Research Article

Biochemical, Hematologic and Oxidative Stress Biomarkers Investigation in Infected Native Breed Calves with Foot and Mouth Disease virus Serotype A

Ramy E. El-Ansary1, Ahmed R. Sofy2, Mohamed A. M. El-Tabakh3, Ahmed F. Afify4, Mostafa El-Gaffary5, Mohamed I. Oraby6*, Mohammed A. Elkhiat6

1Department of Zoology and Entomology, Faculty of Science, Al-Azhar University, Cairo, Egypt; 2Department of Botany and Microbiology, Faculty of Science, Al-Azhar University, Cairo, Egypt; 3Department of Zoology, Faculty of Science, Al-Azhar University, Cairo, Egypt; 4Department of Virology Research, Animal Health Research Institute, Agriculture Research Center, Giza, Egypt; 5Department of Veterinary Clinical Pathology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt; 6Department of internal medicine and infectious diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.

Received | October 24, 2024; Accepted | December 02, 2024; Published | January 20, 2025

*Correspondence | Mohamed I. Oraby, Department of internal medicine and infectious diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt; Email: [email protected]

Citation | El-Ansary RE, Sofy AR, El-Tabakh MAM, Afify AF, El-Gaffary M, Oraby MI, Elkhiat MA (2025). Biochemical, hematologic, and oxidative stress biomarkers investigation in infected native breed calves with foot and mouth disease virus serotype a. Adv. Anim. Vet. Sci. 13(2): 253-261.

DOI | https://dx.doi.org/10.17582/journal.aavs/2025/13.2.253.261

ISSN (Online) | 2307-8316; ISSN (Print) | 2309-3331

Copyright: 2025 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

INTRODUCTION

Many cloven-hoofed animals are susceptible to FMD, a highly contagious transboundary viral disease that results in substantial economic losses because of decreased meat and milk production, young animals mortality, medication expenses, and limitations on the movement of animals from endemic areas (Knight-Jones and Rushton, 2013; Diab et al., 2019; Saravanan et al., 2020; Hassanein et al., 2024). Other symptoms include vesicles or blisters on the tongue, severe frothy salivation, fever, dullness, and anorexia. Some infected animals may not show any symptoms, but they still carry the virus and can infect other animals. Although it increases the risk of abortion in pregnant animals, the illness is typically not fatal in adult cattle (Rich and Winter-Nelson, 2007).

As a member of the Aphthovirus genus, FMDV is a member of the Picornaviridae family. An icosahedral capsid containing around 60 copies of the four structural viral proteins (VP1, VP2, VP3, and VP4) encloses the non-enveloped, single-stranded, positive-sense, non-segmented RNA virus known as FMDV (Domingo et al., 2002; Hassanein et al., 2024). According to Brown et al. (2022); Singanallur et al. (2022); Liu et al. (2021), FMDV is divided into six distinct immunological serotypes: A, O, SAT 1, SAT 2, SAT 3, and Asia. Within these serotypes, over 65 strains, topotypes, and genetic lineages have been identified (Domingo et al., 2002; Jamal and Belsham, 2013). Africa, Europe-South America (Euro-SA), and Asia are the three topotypes of Serotype A that are known to exist.

Clinical symptoms are often used to make the first diagnosis of the disease. In endemic areas, incomplete signs are often disregarded due to natural or vaccine protection (Kitching, 2002). The amount of specific blood metabolites signals the animal’s illness status and level of stress (Rowlands et al., 1973). However, there is a scarcity of research on the effect of experimental FMD infection on bovine blood and serum profiles, which is critical for developing ameliorative methods to alleviate the animal’s biotic stress caused by the infection. Understanding changes in the pattern of clinical, serum biochemical, and haematological parameters during the course of FMD infection is important in developing therapeutic approaches for circumventing stress and thus reducing the negative effect of the infection in the animal (Saravanan et al., 2020).

Clinical signs are frequently used to obtain an early diagnosis of the illness. In endemic locations, partial symptoms are frequently overlooked because of natural or vaccine protection (Kitching, 2002). The concentration of particular blood metabolites indicates the animal’s disease condition and amount of stress (Rowlands et al., 1973). The impact of experimental FMD infection on cow blood and serum profiles, however, has received little attention. This information is crucial for creating remedial strategies to lessen the biotic stress brought on by the infection. Additionally, it is said that the Malnad Gidda, a native breed of India, is immune to several viral diseases, including FMD; however, no thorough study has been done to substantiate this assertion (Ramesha et al., 2002; Das et al., 2012).

Unrestricted animal movement from neighboring countries, the import and transit of live animals and animal products, and the absence of quarantine facilities have all contributed to the discovery of many FMDV serotypes and topotypes in Egypt despite control efforts (Kandeil et al., 2013; Soltan et al., 2017). In order to effectively control the disease, these factors emphasized the need for quick, accurate, sensitive, and efficient diagnostic tests as well as ongoing monitoring of genetic changes in the FMD virus to update FMD vaccine seed strains with currently circulating strains (Hassan et al., 2022a).

Many viral illnesses develop as a result of oxidative stress. Oxidative stress results from an imbalance between oxidants and antioxidants (Ozcan et al., 2015), which causes cellular damage (Marreiro et al., 2017). The stimulation of lipid peroxidation activates protective antioxidant defense systems in cells, resulting in alterations in malondialdehyde (MDA) and antioxidant levels (Uzlu et al., 2016). As a result, antioxidant and oxidative biomarker (MDA) concentrations are assessed to assess oxidative stress in viral infections (Uzlu et al., 2016; Bozukluhan et al., 2021). Stress and pathogenic agents contribute to disease development by increasing free radical generation, reducing antioxidant defences and leading to oxidative stress (Talukder et al., 2015).

Lipid peroxidation indicates oxidative stress, which impairs cell structure and function. Malondialdehyde (MDA), a breakdown product of lipid peroxidation derived from polyunsaturated fatty acids, may detect cellular damage and oxidative stress (Sezer and Keskin 2014; Khoshvaghtı et al., 2014). Under oxidative stress, the MDA level rises significantly (Akyuz et al., 2021). Oxidative stress contributes to the pathophysiology of several illnesses, including foot and mouth disease. The blood MDA level in the diseased group was thought to have rised as a result of stress and cellular degeneration induced by aphthovirus oxidative damage.

Oxidative stress is a state in which the body cannot scavenge free radicals, leading to tissue damage, alterations, and unfavorable effects on the health of animals (Nath et al., 2014). Oxidative processes are linked to a wide range of diseases (Lykkesfeldt and Svendsen, 2007). Cellular level damage was attributed to this mechanism (Halliwell and Gutteridge, 1999). Nevertheless, enzymatic (like Catalase) and non-enzymatic (like copper and zinc) antioxidant mechanisms may mitigate these effects (Erkılıç, et al., 2017). Antioxidants are essential for protecting cells from the damaging effects of reactive oxygen species (ROS) (Khoshvaghti et al., 2014).

Cattle suffer from oxidative stress due to foot and mouth disease, a serious viral infectious disease with a severe clinical course. The number of white blood cells (WBCs) was found to have increased among the haematological parameters tested in infected animals. Among the biochemical markers, MDA, creatinine, and CK enzyme activity were found to have increased, whereas antioxidants, proteins, minerals, and glucose levels were reported to have decreased (Sezar et al., 2024).

To molecularly diagnose and identify the serotype implicated, this study was carried out, with a focus on estimating changes in hematological and serum biochemical markers in cattle affected by FMDV.

MATERIALS AND METHODS

Ethical Statements

This investigation was conducted under the animal ethical guidelines. It was approved by the Veterinary Medicine Cairo University Institutional Animal Care and Use Committee, Faculty of Veterinary Medicine, Cairo University, Egypt (vet cu13102024971).

Blood / Serum Sample Collection

Serum was separated by centrifugation at 3000 g for 10 minutes after 10 mL of blood samples from 25 animals were obtained by jugular venipuncture in a red vacutainer with a clot activator (BD, Franklin, USA). The serum was then maintained at 20°C until serum biochemical parameters were ascertained. A green vacutainer containing heparin as an anticoagulant and RT-PCR for FMDV detection was used to draw a 4 mL blood sample (BD, Franklin, USA).
Thorough study of the blood count. A comprehensive blood count analysis was performed using a three-chamber hematology analyzer (BC-3000 Plus, China).

Biochemical Tests

Using a real semi-automated clinical chemistry analyzer (Microlab 300–ELITech Group, Hollanda), commercial kits were used to measure blood glucose, urea, blood urea nitrogen, creatinine, total cholesterol, total proteins, albumin, aspartate transaminase (AST), triglycerides, alanine transaminase (ALT), MDA, Cat, Zn, and Cu. Every Kit was used according to the manufacturer’s instructions. Cardiac damage was measured using the creatine kinase-myocardial band (CK-MB) kit (Coral Clinical Systems, India) and the immune inhibition technique.

Statistical Analysis

The data was coded and entered using SPSS V.22, a statistical program. The Kolmogorov-Smirnov test for normality, the Shapiro-Wilk test for continuous variables, and parametric test assumptions were checked for data. Arcsine Square Root was used to standardize data on probability and percentiles for normalcy. The mean and standard deviation of the data were displayed. The experimental groups’ recorded physiological parameters were subjected to ANOVA analyses. The control group and sick cattle group had at least three replicates of the analysis (on days 1, 4, 15, and 30 after the onset of symptoms). The post-hoc analysis was assessed using Tukey pairwise comparison using MiniTab V 14, and P-values were deemed significant at <0.05. When feasible, data were visualized using R studio V 2022.02.4.

RESULTS AND DISCUSSION

Clinical Examination of FMDV outbreaks examining the animals’ oral cavities revealed sores, ruptured vesicles, ulcerations on the tongue and gum, destruction on the upper and lower pad region, and wear away on the interdigital space. During the outbreak investigation and sample collection, it was discovered that early-stage FMD-affected animals showed fever, inappetence to anorexia, salivation, and frothiness from the mouth. These creatures were noted to be lame, and vesicles were seen in the gaps between their fingers. Animals with late-stage infections had a reduction in fever with symptoms that were comparable to those in the early stages. On day 30, the animals’ clinical symptoms subsided, they resumed their regular diet, and the wounds on their limbs and buccal regions healed (Figure 1). FMD-affected cattle were falling behind healthy ones regarding nutrition and milk output.

 

Results of hematology are shown in (Table 1 and Figure 2). Hemograms of FMD-infected cattle compared to control animals revealed non-significant decreases in Hb%, RBCs count, and PCV% during the early stages of infection on days 1, 4, and 15, as opposed to day 30 during the late stages of infection or following recovery, when Hb%, RBCs count, and PCV% returned to normal range. In contrast to control animals, WBCs and platelet counts did not significantly rise during infection.

 

Table 1: Biochemical, Hematologic and Oxidative stress biomarkers (mean ± SD values) in infected Native breed Calves with FMD virus Serotype A compared with the normal control through the study period.

	Control	Day 1	Day 4	Day 15	Day 30
Hb %	9.66 ± 0.32abc	8.53 ± 0.99abc	8.18 ± 1.01bc	8.19 ± 0.73c	9.25 ± 0.91a
RBCs (106 / mm3)	5.28 ± 0.23a	5.03 ± 0.75a	4.87 ± 0.71a	4.88 ± 0.61a	5.42 ± 0.54a
PCV %	27.33 ± 1.24ab	27.06 ± 3.56ab	25.7 ± 3.76ab	23.7 ± 5.74b	29.31 ± 3.63a
WBCs (103/mm3)	6.5 ± 0.48a	6.55 ± 1.66a	5.66 ± 1.51a	6.13 ± 1.36a	6.96 ± 1.35a
Platelets (cells/mm3)	200.66 ± 11.02a	264.15 ± 90.45a	251.46 ± 105.77a	272.84 ± 109.86a	275.76 ± 69.01a
Glucose mg/dl	61.66 ± 4.1a	70.7 ± 18.34a	65.83 ± 19.45a	58.74 ± 15.58a	56.29 ± 15.23a
Cholesterol mg/dl	86.41 ± 7.36a	100.34 ± 23.23a	97.81 ± 33.42a	85.03 ± 13.32a	87.47 ± 8.45a
ALT U/l	31.33 ± 2.86abc	30.07 ± 2.3a	27.61 ± 5.18abc	24 ± 3.41bc	24.3 ± 4.51c
AST U/l	107.66 ± 15.1ab	130.15 ± 30.18a	133.84 ± 32.99a	81.69 ± 17.07bc	57.38 ± 12.67c
Urea mg/dl	35.46 ± 1.16a	23.12 ± 4.38b	22.63 ± 5.31b	16.27 ± 4.42c	10.81 ± 2.25d
BUN mg/dl	16.63 ± 0.57a	10.79 ± 2.04b	10.57 ± 2.49b	7.62 ± 2.04c	5.01 ± 1.03d
Creatinine mg/dl	1.02 ± 0.07ab	1.07 ± 0.19b	1.14 ± 0.14ab	1.27 ± 0.14a	1.3 ± 0.12a
T.G. mg/dl	83.66 ± 5.43a	47.74 ± 27.08a	50.82 ± 25.71a	23 ± 10.7b	19.4 ± 6.81b
CK-MB	59.33 ± 4.64bc	98.76 ± 26.79a	89.53 ± 23.65a	70.15 ± 14.05bc	52.92 ± 16.83c
TP (g/dl)	5.56±0.72a	5.35±0.352b	5.13±0.263b	5.36±0.72a	6.08±0.576a
Albumin (g/dl)	2.74±0.29a	2.64±0.31b	2.66±0.297b	2.70±0.29a	3.26±0.360a
Globulin (g/dl)	2.78±0.45a	2.69±0.351b	2.44±0.362b	2.66±0.45b	2.83±0.293a
MDA (nmol/ml)	1.19±0.601e	9.48±3.79a	4.01±0.874b	3.21±0.634c	1.51±0.77d
TAC	0.61±0.326a	0.32±0.111b	0.39±0.05b	0.42±0.15c	0.48±0.055c
Catalase (U/l)	363.12±101.04a	374.80±81.3a	366.34±135.78a	396.74±105.78a	463.73±151.74a
Zn (PPM)	122.55±50.6b	92.19±20.08d	82.80±22e	102.77±22c	140.71±38.4a
Cu (PPM)	81.68±24.6bc	81.43±26.9bc	66.29±11.3c	86.39±11.3b	101.28±14.1a

 

*Means in raw that do not share a letter are significantly different.

 

When comparing the control group to FMD-infected cattle, glucose (mg/d) and cholesterol (mg/dl) did not differ statistically (P>0.05); in fact, the aforementioned parameters did not change substantially (P>0.05) even during the disease (Table 1 and Figure 2).

Day 1 differed substantially (P<0.05) from days 15 and 30, however, the measured levels of ALT (U/l) did not significantly (P>0.05) separate ill and control animals. Conversely, AST (U/l) displays identical results, with the exception that day 30 exhibits a substantial change (P<0.05) in the control group. Day 1 and Day 4 did not substantially differ from each other (P>0.05), but Day 15 and Day 30 did differ statistically (P<0.05) from Day 1 and Day 4 and each other as well. Urea (mg/dl) showed a significant decrease in ill cattle compared to the control (P<0.05). The result for BUN (mg/dl) is the same as that of Urea (mg/dl). Day 1 and Day 4 creatinine (mg/dl) changed (P<0.05) compared to Day 15 and 30, however there was no significant difference (P>0.05) between ill and control cattle. Similar results were noted for T.G. (mg/dl); however, there was a substantial (P<0.05) variation in the control group on days 15 and 30 as well (Table 1 and Figure 2).

The control group’s recorded values of CK-MB revealed that there was no significant relationship (P>0.05) between the records observed on days 15 and 30, but the aforementioned periods differed (P<0.05) with the calculations made on days 1 and 4.

Serum biochemical values analysis for the proteinogram was displayed in (Table 1 and Figure 2). When compared to control, healthy, and recovered cattle on day 30, there was a decrease in total proteins, albumin, and globulin on days 1, 4, and 15.

Changes in the level of oxidants and antioxidants were noted in (Table 1 and Figure 2). Day 1 had a notable increase in MDA, which subsequently steadily dropped between Days 4 and 15, but not at the same rate. Cattle had MDA levels comparable to the control group on day thirty. When compared to the control group, TAC significantly decreased on days 1 and 4, then increased again on days 15 and 30. When compared to the control group, catalase activity did not statistically differ on any of the infection days. Day-1, Day-4, and Day-15 zinc levels significantly decreased in comparison to Day-30 and the control group. Cu level, on the other hand, follows a different trend; it only significantly decreases on day 4 in comparison to the previous infection days and the control group.

 

All cattle with cloven hooves are known to be susceptible to FMD, a contagious viral illness that can result in enormous financial losses for both the livestock community as a whole and individual animal (Knight-Jones and Rushton, 2013).

Examination of hematologic parameters reveals a decrease in erythrogram values in diseased animals compared with the control group and these values returned to normal levels in recovered animals after 30 days of infection. Similar findings were recorded in other reports (Mahmoud and Neamat-Allah, 2016; Nasr El-Deen et al., 2017) however, Nath et al., (2014) reported a change in RBCs only. In the study performed by Kamal and Hassan, (2017), they reported degeneration and necrosis in the kidney cortex and medulla in FMD-affected animals; erythropoietin a hormone produced by the kidney and has a great impact on erythropoiesis might be affected, and hence the reduction in erythrogram.

There are no known serum biochemical benchmarks for cattle that are naturally infected with the FMD virus. According to the current study’s findings, cattle with clinical FMD had considerably greater serum activity of AST, a biomarker of muscle degeneration and necrosis, than calves in good condition.

According to our findings, cattle with acute FMD infection had hyperglycemia. In animals suffering from systemic diseases brought on by stress, hyperglycemia is frequently observed (Paalberg et al., 2002; Gokce et al., 2004). The demise of pancreatic ß-cell islets of Langerhans as a result of FMD viral infection may also be the cause of the elevated glucose level (Sutmoller et al., 2003).

When the FMD virus infects cattle, it can cause hyperglycemia and diabetes through two distinct mechanisms: either the virus directly destroys the pancreatic ß-cells, or the immune system mounts an attack against the virus (Clark, 2003). According to Kamal and Abo Heakal (2018), the FMD virus negatively impacts pancreatic cells, as evidenced by a drop in serum insulin levels and amylase activity that leads to hyperglycemia. Additionally, there is a discernible rise in the clinically-infected cattle’s glucose level, which is consistent with the findings of Mousa and Galal (2013); Nasr El-Deen et al. (2017).

In contrast to (Krupakaran et al., 2009; Sezer et al., 2024), who noted a marked decrease in blood glucose levels in cows infected with FMD. Hyperglycemia is probably brought on by low serum insulin levels as a result of the FMD virus replicating in the pancreas, which destroys the cells that produce insulin (the pancreatic beta cells). Animal breed variations could be the cause of this discrepancy.

According to the results of this study, which are consistent with those of (Nath et al., 2014; Nasr El-Deen et al., 2017), AST, ALT, BUN, and creatinine levels significantly increased in calves with clinical FMD infection, according to the serum biochemical study. This might be explained by the degenerative alterations brought on by the FMD virus’s detrimental effects on the kidney and liver. Furthermore, the higher BUN levels in FMD-infected cattle compared to the control group of animals are probably due to the negative effects of the FMD virus on the renal cells (Constable et al., 2017). Ghanem and Abdel-Hamid (2010), on the other hand, discovered no appreciable differences in AST and ALT levels among clinically infected cattle with FMD.

One of the final products of muscles metabolism is creatinine, a poisonous chemical. Protein catabolism from viral diseases, hunger, and high fever causes serum creatinine levels to rise. It has been noted that when the body loses fluids, blood pressure drops. Thus, renal functions are compromised and prerenal azotemia arises as a result of the glomerular filtration rate decline. Consequently, serum creatinine levels rise (Sezer and Gokce, 2021; Sezar et al., 2024). Serum creatinine levels rise in foot and mouth disease based on injury to soft tissues such the kidney, liver, and heart (Salim et al., 2019). Because the foot and mouth disease-infected animals may have developed renal impairment, the study’s blood creatinine levels were higher than those of the control group.

The observed variation in serum levels of total protein, albumin, and globulin in clinically infected cattle could potentially be attributed to variations in FMD virus serotypes. This hypoproteinemia could be caused by hypoalbuminemia and hyperglobulinemia, which are brought on by decreased feed intake due to appetite loss, pain in the buccal cavity from lesions in the mouth, and a decrease in liver synthesis due to liver damage, maldigestion and protein absorption from gastrointestinal tract lesions, and plasma loss from ulcer exudation (Nasr El-Deen, 2013). All tissues, except bone, contain AST; liver and skeletal muscle have the highest concentrations. Conversely, serum AST activity in muscle-injured cows increases gradually and has a longer half-life than CK (Weber et al., 2019).

Additionally, AST is found in high concentrations in hepatocytes, and an increase in AST in the serum is frequently regarded as a sensitive indicator of hepatocyte damage, even in cases where the damage is subclinical (Hoffmann and Solter, 2008). The current study’s findings demonstrated that skeletal and cardiac muscles in cattle experience varying degrees of injury throughout FMD. While it is common to find myocardial degeneration and necrosis in suckling calves, lambs, and pigs, along with the corresponding mortality, the mechanism of muscular damage caused by FMDV and Myo tropism remains unclear.

Moreover, there was a significant difference between the serum CK-MB activity and that of normal animals in cattle with FMD. This biomarker indicates myocardial damage. One well-known aspect of FMD is myocarditis, which has a high mortality rate in newborn calves and lambs (Constable et al., 2017). According to Ryan et al. (2008), the FMD virus may spread to secondary sites, such as the cardiac muscle of nursing ruminants, following its initial replication in the oropharynx. Viral replication in this tissue is thought to cause cardiac degeneration and necrosis. As markers of myocarditis, CK-MB is released into the bloodstream after cardiac cell damage and its serum levels rise (Aslani et al., 2013; Sobhy et al., 2018). Buffaloes infected with the FMD virus, serotype O, have been shown to have elevated serum CK-MB and AST activities (EL-Deen et al., 2017).

When compared to control data, protein profile levels revealed changes in both early and late diseased animals, with a return to nearly normal levels in the recovered group. According to Rousselle et al. (1997), protein catabolism as a consequence of viral infection and fever may be involved; Gokce et al. (2004) suggested that starvation, liver damage, and protein-losing enteropathy could be the causes of hyperproteinemia and hypoalbuminemia. Protein alterations were also connected to modifications in B-cell functions in the pancreas during clinical illness (Gattani et al., 2011). Furthermore, globulin reduction may be linked to elevated cortisol released during the illness (Mahmoud and Neamat-Allah, 2016).

The current investigation showed that FMD in cattle raises end products of lipid peroxidation, as evidenced by the higher concentration of MDA in the serum of affected animals than of healthy ones. Polyunsaturated lipids are oxidatively damaged by free radicals, and MDA is one of the biomarkers of lipid peroxidation that is thought to be a good indicator of oxidative stress (Singh et al., 2014). Cattle with FMD showed signs of oxidative stress as well as mild myocardial and pancreatic lesions (Soltani et al., 2020). Cattle with FMD infection exhibited a marked increase in MDA levels. The MDA activity of the animals in the recovered stage was marginally similar to that of the control group. One of the key indicators of the cellular process of oxidative stress is the peroxidation of lipids, which produces a variety of compounds, including MDA (Khoshvaghte et al., 2014). Furthermore, according to Zelnikova et al. (2008), the infection itself may release reactive oxygen species (ROS), which can lead to cellular damage (Halliwell et al., 1992). TAC significantly decreased in diseased animals when compared to the control group, in line with the rise in MDA. An increase in ROS causes the body to produce more antioxidants, which are then depleted in an attempt to counteract the overproduction of lipid peroxidation byproducts, which may be related (Nasr El-Deen et al., 2017). TAC provides information about the body’s antioxidant status (Ghiselli et al., 2000). Under infection, a decline is anticipated (Mousa and Galal, 2013). Catalase activity did not differ statistically significantly from the control group in either the diseased or recovered animals, in contrast to MDA and TAC. One antioxidant enzyme, catalase, was suggested to be affected by FMD (Kirkman and Gaetani, 2007). Catalase is important because it helps to destroy H2O2, protecting somatic cells, especially those at inflammatory sites, from the harmful effects of H2O2. (Agar et al., 1986).

When compared to the control group, zinc and copper activities in FMD-infected cattle were lower, and in recovered animals, these activities returned to normal. As components of the antioxidant apparatus, zinc, and copper prevent damage caused by free radicals (Nazifi et al., 2011). Zinc can counteract the redox active products, reducing cellular damage; however, the exact mechanism by which zinc exerts its antioxidant effects remains unclear (Powell, 2000). Additionally, SOD activity decreased in the study conducted by Khoshvaghte et al. (2014), which was linked to FMD infection; copper and zinc are essential for the formation of superoxide dismutase, an antioxidant enzyme that is essential for protecting cells from ROS effects and helping to detoxify “superoxide radicals” (Gonzales et al., 1984; Valentine et al., 2005).

CONCLUSIONS AND RECOMMENDATIONS

While catalase is only slightly altered by FMD, protein and the oxidant-antioxidant system appear to be considerably affected. This impact changes with the stage of the disease. Prevention of foot and mouth disease (FMD) has been declared a global priority by the Food and Agricultural Organization of the United Nations (FAO) and the World Organization for Animal Health (OIE). Effective control tactics, however, need an understanding of FMD distribution and epidemiology, which is why the implementation of simple point-of-care test (POCT) devices for active FMDV detection, monitoring, and characterization is currently an ongoing research endeavor. Affordable livestock imports from Sudan and other sub-Saharan countries are essential to Egypt’s ability to meet the public’s demand for red meat and offset the country’s growing meat shortage caused by the country’s growing population and shrinking meat production sector as a result of the ongoing economic crisis. This need creates a warning against the further spread of animal illnesses, particularly FMDV. Despite the government’s best attempts to avoid it, Egypt is very vulnerable to continued disease introduction because of a lack of quarantining facilities, border-based slaughterhouses, and a breakdown in security forces. Such terrible circumstances might affect the efficacy of disease control efforts and make it harder for the already poor local market to flourish.

ACKNOWLEDGMENTS

We are grateful to the private farms of calves and different owners for allowing us to work on the calves belonging to them and collect samples.

NOVELTY STATEMENTS

This paper presents a comprehensive analysis of hematology, biochemistry and oxidants-antioxidants patterns in cattle during infection with Foot-and-mouth Disease Virus (FMDV) serotype A during FMD outbreaks in 2018 and 2023 in Giza Governorate, Egypt. The study investigated the effect of FMDV infection on several blood parameters, including hemogram (HB%, PCV%, RBCs, WBC and platelets count), serum biochemical parameters (glucose, cholesterol, ALT, AST, urea, BUN, creatinine, triglyceride, CK-MB, total proteins, albumin and globulin), oxidative marker (MDA), enzymatic antioxidant (catalase), TAC and trace elements (Zn and Cu).

AUTHOR’S CONTRIBUTIONS

All authors contributed to the study’s conception, and design. Data collection, clinical examination and experimental study were performed by REE, MAME, AFA and MIO. All biochemical analysis and data analysis were performed by ME and MAE. ARS and ME drafted and corrected the manuscript; REE, AFA, MAE and MIO revised the manuscript. All authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Conflict of Interest

The authors declare no conflict of interest.

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