The effect of different dietary ratios of lysine and arginine in diets with high or low methionine levels on oxidative and epigenetic DNA damage, the gene expression of tight junction proteins and selected metabolic parameters in Clostridium perfringens-challenged turkeys

Katarzyna Ognik; Paweł Konieczka; Dariusz Mikulski; Jan Jankowski

doi:10.1186/s13567-020-00776-y

. 2020 Apr 7;51:50. doi: 10.1186/s13567-020-00776-y

The effect of different dietary ratios of lysine and arginine in diets with high or low methionine levels on oxidative and epigenetic DNA damage, the gene expression of tight junction proteins and selected metabolic parameters in Clostridium perfringens-challenged turkeys

Katarzyna Ognik ¹, Paweł Konieczka ^2,^✉, Dariusz Mikulski ², Jan Jankowski ²

PMCID: PMC7140342 PMID: 32264939

Abstract

Two experiments were performed to investigate the effect of different ratios of arginine (Arg) to lysine (Lys) in diets with low (30% Lys; Experiment 1) and high (45% Lys; Experiment 2) methionine (Met) levels on selected metabolic parameters, oxidative and epigenetic DNA damage, and the mechanisms underlying intestinal barrier integrity in turkeys challenged with Clostridium perfringens. In each experiment, 108 one-day-old Hybrid Converter female turkeys were placed in 6 pens (18 birds per pen) and reared for 42 days. At 34, 36 and 37 days of age, half of the birds were subjected to C. perfringens challenge. A 3 × 2 factorial design with three levels of Arg relative to Lys (90, 100 and 110%; Arg₉₀, Arg₁₀₀ and Arg₁₁₀, respectively) and C. perfringens infection (−, +) was employed. Challenging birds with C. perfringens increased lipid oxidation and the oxidation and methylation of DNA of intestinal mucosa, and down-regulated the activities of DNA-repairing enzymes. Neither the dietary treatment nor the challenge affected the markers of liver function or metabolism. Arg₁₁₀ diets with the high Met level induced DNA oxidation and methylation whereas these processes were downregulated in birds fed Arg₉₀ diets. The results indicate that Arg₉₀ diets with high Met levels have a beneficial influence on the indicators of intestinal barrier integrity in turkeys with necrotic enteritis (NE). Despite the analyzed amino acid ratios interacted with the systems responsible for the maintenance of gut integrity in the host organism, this dietary intervention probably enabled birds to cope with NE.

Introduction

In turkeys, necrotic enteritis (NE) is caused by Clostridium perfringens (C. perfringens) anaerobic bacteria and their toxins, and it causes considerable economic losses in poultry farming [1]. In a post-mortem analysis, the disease manifests by strong inflammation and necrosis of the intestinal mucosa, which impairs nutrient absorption, weakens immune and antioxidant systems and, consequently, compromises growth performance and increases bird mortality [2–4]. Pathological changes associated with NE are also observed in parenchymal organs such as the liver, which can disrupt many biochemical processes. NE can be effectively prevented with organic acids [5] or upon treatment with antibiotics [6].

After the introduction of a ban on the use of antibiotics as growth promoters, poultry nutrition became a viable option for preventing NE. According to many authors, diet has a considerable influence (around 57% relative to the impact of genetic factors which is estimated at 12%) on the gut microbial community [7]. Research has demonstrated that reduced intake or elimination of non-starch polysaccharides (NSP), i.e. complex carbohydrates that increase the viscosity of intestinal digesta, from the diet can intensify fermentation processes and the proliferation of bacteria, including C. perfringens [8]. Bacterial and viral infections exert immunosuppressive effects in poultry [9, 10] and induce reactions that lead to oxidative stress in cells [11, 12]. According to recent research, the supplementation of poultry diets with the appropriate amounts of amino acids, such as arginine (Arg) and methionine (Met), can promote intestinal barrier integrity in many infectious diseases [13–16] because these amino acids stimulate immune and antioxidant systems [17–21]. Tan et al. [14, 22] found that diets supplemented with Arg minimize the damage to intestinal villi and crypts caused by coccidiosis in broiler chickens. Zhang et al. [3] demonstrated that higher levels of l-arginine in the diet improved intestinal barrier integrity and modulated gut microflora in chickens challenged with C. perfringens, producing a consortium that was like to that of healthy controls with higher counts of beneficial bacteria and reduced counts of harmful species. According to Zhang et al. [16], Arg protects the intestinal mucosa by stimulating non-specific immunity, improving intestinal absorption and inhibiting C. perfringens colonization in broilers with inflammatory bowel disease. Munir et al. [9] also demonstrated that Arg could act as an immunoregulator against hydropericardium syndrome virus (HPSV) as well as other poultry pathogens. Our previous study of turkeys [12] revealed that dietary supplementation with Met at a concentration approximately 50% higher than that recommended by the NRC [23] intensified oxidative processes in the intestines, but also stimulated antioxidant mechanisms in the blood and livers of turkeys with HE. However, Ruth and Field [13] argued that dietary supplementation with Met in excess of the recommended levels [23] decreases symptoms of oxidative stress in the intestines of birds with viral and bacterial infections. The cited research is inconclusive and merits further investigation on whether dietary supplementation with the appropriate proportions of Arg and Met can limit the symptoms of oxidative stress, minimize epigenetic alterations that cause DNA damage in turkeys infected with C. perfringens and, consequently, improve intestinal barrier integrity.

According to the NRC [23], the inclusion rate of Arg in turkey diets should reach 90–100% of Lys content, whereas turkey breeding companies [24] recommend higher Arg inclusion rates at 102–105% of Lys content. The Met inclusion rate has been set at 30–38% of Lys content by the NRC [23] and at 36–41% by turkey breeders. Although intestinal barrier and intestinal permeability are important for health and disease, the mucosal barrier and its role in enteric disease are still poorly understood in turkeys. Therefore, the molecular basis of differential responses to infections caused by certain microorganisms in the turkey gut should be elucidated because they are critical for the birds’ health. To the best of our knowledge, the dietary inclusion levels of limiting amino acids (Lys, Arg and Met) and their optimal ratios in the diets of young turkeys challenged with C. perfringens have not been reported in the literature to date. We hypothesized that the optimal concentrations and ratios of Lys, Arg and Met in turkey diets can limit oxidation and methylation of biologically important molecules.

The aim of this study was to determine the effect of different ratios of arginine (Arg) to lysine (Lys) in diets with low (30% Lys; Experiment 1) and high (45% Lys; Experiment 2) methionine (Met) levels on selected metabolic parameters, oxidative and epigenetic DNA damage, and the mechanisms underlying intestinal barrier integrity in turkeys challenged with C. perfringens.

Materials and methods

The study protocol was approved by the Local Ethics Committee (University of Warmia and Mazury, Olsztyn, Poland), and the animals were cared for under guidelines comparable to those laid down by the EU Directive 2010/63/EU.

Birds and housing

A total of 216 one-day-old Hybrid Converter female turkey poults obtained from a commercial hatchery (Grelavi company in Ketrzyn, NE, Poland) were randomly placed in 12 pens on litter (4 m² each; 2.0 m × 2.0 m), and were reared to 42 days of age. The initial BW of 1-day-old poults was 55.7 ± 0.1 g. The birds were divided into 2 subgroups (referred thereafter as Experiment 1 and Experiment 2), each subgroup consisted of 6 pens with 18 birds per pen. At 34, 36 and 37 days of age, half of the birds were subjected to C. perfringens challenge. The temperature and lighting programs were consistent with the recommendations for standard management practices [24].

Experimental design and diets

During the 6-week experiment, birds were fed ad libitum isocaloric diets that met or exceeded their requirements, containing high levels of Lys, approximately 1.80% and 1.65% in two successive feeding periods, consistent with the Lys levels recommended in the Management Guidelines for Raising Commercial Turkeys [24]. The experiments had a completely randomized 3 × 2 factorial design with three levels of Arg (90%, 100% and 110% relative to the content of dietary Lys; Arg₉₀, Arg₁₀₀ and Arg₁₁₀, respectively) and C. perfringens infection (−, +). The diets in Experiment 1 had low Met content (30% Lys), and the diets in Experiment 2 had high Met content (45% of Lys). The AA content of basal diets was determined, and they were mixed with adequate amounts of the above AA. The Lys, Met and Arg content of experimental diets was determined analytically again (Table 1). The diets were offered as crumbles (days 1–28) and pellets (days 29–42).

Table 1.

Analyzed lysine (Lys), arginine (Arg) and methionine (Met) content of turkey diets, g/100 g.

Treatment	Amino acid	Experiments 1 and 2
Treatment	Amino acid	Week 1–4	Week 5–6
Arg₉₀	Lys	1.81	1.67
	Arg	1.59	1.50
	Met	0.53	0.50
Arg₁₀₀	Lys	1.85	1.64
	Arg	1.86	1.64
	Met	0.56	0.52
Arg₁₁₀	Lys	1.89	1.65
	Arg	2.04	1.77
	Met	0.57	0.51

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Clostridium perfringens challenge

At 34, 36 and 37 days of age, birds were infected with 1 mL (per os directly into the crop) of C. perfringens type A strain 56 containing approximately 10⁸ CFU/mL cultured in a brain heart infusion medium (Sigma Aldrich) whereas the non-challenged group received the same dose of sterilized broth medium. The C. perfringens challenge was preceded by administering 1 mL of a coccidia vaccine containing Eimeria (E) species: E. acervulina, 5000 oocytes; E. maxima, 3500 oocytes; E. mitis, 5000 oocytes; E. praecox, 5000 oocytes; E. tenella, 5000 oocytes (Laboratorios HIPRA S.A., Spain) to turkeys at 31 and 34 days of age to make favorable environment in the gut for C. perfringens colonization.

Sample collection and laboratory analysis

At 42 days of age, birds were weighted individually, and 8 turkeys from each treatment were sacrificed by cervical dislocation, and the abdominal cavity was opened for ileal (middle-ileum) tissue collection and processing. Blood samples were taken from 8 birds per group. Blood samples were collected into test tubes with an anticoagulant (heparin) from the wing vein, they were centrifuged at 3000 × g for 10 min, and blood plasma was collected for further analysis.

RNA extraction and real-time quantitative PCR

RNA isolation was performed in accordance with previously developed procedures with some modifications [25]. Briefly; total RNA from the ilium was isolated using the GeneMATRIX Universal RNA Purification Kit (EURX Ltd., Gdańsk, Poland) according to the manufacturer’s protocol. The isolated RNA yield was estimated spectrophotometrically (Nanodrop, NanoDrop Technologies, Wilmington, DE, USA), with integrity assessed electrophoretically by separation on agarose gel. For complementary cDNA synthesis, 800 ng/mL of RNA from ileal tissue was reverse transcribed using the NG dART RT kit (EURX Ltd., Gdańsk, Poland) according to the manufacturer’s instructions. Specific primers for respective genes were designed using Primer 3 software (Whitehead Institute, Cambridge, MA, USA) and synthesized by Genomed (Warsaw, Poland). The respective primer sequences are shown in Table 2.

Table 2.

Genes and primers used in the study.

Gene	Primer	Sequence (5′-3′)	Melting temperature (°C)	Product size (nt)	GenBank access no.
ACTB	Forward	TACCCCATTGAACACGGCAT	58	96	NM_001303173
ACTB	Reverse	CTCCTCAGGGGCTACTCTCA		96	NM_001303173
GAPDH	Forward	AGGATACACAGAGGACCAGGTTG	58	71	NM_001303179
GAPDH	Reverse	CCGCATCAAAGGTGGAGGAATG		71	NM_001303179
ZO-1	Forward	AGAGGCAACTGAACCATAG	58	114	XM_019619275
ZO-1	Reverse	CTGCTGAGAGGCTAATACAA		114	XM_019619275
GLP2	Forward	GCAGTGAAGGAGAAGTGA	58	200	XM_010721176
GLP2	Reverse	GAGGCTGTAAGAAGTAGGA		200	XM_010721176
OCLN	Forward	GCAGATGTCCAGCAGTTA	55	127	XM_019610822
OCLN	Reverse	GTTCACACTCACCTCCTG		127	XM_019610822
TFF2	Forward	AAAATAGCAGCCAGGGAGCG	58	92	XM_010724393
	Reverse	ACTGACGCATTGAAGCAGCA
CLDN15	Forward	GCAAGGAGGCTTCTGAAA	55	161	XM_019618905
	Reverse	CAGTAACTATGTGGCAAGGT
OGG1	Forward	GGGACAAATGGGCACCTG	58	102	XM_010718590
	Reverse	GCAGAGGCAATAGGCTCAG

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ACTB: β-actin, GAPDH: Glyceraldehyde-3-Phosphate Dehydrogenase, ZO-1: Zonula occludens-1, GLP2: Glucagon-like peptide-2, OCLN: Occludin, TFF2: Trefoil Factor 2, CLDN15: Claudin 15, and OGG1: 8-Oxoguanine glycosylase.

Real-time qPCR was performed using the BioRad CFX 96 thermocycler (Bio-Rad Laboratories, Inc., CA, USA) according to the following protocol: one cycle at 95 °C for 15 min (enzyme activation), followed by a PCR including 35 cycles at 95 °C for 10 s (denaturation), 55–58 °C for 10 s (annealing), and 72 °C for 20 s (elongation). A melting curve analysis was performed over 65–95 °C at 0.1 °C/s intervals. Negative controls without the cDNA template were included in each reaction. Real-time qPCR for each cDNA sample was performed in duplicate. Normalized gene expression was calculated using the comparative quantitation option of Rotor qPCR Biorad CFX 96 (Bio-Rad Laboratories, Inc., CA, USA), and determined using the supplied Expression Software Tool. The glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and β-actin (ACTB) genes were selected as endogenous control genes to normalize gene expression.

DNA oxidation and methylation, and metabolic parameters

The levels of 8-hydroxydeoxyguanosine (8-OHdG), endonuclease 1 (APE-1), and glycosylases TDG and ANPG were determined in the wall of the ileum and in the blood of turkeys using OxiSelect diagnostic kits (Cell Biolabs, Inc., San Diego, USA). DNA was isolated from the blood and intestinal wall using QIAGEN kits. Epigenetic changes in the blood and intestinal wall were determined by analyzing global DNA methylation (methylome) using Sigma Aldrich diagnostic kits. The concentration of malondialdehyde (MDA) in the blood of turkeys was determined using kits produced by Cell Biolabs, Inc. (San Diego, USA). The activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx) in the blood of turkeys was determined by spectrometry using Ransel and Ransod diagnostic kits manufactured by Randox (Poland). The plasma concentrations of total cholesterol (TC), triglycerides (TG), uric acid (UA), urea (UREA), total protein (TP), albumin (ALB) and glucose (GLU), and the activity of alanine aminotransferase (ALT), aspartate aminotransferase (AST) and creatine kinase (CK) were measured using an automated biochemistry analyzer (Plasma Diagnostic Instruments Horiba, Kyoto, Japan).

Statistical analysis

Both experiments were performed in a completely randomized 3 × 2 factorial design, and the data were subjected to 2-way ANOVA to examine the following effects: (a) main effect of three levels of Arg (Arg₉₀, Arg₁₀₀ and Arg₁₁₀); (b) main effect of C. perfringens infection (−, +); and (c) interaction between Arg inclusion levels and C. perfringens infection. All data were analyzed using the GLM procedure of STATISTICA software version 12. When a significant interaction effect was noted, Tukey’s test was used to determine differences between the experimental factors. Data variability was expressed as pooled standard errors of the mean (SEM), and P < 0.05 was considered statistically significant.

Results

Experiment 1

Effects of infection

Clostridium perfringens infection did not decrease the BW of turkeys at 6 weeks of age (2.449 vs. 2.367 kg, P = 0.167). The expression of occludin, ZO-1, GLP2, OGG1 and TFF2 genes increased in the wall of the ileum (P < 0.001) in response to C. perfringens infection (Table 3). In comparison with uninfected turkeys, C. perfringens infection increased 8-OHdG levels and decreased the activity of APE-1, TDG and ANPG in the wall of the ileum (P < 0.001). Higher levels of 8-OHdG, a higher percentage of methylated DNA (P < 0.001, respectively) and lower activity of APE-1 (P = 0.003) were also noted in the blood of infected turkeys (Table 4). Clostridium perfringens infection increased the levels of MDA (P = 0.005) and ALB (P < 0.001), and GPx activity (P < 0.001), and decreased the levels of TG (P < 0.001) and UA (P < 0.001), and ALT activity (P < 0.001) (Table 5).

Table 3.

Gene expression in the ileal tissues of 42-day-old turkeys fed diets with different arginine (Arg) to lysine (Lys) ratios and a low methionine (Met) level, challenged withClostridium perfringens—(Experiment 1).

Item	ZO-1	Occludin	GLP2	OGG1	TFF2
Arg₉₀*Infection (−)	0.655	0.005	0.331^b	0.325	0.003
Arg₉₀*Infection (+)	2.191	0.013	1.500^a	0.711	0.009
Arg₁₀₀*Infection (−)	0.762	0.003	0.429^ab	0.142	0.004
Arg₁₀₀*Infection (+)	1.892	0.014	0.933^ab	0.569	0.010
Arg₁₁₀*Infection (−)	0.933	0.007	0.712^ab	0.211	0.004
Arg₁₁₀*Infection (+)	2.434	0.025	1.001^a	1.197	0.011
SEM	0.124	0.002	0.080	0.074	0.0007
Arg level, %
90	1.423	0.009	0.915	0.518^ab	0.006
100	1.327	0.008	0.681	0.355^b	0.007
110	1.684	0.016	0.856	0.704^a	0.008
C. perfringens infection¹
–	0.783^b	0.005^b	0.490^b	0.226^b	0.003^b
+	2.172^a	0.017^a	1.145^a	0.826^a	0.010^a
P value
Arg	0.108	0.052	0.252	0.045	0.420
Infection	0.001	0.001	0.001	0.001	0.001
Arg × infection	0.425	0.295	0.011	0.057	0.868

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Diets contained three levels of Arg relative to Lys (90, 100 and 110%; Arg₉₀, Arg₁₀₀ and Arg₁₁₀, respectively) and a low level of Met (30% dietary Lys).

¹At 34, 36 and 37 days of age, birds were infected with 1 mL (per os directly into the crop) of a culture medium of C. perfringens type A strain 56 containing approximately 10⁸ CFU/mL of bacteria. ^a,bMeans within a row with different superscripts differ significantly (P < 0.05).

Table 4.

Oxidative and epigenetic DNA damage and the activities of repair enzymes in the blood and ileal tissues of 42-day-old turkeys fed diets with different arginine (Arg) to lysine (Lys) ratios and a low methionine (Met) level, challenged withClostridium perfringens—(Experiment 1).

Item	Ileal tissue					Blood
Item	8-OHdG pg/µL DNA	Methylation DNA, %	APE-1 ng/g	TDG ng/g	ANPG ng/g	8-OHdG pg/mL	Methylation DNA, %	APE-1 ng/mL	TDG ng/mL	ANPG ng/mL
Arg₉₀*Infection (−)	24.26^d	14.92^c	1731.0^a	1056.9	39.01	4.424^c	28.66	160.1	83.68	4.197
Arg₉₀*Infection (+)	53.44^b	18.72^ab	933.2^c	596.3	17.78	6.825^a	58.23	146.7	83.99	4.361
Arg₁₀₀*Infection (−)	28.04^d	15.37^bc	1746.2^a	994.5	42.41	5.061^bc	30.14	182.5	100.30	4.747
Arg₁₀₀*Infection (+)	86.21^a	19.55^a	995.3^c	658.9	21.07	6.031^ab	46.46	152.2	92.31	4.601
Arg₁₁₀*Infection (−)	38.08^c	19.00^ab	1382.5^b	876.3	37.38	5.711^abc	30.20	147.4	94.87	4.772
Arg₁₁₀*Infection (+)	84.96^a	13.21^c	1018.2^c	651.0	23.16	6.017^ab	52.06	144.8	93.37	4.978
SEM	3.757	0.493	57.80	33.85	1.673	0.175	2.252	3.025	1.607	0.075
Arg level, %
90	38.85^b	16.82	1332.1	826.6	28.39	5.624	43.44	153.4^ab	83.83^b	4.279^b
100	57.12^a	17.46	1370.7	826.7	31.74	5.546	38.30	167.4^a	96.31^a	4.674^ab
110	59.96^a	16.11	1200.3	763.6	30.27	5.864	41.13	146.1^b	94.12^a	4.875^a
C. perfringens infection¹
–	30.13^b	16.43	1619.9^a	975.9^a	39.60^a	5.065^b	29.67^b	163.3^a	92.95	4.572
+	74.43^a	17.16	982.2^b	635.4^b	20.67^b	6.291^a	52.25^a	147.9^b	89.89	4.647
P value
Arg	0.001	0.329	0.075	0.433	0.356	0.641	0.399	0.004	0.002	0.003
Infection	0.001	0.327	0.001	0.001	0.001	0.001	0.001	0.003	0.292	0.589
Arg × infection	0.001	0.001	0.012	0.119	0.222	0.014	0.221	0.084	0.468	0.523

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Diets contained three levels of Arg relative to Lys (90, 100 and 110%; Arg₉₀, Arg₁₀₀ and Arg₁₁₀, respectively) and a low level of Met (30% dietary Lys).

¹At 34, 36 and 37 days of age, birds were infected with 1 mL (per os directly into the crop) of a culture medium of C. perfringens type A strain 56 containing approximately 10⁸ CFU/mL of bacteria. ^a,b,cMeans within a row with different superscripts differ significantly (P < 0.05).

Table 5.

Metabolic parameters in the blood of 42-day-old turkeys fed diets with different arginine (Arg) to lysine (Lys) ratios and a low methionine (Met) level, challenged withClostridium perfringens—(Experiment 1).

Item	CK U/L	ALT U/L	AST U/L	SOD U/gHb	GPx U/gHb	TP g/L	ALB g/L	UA mmol/L	UREA mmol/L	TC mmol/L	TG mmol/L	MDA µmol/L	GLU mmol/L
Arg₉₀*Infection (−)	0.255	9.15^b	250.1^c	1029.4	14.23^bc	39.61^ab	16.69^b	0.424^ab	1.019	4.069	0.676	1.905^a	9.45^c
Arg₉₀*Infection (+)	0.233	10.52^b	261.4^bc	825.5	17.06^b	41.02^a	18.60^a	0.341^bc	0.789	3.794	0.461	1.886^ab	11.59^ab
Arg₁₀₀*Infection (−)	0.264	12.57^a	300.0^a	1024.8	15.17^bc	28.57^c	13.50^c	0.408^ab	1.171	3.532	0.533	2.014^a	11.78^a
Arg₁₀₀*Infection (+)	0.264	12.71^a	279.1^ab	745.2	31.91^a	34.73^b	18.89^a	0.371^abc	0.942	3.406	0.354	2.089^a	10.02^bc
Arg₁₁₀*Infection (−)	0.275	14.43^a	301.1^a	1082.6	15.30^bc	38.07^ab	18.41^a	0.447^a	1.299	3.250	0.836	1.395^b	11.83^a
Arg₁₁₀*Infection (+)	0.266	6.43^c	248.3^c	1364.5	13.07^c	36.14^ab	19.51^a	0.295^c	1.095	3.410	0.688	2.209^a	9.80^c
SEM	0.006	0.468	4.067	57.66	0.999	0.742	0.325	0.011	0.062	0.070	0.025	0.059	0.215
Arg level, %
90	0.244	9.83^b	255.8^b	927.5^b	15.65^b	40.32^a	17.65^b	0.382	0.904	3.931^a	0.568^b	1.896	10.52
100	0.264	12.64^a	289.5^a	885.0^c	23.54^a	31.65^b	16.19^c	0.390	1.057	3.469^b	0.444^c	2.051	10.90
110	0.271	10.43^ab	274.7^ab	1223.6^a	14.18^b	37.10^ab	18.96^a	0.371	1.197	3.330^b	0.762^a	1.802	10.81
C. perfringens infection¹
–	0.149	12.05^a	283.7^a	1045.6	14.90^b	35.42	16.20^b	0.426^a	1.163	3.617	0.682^a	1.77^b	11.02
+	0.254	9.89^b	262.9^b	978.4	20.68^a	37.30	19.00^a	0.336^b	0.942	3.537	0.501^b	2.06^a	10.47
P value
Arg	0.149	0.001	0.001	0.024	0.001	0.001	0.001	0.638	0.158	0.001	0.001	0.121	0.626
Infection	0.372	0.001	0.001	0.528	0.001	0.054	0.001	0.001	0.077	0.518	0.001	0.005	0.104
Arg × infection	0.734	0.001	0.001	0.074	0.001	0.005	0.001	0.020	0.995	0.348	0.451	0.002	0.000

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Diets contained three levels of Arg relative to Lys (90, 100 and 110%; Arg₉₀, Arg₁₀₀ and Arg₁₁₀, respectively) and a low level of Met (30% dietary Lys).

¹At 34, 36 and 37 days of age, birds were infected with 1 mL (per os directly into the crop) of a culture medium of C. perfringens type A strain 56 containing approximately 10⁸ CFU/mL of bacteria. ^a,b,cMeans within a row with different superscripts differ significantly (P < 0.05).

Effects of dietary ratios of Arg to Lys

Different dietary inclusion levels of Arg had no effect on the BW of turkeys at 6 weeks of age (2.383 vs. 2.429 vs. 2.412 kg, P = 0.808). Diets with the highest Arg content (110% Lys) increased the expression of the OGG1 gene (P = 0.004) in the wall of the ileum. An Arg × infection interaction was noted for the expression of the GLP2 gene in the ileum (P = 0.045): C. perfringens infection increased the expression of the GLP2 gene at the lowest dietary Arg content (90% Lys), but not at the medium or highest Arg content (100% and 110% Lys, respectively) (Table 3).

In comparison with turkeys fed Arg₉₀ diets, diets with higher Arg content increased 8-OHdG levels (P < 0.001) in the ileum. The lowest activity of APE-1 (P = 0.004) was noted in turkeys fed Arg₁₁₀ diets, and the lowest activity of TDG (P = 0.002) and ANPG (P = 0.003) was observed in birds receiving Arg₉₀ diets. An Arg × infection interaction was noted for DNA methylation in the wall of the ileum (P < 0.001): C. perfringens infection decreased DNA methylation at the highest dietary Arg content (Arg₁₁₀), but not at the medium or lowest Arg content (Arg₁₀₀ and Arg₉₀, respectively). An Arg × infection interaction was also found for 8-OHdG levels in the blood (P = 0.014): C. perfringens infection increased 8-OHdG levels at the lowest dietary Arg content (Arg₉₀), but not at the medium or highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively) (Table 4).

Diets with the lowest Arg content increased TP levels in the blood of turkeys (P < 0.001) and decreased AST activity (P < 0.001). In comparison with diets with the lowest and medium Arg inclusion rates, diets with the highest Arg content increased SOD activity (P = 0.024). Turkey fed Arg₉₀ diets were characterized by the lowest ALT activity and the highest TC concentration (P < 0.001). The plasma levels of ALB and TG increased (both P < 0.001) with increasing Arg content. An Arg × infection interaction was noted for ALT and AST activity (both P < 0.001): C. perfringens infection decreased the activity of both enzymes at the highest dietary Arg content (Arg₁₁₀), but not at the medium or lowest Arg content (Arg₁₀₀ and Arg₉₀, respectively). An Arg × infection interaction was observed for TP levels and GPx activity (both P < 0.001): C. perfringens infection increased TP levels and GPx activity at the medium dietary Arg content (Arg₁₀₀), but not at the lowest or highest Arg content (Arg₉₀ and Arg₁₁₀, respectively). An Arg × infection interaction was also found for ALB levels in the blood plasma of turkeys (P < 0.001): C. perfringens infection increased ALB levels at the lowest and medium Arg content (Arg₉₀ and Arg₁₀₀, respectively), but not at the highest Arg content (Arg₁₁₀). The following Arg × infection interaction was noted for the plasma levels of UA and MDA (both P = 0.002): C. perfringens infection increased UA and MDA levels at the highest dietary Arg content (Arg₁₁₀), but not at the lowest or medium Arg content (Arg₉₀ and Arg₁₀₀, respectively). The following Arg × infection interaction was observed for GLU levels in the blood plasma of turkeys (P < 0.001): C. perfringens infection increased GLU levels at the lowest dietary Arg content (Arg₉₀), but not at the medium or highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively) (Table 5).

Experiment 2

Effects of infection

Similarly to Experiment 1, C. perfringens infection had no influence on the BW of turkeys (2.467 vs. 2.392 kg, P = 0.307). Clostridium perfringens infection increased the expression of occludin, ZO-1, GLP2, OGG1 and TFF2 genes (P < 0.001) in the wall of the ileum (Table 6). Similarly to Experiment 1, C. perfringens infection increased 8-OHdG levels and decreased the activity of APE-1, TDG and ANPG in the wall of the ileum (P < 0.001). The infection increased 8-OHdG levels and the percentage of methylated DNA (P < 0.001), and decreased APE-1 activity (P = 0.01) also in turkeys fed diets containing 45% Met. In comparison with uninfected turkeys, C. perfringens infection decreased the activity of ANPG in the blood (P = 0.004) and increased the percentage of methylated DNA in the wall of the ileum (P = 0.004) (Table 7).

Table 6.

Gene expression in the ileal tissues of 42-day-old turkeys fed diets with different arginine (Arg) to lysine (Lys) ratios and a high methionine (Met) level, challenged withClostridium perfringens—(Experiment 2).

Item	ZO-1	Occludin	GLP2	OGG1	TFF2
Arg₉₀*Infection (−)	0.794	0.005	0.375	0.184	0.003
Arg₉₀*Infection (+)	1.918	0.022	1.145	0.666	0.011
Arg₁₀₀*Infection (−)	0.841	0.006	0.385	0.172	0.003
Arg₁₀₀*Infection (+)	2.485	0.014	1.590	0.545	0.009
Arg₁₁₀*Infection (−)	0.838	0.005	0.368	0.283	0.003
Arg₁₁₀*Infection (+)	2.253	0.014	1.219	0.616	0.007
SEM	0.120	0.001	0.091	0.044	0.0007
Arg level, %
90	1.356	0.013	0.760	0.425	0.007
100	1.663	0.010	0.987	0.359	0.006
110	1.545	0.009	0.793	0.450	0.005
C. perfringens infection¹
–	0.824^b	0.005^b	0.376^b	0.213^b	0.003^b
+	2.219^a	0.017^a	1.318^a	0.609^a	0.009^a
P value
Arg	0.134	0.144	0.259	0.532	0.421
infection	0.001	0.001	0.001	0.001	0.001
Arg × infection	0.237	0.078	0.301	0.654	0.283

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Diets contained three levels of Arg relative to Lys (90, 100 and 110%; Arg₉₀, Arg₁₀₀ and Arg₁₁₀, respectively) and a high level of Met (45% dietary Lys).

Table 7.

Oxidative and epigenetic DNA damage and the activities of repair enzymes in the blood and ileal tissues of 42-day-old turkeys fed diets with different arginine (Arg) to lysine (Lys) ratios and a high methionine (Met) level, challenged withClostridium perfringens—(Experiment 2).

Item	Ileal tissue					Blood
Item	8-OHdG pg/µL DNA	Methylation DNA, %	APE-1 ng/g	TDG ng/g	ANPG ng/g	8-OHdG pg/mL	Methylation DNA, %	APE-1 ng/mL	TDG ng/mL	ANPG ng/mL
Arg₉₀*Infection (−)	23.40^d	13.30^b	1708.2^a	983.2^a	38.43^a	4.136^b	29.01	177.9^a	93.44	4.937
Arg₉₀*Infection (+)	79.03^ab	17.69^a	1000.9^b	638.2^c	20.34^b	6.773^a	66.25	148.7^b	91.89	4.416
Arg₁₀₀*Infection (−)	25.92^d	13.44^b	1494.4^a	840.0^ab	35.17^a	5.369^ab	29.02	159.7^ab	91.28	5.053
Arg₁₀₀*Infection (+)	88.68^a	16.21^ab	1008.9^b	691.3^c	21.44^b	5.131^ab	39.83	136.4^b	85.37	4.577
Arg₁₁₀*Infection (−)	38.15^c	14.52^abc	959.9^b	666.9^bc	19.34^b	6.493^a	29.22	150.0^b	97.32	4.686
Arg₁₁₀*Infection (+)	84.28^a	13.01^bc	951.8^b	661.4^c	25.55^b	8.144^a	74.74	159.6^ab	94.07	3.999
SEM	4.152	0.383	48.35	22.98	1.377	0.243	2.863	3.103	1.340	0.102
Arg level, %
90	51.21^b	15.50	1354.6^a	810.7^a	29.38^a	5.454^b	47.63^ab	163.3	92.66	4.677
100	57.30^a	14.82	1251.6^a	765.6^a	28.30^a	5.250^b	34.43^b	148.1	88.32	4.815
110	61.22^a	13.77	955.9^b	664.2^b	22.44^b	7.319^a	51.98^a	154.8	95.70	4.343
C. perfringens infection¹
–	29.16^b	13.75^b	1387.5^a	830.0^a	30.98^a	5.333^b	29.08^b	162.5^a	94.01	4.892^a
+	84.00^a	15.64^a	987.2^b	663.6^b	22.44^b	6.683^a	60.27^a	148.3^b	90.44	4.331^b
P value
Arg	0.001	0.079	0.001	0.001	0.006	0.001	0.001	0.071	0.079	0.116
Infection	0.001	0.004	0.001	0.001	0.001	0.001	0.001	0.010	0.178	0.004
Arg × infection	0.001	0.001	0.001	0.001	0.001	0.003	0.001	0.009	0.789	0.889

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Diets contained three levels of Arg relative to Lys (90, 100 and 110%; Arg₉₀, Arg₁₀₀ and Arg₁₁₀, respectively) and a high level of Met (45% dietary Lys).

¹At 34, 36 and 37 days of age, birds were infected with 1 mL (per os directly into the crop) of a culture medium of C. perfringens type A strain 56 containing approximately 10⁸ CFU/mL of bacteria. ^a,b,cMeans within a row with different superscripts differ significantly (P < 0.05).

Similarly to Experiment 1, C. perfringens infection increased the levels of MDA (P = 0.007) and ALB, and GPx activity (both P < 0.001), and decreased the levels of TG (P = 0.009) and UA, and ALT activity (both P < 0.001). In comparison with uninfected turkeys, infected birds were characterized by lower TP levels (P = 0.003), higher levels of TC (P < 0.001) and GLU (P = 0.006), and higher activity of CK (P < 0.001), AST (P = 0.003) and SOD (P < 0.001) (Table 8).

Table 8.

Metabolic markers in the blood of 42-day-old turkeys fed diets with different arginine (Arg) to lysine (Lys) ratios and a high methionine (Met) level, challenged withClostridium perfringens—(Experiment 2).

Item	CK U/L	ALT U/L	AST U/L	SOD U/gHb	GPx U/gHb	TP g/L	ALB g/L	UA mmol/L	UREA mmol/L	TC mmol/L	TG mmol/L	MDA µmol/L	GLU mmol/L
Arg₉₀*Infection (−)	0.249^d	13.13^a	239.0^c	807.2^c	14.65^d	44.59^a	20.51^b	0.412	1.319^ab	3.727^ab	0.621	1.718^b	6.95^c
Arg₉₀*Infection (+)	0.365^b	11.26^ab	275.4^ab	2234.1^a	20.80^c	36.05^b	18.97^bc	0.280	1.477^a	3.498^b	0.512	1.54^bc	9.43^b
Arg₁₀₀*Infection (−)	0.187^e	15.31^a	247.7^bc	1139.4^c	14.44^d	38.55^b	19.99^b	0.391	1.502^a	2.945^c	0.715	1.279^c	10.25^b
Arg₁₀₀*Infection (+)	0.168^e	6.64^c	303.7^a	2216.3^ab	47.94^b	38.1^b	23.60^a	0.347	1.146^ab	4.063^a	0.646	2.205^a	10.32^b
Arg₁₁₀*Infection (−)	0.236 ^cd	13.64^a	289.3^a	2126.6^ab	12.92^d	37.4^b	18.39^c	0.365	0.738^b	3.358^bc	0.396	1.830^b	12.02^a
Arg₁₁₀*Infection (+)	0.434^a	7.43^c	255.0^bc	1705.9^b	55.60^a	35.75^b	22.58^a	0.317	1.120^ab	4.243^a	0.336	2.119^a	12.10^a
SEM	0.014	0.678	4.438	93.23	2.576	0.676^b	0.305	0.011	0.067	0.079	0.024	0.074	0.290
Arg level, %
90	0.307^b	12.20	257.2^b	15207^c	17.72^b	40.32^a	19.74^b	0.346	1.398^a	3.613	0.566^b	1.629	8.19^c
100	0.177^c	10.98	275.7^a	1677.8^b	31.19^a	38.33^ab	21.80^a	0.369	1.324^a	3.504	0.681^a	1.742	10.28^b
110	0.335^a	10.53	272.2^ab	1916.3^a	34.26^a	36.58^b	20.48^ab	0.341	0.929^b	3.800	0.366^c	1.974	12.06^a
C. perfringens infection¹
–	0.224^b	14.03^a	258.7^b	1357.8^b	14.00^b	40.18^a	19.63^b	0.389^a	1.187	3.343^b	0.577^a	1.609^b	9.74^b
+	0.322^a	8.45^b	278.0^a	2052.1^a	41.45^a	36.64^b	21.72^a	0.315^b	1.248	3.935^a	0.498^b	1.955^a	10.62^a
P value
Arg	0.001	0.408	0.041	0.008	0.001	0.030	0.001	0.466	0.004	0.064	0.001	0.073	0.001
Infection	0.001	0.001	0.003	0.001	0.001	0.003	0.001	0.001	0.605	0.001	0.009	0.007	0.006
Arg × infection	0.001	0.034	0.001	0.001	0.001	0.009	0.001	0.124	0.040	0.001	0.755	0.003	0.002

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Diets contained three levels of Arg relative to Lys (90, 100 and 110%; Arg₉₀, Arg₁₀₀ and Arg₁₁₀, respectively) and a high level of Met (45% dietary Lys).

¹At 34, 36 and 37 days of age, birds were infected with 1 mL (per os directly into the crop) of a culture medium of C. perfringens type A strain 56 containing approximately 10⁸ CFU/mL of bacteria. ^a,b,cMeans within a row with different superscripts differ significantly (P < 0.05).

Effects of dietary ratios of Arg to Lys

An increase in the dietary Arg:Lys ratio to 110% contributed to an increase in the BW of turkeys at 6 weeks of age (2.29 vs. 2.434 vs. 2.564 kg, P = 0.014). Different dietary inclusion levels of Arg, relative to Lys, had no influence on the expression of genes encoding intestinal barrier integrity in turkeys (Table 6). Similarly to Experiment 1, turkeys fed Arg₁₀₀ and Arg₁₁₀ diets had higher 8-OHdG levels in the wall of the small intestine. Turkeys receiving Arg₁₁₀ diets were characterized by the highest 8-OHdG levels and the highest percentage of methylated DNA (both P < 0.001) in the blood. An increase in the Arg content to 110% Lys decreased the activity of APE-1, TDG and ANPG (P < 0.001) in the ileum. An Arg × infection interaction was noted for DNA methylation in the wall of the ileum (P < 0.001): C. perfringens infection increased DNA methylation at the lowest dietary Arg content (Arg₉₀), but not at the medium or highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively). Similarly to Experiment 1, an Arg × infection interaction was observed for 8-OHdG levels in the blood (P = 0.003): C. perfringens infection increased 8-OHdG levels at the lowest dietary Arg content (Arg₉₀) and both Met concentrations (30% or 45% Lys), but not at the medium or highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively). An Arg × infection interaction was also found for the activity of APE-1, TDG and ANPG in the wall of the ileum (P < 0.001): C. perfringens infection decreased the activity of the above enzymes at the lowest and medium dietary Arg content (Arg₉₀ and Arg₁₀₀, respectively) and Met concentration of 45% Lys, but not at the highest Arg content (Arg₁₁₀). The following Arg × infection interaction was noted for APE-1 activity in the blood of turkeys (P = 0.009): C. perfringens infection decreased APE-1 activity at the lowest dietary Arg content (Arg₉₀) and Met concentration of 45% Lys, but not at the medium or highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively) (Table 7).

Similarly to Experiment 1, an increase in the Arg content to 110% Lys increased SOD activity in the blood of turkeys (P = 0.008). Turkeys fed Arg₉₀ diets had lower GPx activity and ALB levels (both P < 0.001) in the blood. An increase in the dietary inclusion rate of Arg (110% Lys) led to an increase in GLU levels and CK activity (both P < 0.001), and a decrease in UREA levels (P = 0.004) in the blood. An Arg × infection interaction was observed for the levels of ALB, TC (both P < 0.001) and MDA (P = 0.003) in the blood of turkeys: C. perfringens infection increased the levels of ALB, TC and MDA at the medium and highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively), but not at the lowest Arg content (Arg₉₀). An Arg × infection interaction was also found for CK activity and UREA levels in the blood plasma of turkeys (P < 0.001, P = 0.04, respectively): C. perfringens infection increased CK activity and UREA levels at the lowest and highest Arg content (Arg₉₀ and Arg₁₁₀, respectively), but not at the medium Arg content (Arg₁₀₀). The following Arg × infection interaction was noted for the activity of AST and SOD in the blood of turkeys (both P < 0.001): C. perfringens infection increased the activity of the above enzymes at the lowest and medium Arg content (Arg₉₀ and Arg₁₀₀, respectively), but not at the highest Arg content (Arg₁₁₀). The following Arg × infection interaction was observed for ALT activity in the blood plasma of turkeys: C. perfringens infection decreased ALT activity at the medium and highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively), but not at the lowest Arg content (Arg₉₀). The following Arg × infection interaction was found for the plasma levels of TP: C. perfringens infection decreased TP levels at the lowest Arg content (Arg₉₀), but not at the medium or highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively). The following Arg × infection interaction was noted for the plasma levels of GLU: C. perfringens infection increased GLU levels at the lowest Arg content (Arg₉₀), but not at the medium or highest Arg content (Arg₁₀₀ and Arg₁₁₀, respectively) (Table 8).

Discussion

Effects of infection

Intestinal barrier integrity plays a key role in protecting birds, in particular turkeys, against pathogenic microflora. Tight junction proteins (TJP) are the key molecules maintaining epithelial cell integrity. They enable the free passage of ions inside cells and prevent pathogens and their toxins from entering cells. sIgA and mucus flow are the main defenders of the intestinal mucosal barrier [26]. Claudin and occludin are integral membrane proteins in tight junctions [27] which form a tight barrier around cells and act as a physical barrier against the free flow of dissolved substances across intercellular spaces. Bacteria, including C. perfringens, secrete toxins and can compromise the tight junction barrier in the intestines, which leads to malabsorption. Therefore, the modulation of bacterial-mucosal cell interactions is of key importance in maintaining gut functional status. In the present report, we observed moderate necrotic lesions in different segments of the gut after C. perfringens administration (Figure 1). This finding confirmed that necrotic model consisting in C. perfringens administration in three periods preceded by coccidia challenge was successful at inducing gut inflammation, without causing bird death. Thus, it provides a good model for studying the specific interactions between diet and host response under challenge conditions. In the present study, the expression of occludin, ZO-1, GLP2, OGG1 and TFF2 genes increased in the wall of the small intestine, which indicates that C. perfringens infection in turkeys compromised intestinal barrier integrity. The expression of the above genes increased in birds fed diets with both low and high Met content, equivalent to 30% and 45% of Lys content, respectively. A review study by Awad et al. [28] indicates that C. perfringens endotoxin (CPE) increases intercellular permeability and disrupts intestinal mucosal barrier function in infected chickens. Cytotoxic CPE binds to claudin receptors and claudin-3 and claudin-4 cell monolayers (Madin-Darby Canine Kidney—MDCK) [29]. It has also been found that claudin proteins play an important role in the regulation of cell signaling. Claudin-1, -3 and -5, CLDN-16, ZO-1 and ZO-2 were expressed in the intestinal epithelium of chickens [30]. Occludin is often transported from tight junctions to cytoplasmic vesicles during the loss of intestinal barrier function [31], which can be stimulated by oxidative stress and inflammation [32]. Cani et al. [33] demonstrated that occludin expression was negatively correlated with the translocation of fluorescein isothiocyanate-dextran from the digestive system to the blood, which indicates that it plays a role in the maintenance of intestinal barrier integrity. Furuse et al. [27] also found that ZO-1 is directly associated with occludin. According to Saitoh et al. [34], CPE can bind to specific claudins to mediate the degradation of TJP and increase permeability across epithelial cells. Necrotic enteritis evokes oxidation processes, and it could be implicated in intestinal malabsorption. In this study, elevated MDA levels and decreased GPx activity in the blood suggest that C. perfringens also induced lipid oxidation in turkeys. Increased MDA concentration in the blood and other tissues, and decreased activity of antioxidant enzymes are indicative of lipid oxidation and impaired antioxidant defense mechanisms [11, 21]. According to Jankowski et al. [21], a higher inclusion rate of Met in turkey diets did not inhibit lipid oxidation during hemorrhagic enteritis. The compromised function of antioxidant defense mechanisms not only leads to lipid oxidation, but also to protein and DNA oxidation. In the current study, C. perfringens infection in turkeys also contributed to oxidative damage and epigenetic alterations leading to DNA damage, which were manifested by an increase in the levels of 8-OHdG in the wall of the small intestine and in the blood, and an increase in the percentage of methylated DNA in the blood. 8-OHdG, an oxidized guanine base adduct, is a major product of the oxidation of DNA bases by reactive oxygen species. Modified guanine can form stable base pairs with cytosine, which leads to its enzymatic methylation. The binding of methyl-binding proteins (MBP) is weakened when 8-OHdG is adjacent to 5-methylcytosine. Frequent conversion of 5-methylcytosine to 5-hydroxymethylcytosine also changes binding affinity for MBP, which leads to epigenetic modifications [35, 36].

**Representative photographs illustrating changes in different intestinal segments of turkeys challenged orally with*C. perfringens***. The typical responses of the host included: A multifocal, minimal to mild hyperemia in the duodenum (blue arrow), and advanced necrosis in connective tissue (green arrow) in the duodenum; B lumpy coating reminiscent of a pseudomembrane (yellow arrow) in the jejunum; C manifested swollen vessels on the jejunum surface (white arrow); D multifocal hyperemia and hemorrhages (red arrow) and fibrinous coating on the surface of the caeca (purple arrow).

This study demonstrated that the high Met level induced DNA methylation in the wall of the ileum, which was not observed in turkeys fed diets with low Met content. According to Young and Shalchi [37], Met is a precursor of S-adenosylmethionine, the main donor of methyl groups in a cell, which is responsible for DNA methylation, and DNA methylation protects microorganisms against the damaging effects of endonucleases and promotes the integrity of genomic DNA which is required for microbial proliferation. DNA methylation is an important physiological process, and its disruptions can lead to the methylation of genes encoding key proteins, such as antioxidant enzymes and DNA repair enzymes [38]. In this study, the activity of DNA repair enzymes (APE-1, TDG, ANPG) decreased in the wall of the small intestine and in the blood of turkeys infected with C. perfringens. In apurinic/apyrimidinic sites, APE1 is the main DNA repair enzyme in base excision repair (BER) and nucleotide excision repair (NER) pathways. In these sites, repair processes are initiated by DNA glycosylase enzymes which recognize modified bases, including OGG1 which recognizes 8-OHdG, ANPG which recognizes εA and εG, and TDG which recognizes εC. These enzymes remove the damaged base from the DNA strand at the site of damage [39]. In this experiment, TG levels in the blood decreased in infected turkeys fed diets with a 30% and 45% Met:Lys ratio. In the experiment performed by Abudabos et al. [40], C. perfringens infection in broilers did not affect GLU, TC or TG levels. According to Amad et al. [41], the infection did not lead to changes in the blood biochemistry of chickens. In our study, C. perfringens infection in turkeys administered diets with high and low Met content decreased the activity of liver enzyme ALT and UA. Numerous authors have demonstrated that viral and bacterial infections provoke hypertransaminasemia, but AST and ALT levels are quickly normalized or even decreased [42]. In infected turkeys, high-Met diets also increased TC and GLU concentrations, increased the activity of AST, SOD and CK, and decreased TP levels. These observations could be attributed to the effects of Met, rather than the infection because according to some authors, high dietary levels of Lys and Met can induce hypercholesterolemia in birds [43]. Previous studies of turkeys [21] and chickens [37] suggest that an increase in the dietary inclusion levels of Met can promote bacterial proliferation. Methionine could be a donor of methyl groups to the 5′-terminus of viral or bacterial mRNA, which promotes the rapid proliferation of pathogens [44]. Increased proliferation of C. perfringens under the influence of higher dietary Met content probably induced metabolic changes, including increased activity of AST, SOD and CK. The activity of these enzymes usually increases in response to induced oxidative stress [45]. Even though intestinal barrier integrity was compromised in young turkeys, C. perfringens infection had no effect on the growth performance of birds fed diets with high or low Met content. In many studies [46, 47], performance parameters decreased in C. perfringens–challenged chickens administered diets formulated according to NRC [23] recommendations.

Effects of dietary ratios of Arg to Lys

Recent research has demonstrated that higher levels of amino acid influence GIT development and immune system in healthy and challenged broilers [14, 48]. According to the cited authors, higher intake of readily digestible amino acids can compensate for impaired intestinal absorption in challenged birds. Arginine, the key precursor of polyamine synthesis, can stimulate the proliferation, migration and apoptosis of intestinal cells, and promote mitotic processes in intestinal crypts and villi [49]. Tan et al. [14] found that the density of the intestinal mucosa increases linearly with a rise in dietary Arg levels, which could be attributed to the indirect effect of polyamines. However, it remains unknown whether Arg directly affects the replication of goblet cells or enterocytes.

Arginine is also a precursor of nitric oxide (NO), and it inhibits the replication of Eimeria parasites in the intestinal epithelium of chickens with coccidiosis [50]. In the present study, the administration of Arg₁₁₀ diets containing 30% Met increased the expression of the OGG1 gene which conditions intestinal barrier integrity, but the above correlation was not observed in turkeys fed Arg₁₁₀ diets containing 45% Met. OGG1 is the key repair enzyme which removes 8-OHdG from cellular DNA. The results of this study confirm that these amino acids regulate gene expression and the production of molecules that are essential for healthy gut function, including polyamines and NO [51, 52]. The role of Arg in mucin production and immune function has been extensively researched [14, 16] demonstrated that high levels of l-arginine limit disruptions in intestinal barrier integrity, which decreases the mRNA expression of claudin-1 and increases the mRNA expression of occludin.

The present findings indicate that Arg₉₀ diets containing both 30% and 45% Met minimize DNA oxidation in the intestines. However, DNA oxidation and methylation was intensified in turkeys fed Arg₁₁₀ diets, in particular diets containing 45% Met. At the same time, when the dietary inclusion level of Arg was increased to 110% of Lys content, oxidative and epigenetic changes were intensified in the intestines or in the blood, which was manifested by an increase in 8-OHdG levels and in the percentage of methylated DNA, and a decrease in the levels of DNA repair enzymes. According to Gao et al. [53], higher levels of Arg in poultry diets inhibit DNA oxidation and methylation. Therefore, the observed effect could be attributed to a higher dietary inclusion rate of Met. In the present study, Arg₁₁₀ diets containing both 30% and 45% Met increased SOD activity in the blood of turkeys. Enhanced oxidation potentially mobilized the antioxidant enzyme to catalyze the dismutation of superoxide radicals in cells. Adverse changes were observed in selected blood biochemical parameters in turkeys fed Arg₁₁₀ diets with a 30% Met:Lys ratio (higher TG and ALB levels) and a 45% Met:Lys ratio (higher CK activity and lower UREA concentration). These results are surprising since according to the literature, higher dietary supplementation levels of Arg decrease the plasma concentrations of GLU, TG and TCs and can promote the treatment of metabolic syndrome disorders [54]. In the current study, Arg₉₀ diets with a 30% Met:Lys ratio had a favorable impact on liver metabolism by decreasing AST and ALT activity and increasing TP levels in the blood of turkeys. However, these diets also increased TC levels. Arg₉₀ diets with a 45% Met:Lys ratio also decreased AST activity and inhibited oxidative processes, as demonstrated by a decrease in SOD and GPx activity and albumin levels. A review study by Fouad et al. [55] revealed that adequate dietary levels of Arg minimize oxidative stress, improve lipid and protein metabolism, and boost immunity in birds. In this study, diets with graded levels of Arg and a 30% Met:Lys ratio had no effect on the growth performance of turkeys, whereas Arg₁₁₀ diets with a 45% Met:Lys ratio improved their growth rate. Adedokun et al. [56] reported higher feed conversion in challenged broiler chickens fed diets with increased concentrations of Lys, Met, threonine, isoleucine, tryptophan and valine. Jahanian and Khalifeh-Gholi [57] found that an increase in the dietary inclusion rate of Met improved FCR when the Arg content of chicken diets was increased to 110% of the level recommended by the NRC [23].

In turkeys infected with C. perfringens, fed diets with high Lys content, Arg content should be decreased to 90% Lys and Met content should be increased to 45% Lys. The above dietary amino acid ratios contribute to suppressing oxidative processes and epigenetic alterations in important molecules in the wall of the ileum and in the blood, and maintaining intestinal barrier integrity; they also exert a beneficial influence on metabolic parameters. Even though the analyzed amino acid ratios interacted with the systems responsible for the maintenance of gut integrity in the host organism, this dietary intervention probably enabled birds to cope with NE.

Acknowledgements

We thank Marzena Mikulska from University of Warmia and Mazury in Olsztyn for assistance in statistical analysis.

Abbreviations

8-OHdG: 8-hydroxydeoxyguanosine
ALP: albumin
ALT: alanine aminotransferase
APE-1: endonuclease 1
Arg: arginine
BWG: body weight gain
CK: creatine kinase
CLDN15: Claudin 15
GLP2: Glucagon-like peptide-2
GPx: glutathione peroxidase
Lys: lysine
Met: methionine
NE: necrotic enteritis
NSP: non-starch polysaccharides
OCLN: Occludin
SOD: superoxide dismutase
TC: total cholesterol
TFF2: Trefoil Factor 2
TG: triglycerides
TP: total protein
UA: uric acid
ZO-1: Zonula occludens-1

Authors’ contributions

KO performed analyzes regarding oxidative responses and drafted the manuscript. PK designed the challenge concept, performed turkey trial, performed analyzes regarding genes expression, edited the manuscript and responded to review. DM performed the turkey trial and interpreted statistical data. JJ designed the study concept, interpreted results, and edited the manuscript. All authors read and approved the final manuscript.

Authors’ information

KO; grant co-holder, PK; post-doc in the grant, DM; grant co-holder; JJ; grant supervisor.

Funding

This work was supported by the National Science Centre, Grant No. 2017/27/B/NZ9/01007.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate

The experimental procedure was approved by the Local Ethics Committee for Experiments on Animals in Olsztyn, Poland (approval no 82/2017).

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Katarzyna Ognik, Email: kasiaognik@poczta.fm.

Paweł Konieczka, Email: pawel.konieczka@uwm.edu.pl.

Dariusz Mikulski, Email: darekm@uwm.edu.pl.

Jan Jankowski, Email: janj@uwm.edu.pl.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

[CR1] 1.Wade B, Keyburn A. The true cost of necrotic enteritis. World Poult. 2015;31:16–17. [Google Scholar]

[CR2] 2.Timbermont L, Haesebrouck F, Ducatelle R, Van Immerseel F. Necrotic enteritis in broilers: an updated review on the pathogenesis. Avian Pathol. 2011;40:341–347. doi: 10.1080/03079457.2011.590967. [DOI] [PubMed] [Google Scholar]

[CR3] 3.Zhang B, Lv Z, Li Z, Wang W, Li G, Guo Y. Dietary l-arginine supplementation alleviates the intestinal injury and modulates the gut microbiota in broiler chickens challenged by Clostridium perfringens. Front Microbiol. 2018;9:1716. doi: 10.3389/fmicb.2018.01716. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR4] 4.Hardy SP, Benestad SL, Hamnes IS, Moldal T, David B, Barta JR, Reperant J-M, Kaldhusdal M. Developing an experimental necrotic enteritis model in turkeys—the impact of Clostridium perfringens, Eimeria meleagrimitis and host age on frequency of severe intestinal lesions. BMC Vet Res. 2020;16:63. doi: 10.1186/s12917-020-2270-5. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR5] 5.Papatsiros VG, Katsoulos PD, Koutoulis KC, Karatzia M, Dedousi A, Christodoulopoulos G. Alternatives to antibiotics for farm animals. CAB Rev. 2013;8:32. doi: 10.1079/PAVSNNR20138032. [DOI] [Google Scholar]

[CR6] 6.Koutoulis KC, Pappas I, Filioussis G, Athanasiou L. Pharmacokinetics and clinical assessment of amoxicillin for the control of necrotic enteritis in broiler-breeders under field conditions. Avian Biol Res. 2015;8:89–96. doi: 10.3184/175815515X14292912200460. [DOI] [Google Scholar]

[CR7] 7.Tomasello G, Tralongo P, Damiani P, Sinagra E, Di Trapani B, Zeenny MN, Hussein IH, Jurjus A, Leone A. Dismicrobism in inflammatory bowel disease and colorectal cancer: changes in response of colocytes. World J Gastroenterol. 2014;20:18121–18130. doi: 10.3748/wjg.v20.i48.18121. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR8] 8.Annett CB, Viste JR, Chirino-Trejo M, Classen HL, Middleton DM, Simko E. Necrotic enteritis: effect of barley, wheat and corn diets on proliferation of Clostridium perfringens type A. Avian Pathol. 2002;31:598–601. doi: 10.1080/0307945021000024544. [DOI] [PubMed] [Google Scholar]

[CR9] 9.Munir K, Muneer MA, Masaoud E, Tiwari A, Mahmud A, Chaudhry RM, Rashid A. Dietary arginine stimulates humoral and cell-mediated immunity in chickens vaccinated and challenged against hydropericardium syndrome virus. Poult Sci. 2009;88:1629–1638. doi: 10.3382/ps.2009-00152. [DOI] [PubMed] [Google Scholar]

[CR10] 10.Tykalowski B, Smialek M, Koncicki A, Ognik K, Zdunczyk Z, Jankowski J. The immune response of young turkeys to haemorrhagic enteritis virus infection at different levels and sources of methionine in the diet. BMC Vet Res. 2019;15:387. doi: 10.1186/s12917-019-2138-8. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR11] 11.Wang HF, Zhong X, Shi WY, Guo B. Study of malondialdehyde (MDA) content, superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities in chickens infected with avian infectious bronchitis virus. Afr J Biotechnol. 2011;10:9213–9217. doi: 10.5897/AJB11.782. [DOI] [Google Scholar]

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PERMALINK

The effect of different dietary ratios of lysine and arginine in diets with high or low methionine levels on oxidative and epigenetic DNA damage, the gene expression of tight junction proteins and selected metabolic parameters in Clostridium perfringens-challenged turkeys

Katarzyna Ognik

Paweł Konieczka

Dariusz Mikulski

Jan Jankowski

Abstract

Introduction

Materials and methods

Birds and housing

Experimental design and diets

Table 1.

Clostridium perfringens challenge

Sample collection and laboratory analysis

RNA extraction and real-time quantitative PCR

Table 2.

DNA oxidation and methylation, and metabolic parameters

Statistical analysis

Results

Experiment 1

Effects of infection

Table 3.

Table 4.

Table 5.

Effects of dietary ratios of Arg to Lys

Experiment 2

Effects of infection

Table 6.

Table 7.

Table 8.

Effects of dietary ratios of Arg to Lys

Discussion

Effects of infection

Figure 1.

Effects of dietary ratios of Arg to Lys

Acknowledgements

Abbreviations

Authors’ contributions

Authors’ information

Funding

Availability of data and materials

Ethics approval and consent to participate

Competing interests

Footnotes

Contributor Information

References

Associated Data

Data Availability Statement

ACTIONS

PERMALINK

RESOURCES

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