Research Article

Effect of Trypanosoma evansi on the Efficiency of Pasteurella multocida Vaccination

Safaa M. Barghash1*, Amani A. Hafez2

1Parasitology Unit, Animal and Poultry Health Department, Animal Production and Poultry Division, Desert Research Center, 1-Mathaf El-Mataria St. El-Naam, P.O. Box 11753, Cairo, Egypt; 2Infectious Diseases Unit, Animal and Poultry Health Department, Animal Production and Poultry Division, Desert Research Center, El-Naam, Egypt.

Received | October 03, 2021; Accepted | October 25, 2021; Published | March 24, 2022

*Correspondence | Safaa M. Barghash, Associate Professor of Parasitology, Parasitology Unit, Animal and Poultry Health Department, Animal Production and Poultry Division, Desert Research Center, 1-Mathaf El-Mataria St. El-Naam, P.O. Box 11753, Cairo, Egypt; Email: barghash_7@yahoo.com

Citation | Barghash SM, Hafez AA (2022). Effect of Trypanosoma evansi on the efficiency of Pasteurella Multocida vaccination. Adv. Anim. Vet. Sci. 10(4):911-918.

DOI | https://dx.doi.org/10.17582/journal.aavs/2022/10.4.911.918

ISSN (Online) | 2307-8316

Copyright: 2022 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

Trypanosoma evansi is the most ubiquitous protozoan parasite with a wide geographical distribution (Juyal et al., 2005; Gillingwater et al., 2007). It is highly pathogenic with a high prevalence among several domestic animals and wild mammals and rarely in humans (Hoare, 1972; Joshi et al., 2005), causing a variety of types of pathogenicity (Lun et al., 1992). Respiratory tract diseases included hemorrhagic septicemia, are among the emerging health hazards to domestic animals worldwide and are incurring a considerable loss of life and production (Mochabo et al., 2006; Intisar et al., 2009). Pasteurella multocida is a Gram-negative bacillus in the pasteurellaceae family considered a common inhabitant of the upper respiratory tract, which may cause disorders in association with other microorganisms (Wilson and Ho, 2013). Pasteurellosis due to P. multocida type A is an acute fatal respiratory disease in animals that suffer from malnutrition, gastrointestinal parasitism, and exposure to cold (Abubakar et al., 2010). It is associated with hemorrhagic septicemia in camels and is known as Pneumonic Head (Kebede and Gelaye, 2010).

Pathogenic trypanosomes induce generalized immunosuppression of humoral antibodies and T-cell mediated immune responses (Stijlemans et al., 2017; Magez et al., 2020). As a result, in the long term, the host immune responses fail and succumb to either the overwhelming parasite load or to secondary infection, consequently leading to the occurrence of trypanosome-induced immunopathology (Eyob and Matios, 2013; Onyilagha and Uzonna, 2019). Several studies undertaken to investigate the influence of T. evansi infection on production in livestock suggested that the capacity to mount the immune response against Theileria, Anaplasma and Babesia may be immunosuppressed in T. evansi infected camel. It demonstrated that T. evansi infection lowers the immune responsiveness of camels to concurrent immunizations (Holland et al., 2003; El-Naga and Barghash, 2016). Also, T. evansi infection might interfere with the protective immunity development upon heterologous vaccinations causing poor protection of Pasteurella-vaccinated buffaloes in T. evansi-endemic areas of Vietnam (Holland et al., 2001). The generation of suppressor T-cells and macrophages altered antigen handling and presentation are mechanisms involved in trypanosome-mediated immunosuppression (Sileghem and Flynn, 1994). Phospholipases, neuraminidases, and proteases are trypanosome enzymes involved in membrane fluidity and causes cellular damage (Fung et al., 2007).

Likewise, experimental infections in buffalo and pigs have shown reduced cellular, in addition to humoral responses after vaccination against classical swine fever and P. multocida in T. evansi infected animals compared to uninfected animals (Holland et al., 2001, 2003). It indicated by a lost capacity to mount humoral and cell-mediated immune responses against heterologous antigens in cattle and buffaloes (Desquesnes et al., 2013). It would be responsible for the failure of the vaccination campaigns against foot and mouth disease (FMD) and hemorrhagic septicemia (Singla et al., 2010, 2012; Çokçalışkan et al., 2019). It also affects immune responses in sheep by delaying and depressing the number of lymphoblasts induced by P. haemolytica vaccine administration (Onah et al., 1997), as well as pigs by interfering with their immune response to the classical swine fever (CSF) vaccine (Holland et al., 2003). In Egypt, no vaccines are available against P. multocida in camels, but one commercial vaccine (A: Pneumobac® vaccine), is used for sheep and cattle vaccination. The present study aimed to investigate if T. evansi induced immunosuppression in experimental rats may interfere with the development of immunity after vaccination against P. multocida infection and confirmed the result with the histopathology of the lung. Also, to evaluate and compare the protective efficacies of P. multocida vaccines, the formalin-killed whole-cell antigen (FKA) prepared from local P. multocida strain isolated from camel, and the commercial vaccine (Pneumo-bac®, VSVRI).

MATERIALS AND METHODS

Ethical approval

The current experiment was conducted in compliance with internationally accepted principles of the European Directive 2010/63/EU for laboratory animal use, the Declaration of Helsinki (1964), and the National Institutes of Health guide (NIH Publications No. 8023 revised 1978). Also, it was following International Guiding for Biomedical Research Involving Animals, 2012. 

T. evansi strain

It was obtained from a naturally infected camel at Ras-Sudr (South-Sinai, Egypt), and maintained in the laboratory by the continuous passage in white Swiss mice, then purified, sequenced, and BLASTn with the existing sequence of T. evansi in the GenBank database and identified with an accession number of MZ198121. Parasitemia level was calculated daily until giving parasitemia of approximately 105 Trypanosoma/ml, according to Hoare (1972).

Bacterial strain

P. multocida strain was isolated from a pneumonic lung obtained from a freshly slaughtered camel from South-East Egypt, according to Jakeen et al. (2016). It is identified and referenced in the GenBank database under the accession number MW925053. 

Vaccines

Two vaccines against P. multocida are evaluated in the present study; one commercial for sheep and goats (Pneumobac, VSVRI) (A) purchased from Veterinary Serum and Vaccine Research Institute (Abbasia, Cairo, Egypt). Another one is formalin-killed Vaccine (B) from P. multocida local strain obtained from camel and prepared according to Ruzauskas (2005) and Roetzera et al. (2017).

Bacterial infection challenge

P. multocida was grown on dextrose starch agar plates overnight at 37°C. The cells were harvested in 0.01 M phosphate-buffered saline (PBS), centrifuged, washed twice in PBS, and diluted to a final concentration of 3.6 × 1010/ml, according to Ahmed et al. (2016).

Experimental animals and design

Eighty male Swiss Albino Wister rats weighing 200 g from Serum and Vaccine Research Institute, Abbasia, Cairo, Egypt, were kept in well-ventilated plastic cages. They were exposed to 12 hours light and dark cycles, watered and fed with pellets and fresh vegetables throughout the experimental period. The animals were allowed 10-days of acclimatization before the experiment. They were classified into eight groups of ten rats per cage and subjected to treatments, as illustrated in detail in Table 1. All rats were observed daily for signs and symptoms. 

Biological analysis

Blood samples were collected after 1st immunization for haematological examination at 0, 15, 30, 45, 60, 75, and 90 days, and sera were frozen at –20 °C until used. The haematological investigation and biochemical analyses: For glucose, bilirubin, uric acid, creatinine, total protein, albumin, liver enzyme alanine transferase (ALT), aspartate transferase (AST), and alkaline phosphatase (ALP) were estimated following standard methods, using commercial test kits (Spectrum, Egypt). Tissue specimens from lungs were fixed in 10% neutral buffer formalin solution. After complete fixation, they were dehydrated in ethyl alcohol, embedded in paraffin, sectioned at 5μm thicknesses, stained with Hematoxylin-Eosin stain for general histopathological examination, according to Bancroft and Stevens (1966).

Vaccine efficiency

The antibody productions were evaluated using optical density as an indicator for the efficiency of the tested vaccines against P. multocida to generate an immune response. Sera samples were assayed for antibodies against P. multocida by enzyme-linked immune-sorbent assay (ELISA). The plates were read at 405 nm spectrophotometrically using an ELISA reader (BioTek ELX800, with software Gen52.00).

Cytokine determination

ELISA was used to determine IL6, IL10, IL12, TNF-α, and IFN-γ titers at 0, 15, 30, 45, 60, 75, and 90 days in the sera of the immunized rats. The levels of tumour necrosis factor (TNF-α) were quantified by sandwich ELISA, with Ray BroR Rat Kit TNF-α (KOMA BIOTECH INC). IBL Rat ELISA set IL6, IL10, IL12, and Interferon-Gamma (IFN-γ) (Immunological Laboratories Inc., Meme Minneapolis, Minnesota, USA), following manufacturer instructions.

Data analysis

The absorbance value of ELISA for evaluation of antibody levels and detection of cytokines were statistically analyzed for difference among groups by performing ANOVA. A P-value < 0.05 was considered statistically significant.

RESULTS AND DISCUSSION

Clinical observation

In the present study, no death in (N) rats, contrary to rats in (T) that died on the third week and after 36 hours in (P). On the other hand, rats in (TP) gave clues of dullness after 24 hours, and three rats died then all rats after 48 hours. Concerning groups (AP, BP); no death but after challenge in group AP (five rats died), and three died from group BP. In the same experiment, rats in groups (TPA, TPB) were regularly examined every hour for the appearance of symptoms after the challenge. After 24 hours, the signs of dullness developed compared to the healthy ones, followed

 

Table 1: The status of the experimental groups before and after vaccination.

Group	Code	Status
G1	N	Injected subcutaneously (SC) with 2 mL of sterile PBS and kept as -Ve group.
G2	T	Infected intraperitoneally (IP) with 0.1 mL of blood from infected mice containing 3 x 105 trypanosomes (+Ve T. evansi).
G3	P	IP injected with P. multocida 0.5 mL of 3.6 × 1010 bacterial cells/dose (+Ve P. multocida).
G4	TP	IP route infected with P. multocida of approximately 3.6 × 1010 bacterial cells/dose at the same time 100 µl infected blood with T. evansi/ rat.
G5	AP	Vaccinated (S/C) with two doses of commercial vaccine A, After three weeks booster dose was administered then challenge (I/P) with live P. multocida specific strain at 1×10-3dilution.
G6	BP	Vaccinated (S/C) with two doses of vaccine B, adjuvant with 0.5% aluminium potassium sulfate prepared from a local strain isolated from camel against P. multocida at 4 × 109 bacterial cells/ dose followed by a booster dose which was given three weeks after the first one, then challenge (I/P) with live P. multocida specific strain at 1×10-3dilution.
G7	TPA	Contained infected rats with 0.1 mL of 3x105 T. evansi, then vaccinated (S/C) with two doses of vaccine A; the booster dose of commercial vaccine was three weeks after the first dose, then challenge with 0.5 ml P. multocida at 4 ×109 bacterial cells/ dose.
G8	TPB	Infected rats with 0.1 mL of 3x 105 T. evansi were vaccinated (S/C) with two doses of vaccine B, followed by the booster dose at three weeks after the first dose, then challenge with 0.5 ml P. multocida at 4 × 109 bacterial cells/ dose.

 

by the death of all rats after 72 hours. Dead rats had gross lesions and severed congestion with an abscess in all internal organs.

The effect of T. evansi on rats inoculated with single P. multocida and with that vaccinated against pasteurellosis was studied. Haematological analysis and clinic-biochemical results of the infected and treated rats revealed a significant difference (p≤0.05) between the groups, harboured T. evansi infection and those only vaccinated and challenged with P. multocida groups until the end of the experimental period (Figure 1). Whereas, T. evansi delayed and depressed the increases in HB and RBCs output in the single infected group with T. evansi (T), mixed infections (TP), and in vaccinated groups (TPA, TPB) in contrary to total WBCs levels that elevated in these groups. In the non-infected group (N), the total cellular output peaked at more than two times the T. evansi infection values after primary infection but smaller after injection with P. multocida. 

 

 

On the other hand, the output of biochemical tests revealed significant differences between groups with and without trypanosomosis. It peaked at vaccinated groups with T. evansi (TPA, TPB) compared to the pre-vaccination values without T. evansi (AP, BP) and more than a single infection with T. evansi (T). It was three times more in single T. evansi and 5-30 times in P. multocida vaccinated one (P). In response to the infection with T. evansi, the levels of Urea, Creatinine, ALT, AST, ALP, and T. Protein showed sharply elevation in T. evansi infected groups (T), (TP), (TPA), and (TPB) compared to P. multocida and vaccinated groups (P, AP, and BP). 

Evaluation of the two vaccines using ELISA

HS-specific antibody responses

The effects of T. evansi infection on the antibody titers against the two vaccines are illustrated in Figure 2. Antibodies following primary vaccination with a single B-vaccine were detected as early as day 7 (0.312±0.00). After the first week, a higher titer in the BP group (0.758±0.006) than AP group (0.527±0.014), and very low titers at TPB group (0.307±0.004) and TPA group (0.359±0.008) were patent. The highest antibody titers after 21 days reached 0.861±0.009 was at BP group than 0.598±0.033 at AP group, whereas the lowest titers were recorded at (0.290±0.023) and (0.355±0.010) of TPB and TPA groups, respectively.

 

Protective efficacy of vaccines

The results of the protective efficacy of vaccines were evaluated in rats after a challenge with P. multocida specific strain. Animals were challenged on day 28 (2 weeks after second and final immunization) with P. multocida strain at a dose of 1.5×107 CFU/mL (IP) and observed for 14 days post-challenge. The results showed that the mortality rate in T. evansi plus A-vaccine (TPA) and T. evansi plus B-vaccine (TPB) (100%) was higher than that in BP which vaccinated only with two doses of B-vaccine (30%) and AP which vaccinated only with two doses of A-vaccine (50%) in an inactivated oil adjutant polyvalent Pasteurella vaccine.

Changes in serum cytokines titres

To investigate the cellular immune response of different immunogens: Th1 cytokines (IL12, IFN-γ, TNF-α) and Th2 cytokines (IL6 and IL10) levels were determined in the eight groups (Figure 3). Also, to correlate the clinical findings with the immunological response observed during vaccination against P. multocida in T. evansi infected rats. Besides, to identify potential immunological pathogenesis markers that can stimulate antibody production circulating in the present study. The values of TNF-α and IL6 were consistently higher in all groups than in the negative control group and, no differences between commercial and local vaccinated groups. IL12 level in the B group was extremely statistically significantly higher than that in other immunized and control groups (P=0.0001). The present results also showed that sera produced higher levels of TNF-α, IL12, IFN-γ in all groups (except A, B). There is a correlation with no difference between TNF-α, IL12, IFN-γ levels, and IL6 levels that belong to Th2 cytokines, with IL10, which behaved the opposite. However, IL10 produced with high levels only in vaccinated groups than lower levels in other groups.

Histopathological examination

The changes were seen microscopically in the lungs and were consistent with trypanosome infection. The results of the histopathological abnormalities in the lungs are shown in Figure 4. It was more severe and evident in vaccinated groups with trypanosome infection than others. All groups were associated with no weight loss in rats compared to the T. evansi infected groups. The lung of G2 (T) showed peribronchitis with peribronchial mononuclear cell infiltrations (arrowhead) and peribronchial congested blood vessel (arrow) (H and E X 200). Whereas in G3 (P), the lung shows broncho interstitial pneumonia representing by bronchitis (arrowhead) and severe interstitial inflammatory reaction, congestion and leucocytic cell infiltrations (H and E X 200). Mixed infections in G4 (PT) causes change vasculitis representing by congestion (arrow) and thick wall muscle layer (arrowhead) (H and E X 200). Sections of lungs in vaccinated groups G5 (AP) and G6 (BP) showed less diffuse interstitial pneumonia with marked interstitial thickening (arrowhead) and mononuclear cells infiltration (arrow) (H and E X 400). In contrast, lungs in infected and vaccinated groups: G7 (TPA) and G8 (TPB) show interstitial pneumonia representing by severe interstitial inflammatory reaction; congestion, oedema (arrowhead), alveolar haemorrhage, and leucocytic cell infiltrations (arrow) (H and E X 100).

 

Trypanosomosis is a disease affecting the immune system of the host animal (Singla and Juyal, 1992; Lutje and Mertens, 1995). Although the immune system is designed to protect a host from pathogens, it can sometimes be overwhelmed, respond inappropriately, or result in immune-mediated disease with clinical signs or succumbs to either the overwhelming parasite load or secondary infection (Stijlemans et al., 2007; Gupta et al., 2009). T. evansi is occasionally accompanied by P. multocida when animals are weakened due to stress caused by a parasite, viral and bacterial infection, or change in climatic conditions (Kebede and Gelaye, 2010; Singla et al., 2015; ElNaga and Barghash, 2016). T. evansi as purely extracellular parasites survives, multiply, and differentiates in extracellular fluids of the mammalian host, including the aggressive vascular environment. Thus, these parasites are permanently confronted with the multiple components of the host immune system ranging from innate to adaptive immune defences (Magez et al., 2020).

 

To determine whether T. evansi induces immunosuppression or may induce immunosuppression, the present investigation was intended to characterize the clinical phases of trypanosomosis in experimentally infected rats, with the difference in the regulation of cytokine expression. The diagnostic potential of IFN-γ, TNF-α, IL12, IL6, and IL10 as biomarkers of the clinical phase of infections compared to parasitological and biochemical levels was studied. Analysis of the results showed an imbalanced immune response in the eight groups, suggesting that an uncontrolled immune response is associated with the present T. evansi. In some helminthic infections (Finkelman et al., 1991; Lange et al., 1994), the Th1 (produce IL12, IFN-γ) and Th2 (express IL6, IL10) cytokine secretion patterns down-regulate each other (Pearce et al., 1991). But the co-expression of IFN-γ, TNF-α, IL12, IL6 at high levels in contrary to IL10 levels in the present study suggests that the immune response may be due to a complex mixture of antigens in the blood of rats which probably contain distinct epitopes for the two pathogens as reported by McManus and Bryant (1995). Besides, secondary infections cause more severe complications. But in the present study, the immunosuppressive cytokine, IL10, is overexpressed. It inhibited the production of proinflammatory cytokines (IL6 and TNF-α) as reported by Kirchberger et al. (2007). IL6 is produced by antigen-presenting cells such as macrophages, dendritic cells, and B cells. Also, it is produced by non-hematopoietic cells as fibroblasts in response to external stimuli such as TNF-α, platelet-derived growth factor, or microbial components. IL6 receptors are only present on directly activated B-cells which increase IgM and IgG antibodies (Jones, 2005). Trypanosome killing is assumed to occur via the induction of classically activated macrophages that produce high levels of inflammatory compounds such as tumour necrosis factor α (TNF-α) and reactive oxygen intermediates (Vincendeau and Boutwill, 2005).

Despite several previous studies on T. evansi infection that showed a correlation between the intensity of inflammation and the level of parasitemia, the circulating trypanosomes in some studies failed to show that because the immune response was directed against both parasites and self-antigens (Soares and Santos, 1999). However, these pathogens defy humoral immunity through a subtle mechanism of antigenic variation (Mosa, 2020). The antibodies directed against the specific surface-exposed epitopes of the VSG coat opsonize the parasites. Besides, the immune complexes are efficiently phagocytosed and destroyed, mainly in the liver, by the macrophages (Barghash, 2019). It may be responsible for the high levels of production in the infected groups with T. evansi (single, mixed infection, and that vaccinated against P. multocida). Also, the VSG may be released from the dead trypanosomes activated macrophages to secrete proinflammatory molecules like TNF-α, IL6, IL12, and IL10, as a response of the host immune system. It is involved in the first peak of parasitemia by the toxic nature of TNF-α for both the host cell and the parasite (Finkelman et al., 1991). A previous study has highlighted the capability of T. evansi in pro-inflammation or anti-inflammation activities (El Sayed et al., 2017). The elevated IL10 levels are correlated with poor survival (Kubatzky, 2012). Among other factors such as lipopolysaccharide, outer membrane proteins and their capsule, the protein toxin (PMT) of P. multocida is an important virulence factor that determined the immunological response of the host’s immune system in agreement with Stijlemans et al. (2018).

The present results showed a correlation in analysis between inflammatory cytokine production in commercial and locally prepared vaccines against P. multocida. It also showed the displayed negative correlation between IFN-γ and IL-10 levels in serum and positive correlation with other cytokines indicates a controlled inflammatory response in infected and vaccinated groups. The elevated levels of IL-10 that produced in vivo experimental infection were correlated with poor survival in rats and accompanied with severe pathological changes which increased in rats of TPA and TPB vaccine groups. It is in agreement with primary and secondary infections that elicited similar responses included elevated levels of IL10. Notably, various studies have shown that polyclonal B cell activation, generation of suppressor T-cells and macrophages, and altered antigen handling and presentation are all mechanisms that could be involved in trypanosome-mediated immuno-suppression (Sileghem and Flynn, 1994). In the present study, cytokines responsible for B-cell activation and T-cell suppression were released.

During trypanosome infections; TNF-α secreted by classically activated macrophages is involved in both parasitemia control and infection-associated pathologies like anaemia, organ lesion, and fever. These findings support the hypothesis that a lack of efficient regulation between IFN-γ and IL10 cytokine productions associated with immune-regulation of effector responses may lead to immunopathogenesis as reported before (Raes et al., 2002). In the current study, lymph nodes and spleen were remarkably reactive in fulminated parasitemia. It may account for the generalized lymphoid tissue hyperplasia characteristic of T. evansi infections, while the immune system became depleted of lymphoid cells in the late stages, in agreement with Ghaffar et al. (2016).

Regarding histopathological studies, lungs in experimental single and mixed infections and after vaccination against P. multocida in the presence of T. evansi in rats appeared oedema, congestion, emphysema, and infiltration with inflammatory cells accompanied with alveolar haemorrhage. These changes were due to vasodilatation and exudation mainly caused by the inflammatory response. Also, it may be due to an immune complex deposition and complement cascade reaction, as reported by Abd El-Baky and Salem (2011). These changes in the infected lung tissue were similar to those seen in the lung of various infected animals with T. evansi (Biswas et al., 2001; Otto et al., 2010; Barghash et al., 2018; Barghash, 2021).

In summary, the present study revealed the possible use of cytokines as immunological markers of clinical evolution in the sera of rats’ harbouring trypanosomosis. It assessed the levels of antibodies administered by the local prepared and commercial vaccines against Pasteurellosis (alone or accompanied with T. evansi) using ELISA assay. The immune response depended on gross and microscopic lesion scoring of the lung, mortality, and haemo-biochemical changes. Cytokines levels were significantly reduced in T. evansi infected animals and responded against P. multocida. The inductive capacity to mount immune responses against the heterologous antigens was suppressed in T. evansi-infected animals. Consequently, T. evansi infection interfered with that or might inhibit total cytokines may play a role in the induction of immunosuppression by the parasite. We advise that the treatment with anti-trypanosomal drugs may help in reducing the failure of vaccination programs.

ACKNOWLEDGMENTS

The authors gratefully acknowledge the scientific support of the Desert Research Center (DRC) in Cairo, Egypt.

Novelty Statement

This study has examined the effect of T. evansi on vaccination against Pasteurellosis, besides the efficiency of imported commercial vaccine compared to the local in vitro prepared one. It also supported the possible use of cytokines as immunological markers.

AUTHOR’S CONTRIBUTION

SB had the idea, planned, designed the work, prepared T. evansi strain, and analyzed the clinical results. AH has prepared P. multocida strain, formol-killed vaccine, and challenge. Except that, this work is a product of the two members who have contributed in equal degrees to the analytical methods used, to the research concept, and the experimental infection. The two authors have contributed to writing and approved the manuscript.

Conflict of interest

The authors have declared no conflict of interest.

REFERENCES

Abd El-Baky AA, Salem SI (2011). Clinicopathological and cytological studies on naturally infected camels and experimentally infected rats with Trypanosoma evansi. World Appl. Sci. J., 14(1): 42–50.

Abubakar MS, Fatihu MY, Ibrahim NDG, Oladele SB, Abubakar MB (2010). Camel pneumonia in Nigeria: Epidemiology and bacterial flora in normal and diseased lung. Afr. J. Microbiol. Res., 4: 2479–2483.

Ahmed S, Ahmed B, Mahmoud G, Nemr W, Abdel-Rahman E (2016). Comparative study between formalin-killed vaccine and developed gamma irradiation vaccine against Mannheimia haemolytica in rabbits. Turk. J. Vet. Anim. Sci., 40: 219–224. https://doi.org/10.3906/vet-1504-34

Bancroft JD, Stevens A (1996). Theory and practice of histological techniques. Churchill Living stone, New York.

Barghash SM (2019). Advanced studies on Trypanosoma evansi: Does Trypanosoma evansi cause cancer or behave like a cancerous cell? Mendeley Data, V1.

Barghash SM (2021). Antitrypanosomal activity of essential oils extracted from Rosmarinus officinalis and Salvia fruticosa. Eur. J. Biomed. Pharm. Sci., 8(4): 37–45.

Barghash SM, Sobhy HM, Nono RS, Razin EA (2018). Activity of human plasma proteins on trypanosomiasis. Eur. J. Biomed. Pharm. Sci., 5: 87–97.

Biswas D, Choudhury A, Misra KK (2001). Histopathology of Trypanosoma (Trypanozoon) evansi infection in bandicoot rat. I. Visceral organs. Exp. Parasitol., 99(3): 148–159. https://doi.org/10.1006/expr.2001.4664

Çokçalışkan C, Göktuna PT, Türkoğlu T, Uzunlu E, Gündüzalp C, Uzun AE, Sareyyüpoğlu B, Kürkçü A, Gülyaz V (2019). Effect of simultaneous administration of foot-and-mouth disease (FMD) and anthrax vaccines on antibody response to FMD in sheep. Clin. Exp. Vaccine Res., 8(2): 103–109. https://doi.org/10.7774/cevr.2019.8.2.103

Desquesnes M, Holzmuller P, Lai DH, Dargantes A, Lun ZR, Jittaplapong S (2013). Trypanosoma evansi and surra: a review and perspectives on origin, history, distribution, taxonomy, morphology, hosts, and pathogenic effects. Biomed. Res. Int., https://doi.org/10.1155/2013/194176

El Sayed RA, Barghash SM, El-Alfy NM, Abou-Elnour BM, Sadek AM (2017). Physiological, immunological and histopathological comparison of Echinococcus granulosus (G6) camel strain by different viability status using secondary cyst development in rat. Int. J. Adv. Res., 5(2): 2119–2131. https://doi.org/10.21474/IJAR01/3385

ElNaga TR, Barghash SM (2016). Blood parasites in camels (Camelus dromedarius) in northern west coast of Egypt. J. Bacter. Parasitol., 7: 258. https://doi.org/10.1016/j.parepi.2016.07.002

Eyob E, Matios L (2013). Review on camel trypanosomosis (surra) due to Trypanosoma evansi: Epidemiology and host response. J. Vet. Med. Anim. Health, 5(12): 334–343.

Finkelman FD, Pearce JF, Urban JR, Sher A (1991). Regulation and biological function of helminth induced cytokine responses. Immunol. Today, 12(A): 62–66. https://doi.org/10.1016/S0167-5699(05)80018-0

Fung S, Reid A, Inoue, Lun S (2007). Immunization with recombinant beta-tubulin from Trypanosoma evansi induced protection against Trypanosoma evansi, T. equiperdum and T. brucei infection in mice. Para. Immunol., 29(4): 191–201. https://doi.org/10.1111/j.1365-3024.2006.00933.x

Ghaffar MA, El-Melegy M, Afifi AF, Bahaa El Deen W, El-Kady N, Atia AF (2016). The histopathological effects of Trypanosoma evansi on experimentally infected mice. Meno. Med. J., 29(4): 868–873.

Gillingwater K, Büscher P, Brun R (2007). Establishment of a panel of reference Trypanosoma evansi and Trypanosoma equiperdum strains for drug screening. Vet. Parasitol., 148(2): 114–121. https://doi.org/10.1016/j.vetpar.2007.05.020

Gupta MP, Kumar H, Singla LD (2009). Trypanosomosis concurrent to tuberculosis in black bucks. Indian Vet. J., 86: 727–728.

Hoare CA (1972). The trypanosomes of mammals. Blackwell Scientific Publication, Oxford, pp. 1–749.

Holland WG, Do TT, Huong NT, Dung NT, Thanh NG, Vercruysse J, Goddeeris BM (2003). The effect of Trypanosoma evansi infection on pig performance and vaccination against classical swine fever. Vet. Parasitol., 111: 115–123. https://doi.org/10.1016/S0304-4017(02)00363-1

Holland WG, My LN, Dung TV, Thanh NG, Tam PT, Vercruysse J, Goddeeris BM (2001). The influence of T. evansi infection on the immuno-responsiveness of experimentally infected water buffaloes. Vet. Parasitol. 102(3): 225–234. https://doi.org/10.1016/S0304-4017(01)00534-9

Intisar KS, Ali YH, Khalafalla AI, Mahasin EAR, Amin AS (2009). Natural exposure of dromedary camels in Sudan to infectious bovine rhinotracheitis virus (bovineherpes virus 1). Acta Trop., 111: 243–246. https://doi.org/10.1016/j.actatropica.2009.05.001

Jakeen KE, Samah SA, Soumaya AE, Ashgan MH, Abdullah AA, Moussa IM (2016). Comparative studies for serodiagnosis of haemorrhagic septicaemia in cattle sera. Saudi J. Biol. Sci., 23: 48–53. https://doi.org/10.1016/j.sjbs.2015.06.011

Jones SA (2005). Directing transition from innate to acquired immunity: Defining a role for IL-6. J. Immunol., 175: 3463–3468. https://doi.org/10.4049/jimmunol.175.6.3463

Joshi PP, Shegokar VR, Powar RM, Herder S, Katti R, Dani R, Bhargava A, jannin J, Truc P (2005). Human trypanosomiasis caused by Trypanosoma evansi in India: The first case report. Am. Trop. Med. Hyg., 37: 491– 495. https://doi.org/10.4269/ajtmh.2005.73.491

Juyal PD, Singla LD, Kaur P (2005). Management of surra due to Trypanosoma evansi in India: An overview. In: Infectious Diseases of Domestic Animals and Zoonosis in India, Tandon V and Dhawan BN (Eds). Proc. Natl. Acad. Sci. India B Biol. Sci., 75 (Special issue): 109–120.

Kebede F, Gelaye E (2010). Studies on major respiratory diseases of camel (Camelus dromedarius) in Northeastern Ethiopia. Afr. J. Microbiol. Res., 4: 1560–1564.

Kirchberger S, Leroch M, Huynen MA, Wahl M, Neuhaus HE, Tjaden J (2007). Molecular and biochemical analysis of the plastidic ADP-glucose transporter (ZmBT1) from Zea mays. J. Biol. Chem., 282: 22481–22491. https://doi.org/10.1074/jbc.M702484200

Kubatzky KF (2012). Pasteurella multocida and immune cells. Curr. Trop. Microbiol. Immunol., 361: 53–72. https://doi.org/10.1007/82_2012_204

Lange AM, Yutanawiboonchai W, Scott P, Abraham D (1994). IL-4- and IL-5-dependent protective immunity to Onchocerca volvulus infective larvae in BALB/c BYJ mice. J. Immunol., 153: 205–211.

Lun ZR, Brun R, Gibson W (1992). Kinetoplast DNA and molecular Karyotypes of Trypanosoma evansi and Trypanosoma equiperdum from China. Mol. Biochem. Parasitol., 50: 189–196. https://doi.org/10.1016/0166-6851(92)90215-6

Lutje V, Mertens B (1995). Trypanosoma congolense: proliferative responses and interleukin production in lymph node cells of infected cattle. Exp. Parasitol., 81(2): 154–164. https://doi.org/10.1006/expr.1995.1104

Magez S, Torres JEP, Obishakin E, Radwanska M (2020). Infections with extracellular trypanosomes require control by efficient innate immune mechanisms and can result in the destruction of the mammalian humoral immune system. Front. Immunol., 2020. https://doi.org/10.3389/fimmu.2020.00382

McManus DP, Bryant C (1995). Biochemistry, physiology and molecular biology of Echinococcus. In: R.C.A. Thompson and A.J. Lymbery (ed.), the biology of Echinococcus and hydatid disease. CAB International, Wallingford, United Kingdom. pp. 355–410.

Mochabo KOM, Kitala PM, Gathura PB, Ogara WO, Ereqae EM, Kaitho TD, Catley A (2006). The socio-economic impact of important camel diseases as perceived by a pastoralist community in Kenya. Onderstepoort. J. Vet. Res., 73: 269–274.

Mosa AI (2020). Antigenic variability. Front. Immunol., https://doi.org/10.3389/fimmu.2020.02057

Onah DN, Hopkins J, Luckins AG (1997). Effects of Trypanosoma evansi on the output of cells from a lymph node draining the site of Pasteurella haemolytica vaccine administration. J. Com. Pathol., 117(1): 73–82. https://doi.org/10.1016/S0021-9975(97)80067-9

Onyilagha C, Uzonna JE (2019). Host immune responses and immune evasion strategies in African trypanosomiasis. Front. Immunol., 10: 2738. https://doi.org/10.3389/fimmu.2019.02738

Otto MA, da Silva AS, Gressler LT, Farret MH, Tavares KC, Zanette RA, Miletti LC, Monteiro SG (2010). Susceptibility of Trypanosoma evansi to human blood and plasma in infected mice. Vet. Parasitol., 168(1-2): 1–4. https://doi.org/10.1016/j.vetpar.2009.10.020

Pearce EJ, Caspar P, Grzych JM, Lewis FA, Sher A (1991). Downregulation of Th1 cytokine production accompanies induction of Th2 responses by a parasitic helminth, Schistosoma mansoni. J. Exp. Med., 173: 159–166. https://doi.org/10.1084/jem.173.1.159

Raes G, De Baetselier P, Noël W, Beschin A, Brombacher F, Gholamreza HG (2002). Differential expression of FIZZ1 and Ym1 in alternatively versus classically activated macrophages. J. Leuk. Biol., 71(4): 597–602.

Roetzera A, Bernd Jilmab B, Eibl MM (2017). Vaccine against toxic shock syndrome in a first in man clinical trial. Expert. Rev. Vaccine, 16(2): 81–83. https://doi.org/10.1080/14760584.2017.1268921

Ruzauskas M (2005). Development and assay of inactivated Pasteurella vaccine for rabbits. Biologia, 2: 35–39.

Sileghem CM, Flynn NZ (1994). The role of the macrophage in induction of immunosuppression in Trypanosoma congolense- infected cattle. Int. Livest. Res. Inst., 74(2): 310–316.

Singla LD and Juyal PD (1992). Immunomodulatory effects of levamisole against Trypanosoma evansi infection in cow-calves: Serum gamma-globulins. J. Vet. Parasitol., 6(2): 9–14.

Singla LD, Juyal PD and Sharma NS (2010). Immune responses to haemorrhagic septicaemia (HS) vaccination in Trypanosoma evansi infected buffalo-calves. Trop. Anim. Hlth. Prod., 42: 589-595. https://doi.org/10.1007/s11250-009-9461-1

Singla LD, Juyal PD, Sharma NS (2012). Responses to haemorrhagic septicaemia vaccination in Trypanosoma evansi infected buffalo-calves. J. Vet. Parasitol., 26(1): 39–43.

Singla LD, Singla N and Parshad VR (2015). Development of concurrent infection of notoedric mange in rabbits infected with Trypanosoma evansi. Scand. J. Lab. Anim. Sci., 41(2): 1-6.

Soares M, Santos R (1999). Immunopathology of cardiomyopathy in the experimental chagas disease. Memórias do instituto Oswaldo Cruz, 94(1): 257. https://doi.org/10.1590/S0074-02761999000700043

Stijlemans B, Baral T, Guilliams M (2007). A glycosylphosphatidy Inositol-based treatment alleviates trypanosomiasis-associated immunopathology. J. Immunol., 179(6): 4003–4014. https://doi.org/10.4049/jimmunol.179.6.4003

Stijlemans B, Radwanska M, De Trez C, Magez S (2017). African trypanosomes undermine humoral responses and vaccine development: link with inflammatory responses? Front. Immunol., 8: 582. https://doi.org/10.3389/fimmu.2017.00582

Stijlemans B, De Baetselier P, Magez S, Van Ginderachter JA, De Trez C (2018). African trypanosomiasis-associated anemia: The contribution of the interplay between parasites and the mononuclear phagocyte system. Front. Immunol., 9: 218. https://doi.org/10.3389/fimmu.2018.00218

Vincendeau P, Boutwill B (2006). Immunology and immunopathology of African trypanosomiasis. Anais da Academia Brasileira de Ciências, 78(4): 645–665. https://doi.org/10.1590/S0001-37652006000400004

Wilson BA, Ho M (2013). Pasteurella multocida from zoonosis to cellular microbiology. Clin. Micro Rev., 26(3): 631–655. https://doi.org/10.1128/CMR.00024-13