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İnsan parechoviruslarının özellikleri, epidemiyolojisi ve klinik önemi

Yıl 2019, Cilt: 44 Sayı: 3, 1118 - 1130, 30.09.2019
https://doi.org/10.17826/cumj.528673

Öz

İnsan Parechoviruslar (Human Parechovirus; HPeV) tek iplikli, pozitif polariteli RNA viruslarıdır.  Başlangıçta klinik ve morfolojik özelliklerine göre insan enterovirusları içerisinde Echovirus 22 ve 23 olarak tanımlansalar da, genom organizasyonu, yapı ve replikasyonlarında birkaç farklı özellikleriyle enteroviruslar ve diğer picornavirus gruplarından farklı oldukları gösterilmiştir. HPeV’ler genetik ve antijenik heterojenlik göstermekte ve birçok tipi dünyanın her yerinde bulunan insan popülasyonunda yaygın bir şekilde bulunmaktadır. HPeV1 en yaygın genotip olup sıklıkla gastrointestinal ve solunum yolu hastalıklarına neden olmaktadır. HPeV3 enfeksiyonu yenidoğanlarda ve 3 aydan daha küçük infantlarda sepsis, meningoensefalit, nörolojik sekellere ve ölümlere yol açmaktadır. Küçük infantlarda tipik klinik tablo, ateş, şiddetli sinirlilik ve kızarıklıktan oluşur ve sıklıkla “ateşli, kırmızı döküntülü, kızgın bebekler” tanımına sebep olmaktadır. Günümüzde HPeV’lerin tanısı için en duyarlı metod real-time polimeraz zincir reaksiyonudur. Enfeksiyonlarının tedavisinde şimdiye kadar kadar herhangi bir spesifik antiviral tedavi mevcut olmayıp monoklonal antikorların kullanımı değerlendirilmektedir.  HPeV’ler üzerine yapılacak daha fazla çalışma ile bu virusların spesifik karakteristiklerinin anlaşılmasına ve uygun tedavi stratejilerinin geliştirilmesine ihtiyaç vardır.

Kaynakça

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Characteristics, epidemiology and clinical importance of human parechoviruses

Yıl 2019, Cilt: 44 Sayı: 3, 1118 - 1130, 30.09.2019
https://doi.org/10.17826/cumj.528673

Öz

Human parechoviruses (HPeVs) are single-stranded, positive-sense RNA viruses. Although originally described as echovirus 22 and 23 within human enteroviruses because of their clinical and morphological properties, they have since been shown to be distinct from this and other picornavirus groups in several features of their genome organisation, structure and replication. HPeVs show genetic and antigenic heterogeneity and a number of distinct types are known to circulate widely in human populations throughout the world. HPeV1 causes mostly gastrointestinal and respiratory tract infections. HPeV3 can cause sepsis and meningoencephalitis in neonates and infants younger than 3 months, which could lead to neurological sequelae and death. In young infants, the typical clinical presentation includes fever, severe irritability, and rash, often leading to descriptions of “hot, red, angry babies”. Nowadays, the most sensitive method for detecting HPeV is real-time polymerase chain reaction assays. In the treatment of infections, no specific antiviral therapy has been available so far and the use of monoclonal antibodies is still being evaluated. More research is therefore needed to understand the specific characteristics of this viruses and to develop appropriate treatment strategies.

Kaynakça

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  • 2. Picornaviridae.com, http://www.picornaviridae.com/(Erişimi tarihi:06.02.2018)
  • 3. Racaniello Vincent R. Picornaviridae: the viruses and their replication. In: Knipe DM, Howley PM, editors. Fields virology. 6th ed., vol. 1. Philadelphia: Lippincott Williams and Wilkins; 2013. p. 610.
  • 4. Hyypiä T, Horsnell C, Maaronen M, Khan M, Kalkkinen N, Auvinen P. et al. A distinct picornavirus group identified by sequence analysis. Proc Natl Acad Sci USA. 1992; 89(18): 8847-51.
  • 5. Cristanziano VD, Bottcher S, Diedrich S, Timmen-Wego M, Knops E, Lubke N, et al. Detection and characterization of enteroviruses and parechoviruses in healthy people living in the South of Cote d'Ivoire. J Clin Virol. 2015; 71(1): 40-3.
  • 6. Chuchaona W, Khamrin P, Yodmeeklin A, Saikruang W, Kongsricharoern T, Ukarapol N, et al. Detection and characterization of a novel human parechovirus genotype in Thailand. Infect Genet Evol. 2015; 31(1): 300-4.
  • 7. Nateri AS, Hughes PJ, Stanway G. In vivo and in vitro identification of structural and sequence elements of the human parechovirus 5' untranslated region required for internal initiation. J Virol. 2000; 74(14): 6269-77.
  • 8. Nateri AS, Hughes PJ, Stanway G. Terminal RNA replication elements in human parechovirus 1. J Virol. 2002; 76(24): 13116-22.
  • 9. Stanway G, Kalkkinen N, Roivainen M, Ghazi F, Khan M, Smyth M, Meurman O, Hyypiä T. Molecular and biological characteristics of echovirus 22, a representative of a new picornavirus group. J Virol. 1994; 68(12): 8232-8.
  • 10. Harvala H, Simmonds P. Human parechoviruses: biology, epidemiology and clinical significance. J Clin Virol. 2009; 45(1): 1-9.
  • 11. Wildenbeest JG, Harvala H, Pajkrt D, Wolthers KC. The need for treatment against human parechoviruses: how, why and when? Expert Rev Anti Infect Ther. 2010; 8(12): 1417-29.
  • 12. Schultheiss T, Emerson SU, Purcell RH, Gauss-Muller V. Polyprotein processing in echovirus 22: a first assessment. Biochem Biophys Res Commun. 1995. 26; 217(1): 1120–7.
  • 13. Krogerus C, Samuilova O, Poyry T, Jokitalo E, Hyypia T. Intracellular localization and effects of individually expressed human parechovirus 1 non-structural proteins. J Gen Virol. 2007. 88(Pt 3): 831–41.
  • 14. Simmonds P, Welch J. Frequency and dynamics of recombination within different species of human enteroviruses. J Virol. 2006; 80(1): 483–93.
  • 15. Simmonds P. 2006. Recombination and selection in the evolution of picornaviruses and other Mammalian positive-stranded RNA viruses. J Virol. 80: 11124–40.
  • 16. Benschop KS, Williams CH, Wolthers KC, Stanway G, Simmonds P. Widespread recombination within human parechoviruses: analysis of temporal dynamics and constraints. J Gen Virol. 2008; 89(Pt 4): 1030–5.
  • 17. Benschop KS, de VM, Minnaar RP, Stanway G, van der Hoek L, Wolthers KC, Simmonds P. Comprehensive full-length sequence analyses of human parechoviruses: diversity and recombination. J Gen Virol. 2010(Pt 1); 91: 145–54.
  • 18. Swiss Institute of Bioinformatics. 2011. ViralZone. Swiss Institute of Bioinformatics, Lausanne, Switzerland. http://www.expasy.org/viralzone.
  • 19. Faria NR, de Vries M, van Hemert FJ, Benschop K, van der Hoek L. Rooting human parechovirus evolution in time. BMC Evol Biol. 2009; 15;9: 164.
  • 20. Drake JW, Holland JJ. Mutation rates among RNA viruses. Proc Natl Acad Sci USA. 1999; 23; 96(24): 13910-3.
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  • 60. Wolthers KC, Benschop KS, Schinkel J, Molenkamp R, Bergevoet RM, Spijkerman IJ, et al. Human parechoviruses as an important viral cause of sepsislike illness and meningitis in young children. Clin Infect Dis. 2008; 1;47(3): 358-63.
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  • 62. Boivin G, Abed Y, Boucher FD. Human parechovirus 3 and neonatal infections. Emerg Infect Dis. 2005; 11: 103–5.
  • 63. Levorson RE, Jantausch BA, Wiedermann BL, Spiegel HM, Campos JM. Human Parechovirus -3 infection: emerging pathogen in neonatal sepsis 2. Pediatr Infect Dis J. 2009; 28(1): 545–47.
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  • 66. Harvala H, McLeish N, Kondracka J, McIntyre CL, McWilliam Leitch EC, Templeton K. et al. Comparison of human parechovirus and enterovirus detection frequencies in cerebrospinal fluid samples collected over a 5-year period in edinburgh: HPeV type 3 identified as the most common picornavirus type. J Med Virol. 2011; 83(5): 889-96.
  • 67. Ito M, Yamashita T, Tsuzuki H, Kabashima Y, Hasegawa A, Nagaya S, et al. Detection of human parechoviruses from clinical stool samples in Aichi, Japan. J Clin Microbiol 2010; 48(8): 2683-8.
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Toplam 93 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm Derleme
Yazarlar

Semih Tokak 0000-0003-2239-0014

Mehmet Özdemir 0000-0002-9316-771X

Yayımlanma Tarihi 30 Eylül 2019
Kabul Tarihi 27 Nisan 2019
Yayımlandığı Sayı Yıl 2019 Cilt: 44 Sayı: 3

Kaynak Göster

MLA Tokak, Semih ve Mehmet Özdemir. “İnsan parechoviruslarının özellikleri, Epidemiyolojisi Ve Klinik önemi”. Cukurova Medical Journal, c. 44, sy. 3, 2019, ss. 1118-30, doi:10.17826/cumj.528673.