Abstract
The purpose of the current experiment was to test the immunization against Coenurus cerebralis in sheep. Sixteen animals (6 months old, from 1 October 2020 to 30 March 2021 in Najaf city) were recruited to perform the experiment, in which eight of them were injected twice at 21-day interval using the cellular metabolic antigen of C. cerebralis protoscolex cultivated and then emulsified by complete Freund's adjuvant (CFA). The shots were injected intramuscularly at a dose of 1 ml (15 mg of antigenic protein determined in a separate experiment). The second group of eight sheep served as controls (injected intramuscularly with 1 ml sterile saline only at the days of injections). Blood samples were collected from all animals at day-0 (before injection) and at day 10, 18, and 24 after the first injection, and at day10, 16, 26, 40, 48, 53, 61, 80, 85, and 89 after the second injection. Serum activity was studied by indirect enzyme-linked immunosorbent assay (iELISA). The findings, by iELISA, revealed that the cellular antigen of C. cerebralis protoscolices is an active stimulator of antibody response. Day-10 (after the first injection) showed significantly (P<0.05) 3.4 to 9.9 time-higher antibody levels compared to those from day-0. This elevation in the titer of antibodies was increased after receiving the second dose showing 6.3 to 12 time-higher antibody presence even at the final days of blood collection compared to those from day-0. No changes were noticed in the sera of the control animals. The obtained data allow us to conclude that metabolites synthesized by cultivation are active immunogenic components that activate the humoral part of the immune system manifested by the increases in the antibody titers. This gives a solid ground for future work regarding alternative methods of discovering immunization techniques against cestodes.
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Protoscolex metabolites of Coenurus cerebralis as antigenic-produced humoral immune response in sheep
Sura Saad Hamada Alkhuzaie
Department of Veterinary Microbiology, College of Veterinary Medicine, University of Al-Qadisiyah, Al-Diwaniyah, Iraq
sora.hamada@qu.edu.iq, 0000-0003-0162-1397
Abstract
The purpose of the current experiment was to test the immunization against Coenurus cerebralis in sheep. Sixteen animals (6 months old, from 1 October 2020 to 30 March 2021 in Najaf city) were recruited to perform the experiment, in which eight of them were injected twice at 21-day interval using the cellular metabolic antigen of C. cerebralis protoscolex cultivated and then emulsified by complete Freund's adjuvant (CFA). The shots were injected intramuscularly at a dose of 1 ml (15 mg of antigenic protein determined in a separate experiment). The second group of eight sheep served as controls (injected intramuscularly with 1 ml sterile saline only at the days of injections). Blood samples were collected from all animals at day-0 (before injection) and at day 10, 18, and 24 after the first injection, and at day10, 16, 26, 40, 48, 53, 61, 80, 85, and 89 after the second injection. Serum activity was studied by indirect enzyme-linked immunosorbent assay (iELISA). The findings, by iELISA, revealed that the cellular antigen of C. cerebralis protoscolices is an active stimulator of antibody response. Day-10 (after the first injection) showed significantly (P<0.05) 3.4 to 9.9 time-higher antibody levels compared to those from day-0. This elevation in the titer of antibodies was increased after receiving the second dose showing 6.3 to 12 time-higher antibody presence even at the final days of blood collection compared to those from day-0. No changes were noticed in the sera of the control animals. The obtained data allow us to conclude that metabolites synthesized by cultivation are active immunogenic components that activate the humoral part of the immune system manifested by the increases in the antibody titers. This gives a solid ground for future work regarding alternative methods of discovering immunization techniques against cestodes.
Keywords: Antibody, Coenurus cerebralis, ELISA, Protoscolex, Sheep.
نواتج أیض الرؤیسات للطور الیرقی للمرأسة المخیة کمواد مستضدیة للاستجابة المناعیة الخلطیة فی الأغنام
سرى سعد حمادة الخزاعی
فرع الأحیاء المجهریة البیطریة، کلیة الطب البیطری، جامعة القادسیة، محافظة الدیوانیة، العراق.
الخلاصة
کان الغرض من التجربة الحالیة هو اختبار التحصین ضد أکیاس المرأسة المخیة فی الأغنام. تم استخدام ستة عشر حیوانا (بعمر 6 أشهر) (للفترة من بدایة شهر تشرین الأول 2020 ولغایة نهایة شهر أذار 2021 فی مدینة النجف) لإجراء التجربة، حیث تم حقن ثمانیة منهم مرتین بفاصل 21 یوما باستخدام مستضد التمثیل الغذائی الخلوی لرؤیسات المرأسة المخیة المزروع والمستحلب بواسطة المرسب الکامل. تم الحقن العضلی بجرعة 1 مل (15 ملغ من البروتین المستضدی تم تحدید الترکیز فی تجربة منفصلة). المجموعة الثانیة من ثمانیة أغنام کانت بمثابة مجموعة سیطرة (حقنت عضلیا بمحلول ملحی معقم 1 مل فقط فی أیام الحقن). تم جمع عینات الدم من جمیع الحیوانات فی الیوم 0 (قبل الحقن) وفی الیوم 10 و 18 و 24 بعد الحقن الأول وفی الیوم 10 و 16 و 26 و 40 و 48، 53 و61 و 80 و 85 و 89 بعد الحقن الثانی. تمت دراسة نشاط المصل عن طریق فحص الامتصاص المناعی غیر المباشر المرتبط بالإنزیم. کشفت النتائج أن المستضد الخلوی لرؤیسات المرأسة المخیة هو محفز نشط لاستجابة الأجسام المضادة. أظهر الیوم 10 (بعد الحقن الأول) مستویات أضداد أعلى بشکل ملحوظ (أ<0.05) 3.4 إلى 9.9 مرة مقارنة بتلک الموجودة فی الیوم صفر. لوحظت زیادة هذا الارتفاع فی عیار الأجسام المضادة بعد تلقی الجرعة الثانیة مما أظهر وجود أجسام مضادة أعلى من 6.3 إلى 12 مرة حتى فی الأیام الأخیرة من جمع الدم مقارنة بتلک الموجودة فی الیوم 0. لم یلاحظ أی تغییرات فی مصل حیوانات السیطرة. تسمح لنا البیانات التی تم الحصول علیها بالاستنتاج أن المستضدات التی یتم تحضیرها عن طریق الزراعة هی مکونات مناعیة نشطة والتی تنشط الجزء الخلطی من الجهاز المناعی الذی یتجلى فی الزیادة فی عیار الأجسام المضادة. وهذا یعطی أرضیة صلبة للعمل المستقبلی فیما یتعلق بالطرق البدیلة لاکتشاف تقنیات التحصین ضد الدیدان الشریطیة.
Introduction
Taenia multiceps (Multiceps multiceps) is a taeniid cestode which infests the small intestine of dogs, coyotes, foxes, and jackals as final host during its adult phase (1). C. cerebralis larval stage is commonly located in the nervous systems of small ruminants such as sheep, goats and large ruminants such as buffaloes, cattle, camels, and equids leading to cerebral coenurosis marked by neurological abnormalities (2,3). Non-cerebral coenurosis has also been identified in other parts of the body such as in the muscular tissues and visceral organs of the affected intermediate hosts (4,5). Small ruminants have a very high infestation risk with C. cerebralis (6). In small ruminants, coenurosis is linked to disease burden, fatalityand major economic losses (7). Reports of human infection have been identified in Egypt, Canada, France, and the United States. Infection occurs by the fecal-oral path, which involves contaminated food and/or water with the infective stage (eggs) (6).
Clinical signs, epidemiological occurrences, histological defects and morphological characteristics of C. cerebralis have generally been used to diagnose taeniid tapeworms (8). The important aspects for morphometric recognition are hook number, sizeand shape (9); nevertheless, these parameters are subject to errors particularly in the situation of sterile, young or degraded coenurior also in the maturity phase. Molecular tests have been extensively utilized in research relating to population biology, epidemiological and phylogenetic studies as well as in distinguishing the identity of cysts of different taeniids (10).
Small ruminant production is regarded as a critical component of long-term economic growth in the developing countries. Nevertheless, these infections have been identified as a significant serious obstacle for the livestock farming industries leading to stagnant economic growth (11). The purpose of the current experiment was to test the immunization against Coenurus cerebralis in sheep.
Materials and methods
Samples and experimental design
Sixteen sheep (6 months old) (From 1 October 2020 to 30 March 2021 in Najaf city) were recruited to perform the experiment, in which eight of them were injected twice at 21-day interval using the cellular metabolic antigen of C. cerebralis protoscolex. The second group of eight sheep served as controls (12). Blood samples were collected from all animals at day-0 (before injection) and at day 10, 18, and 24 after the first injection, and at day 10, 16, 26, 40, 48, 53, 61, 80, 85, and 89 after the second injection.
Production of protoscolex metabolites
Metabolites for experimental antigenicity were obtained by cultivating C. cerebralis protoscolex cells in a Heraeus CO2 based incubator at 37˚C using automated control of the gases (CO2 - 5%, O2 - 95%) at 70% humidity in RPMI-1640 medium. The antigens were then emulsified by CFA. The metabolites synthesized in the process of cultivation of C. cerebralis protoscolex cells are active immunogens that activate the humoral component of immune system, which is manifested by synthesis of specific antibodies and gives grounds to speak about an alternative method of obtaining immune drugs from cestodes.
Experiment
The shots were injected intramuscularly at a dose of 1 ml (15 mg of antigenic protein determined in a separate experiment which discussed in production of protoscolex metabolites) in the treatment groups. The control sheep were injected intramuscularly with 1 ml sterile saline only at the days of injections.
IELISA
Serum activity was studied by iELISA. After determining the optimal antigen concentration, solid phase sensitization was performed using the cellular antigen. The conjugate in the reaction was antibodies based on peroxidase labeling prepared against sheep serum lgG (13). The reaction was evaluated using an automated colorimetrical enzyme-immunoassay analyzer 340/ATC (STL-Labsistems, Austria), at 492 nm of a wavelength to measure the optical density (OD) (14).
Results
The findings, by iELISA, revealed that the cellular antigen of C. cerebralis protoscolices is an active stimulator of antibody response. Day-10 (after the first injection) showed significantly (P<0.05) 1.6 to 2.1 time-higher antibody levels compared to those from day-0 (Table 1).
Table 1: Antibody titers in sheep injected with cellular antigens of C. cerebralis protoscoleces
Days of study |
Optical density in IER* in experimental animals |
Mean ± SE |
||
10** |
2.107 |
1.822 |
1.611 |
2.383±0.05 |
18 |
2.322 |
2.011 |
1.980 |
2.104±0.01 |
24 |
2.111 |
2.321 |
2.032 |
2.154±0.04 |
31\10*** |
2.211 |
2.377 |
1.911 |
2.166±0.016 |
37\16 |
2.011 |
1.711 |
1.924 |
1.882±0.052 |
47\26 |
2.110 |
2.011 |
2.111 |
2.077±0.061 |
61\40 |
2.326 |
2.222 |
2.300 |
2.282±0.043 |
69\48 |
2.439 |
2.441 |
2.654 |
2.511±0.053 |
74\53 |
2.654 |
2.352 |
2.454 |
2.486±0.034 |
82\61 |
2.591 |
2.524 |
2.311 |
2.475±0.054 |
101\80 |
2.422 |
2.655 |
2.611 |
2.562±0.044 |
106\85 |
2.510 |
2.811 |
2.721 |
2.680±0.056 |
* IER: Immunoenzymatic reaction (P≤ 0.001). ** First Injection. *** Second injection
This elevation in the titer of antibodies was increased after receiving the second dose showing 0.151 to 0.291 time-higher antibody presences even at the final days of blood collection compared to those from day-0. No changes were noticed in the sera of the control animals (Table 2).
Table 2: IER values with sera of control sheep
Days of study |
Optical density in IER* in experimental animals |
Mean±SE |
||
0 |
0.241 |
0.211 |
0.196 |
0.216±0.033 |
15 |
0.251 |
0.234 |
0.211 |
0.227±0.051 |
29 |
0.291 |
0.218 |
0.244 |
0.251±0.045 |
38 |
0.284 |
0.204 |
0.214 |
0.234±0.044 |
43 |
0.231 |
0.233 |
0.197 |
0.220±0.036 |
51 |
0.288 |
0.190 |
0.188 |
0.224±0.043 |
58 |
0.289 |
0.241 |
0.231 |
0.253±0.045 |
77 |
0.281 |
0.151 |
0.244 |
0.225±0.056 |
110 |
0.280 |
0.177 |
0.213 |
0.223±0.046 |
* IER: Immunoenzymatic reaction (P≤ 0.001).
Discussion
Even through these species-specific variations, cestode has been revealed to convert/regulate the host reaction to their body parts (immunoregulation). These organisms, nevertheless, may change the immune reaction to antigens, such as vaccinations with long-term persistent infection. They've also been linked to a change in the incidence of inflammatory bowel disease, diabetes, and arthritis (15-20). Since parasites have the ability to control the host immune response, which can be partly restored by anthelmintic medications, there has been a lot of curiosity more about the pathways behind helminth-induced immune modulations and the parasite-encoded compounds that could be causing it. The excretory/secretory products of helminth parasites have gotten the most interest, since they may be used as alternative therapeutics for inflammatory and autoimmune diseases or as candidates for anthelmintic vaccinations, diagnostic tools, and medications (21).
Our results indicate high antibody response as it identified by the ELISA method. This agrees with the fact that metabolites of the C. cerebralis protoscolex cells may provide a strong immunogenic agent that could give a solid protection against the cystic stage of the cestode (21). Coenurosis is a lethal central nervous system condition triggered by the larval coenurus of the tapeworm T. multiceps in both sheep and humans. Despite the availability of medication and preventive services, controlling coenurosis remains a difficult task. Li et al (22) have exhibited a significant genome sequence of T. multiceps, length of 44.8 Mb and an effective assembly of 240 Mb 96% of the genome utilizing Pacbio single-molecule real-time and Hi-C results. Furthermore, they have discovered many genes that encode proteins participating in proglottid development and associations with the host central nervous system, which may help T. multiceps adjust to its parasitic lifestyle. They have suggested that their research not only sheds light on the genetics and development of T. multiceps, but also establishes a range of species-specific gene targets that could be used to establish new coenurosis treatments and controls. Exactly, this agrees with our findings in which metabolites of the cells belong to the C. cerebralis protoscolex have led to the production of immune responses represented by the increases in the circulating antibodies.
The identification of helminth-secreted extracellular vesicles (EVs) has proposed a new model in the research of host-parasite communication. EVs are generated by a wide range of cell types and organisms, such as parasites. EVs are a cell-to-cell exchange system that happens at homeostasis by the movement of genetic information, proteins, lipids, and signals. Some studies have identified those vesicles as immunogenic materials to produce protection against certain parasites (21-26).
Conclusion
The obtained data allow us to conclude that metabolites synthesized by cultivation are active immunogenic components that activate the humoral part of the immune system manifested by the increases in the antibody titers. This gives a solid ground for future work regarding alternative methods of discovering immunization techniques against cestodes.
Acknowledgments
The authors thank Professor Jabbar Ahmed Alssady, Dean of College of Veterinary Medicine, University of Al-Qadisiyah, Iraq, for technical assistance.
Conflict of interests
The authors have not received any funding or benefits from industry, agency of financing, or elsewhere to conduct this study.