2) were kindly donated by Dr. Shiyan Qiao (China Agricultural University, China). Cells were grown in Dulbecco's Modified Eagle's medium/Ham's nutrient mixture F-12 (DEME/F12) containing 1% streptomycin (10,000 g/mL)/penicillin (10,000 U/mL), 10% fetal bovine serum, 1% insulin/transferrin/selenium (ITS) and 5 µg/L epidermal growth factor. Cells were cultured in a 95% humidified atmosphere with 5% CO 2 at 37°C. IPEC-J2 cells (1 × 10 6 cells per well) were seeded onto 6-well plates and incubated in medium without antibiotics to about 80% confluence. Before infection, ETEC K88 (2 × 10 8 CFU/mL) was pre-incubated with 5 mg/mL anti-ETEC K88 IgY, 5 mg/mL non-specific IgY and PBS at 37°C for 1 h, respectively. Then, preincubated ETEC K88 cells were used for infection in IPEC-J2 cells (n = 3) for 2 h in 5% CO 2 atmosphere at 37°C. Unbound bacteria were removed by three washings with sterile PBS. IPEC-J2 cells were lysed with 1 mL of 0.1% Triton X-100 for 5-10 min, serially diluted, plated onto MacConkey-agar plates and incubated at 37°C for 16 h. Initial and final bacterial colonies were counted.

To evaluate the alteration of ETEC K88 cell ultrastructure and membrane morphology, transmission electron microscopy (TEM) was performed as described previously , with minor modifications. Briefly, ETEC K88 cells (10 7 CFU/mL) were incubated with 5 mg/mL of sterilized IgY.

The negative and blank controls included 5 mg/mL of nonspecific IgY and sterile PBS, respectively. After centrifugation, bacterial cells were fixed with 2.5% (v/v) glutaraldehyde in PBS (0.1 mol/L, pH 7.4) at 4°C for 2-4 h, covered with 1% agarose, and washed with PBS three times. Cells were then fixed with 1% osmium tetroxide at room temperature for 2 h, dehydrated with acetone, and embedded in Epon. Thin sections were stained with uranium acetic acid and lead citrate for 15 min and observed by using TEM (Model JEM-1230, JEOL, Japan).

All mouse experiments were approved and performed according to the guidelines of the Institutional Animal Care and Use Committee at China Agricultural University (Beijing, China). Pathogen-free, female C57BL/6J mice (4-6 weeks of age, 17.12 ± 0.39 g initial body weight) were obtained from Beijing HFK Bioscience Co., Ltd. (Beijing, China). All mice were housed in the same humidity-and temperature-controlled room with 12 h light/dark cycle. All mice were kept in a laminar flow cabinet individually and feed and water were provided ad libitum.

Mice (n=60) were divided randomly into 6 treatments (10 mice per treatment) according to their body weight after a 3-day adaptation period. Treatments were as follows: uninfected control (neither IgY nor ETEC K88 infection), ETEC K88 infected control, mice challenged with ETEC K88 and treated with 250 mL of high-dose (32 mg/mL), medium-dose (16 mg/ mL) or low-dose (8 mg/mL) anti-ETEC IgY or 250 mL of nonspecific IgY (16 mg/mL). Prior to experimental infection, mice in the control and ETEC group were pre-treated with 250 mL of sterile PBS by gavage, whereas mice in test groups were pretreated with 250 mL of a solution containing 32, 16 or 8 mg/mL of anti-ETEC IgY, or 16 mg/mL of non-specific IgY once daily by oral gavage for 5 consecutive days. The following day, except for the control group, all mice were inoculated orally with 300 mL of ETEC K88 (5×10 10 CFU/mL). Mice were fasted (feed and water) for 4 h before challenge, and deprived of feed and water for 3 h after challenge. After challenge, mice in the control and ETEC group continued to be treated with sterile PBS by oral gavage, whereas mice in test groups continued to receive their assigned doses of IgY for 3 d.

After challenge, clinical signs of mice were observed daily using a scoring system that was reported previously (Warren et al., 2013; Pizarro-Guajardo et al., 2017) . Stool scores were as follows: 0, normal stool (dry stool, intact granules); 1, mild diarrhea stool (slight sticky stool, adhesion to filter paper); 2, moderate diarrhea stool (soft stool, no formation of feces, no separation of fecal water); 3, severe diarrhea stool (liquid stool). Mice with a fecal score greater than 1 were considered to have diarrhea. Body weight and survival rate of mice were recorded daily for 4 days after ETEC inoculation.

Fresh fecal samples were taken from six same mice (selected randomly from each group) for each of the 4 days after ETEC K88 challenge. The bacterial load of E. coli was measured on MacConkey agar plates (OXOID, Hampshire, UK). A second fecal sample was kept in a freezer at -80°C for analysis of the concentration of short chain fatty acid (SCFA). At day 4 postinfection, blood samples of mice were collected. Serum was obtained by centrifugation (3000×g, 15 min) and stored at -80°C for further analysis.

Intestinal tissues collected from the middle of duodenum, jejunum and ileum were flushed gently with normal saline (0.9% sodium chloride), fixed in 4% paraformaldehyde, and embedded in paraffin for morphological and pathological analysis. Another section of jejunal tissue was collected, snap-frozen in liquid nitrogen, and stored at -80°C for secretory immunoglobulin A (sIgA) analysis. Cecal contents were collected and stored at -80°C for analysis of microbial composition and SCFA content.

Fresh fecal samples were collected each day from mice after challenge, resuspended in sterile physiological saline solution, and homogenized. The bacterial load of E. coli strain was counted by plating 10-fold serial dilutions of homogenates on MacConkey plates, and incubated at 37°C for 24 h. Results were expressed as log 10 CFU/g of feces. Total bacteria and E. coli numbers in cecal contents were determined by quantitative reverse-transcription PCR (RT-qPCR) method as described in our previous study (Han et al., 2019 ).

Concentrations of SCFA in feces and cecal contents were determined by ion chromatography (ICS 3000, Thermo, USA). Samples were thawed and thoroughly mixed before analysis. Thawed sample was weighed (about 80 mg) into 8 mL of doubledistilled water. The mixture was incubated in an ultrasonic bath for 20 min, and then centrifuged at 10,000 × g for 15 min. The resulting suspension was diluted (1:8) in distilled water. The extracted sample that was filtered through a 0.22-mm filter (100 mL) was injected into ion chromatography and analyzed using AS11 analytical column (250 mm× 4 mm).

An automatic biochemistry analyzer (Hitachi, Ltd., Japan) was used to measure concentrations of serum albumin (ALB), globulin (GLB), albumin to globulin ratio (A/G), total protein (TP), urea nitrogen (UN), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) according to commercial kits and manufacturer's instructions. All the kits were obtained from Biosino Biotechnolgy and Science Inc. (Beijing, China).

Serum cytokines, including IL-10, IFN-g, IL-1b, IL-12p70, IL-2, IL-4, IL-6, IL-5, growth regulates oncogenes (KC/GRO) and TNF-a, were measured using V-PLEX proinflammatory Panel 1 (mouse) kit (Meso Scale Discovery) by a Meso QuickPlex SQ 120 instrument (Meso Scale Discovery) follow the instruction. The mRNA relative expression of TNF-a, IL-10 and IL-1b in jejunum of mice were determined using RT-qPCR. The gene for b-actin was used as an endogenous reference. The relative expression of genes was expressed using the 2 −DDCt (Yu et al., 2020) . The primers are listed in Table S1 .

Concentrations of D-lactate, diamine oxidase (DAO) and immunoglobulins in serum and sIgA in jejunal tissues were determined using corresponding commercially available mouse ELISA kits (Beijing Yonghui Biotechnology Co., Ltd., China) according to procedures described by manufacturers.

Random segments of duodenum, jejunum and ileum were excised and fixed with 4% paraformaldehyde, embedded in paraffin, sectioned into 5-mm slices and stained with hematoxylin and eosin (HE) according to standard procedures. Villus height and crypt depth were measured as described previously (Tsirtsikos et al., 2012) . The ratio of villus height to crypt depth (V/C ratio) was calculated. Stained sections were observed microscopically by a single scorer blinded to treatments using a scoring system (Barthel et al., 2003; Li et al., 2016) . The severity of epithelial cell necrosis, inflammatory cell infiltration, central chylous tube dilatation, and submucosal edema in each intestinal tissue section was assessed according to the following degrees: 0, none;1, mild; 2, gentle; 3, severe.

Proliferation of intestinal T lymphocytes and subtypes was analyzed according to the conventional method for immunohistochemical analysis (Tu et al., 2016) . Briefly, jejunal tissues were fixed in 4% paraformaldehyde, serial dehydrated by a gradient of ethanol, and embedded in paraffin. Sections were dewaxed, rehydrated and washed with PBS, and underwent heatinduced epitope retrieval with preheated epitope retrieval solutions (10 mM citrate buffer, pH 6.0 for CD3 and CD8; EDTA buffer, pH 9.0 for CD4). Endogenous peroxidase activity was quenched and blocked. Sections were incubated at 4°C overnight with corresponding primary mouse monoclonal antibody: mouse anti-CD3 (1:100, Abcam, Cambridge, UK), mouse anti-CD4 (1:200, Santa Cruz Biotechnology, Canada), mouse anti-CD8 (1:200 Abcam, Cambridge, UK). After incubation, sections were washed with PBS and incubated with horseradish peroxidase conjugated goat anti-mouse/rabbit IgG antibody for 50 min at 37°C, developed with diaminobenzidine, and counterstained with hematoxylin. After sealing with neutral gum, sections were observed with a microscope. Negative control was performed without primary antibodies.

Differences in survival rates were analyzed by the chi-square test using SAS (SAS 9.4 software; SAS Inst. Inc., Cary, NC). Other data were analyzed using ANOVA and GLM procedure, and statistical differences among treatments were compared using Student-Neuman-Keuls multiple-range test. Data are expressed as least square means with standard error of the mean (SEM). Statistical significance and tendency were considered as P < 0.05 and 0.05 ≤ P < 0.10, respectively. *P < 0.05, **P<0.01 and ***P < 0.001.

To evaluate the antibacterial activity of IgY, killing curves were performed. Results show that anti-ETEC IgY inhibited the growth of ETEC K88 in a dose-dependent manner ( Figure 1) . Moreover, the bacteriostatic effect was enhanced with the increase of anti-ETEC IgY concentration, which agrees with previous reports (Zhen et al., 2008; Sui et al., 2011) .

To determine whether IgY could inhibit bacterial adhesion and damage the cell morphology and integrity of ETEC, adherence inhibition and TEM assay were performed. Results showed that, compared with the ETEC infection group, anti-ETEC IgY and non-specific IgY decreased adhesion of ETEC K88 to IPEC-J2 cells (P < 0.05), and anti-ETEC IgY expressed greater antibacterial activity than non-specific IgY ( Figure 2 ). ETEC K88 cells in the control and non-specific IgY groups had an intact morphology and a smooth surface. However, after treatment with anti-ETEC IgY, some ETEC K88 cell walls were thinner, blurred, or even missing ( Figure 3 ).

The schematic diagram of the experimental design for the protective effects of anti-ETEC IgY on mice infected with ETEC K88 is shown in Figure 4A . To make a risk assessment of IgY and investigate whether anti-ETEC IgY administrated orally could relieve negative effects induced by ETEC in mice, we firstly monitored clinical signs of mice daily. After ETEC K88 challenge, mice showed different degrees of clinical signs, which included lethargy, appetite loss, curled up body posture, shivering, and soft stools, while mice in the control group did Figure 4B ). Mice in ETEC K88-infected group had lower body weight gains (P < 0.05; Figure 4C ) and higher fecal scores at day 1 and day 2 post-infection (P < 0.05; Figure 4D ) than control mice. However, mice pretreated with high-and medium-dose anti-ETEC IgY attenuated the reduction of body weight and were similar with control mice (P > 0.05). On day 1 post infection, fecal scores of mice in both high-and medium-dose anti-ETEC IgY groups were lower than in the ETEC K88 and non-specific IgY groups (P < 0.05). On day 2 post infection, the fecal score of mice in medium-dose anti-ETEC IgY group was lower than in the ETEC K88 group (P < 0.05). Results indicated that high-, and medium-dose anti-ETEC IgY could ameliorated ETEC-induced clinical signs more effectively.

To study whether this positive effects of anti-ETEC IgY on clinical signs of challenged mice was caused by a difference in bacteria removal efficiency, the viable cell counts of E. coli in fresh feces of mice from day 1 and 2 after infection were measured. On day 1 post infection, compared with control group, the numbers of E. coli in feces of all challenged mice were increased (P < 0.05; Figure 5A ). Numbers of E. coli in feces of mice treated with different doses of anti-ETEC IgY decreased compared with the ETEC-infected group (P < 0.05), and numbers of E. coli in feces of mice treated with high-and medium-dose anti-ETEC IgY were lower than the non-specific IgY group (P < 0.05). On day 2 post infection, no significant differences were observed in the number of E. coli in feces among anti-ETEC IgY treated and ETEC-infected groups.

In terms of SCFAs, compared with the control group, ETEC K88 infection decreased (P < 0.05) the concentrations of acetic acid, propionic acid, and butyric acid in the feces of mice infected with ETEC (P < 0.05; Figures 5B-D) . Similarly, propionic acid and butyric acid contents in the feces of infected mice treated with non-specific IgY were decreased compared with controls. Acetic acid contents in feces of infected mice treated with highand medium-dose anti-ETEC IgY were increased compared with the ETEC-infected group. Moreover, the concentrations of SCFA in feces of mice treated with high-and medium-dose anti-ETEC IgY returned to the normal levels in the control group. The amount of E. coli in cecal contents of ETEC-infected mice increased (P < 0.05) compared with control. However, oral gavage with IgY partially mitigated the bacteria load and were similar to control ( Figure 5E ). Concentrations of butyric acid were decreased in cecal contents of ETEC-infected mice and infected mice treated with non-specific IgY compared with the control group (P < 0.05; Figure 5H ). Mice treated with high-and medium-dose anti-ETEC IgY had greater butyric acid levels in cecal contents compared with ETEC-infected mice (P < 0.05). No differences were observed on the concentrations of acetic acid and propionic acid among treatments ( Figures 5F, G) . These results indicated that anti-ETEC IgY improved bacteria removal efficiency, and positively affected the microbial metabolites.

To evaluate the effects of different doses of anti-ETEC IgY on liver function and immunity in ETEC-infected mice, we determined serum indicators. As shown in Table 1 , compared with the control group, serum globulin and aspartate transaminase (AST) contents increased, and albumin to globulin ratio decreased in ETEC-infected mice, and serum AST contents increased in mice treated with non-specific IgY group (P < 0.05). Serum AST level in mice treated with medium-dose anti-ETEC IgY was lower than that in ETEC-infected mice (P <0.05), and similar to the normal levels of the control group.

Compared with the control group, ETEC K88 infection increased serum immunoglobulin IgG and IgA concentrations in mice (P < 0.05; Table 2 ). Serum IgG concentrations in infected mice treated with anti-ETEC IgY were decreased (P < 0.05) compared with ETEC-infected mice and were similar to the normal levels of the control mice. Serum IgA concentrations in infected mice treated with high-and medium-dose anti-ETEC IgY were lower than in ETEC-infected mice and were not different from control mice. Concentration of sIgA in jejunum of mice treated with medium-dose anti-ETEC IgY was increased compared with ETEC-infected mice and infected mice treated with non-specific IgY (P < 0.05). Results suggested that ETEC could reduce liver damage and immune overreaction, but this phenomenon was partly recovered by high-or medium-dose anti-ETEC IgY. . Fecal scoring scale was performed from 0 to 3 (0, dry stool; 1, slight sticky stool; 2, soft stool; 3, liquid stool). Values reported are least squares mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001, ns, not significant.

To test the anti-inflammatory effects of IgY on ETEC-induced enteritis, we evaluated the secretion and mRNA expression of inflammatory cytokines. Compared with the control group, the concentration of IL-1b in serum of mice in ETEC-infected group increased (P < 0.05), and concentration of IL-4 decreased (P < 0.05; Table 3 ). Mice treated with different doses of anti-ETEC IgY had lower IFN-g and IL-1b concentrations in serum than in ETEC-infected mice (P < 0.05). Concentrations of IL-1b Values with different superscripts within a row differ (P < 0.05), n=6. Mice in control group were not challenged with ETEC K88. Mice in ETEC group were challenged with ETEC K88 and treated with PBS. Mice in IgY groups were challenged with ETEC K88 and treated with 250 mL of high-, medium-or low-doses anti-ETEC IgY or 250 mL of non-specific IgY. Values with different superscripts within a row differ (P < 0.05), n=6. Mice in control group were not challenged with ETEC K88. Mice in ETEC group were challenged with ETEC K88 and treated with PBS. Mice in IgY groups were challenged with ETEC K88 and treated with 250 mL of high-, medium-or low-doses of anti-ETEC IgY or 250 mL of non-specific IgY.

were lower than that of mice treated with non-specific IgY (P < 0.05). Serum IL-10 content of mice treated with medium-dose anti-ETEC IgY was higher and KC/GRO content was lower than mice in the ETEC-infected group (P < 0.05), and that were similar to the control mice.

Consistent with the results of cytokines in serum, ETECinfected mice had a greater mRNA relative expression of TNF-a, and a lower mRNA relative expression of IL-10 in jejunum than those in control mice ( Figures 6A, B) . Fortunately, compared with ETEC-infected mice, mice treated with high-dose anti-ETEC IgY decreased TNF-a mRNA relative expression (P < 0.05; Figure 6A ). Specific and non-specific IgY all reduced IL-1b mRNA relative expression in jejunum of mice (P < 0.05; Figure 6C ). These results indicated that oral administration of ETEC specific IgY is efficacious in reducing intestinal inflammation associated with ETEC infection in mice.

Following inflammation, we investigated whether IgY could ameliorate ETEC-induced intestinal permeability. Results showed that concentrations of D-lactate ( Figure 7A ) and DAO ( Figure 7B ) in serum of mice in the ETEC-infected group were higher than mice in the control group (P < 0.05), while the increases were limited in those from high-and medium-dose anti-ETEC IgY groups (P < 0.05). Compared with the nonspecific IgY group, anti-ETEC IgY could reduce intestinal permeability more effectively. Taken together, these results demonstrated that prophylactic administration of anti-ETEC IgY relieves intestinal inflammation and permeability induced by ETEC.

To further evaluate the status of intestinal injury risk, intestinal morphological analysis and histopathological scores were performed. Villus height and V/C ratio decreased and the crypt depth increased in the jejunum and ileum of the ETECinfected mice compared with controls (P < 0.05; Table 4 ). Oral administration of different doses of IgY improved jejunum and ileum tissue morphology of challenged mice in varying degrees. Mice treated with high and medium-doses anti-ETEC IgY had higher villi height and V/C ratio in jejunum and ileum than mice in ETEC-infected group (P < 0.05), and were not different from control mice.

Infection with ETEC K88 caused the jejunum, ileum and colon of mice to present submucosal edema, central chylous duct Values with different superscripts within a row differ (P < 0.05), n=5. Mice in control group were not challenged with ETEC K88. Mice in ETEC group were challenged with ETEC K88 and treated with PBS. Mice in IgY groups were infected with ETEC K88 and treated with 250 mL of high-, medium-or low-doses anti-ETEC IgY or 250 mL of non-specific IgY. dilatation, leucocyte infiltration and epithelial damage ( Figures 8A-C) . Oral administration of the high dose of anti-ETEC IgY tended to reduce total colon histopathological score of mice (P = 0.07) compared with ETEC-infected group.

To further determine how IgY modulates immune response of ETEC-infected mice, we analyzed the effects of IgY on lymphocytes in jejunum. Different types of jejunal lymphocytes were labeled, localized, and counted and different lymphocyte populations were shown in brown area ( Figure 9A ). ETEC K88 challenge increased number of T lymphocytes (CD3 + ), T helper lymphocytes (CD4 + ) and T suppressor/cytotoxic lymphocytes (CD8 + ) compared with control group (P < 0.05; Figure 9B ). Different doses of anti-ETEC IgY all attenuated the increase in the number of T lymphocytes (CD3 + , CD4 + and CD8 + ). Non-specific IgY attenuated the increase in number of CD3 + lymphocytes induced by ETEC K88 challenge (P < 0.05). Compared with the non-specific IgY group, high and medium-doses anti-ETEC IgY inhibited the increase in number of CD3 + and CD8 + lymphocytes (P < 0.05), and CD8 + lymphocytes concentrations nearly returned to the normal level of the control group.

ETEC is one of the pathogens that causes moderate-to-severe intestinal inflammation, diarrhea, and even death among young animals and human infants (Mondal et al., 2009; Shah et al., 2009 ). In the current study, we investigated the bacteriostatic activity of IgY against ETEC K88 in vitro, and evaluated the protective effects of anti-ETEC against ETEC infection in vivo. Results suggested that oral administration of anti-ETEC specific IgY is efficacious in reducing morbidity and intestinal inflammation associated with ETEC infection in mice. Experiments in vitro showed that anti-ETEC IgY could cause agglutination of bacteria and effectively inhibit the growth of ETEC K88, reduce the adherence of ETEC K88 to IPEC-J2 cells, and destroy the integrity of the ETEC K88 bacterial cell wall.

FIGURE 7 | D-Lactate (A) and diamine oxidase (B) contents in serum of control (neither IgY nor ETEC infection) mice, ETEC-infected mice, ETEC-infected mice treated with high-, medium-or low-doses anti-ETEC IgY or ETEC-infected mice treated with non-specific IgY. Values are expressed as least squares mean ± SEM, n =6. *P < 0.05, ***P < 0.001. # P <0.05 compared to control group. Values with different superscripts within a row differ (P < 0.05), n=6. Mice in control group were not challenged with ETEC K88. Mice in ETEC group were challenged with ETEC K88 and treated with PBS. Mice in IgY groups were challenged with ETEC K88 and treated with 250 mL of high-, medium-or low-doses anti-ETEC IgY or 250 mL of non-specific IgY.

These findings are consistent with Lee et al. (2002) , who found that anti-Salmonella IgY can bind to antigens expressed on the surface of Salmonella, resulting in surface structure alterations of the bacteria. These findings may contribute to why specific IgY antibody acts as a bacteriostatic factor in the absence of other factors such as serum complement.

To evaluate the preventive effect of IgY against ETEC K88 infection, we established a mouse model of intestinal inflammation induced by ETEC K88 similar to that reported previously (Yu et al., 2020) . Mice exhibited typical clinical signs of ETEC infection which included curled up body posture, shivering, diarrhea, weight loss, intestinal inflammation, and death, which indicates that this model can be used to evaluate the efficacy of IgY against ETEC K88 infection. Both high and medium-doses anti-ETEC IgY effectively relieved the weight loss and the severity of diarrhea. This is in accord with a previous report, that found anti-S. typhimurium IgY provided effective protection against S. typhimurium-induced intestinal infection (Li et al., 2016) . Results in this study suggest that oral administration of specific IgY was able to improve clinical signs.

Gut microbiota plays an important role in maintaining intestinal microecological balance. Fecal E. coli number of mice infected with ETEC K88 increased sharply, but mice treated with anti-ETEC IgY reduced fecal E. coli load on day 1 post infection. Similarly, Rahimi et al. (2007) found that IgY against Salmonella enteritis could reduce excretion of Salmonella in the feces of Salmonella-infected laying hens, and reduce its colonization in hen's cecum. Other researchers (Yi et al., 2017) reported that infecting mice with E. coli O157:H7 increased the number of E. coli and decreased the number of Lactobacillus in cecum. Results suggest that anti-ETEC IgY can promote pathogen excretion, thereby reducing their colonization in mice intestine. Increased bacteria removal efficiency may contribute to the positive effects of anti-ETEC IgY on clinical signs of challenged mice.

Metabolites of intestinal bacteria are vital to maintain integrity of the intestinal barrier function. SCFAs produced by intestinal microbial fermentation of carbohydrates have diverse functional roles in various physiologic processes (Koh et al., 2016) . In the present study, ETEC K88 infection reduced levels of acetic acid, propionic acid, and butyric acid in feces of mice. High-and medium-doses anti-ETEC IgY were more effective than low dose of anti-ETEC IgY and non-specific IgY at restoring SCFA concentrations. These results imply that anti-ETEC IgY can effectively improve metabolism of intestinal microbiota. We also investigated effects of IgY on biochemical indices in serum of ETEC K88 challenged mice. ALB plays a vital role in maintaining normal osmotic pressure of blood and ensures nutrient supply to the body. Liver is rich in enzymes that are involved in protein synthesis and catabolism. ALT and AST in serum are important transaminases and often used as an enzymatic index to evaluate liver function (Zhu et al., 2016) . When the liver has pathological changes or injuries, concentration of GLB, ALT and AST in serum increased. We found that ETEC K88 challenge significantly increased GLB content and decreased the ratio of ALB to GLB in serum. Oral gavage with anti-ETEC IgY partially mitigated the increase of GLB and AST and the decrease of the ratio of ALB to GLB induced by ETEC K88 challenge. These findings suggest that anti-ETEC IgY can partially relieve liver damage of mice induced by ETEC K88.

Immunoglobulins are immune effector molecules that play an important role in resisting the infection of external pathogens and can reflect immune level of the body. A previous study demonstrated that serum IgG, IgA and IgM levels significantly increased in piglets challenged with Salmonella or E. coli (Szaboé t al., 2008) . In the present study, we found that IgA and IgG content in serum of ETEC-infected mice increased significantly compared with non-infected mice. Oral gavage with high-and medium-doses anti-ETEC IgY effectively mitigated the increased IgA and IgG secretion caused by ETEC K88 challenge. In addition, sIgA plays an important role in antibody-mediated humoral immunity and maintaining intestinal mucosal homeostasis by binding to pathogenic bacteria which prevents bacterial invasion and adhesion (Fagarasan, 2008) . The sIgA content of the jejunum in mice treated with anti-ETEC IgY increased in varying degrees. Similarly, Liu et al. (2017) found that ETEC infection decreased mRNA expression of the polymeric immunoglobulin receptor involved in sIgA transport in mouse intestinal epithelial cells, which increased contents of sIgA in jejunum and ileum of mice Values are least squares means ± SEM, n=5. *P < 0.05, **P < 0.01, ***P < 0.001.

after challenge. This observation was consistent with the trend of sIgA content in jejunum of ETEC-infected mice in our study. These data suggested that anti-ETEC IgY modulated the body's inflammatory response and promoted pathogen excretion in ETEC K88 infected mice. ETEC infection activates the body's immune system. The immune response elicits an increase in IL-1b, TNF-a, IL-6 and other pro-inflammatory cytokines to resist invasion of exogenous pathogens which produces on inflammatory response. Excessive expression of pro-inflammatory cytokines seriously damages health of the body (Yu et al., 2018) . In this study, ETEC K88 challenge increased the secretion of proinflammatory cytokine IL-1b and the expression of TNF-a and IL-1b, decreased the secretion of anti-inflammatory cytokine IL-4 and the expression of IL-10 in jejunum of mice. This may be due to higher levels of pro-inflammatory cytokines that inhibited anti-inflammatory cytokine production in mice, in a negative feedback regulation of the immune system (Gao et al., 2013) . Our study found that mice pretreated with specific IgY effectively inhibited ETEC-induced inflammatory response.

Maintaining integrity of the intestinal epithelial barrier is very important for defense against pathogen invasion and inflammation (Fasano and Shea-Donohue, 2005; Liu et al., 2017) . Serum D-lactate and DAO have been used as markers for reflecting intestinal permeability and barrier function (Wijtten et al., 2011) . In the present study, Anti-ETEC IgY effectively inhibited the increase of D-lactate and DAO levels in serum of mice compared with ETEC-infected mice. The highand medium-doses anti-ETEC IgY were more effective than lowdose anti-ETEC IgY and non-specific IgY. Previous studies have reported that pathogens such as ETEC or Salmonella can increase concentration of D-lactate and DAO in serum and exacerbate the intestinal permeability (Yang et al., 2014; Xia et al., 2015) . Our results indicate that anti-ETEC IgY improves the reduced intestinal permeability and enhances intestinal barrier function in ETEC K88 infected mice, which is consistent with our previous study (Han et al., 2019) .

Intestinal morphology is an important indicator to evaluate digestive and absorptive functions of the gut. ETEC causes intestinal inflammation, and damages to intestinal tissues that results in bacterial invasion and enteric infection (Johnson et al., 2010) . In the present study, ETEC K88 infection caused damage to the jejunum and ileum. Oral administration of different doses of anti-ETEC IgY reversed these negative impacts to varying degrees. This may be due to the preventive effects of anti-ETEC IgY in decreasing intestinal permeability and inflammatory responses. These results suggest that anti-ETEC IgY effectively relieve villous atrophy and crypt hyperplasia of jejunal and ileal tissue, thus improving intestinal tissue morphology in mice challenged with ETEC K88.

To further investigate potential mechanisms through which IgY exert protection, we also surveyed effects of IgY on the mucosal immune response during ETEC K88 infection. T lymphocytes in intestines are composed of two main subpopulations, namely CD4 + lymphocytes (T helper lymphocytes) and CD8 + lymphocytes (T suppressor/cytotoxic lymphocytes). Pathogen infection can mobilize intestinal mucosal immune responses to defend against the pathogen invasion. Previous reports have shown that bioactive substances including fructo-oligosaccharide and spray-dried porcine plasma (containing immunoglobulin G) can regulate the immune response of intestinal-associated lymphoid tissue in animals (Peŕez-Bosque et al., 2004; Watzl et al., 2005) . Another study showed that IgY modulates the immune response against bovine rotavirus infection at the mucosal level in newborn calves (Vega et al., 2011) , but the immuno-modulatory functions of IgY during infection are still unclear. In our study, ETEC K88 challenge increased T lymphocytes (CD3 + ), T helper lymphocytes (CD4 + ) and T suppressor/cytotoxic lymphocytes (CD8 + ) in the jejunum of mice, that probably due to ETEC K88 excessive stimulated the mucosal immune system. Nevertheless, anti-ETEC IgY notably inhibited excessive proliferation of jejunal T lymphocytes caused by ETEC K88 infection. Compared with non-specific IgY, anti-ETEC IgY was more effective in regulating the immune response of intestinal mucosa. This effect is similar with that observed by Li et al. (2016) who found that IgY played an important immunomodulatory role in mice challenged with S. typhimurium. Hence, the data suggest that IgY can alleviate excessive immune stresses induced by ETEC K88 infection, so that homeostasis of the intestinal environment is maintained.

In summary, we successfully established an ETEC-infected mouse model of intestinal inflammation. We found that specific IgY exhibited strong anti-infective activity in vitro, and effectively ameliorated the ETEC K88-induced inflammation response, mucosal morphology damage and intestinal epithelial barrier injury. Anti-ETEC IgY decreased fecal and cecal bacterial load, and modulated the intestinal mucosal immune response. In addition, the overall effects of high-(32 mg/mL) and medium-(16 mg/mL) dose anti-ETEC IgY were more effective than low-(8 mg/mL) dose anti-ETEC IgY and non-specific IgY. Our results suggest that anti-ETEC IgY has a positive effect in improving intestinal health and regulating immune response. Consequently, anti-ETEC IgY may be a prophylactic immunotherapy agent against infection of intestinal tissues by pathogenic bacteria.

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

The animal study was reviewed and approved by Institutional Animal Care and Use Committee at China Agricultural University.

SH: Conceptualization, methodology, validation, formal analysis, investigation, data curation and writing-original draft preparation. YW: Conceptualization, methodology and formal analysis. FY: Validation and formal analysis. PH: Conceptualization, writingreview and editing, supervision, project administration and funding acquisition. All authors contributed to the article and approved the submitted version.

The authors declare that all sources of funding received for the research have been submitted.

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The financial support from the National Key Research and Development Program of China (2017YFC1600300) is gratefully acknowledged.

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcimb.2021. 662710/full#supplementary-material Conflict of Interest: Author FY was employed by Hubei Shendi Biological Technology Co., LTD.The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.Copyright © 2021 Han, Wen, Yang and He. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.