Μετάδοση των Ροταϊών ανάμεσα σε μηρυκαστικά, σκύλους και ανθρώπους: Τωρινά δεδομένα και παρατηρήσεις
Δημοσιευμένα:
Jan 29, 2018
Λέξεις-κλειδιά:
Βοοειδή σκύλοι αίγες άνθρωποι ροταϊοί πρόβατα μετάδοση
Περίληψη
Οι ροταϊοί θεωρούνται ένας σημαντικός αιτιολογικός παράγοντας διάρροιας σε ανθρώπους και σε διάφορα είδη ζώων, προκαλώντας σοβαρές οικονομικές απώλειες σε εκτρεφόμενα ζώα, ιδιαίτερα χοίρους και μηρυκαστικά. Το γεγονός αυτό σε συνδυασμό με τη γενετική ποικιλομορφία που χαρακτηρίζει τα μέλη της ομάδας των ροταϊών, δημιουργεί ανησυχίες σχετικά με τη δυνατότητα μετάδοσης των στελεχών του ιού, μεταξύ των διαφόρων ειδών ζώων και ανθρώπων. Οι μελέτες και τα δεδομένα που έχουν παρουσιαστεί τα τελευταία χρόνια σχετικά με την παρουσία των ροταϊών στα μηρυκαστικά και την επιδημιολογία τους σε σχέση με τους ανθρώπους και τους σκύλους με τους οποίους έρχονται σε στενή επαφή, είναι περιορισμένα. Σε αυτή την επισκόπηση παρουσιάζουμε όλες τις τελευταίες πληροφορίες σχετικά με την κατανομή των γενοτύπων των ροταϊών σε μηρυκαστικά, σκύλους και ανθρώπους.
Λεπτομέρειες άρθρου
- Πώς να δημιουργήσετε Αναφορές
-
VALIAKOS, G., CHATZOPOULOS, D. C., & TSOKANA, C. N. (2018). Μετάδοση των Ροταϊών ανάμεσα σε μηρυκαστικά, σκύλους και ανθρώπους: Τωρινά δεδομένα και παρατηρήσεις. Περιοδικό της Ελληνικής Κτηνιατρικής Εταιρείας, 68(2), 123–130. https://doi.org/10.12681/jhvms.15596
- Τεύχος
- Τόμ. 68 Αρ. 2 (2017)
- Ενότητα
- Review Articles
Αυτή η εργασία είναι αδειοδοτημένη υπό το CC Αναφορά Δημιουργού – Μη Εμπορική Χρήση 4.0.
Οι συγγραφείς των άρθρων που δημοσιεύονται στο περιοδικό διατηρούν τα δικαιώματα πνευματικής ιδιοκτησίας επί των άρθρων τους, δίνοντας στο περιοδικό το δικαίωμα της πρώτης δημοσίευσης.
Άρθρα που δημοσιεύονται στο περιοδικό διατίθενται με άδεια Creative Commons 4.0 Non Commercial και σύμφωνα με την άδεια μπορούν να χρησιμοποιούνται ελεύθερα, με αναφορά στο/στη συγγραφέα και στην πρώτη δημοσίευση για μη κερδοσκοπικούς σκοπούς.
Οι συγγραφείς μπορούν να καταθέσουν το άρθρο σε ιδρυματικό ή άλλο αποθετήριο ή/και να το δημοσιεύσουν σε άλλη έκδοση, με υποχρεωτική την αναφορά πρώτης δημοσίευσης στο J Hellenic Vet Med Soc
Οι συγγραφείς ενθαρρύνονται να καταθέσουν σε αποθετήριο ή να δημοσιεύσουν την εργασία τους στο διαδίκτυο πριν ή κατά τη διαδικασία υποβολής και αξιολόγησής της.
Λήψεις
Τα δεδομένα λήψης δεν είναι ακόμη διαθέσιμα.
Αναφορές
Alkan F, Gulyaz V, Ozkan Timurkan M, Iyisan S, Ozdemir S, Turan N, Buonavoglia C, Martella V (2012) A large outbreak of enteritis in goat flocks in Marmara, Turkey, by G8P[1] group A rotaviruses. Arch Virol 157(6):1183–1187.
Banyai K, Laszlo B, Duque J, Steele AD, Nelson EA, Gentsch JR, Parashar UD (2012) Systematic review of regional and temporal trends in global rotavirus strain diversity in the pre rotavirus vaccine era: insights for understanding the impact of rotavirus vaccination programs. Vaccine 30 Suppl 1:A122-130.
Chasey D, Banks J (1984) The commonest rotaviruses from neonatal lamb diarrhoea in England and Wales have atypical electropherotypes. Vet Rec 115(13):326–327.
Chatzopoulos DC, Athanasiou LV, Spyrou V, Fthenakis GC, Billinis C (2013) Rotavirus infection in domestic animals. J Hellenic Vet Med Soc 64:145-160.
Chatzopoulos DC, Sarrou S, Vasileiou NGC, Ioannidi KS, Peteinaki E, Valiakos G, Tsokana K, Papadopoulos E, Spyrou V, Giannakopoulos A, Sbiraki A, Lacasta D, Bueso JP, Athanasiou LV, Billinis C (2015) Dissemination of intestinal pathogens between lambs and puppies in sheep farms, Small Rumin Res accepted for publication.
Chen Y, Zhu W, Sui S, Yin Y, Hu S, Zhang X (2009) Whole genome sequencing of lamb rotavirus and comparative analysis with other mammalian rotaviruses. Virus Genes 38(2):302–310.
Cunliffe NA, Gondwe JS, Broadhead RL, Molyneux ME, Woods PA, Bresee JS, Glass RI, Gentsch JR, Hart CA (1999) Rotavirus G and P types in children with acute diarrhea in
Blantyre, Malawi, from 1997 to 1998: predominance of novel P[6]G8 strains. J Med Virol 57:308-312.
de Beer M, Steele D (2002) Characterization of the VP7 and VP4 genes of a South African group A caprine rotavirus. GenBank record.
De Grazia S, Martella V, Giammanco GM, Gomara MI, Ramirez S, Cascio A, Colomba C, Arista S (2007) Canine-origin G3P[3] rotavirus strain in child with acute gastroenteritis. Emerg Infect Dis 13:1091-1093.
Do LP, Doan YH, Nakagomi T, Gauchan P, Kaneko M, Agbemabiese C, Dang AD, Nakagomi O (2015) Whole genome analysis of Vietnamese G2P[4] rotavirus strains possessing the NSP2 gene sharing an ancestral sequence with Chinese sheep and goat rotavirus strains. Microbiol Immunol 59(10):605-613.
Donato CM, Manuelpillai NM, Cowley D, Roczo-Farkas S, Buttery JP, Crawford NW, Kirkwood CD (2014) Genetic characterization of a novel G3P[14] rotavirus strain causing gastroenteritis in 12 year old Australian child Infect Genet Evol 25:97-109.
Dóró R, Laszlo B, Martella V, Leshem E, Gentsch J, Parashar U, Bányai K (2014) Review of global rotavirus strain prevalence data from six years post vaccine licensure surveillance: is there evidence of strain selection from vaccine pressure? Infect Genet Evol 28:446-461.
Dóró R, Farkas SL, Martella V, Bányai K (2015) Zoonotic transmission of rotavirus: surveillance and control. Expert Rev Anti Infect Ther 13(11):1337-1350.
Estes MK, Kapikian AZ (2007) Rotaviruses. In: (eds: Knipe DM, Howley PM) Fields’ Virology, 5th edn. Kluwer, Philadelphia, pp. 1917-1974.
Fitzgerald TA, Munoz M, Wood AR, Snodgrass DR (1995) Serological and genomic characterisation of group A rotaviruses from lambs. Arch Virol 140(9):1541–1548.
Galindo-Cardiel I, Fernandez-Jimenez M, Lujan L, Buesa J, Espada J, Fantova E, Blanco J, Segales J, Badiola JJ (2011) Novel group A rotavirus G8 P[1] as primary cause of an ovine diarrheic syndrome outbreak in weaned lambs. Vet Microbiol 149(3–4): 467–471.
Gazal S, Taku AK, Kumar B (2012) Predominance of rotavirus genotype G6P[11] in diarrhoeic lambs. Vet J. 193(1):299–300.
Gentsch JR, Laird AR, Bielfelt B, Griffin DD, Banyai K, Ramachandran M, Jain V, Cunliffe NA, Nakagomi O, Kirkwood CD, Fischer TK, Parashar UD, Bresee JS, Jiang B, Glass RI (2005) Serotype diversity and reassortment between human and animal rotavirus strains: implications for rotavirus vaccine programs. J Infect Dis 192:146-159.
Ghosh S, Alam MM, Ahmed MU, Talukdar RI, Paul SK, Kobayashi N (2010) Complete genome constellation of a caprine group A rotavirus strain reveals common evolution with ruminant and human rotavirus strains. J Gen Virol 91(9):2367–2373.
Hu L, Ramani S, Czako R, Sankaran B, Yu Y, Smith DF, Cummings RD, Estes MK, Venkataram Prasad BV, 2015. Structural basis of glycan specificity in neonate-specific
bovine-human reassortant rotavirus. Nat Commun 6. Khafagi MH, Mahmoud MA, Habashi AR (2010) Prevalence of rotavirus infections in small ruminants. Glob Vet. 4(5):539–543.
Kokkinos P.A.,•Ziros P.G., Monini M.,•Lampropoulou P., Karampini A., Papachatzi E., Mantagos S., Ruggeri F.M., Vantarakis A. (2013) Rare Types of Rotaviruses Isolated from Children with Acute Gastroenteritis in Patras, Greece, Intervirology 56:237-241.
Konstantopoulos A, Tragiannidis A, Fouzas S, Kavaliotis I, Tsiatsou O, Michailidou E et al. Burden of rotavirus gastroenteritis in children <5 years of age in Greece: hospital-based prospective surveillance (2008–2010). BMJ Open. 2013; 3(12):e003570.
Koukou D, Chatzichristou P, Trimis G, Siahanidou T, Skiathitou AV, Koutouzis EI, Syrogiannopoulos GA, Lourida A, Michos AG, Syriopoulou VP (2015) Rotavirus Gastroenteritis in a Neonatal Unit of a Greek Tertiary Hospital: Clinical Characteristics and Genotypes. PLoS One 10:e0133891.
Lee JB, Youn SJ, Nakagomi T, Park SY, Kim TJ, Song CS, Jang HK, Kim BS, Nakagomi O (2003) Isolation, serologic and molecular characterization of the first G3 caprine rotavirus. Arch Virol 148:643–657.
Legrottaglie R, Volpe A, Rizzi V, Agrimi P (1993) Isolation and identification of rotaviruses as aetiological agents of neonatal diarrhoea in kids. Electro-phoretical characterization by PAGE. New Microbiol 16:227–235.
Liu F, Xie JX, Liu CG, Wang KG, Zhou BJ, Wen M (2012) Full genomic sequence and phylogenetic analyses of a caprine G10P[15] rotavirus A strain XL detected in 2010. GenBank record.
Louge Uriarte EL, Badaracco A, Matthijnssens J, Zeller M, Heylen E, Manazza J, Miño S, Van Ranst M, Odeón A, Parreño V (2014) The first caprine rotavirus detected in Argentina displays genomic features resembling virus strains infecting members of the Bovidae and Camelidae. Vet Microbiol 171(1-2):189-197.
Marton S, Mihalov-Kovács E, Dóró R, Csata T, Fehér E, Oldal M, Jakab F, Matthijnssens J, Martella V, Bányai K (2015) Canine rotavirus C strain detected in Hungary shows marked genotype diversity. J Gen Virol 96:3059-3071.
Matthijnssens J, Potgieter CA, Ciarlet M, Parreno V, Martella V, Banyai K, Garaicoechea L, Palombo EA, Novo L, Zeller M, Arista S, Gerna G, Rahman M, Van Ranst M (2009) Are human P[14] rotavirus strains the result of interspecies transmissions from sheep or other ungulates that belong to the mammalian order Artiodactyla? J Virol 83(7):2917–2929.
Matthijnssens J, Ciarlet M, McDonald SM, Attoui H, Banyai K, Brister JR, Buesa J, Esona MD, Estes MK, Gentsch JR, Iturriza-Gomara M, Johne R, Kirkwood CD, Martella V, Mertens PP, Nakagomi O, Parreno V, Rahman M, Ruggeri FM, Saif LJ, Santos N, Steyer A, Taniguchi K, Patton JT, Desselberger U, Van Ranst M (2011a) Uniformity of rotavirus strain nomenclature proposed by the Rotavirus Classification Working Group (RCWG). Arch Virol 156:1397–1413.
Matthijnssens J, De Grazia S, Piessens J, Heylen E, Zeller M, Giammanco GM, Banyai K, Buonavoglia C, Ciarlet M, Martella V, Van Ranst M (2011b) Multiple reassortment and interspecies transmission events contribute to the diversity of feline, canine and feline/canine-like human group A rotavirus strains. Infect Genet Evol 11:1396-1406.
Matthijnssens J., Nakagomi O., Kirkwood C.D., Ciarlet M., Desselberger U., Van Ranst M. (2012) Group A rotavirus universal mass vaccination: how and to what extent will selective pressure influence prevalence of rotavirus genotypes? Expert Rev Vaccines, 11,1347-1354.
Matthijnssens J, Zeller M, Heylen E, De Coster S, Vercauteren J, Braeckman T, Van Herck K, Meyer N, Pirçon JY, Soriano-Gabarro M, Azou M, Capiau H, De Koster J, Maernoudt AS, Raes M, Verdonck L, Verghote M, Vergison A, Van Damme P, Van Ranst (2014) Higher proportion of G2P[4] rotaviruses in vaccinated hospitalized cases compared with unvaccinated hospitalized cases, despite high vaccine effectiveness against heterotypic G2P[4] rotaviruses Clin. Microbiol. Infect. 10, O702-710.
Mihalov-Kovacs E, Gellert A, Marton S, Farkas SL, Feher E, Oldal M, Jakab F, Martella V, Banyai K (2015) Candidate new rotavirus species in sheltered dogs, Hungary. Emerg Infect Dis 21:660-663.
Munoz M, Alvarez M, Lanza I, Carmenes P (1995) An outbreak of diarrhea associated with atypical rotaviruses in goat kids. Res Vet Sci 59:180–182.
Munoz M, Alvarez M, Lanza I, Carmenes P (1996) Role of enteric pathogens in the aetiology of neonatal diarrhoea in lambs and goat kids in Spain. Epidemiol Infect 1 17(1):203–211.
Ndze VN, Esona MD, Achidi EA, Gonsu KH, Doro R, Marton S, Farkas S, Ngeng MB, Ngu AF, Obama-Abena MT, Banyai K (2014) Full genome characterization of human Rotavirus A strains isolated in Cameroon, 2010-2011: diverse combinations of the G and P genes and lack of reassortment of the backbone genes. Infect Genet Evol 28:537-560.
Papp H, Laszlo B, Jakab FB, Ganesh B, De Grazia S, Matthijnssens J, Ciarlet M, Martella V, Banyai K, (2013) Review of group A rotavirus strains reported in swine and cattle. Vet Microbiol 165(3-4):190-199.
Parashar UD, Gibson CJ, Bresee JS, Glass RI (2006) Rotavirus and severe childhood diarrhea. Emerg Infect Dis 12:304-306.
Pratelli A, Martella V, Tempesta M, Buonavoglia C (1999) Characterization by polymerase chain reaction of ruminant rotaviruses isolated in Italy. New Microbiol 22:105–109.
Schoenian S (2007) Diarrhea (scours) in small ruminants. Comp Ext J Maryland University. http://www.sheepandgoat.com/articles/scours.html.
Settembre EC, Chen JZ, Dormitzer PR, Grigorieff N, Harrison SC (2011) Atomic model of an infectious rotavirus particle. EMBO J 30:408-416.
Shen S, Burke B, Desselberger U (1993) Nucleotide sequences of the VP4 and VP7 genes of a Chinese lamb rotavirus: evidence for a new P type in a G10 type virus. Virology 197(1):497–500.
Sieg M, Ruckner A, Kohler C, Burgener I, Vahlenkamp TW (2015) A bovine G8P[1] group A rotavirus isolated from an asymptomatically infected dog. J Gen Virol 96:106-114.
Tacharoenmuang R, Komoto S, Guntapong R, Ide T, Haga K, Katayama K, Kato T, Ouchi Y, Kurahashi H, Tsuji T, Sangkitporn S, Taniguchi K (2015) Whole Genomic Analysis of an Unusual Human G6P[14] Rotavirus Strain Isolated from a Child with Diarrhea in Thailand: Evidence for Bovine-To-Human Interspecies Transmission and Reassortment Events. PLoS ONE 10(9):e0139381.
Tam KI, Roy S, Esona MD, Jones S, Sobers S, Morris-Glasgow V, Rey-Benito G, Gentsch JR, Bowen MD, (2014) Full genomic characterization of a novel genotype combination, G4P[14], of a human rotavirus strain from Barbados. Infect Genet Evol 28:524-529.
Theil KW, Lance SE, McCloskey CM (1996) Rotaviruses associated with neonatal lamb diarrhea in two Wyoming shed-lambing operations. J Vet Diagn Invest 8(2):245–248.
Timurkan MO, Alkan F (2012) Molecular characterization of VP4, VP6, VP7 and NSP4 genes of group A rotavirus strains in different animal species in Turkey. GenBank record.
Trimis G, Koutsoumbari I, Kottaridi C, Palaiologou N, Assimakopoulou E, Spathis A et al. Hospitalbased surveillance of rotavirus gastroenteritis in the era of limited vaccine
uptake through the private sector. Vaccine. Oct 6 2011; 29(43):7292–7295.
Wani SA, Bhat MA, Nawchoo R, Munshi ZH, Bach AS (2004) Evidence of rotavirus associated with neonatal lamb diarrhea in India. Trop Anim Health Prod 36(1):27–32.
Wu FT, Banyai K, Lin JS, Wu HS, Hsiung CA, Huang YC, Hwang KP, Jiang B, Gentsch JR (2012) Putative canine origin of rotavirus strain detected in a child with diarrhea, Taiwan. Vector Borne Zoonotic Dis 12:170-173.
Zhang Z, Jia ZJ, Xiao F, Ye RF, Zhao J, Liu JL, Yang JH (2011) Full genomic analysis of lamb rotavirus strain Lamb-cc. GenBank record.
