مقایسه الگوی الکتروفورتیک پروتئین‌های لینگواتولا سراتا در نشخوارکنندگان اهلی و سگ به روش SDS- PAGE

نوع مقاله : مقاله پژوهشی

نویسندگان

1 گروه پاتوبیولوژی، دانشکده دامپزشکی، دانشگاه رازی، کرمانشاه، ایران

2 گروه پاتوبیولوژی، دانشکده دامپزشکی، دانشگاه ارومیه، ارومیه، ایران

3 گروه علوم درمانگاهی، دانشکده دامپزشکی، واحد شهرکرد، دانشگاه آزاد اسلامی، شهرکرد، ایران

چکیده

زمینه مطالعاتی: لینگواتولا سراتا یک انگل مشترک انسان و دام است و طیف وسیعی از حیوانات از جمله انسان را تحت تأثیر قرار می دهد و بیماری‌های متعددی ایجاد می‌نماید. فرم بالغ این انگل در مجاری فوقانی تنفسی سگ‌سانان زندگی می‌کند و طیف وسیعی از علف خواران به ویژه نشخوارکنندگان به عنوان میزبان واسط عمل می‌کنند که نوچه انگل در اندام‌های احشایی به ویژه غدد لنفاوی مزانتریک آن‌ها یافت می‌شود. هدف از این مطالعه بررسی مقایسه الگوی الکتروفورتیک پروتئین‌های لینگواتولا سراتا فرم بالغ و نوچه به‌دست آمده از میزبان‌های مختلف بود.
روش کار: در این مطالعه لینگواتولا سراتا بالغ جنس نر و ماده از مجاری فوقانی تنفسی سگ‌های تلف شده در اثر تصادف جاده‌ای و نوچه لینگواتولا سراتا از غدد لنفاوی مزانتریک بز، گاومیش، گوسفند، گاو و شتر کشتار شده در کشتارگاه جداسازی و به‌صورت جداگانه ذخیره شد. پس از تهیه عصاره غلظت پروتئین‌های نمونه‌های انگلی به روش برادفورد مورد سنجش قرار گرفت و در نهایت با استفاده از روش SDS- PAGE، الگوی الکتروفورتیک پروتئین‌های انگل در نشخوارکنندگان مختلف و سگ مورد بررسی قرار گرفت.
نتایج: در الکتروفورز پروتئین‌های سوماتیک گروه‌های مختلف نوچه‌ها، 2 باند پپتیدی به‌خوبی واضح با وزن-های تقریبی 62 و 53 کیلودالتون در ژل SDS-PAGE مشاهده شد. در اشکال بالغ، تنها باند پپتیدی با وزن تقریبی 62 کیلودالتون حضور داشت.
نتیجه‌گیری نهایی: نتایج حاصله نشان می‌دهد حضور باند پپتیدی با وزن تقریبی 62 کیلودالتون در تمام گروه‌های مورد مطالعه، ممکن است نشان‌دهنده برخی ویژگی‌های بیولوژیک آن باشد و به ویژه چنانچه با سویه-های متفاوت انگل مواجه باشیم این تفاوت‌ها تعیین کننده است و می‌تواند در طراحی آزمون‌های سرولوژیکی کارآمد جهت تشخیص آلودگی‌ها در میزبان‌های مختلف مفید باشد.

کلیدواژه‌ها


عنوان مقاله [English]

Comparison of electrophoretic pattern of Linguatula serrata proteins obtained from domestic ruminants and dogs by SDS-PAGE

نویسندگان [English]

  • Farid Rezaei 1
  • Mosa Tavassoli 2
  • Maryam Karimi-Dehkordi 3
1 Department of Pathobiology, Faculty of Veterinary Medicine, Razi University, Kermanshah, Iran
2 Department of Pathobiology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran
3 Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran
چکیده [English]

Introduction: The phylum Pentastomida contains a highly specialized taxon with more than 120 species which infect the respiratory tracts of reptiles and other vertebrates. The species of Pentastomida, a still-enigmatic group of worm-like, linguatula serrata belongs to the bloodsucking parasites that inhabit the upper respiratory tract of terrestrial, carnivorous vertebrates, mostly reptiles and birds; L. serrata, commonly called tongue worms, typically inhabit canids and felids. The intermediate hosts of these parasites are usually sheep, cattle, other ruminants or rodents. The hosts ingest the eggs, and the first instar larva hatches within their intestines, penetrates the mucosa, and retreats into the tissue, where it encysts and molts to the third larval stage. The parasite is tongue shaped, lightly convex dorsally and flattened ventrally. Males measure 1.8–2 cm, while females measure 8–13 cm in length. The nymph of L. serrata is characterised by the possession of a saw-like cuticle with multiple transverse grooves, a ventral buccal apparatus with two pairs of peribuccal hooks and acidophilic glands, a complete digestive system and primordial genital organs. Moreover, in degraded nymphs, the hooks and remnants of the cuticle are often the only findings that allow the diagnosis of the infestation. Humans may be infected with linguatula either by ingestion of nymphs of L. serrate resulting in a condition called nasopharyngeal linguatulosis or Halzoun syndrome or by ingestion of infective eggs which develop in internal organs resulting in visceral linguatulosis. Halzoun syndrome is a rare clinical disease that manifests as an acute allergic-like reaction involving the upper respiratory tract and nasopharyngeal mucosa after the consumption of raw sheep or goat liver, a popular food presentation in Lebanon and other countries of the Eastern Mediterranean region. L. serrata is a common human and animal parasite and affects a wide range of animals, including humans, and causes various diseases in humans. In Iran, this parasite reported from definitive and intermediate hosts in different regions. Also some reports from human Halzoun syndrome it exists in Iran. Diagnosis in final host will be done by clinical signs and separating of the parasite eggs in feces, nasal secretions and animal’s saliva. The diagnosis in intermediate hosts will be done by biopsy. Compression of the electrophoretic pattern of adult and nymph L. serrate proteins obtained from different hosts.
Material and Methods: In this study, adult male and female of l. serrate were isolated from the upper respiratory tract of dogs killed by road accident and linguatula nymphs isolated from mesenteric lymph nodes of goats, buffaloes, sheep, cattle and camels. Obtained parasites were separately stored. Collected nymphs of the parasite were washed separately 3 times with 0.85% saline (sterile) and phosphate-buffered saline. The nymph and adult Mouth parts parasites were sonicated on ice with ultrasonicator. After preparing the extract, the protein concentration of parasitic samples was measured by Bradford method and finally, by SDS-PAGE method, the electrophoretic pattern of parasite proteins in different ruminants and dogs was investigated. SDS-PAGE of somatic proteins was performed in different percentage polyacrylamide gels using a discontinuous system as described by Laemmli. The prepared proteins were run on SDS–polyacrylamide gels, composed of 4 % resolving gel and 12 % stacking gel, under reducing conditions using the discontinuous buffer system. For size estimation in SDS-PAGE, a prestained protein marker at a range of 11-180KDa molecular weight (PS10 plus) was used.
Results and Discussion: Electrophoresis of protein extracts from Mouth parts of different groups of nymphs obtained from different ruminants and adult forms of male and female L. serrata by SDS-PAGE showed a wide range of peptide bands between 8 kDa and 200 kDa. Electrophoresis of Mouth parts of larvae somatic proteins of different groups of parasites (separated from goat, cattle, buffalo, sheep and camel) showed 2 very clear peptide bands with approximate weights of 62 and 53 kDa in SDS-PAGE gel. For proteins prepared from the Mouth parts of cattle and buffaloes, the fine peptide bands did not show much density and were not clear. The status of these bands in the proteins prepared from the oral appendages of camel showed a different pattern from that of other ruminants. It differed from other ruminants in that these bands were clearer than those obtained from cattle and buffaloes and weaker than those from goats and sheep. In male and female adult forms (separated from dog), only the peptide band weighing approximately 62 kDa was present. In the present study, as expected, due to the multicellularity of L. serrate, a wide range of peptide bands in the range of 8 to 200 kDa were found in all samples analyzed by SDS-PAGE. However, there were only two peptide bands in the samples prepared from the oral appendages of the parasitic nodules (about 62 kDa band and about 53 kDa band) and one peptide bond in the proteins prepared from the adult male and female oral appendages (About 62 kDa) were well stained and quite clear, indicating a predominance of peptide concentrations in the mentioned bands.
Conclusion: The prevalence of Linguatulosis is important in ruminants because without any specific clinical symptoms, it leads to reduction of animal productions and hidden economic loss, as well as public health hazards. The results show that the presence of a peptide band with an approximate weight of 62 kDa in all study groups may indicate some of its biological characteristics, especially if we encounter different strains of the parasite is decisive and can be useful in designing efficient serological tests to detect infections in different hosts.

کلیدواژه‌ها [English]

  • Linguatula serrata
  • Electrophoretic
  • Dog
  • Domestic ruminants
  • SDS-PAGE
Alborzi AR, Bahrami S and Khajeh F, 2021. A Preliminary Study on the Antigenic Proteins of Linguatula serrata Nymphal Stage in Sheep with Visceral Linguatulosis. Archives of Razi Institute. https://dx.doi.org/10.22092/ari.2021.352744.1578
Alcala-Canto Y, Alberti-Navarro A and Ibbara-Velarde F, 2007. Serine protease activity demonstrated in larval stage of the pentastomid Linguatula serrata. Parasitology Research 100: 1011-1014.
Barton DP, Baker A, Porter M, Zhu X, Jenkins D and Shamsi S, 2020. Verification of rabbits as intermediate hosts for Linguatula serrata (Pentastomida) in Australia. Parasitology Research 119 (5) 1553-1562.
Buckle AC, Knox DP and Riley J, 2002. Proteins and proteinases in the in vitro released products (IVRP) of tissue-invasive and lung-dwelling larvae of the pentastomid Procephalus crotali. Parasitology 124: 391-399.
Farshchi S, Alikhani MY, Choresh KS, Khaledi A, Farrash BR and Choresh KS, 2018. Prevalence of Linguatula serrata nymphs in goats slaughtered in Mashhad slaughterhouse, Iran. Avicenna Journal of Clinical Microbiology and Infection 5(3) 52-54.
Hajipour N, Soltani M and Mirshekar F, 2019.  Effect of age, sex, and season on the prevalence of Linguatula serrata infestation in mesenteric lymph nodes of goats slaughtered in Tabriz, Iran. Tropical Animal Health and Production 51: 879–885.
Hajipour N, Tavassoli M, Eslamlo AA and Javadi SH, 2018. Investigation of histopathological changes caused by adult stage of Linguatula serrata in dog. Comparative Clinical Pathology 27(3) 717-20.
Hajipour N, Tavassoli M, Tayefi-Nasrabadi H and Seyedi S, 2016. Comparative evaluation of somatic proteins of the nymphal stage of Linguatula serrata isolated from goats and cattle in northwest Iran. Bulgarian Journal of Veterinary Medicine 19 (3) 242-6.
Hamid T, Hossein YD, Mehran BB, Masood FS and Hamid E, 2012. A case report of Linguatula serrata infestation from rural area of Isfahan city, Iran. Advanced Biomedical Research 1: 42-44.
Islam R, Hossain MS, Alam Z, Islam A, Khan AH, Kabir ME, Hatta T, Alim A  and Tsuji N, 2018. Linguatula serrata, a food-borne zoonotic parasite, in livestock in Bangladesh: Some pathologic and epidemiologic aspects. Veterinary Parasitology: Regional Studies and Reports 13: 135-140.
Koehsler M, Walochnik J, Georgopoulo M, Pruente C, Boeckeler W, Auer H, Barisani-Asenbauer T, 2011. Linguatula serrata tongue worm in human eye, Austria. Emerging Infectious Diseases 17(5) 870-872.
Machado MA, Makdissi FF, Canedo LF, Martino RB and Crescentini F, 2006. Unusual case of pentastomiasis mimicking liver tumor. Journal of Gastroenterology and Hepatology 21: 1218-1220.
Mairena H, Solano M and Venegas W, 1989. Human dermatitis caused by a nymph of Sebekia. American Journal of Tropical Medicine and Hygiene 41: 352–354.
Mohammadi MA, Bamorovat M, Sharifi I, Mostafavi M, Zarandi MB, Kheirandish R, Karamoozian A, Khatami M and Zadeh SH, 2020. Linguatula serrata in cattle in southeastern Iran: Epidemiological, histopathological and phylogenetic profile and its zoonotic importance. Veterinary Parasitology: Regional Studies and Report, 22: 100465. doi: 10.1016/j.vprsr.2020.100465
Mohanta UK and Itagaki,T, 2017. Molecular characterization and phylogeny of Linguatula serrata (Pentastomida: Linguatulidae) based on the nuclear 18S rDNA and mitochondrial cytochrome c oxidase I gene. Journal of Veterinary Medical Science 79(2) 398-402.
Morales PM, Carrillo MP, González M. and Carvallo FC, 2020.  Histopathological lesions compatible with nymphs of Linguatula serrata in bovine liver. Austral Journal of Veterinary Sciences 52(1) 19-23.
Musharrafıeh U, Hamadeh G, Touma A and Fares J, 2018. Nasopharyngeal linguatulosis or halzoun syndrome: clinical diagnosis and treatment. Revista da Associação Médica Brasileira 64(12) 1081-1084.
Nagamori Y, Ramachandran A, Kuzma C, Nafe L and Johnson EM, 2019. A zoonotic parasite, Linguatula serrata, infection in a dog imported from Ethiopia to the United States. Veterinary Parasitology: Regional Studies and Reports 16: 100273. https://doi.org/10.1016/j.vprsr.2019.100273
Naude T, Pant S, Tavassoli M, Sarker S and Ghorashi SA, 2018.  The complete mitochondrial genome of Linguatula serrata (tongue worm) isolated from a dog and phylogenetic analysis. Mithocondrial DNA Part B: Resources 3(1) 357-358.
Sarmadian H, Nasiri Z, Saeedinia S, Moradi Y, Eshrati B, Ghasemikhah R, Salehi MM and Zamani M, 2020. Clinical manifestation and epidemiological findings of human linguatula serrate infection in Iran: systematic review. Journal of Parasitic Diseases 23: 1-9.
Shamsi S, Barton DP, Zhu X and Jenkins DJ, 2020. Characterisation of the tongue worm, Linguatula serrata (Pentastomida: Linguatulidae), in Australia. International Journal for Parasitology: Parasites and Wildlife 11: 149-57.
Tabaripour R, Shokri A, Teshnizi SH, Fakhar M and Keighobadi M, 2019. Status of Linguatula serrata infection in livestock: A systematic review with meta-analysis in Iran. Parasite Epidemiology and Control 7: 1-13.
Yazdani R, Sharif I, Bamorovat M and Mohammadi MA, 2014. Human linguatulosis caused by Linguatula serrata in the city of Kerman, South-eastern Iran: case report. Iranian Journal of Parasitology 9(2) 282-285