Skip to main content
Top
Published in: Archives of Virology 11/2015

01-11-2015 | Brief Report

Molecular epidemiology of coxsackievirus type B1

Authors: Ichrak Abdelkhalek, Mohamed Seghier, Ahlem Ben Yahia, Henda Touzi, Zina Meddeb, Henda Triki, Dorra Rezig

Published in: Archives of Virology | Issue 11/2015

Login to get access

Abstract

Coxsackievirus type B1 (CVB1) has emerged globally as the predominant enterovirus serotype and is associated with epidemics of meningitis and chronic diseases. In this report, the phylogeny of CVB1 was studied based on the VP1 sequences of 11 North African isolates and 81 published sequences. All CVB1 isolates segregated into four distinct genogroups and 10 genotypes. Most of the identified genotypes of circulating CVB1 strains appear to have a strict geographical specificity. The North African strains were of a single genotype and probably evolved distinctly. Using a relaxed molecular clock model and three different population models (constant population, exponential growth and Bayesian skyline demographic models) in coalescent analysis using the BEAST program, the substitution rate in CVB1 varied between 6.95 × 10−3 and 7.37 × 10−3 substitutions/site/year in the VP1 region. This study permits better identification of circulating CVB1, which has become one of the most predominant enterovirus serotypes in humans.
Literature
1.
go back to reference Pallansch M, Roos R (2007) Enteroviruses: polioviruses, coxsackieviruses, echoviruses, and newer enteroviruses. In: Knipe DM, Howley PM (eds) Fields virology, 5th edn. Lippincott Williams and Wilkins, Philadelphia, pp 839–894 Pallansch M, Roos R (2007) Enteroviruses: polioviruses, coxsackieviruses, echoviruses, and newer enteroviruses. In: Knipe DM, Howley PM (eds) Fields virology, 5th edn. Lippincott Williams and Wilkins, Philadelphia, pp 839–894
2.
go back to reference Laitinen OH, Honkanen H, Pakkanen O, Oikarinen S, Hankaniemi MM, Huhtala H, Ruokoranta T, Lecouturier V, André P, Harju R, Virtanen SM, Lehtonen J, Almond JW, Simell T, Simell O, Ilonen J, Veijola R, Knip M, Hyöty H (2014) Coxsackievirus B1 is associated with induction of β-cell autoimmunity that portends type 1 diabetes. Diabetes 63(2):446–455. doi:10.2337/db13-0619 CrossRefPubMed Laitinen OH, Honkanen H, Pakkanen O, Oikarinen S, Hankaniemi MM, Huhtala H, Ruokoranta T, Lecouturier V, André P, Harju R, Virtanen SM, Lehtonen J, Almond JW, Simell T, Simell O, Ilonen J, Veijola R, Knip M, Hyöty H (2014) Coxsackievirus B1 is associated with induction of β-cell autoimmunity that portends type 1 diabetes. Diabetes 63(2):446–455. doi:10.​2337/​db13-0619 CrossRefPubMed
3.
go back to reference Oikarinen S, Tauriainen S, Hober D, Lucas B, Vazeou A, Sioofy-Khojine A, Bozas E, Muir P, Honkanen H, Ilonen J, Knip M, Keskinen P, Saha MT, Huhtala H, Stanway G, Bartsocas C, Ludvigsson J, Taylor K, Hyöty H (2014) Virus antibody survey in different European populations indicates risk association between coxsackievirus B1 and type 1 diabetes. Diabetes 63(2):655–662. doi:10.2337/db13-0620 CrossRefPubMed Oikarinen S, Tauriainen S, Hober D, Lucas B, Vazeou A, Sioofy-Khojine A, Bozas E, Muir P, Honkanen H, Ilonen J, Knip M, Keskinen P, Saha MT, Huhtala H, Stanway G, Bartsocas C, Ludvigsson J, Taylor K, Hyöty H (2014) Virus antibody survey in different European populations indicates risk association between coxsackievirus B1 and type 1 diabetes. Diabetes 63(2):655–662. doi:10.​2337/​db13-0620 CrossRefPubMed
4.
go back to reference Kim H, Kang B, Hwang S, Hong J, Chung J, Kim S, Jeong YS, Kim K, Cheon DS (2013) Molecular characteristics of human coxsackievirus B1 infection in Korea, 2008–2009. J Med Virol 85(1):110–115. doi:10.1002/jmv.23359 CrossRefPubMed Kim H, Kang B, Hwang S, Hong J, Chung J, Kim S, Jeong YS, Kim K, Cheon DS (2013) Molecular characteristics of human coxsackievirus B1 infection in Korea, 2008–2009. J Med Virol 85(1):110–115. doi:10.​1002/​jmv.​23359 CrossRefPubMed
5.
go back to reference Khetsuriani N, Lamonte A, Oberste MS, Pallansch M (2006) Neonatal enterovirus infections reported to the National Enterovirus Surveillance system in the United States, 1983–2003. Pediatr Infect Dis J 25:889–893CrossRefPubMed Khetsuriani N, Lamonte A, Oberste MS, Pallansch M (2006) Neonatal enterovirus infections reported to the National Enterovirus Surveillance system in the United States, 1983–2003. Pediatr Infect Dis J 25:889–893CrossRefPubMed
6.
go back to reference Khetsuriani N, Lamonte-Fowlkes A, Oberst S, Pallansch MA, Centers for Disease Control and Prevention (2006) Enterovirus surveillance—United States, 1970–2005. MMWR Surveill Summ 55:1–20PubMed Khetsuriani N, Lamonte-Fowlkes A, Oberst S, Pallansch MA, Centers for Disease Control and Prevention (2006) Enterovirus surveillance—United States, 1970–2005. MMWR Surveill Summ 55:1–20PubMed
7.
go back to reference Centers for Disease Control and Prevention (CDC) (2008) Increased detections and severe neonatal disease associated with coxsackievirus b1 infection—United States, 2007. MMWR 57:553–556 Centers for Disease Control and Prevention (CDC) (2008) Increased detections and severe neonatal disease associated with coxsackievirus b1 infection—United States, 2007. MMWR 57:553–556
8.
go back to reference Wikswo ME, Khetsuriani N, Fowlkes AL, Zheng X, Peñaranda S, Verma N, Shulman ST, Sircar K, Robinson CC, Schmidt T, Schnurr D, Oberste MS (2009) Increased activity of Coxsackievirus B1 strains associated with severe disease among young infants in the United States, 2007–2008. Clin Infect Dis 49(5):e44–e51. doi:10.1086/605090 CrossRefPubMed Wikswo ME, Khetsuriani N, Fowlkes AL, Zheng X, Peñaranda S, Verma N, Shulman ST, Sircar K, Robinson CC, Schmidt T, Schnurr D, Oberste MS (2009) Increased activity of Coxsackievirus B1 strains associated with severe disease among young infants in the United States, 2007–2008. Clin Infect Dis 49(5):e44–e51. doi:10.​1086/​605090 CrossRefPubMed
10.
go back to reference Muir P, Kammerer U, Korn K, Mulders MN, Poÿry T, Weissbrich B, Kandolf R, Cleator GM, Van Loon AM (1998) Molecular typing of enteroviruses: current status and future requirements. Clin Microbiol Rev 11(1):202–227PubMedCentralPubMed Muir P, Kammerer U, Korn K, Mulders MN, Poÿry T, Weissbrich B, Kandolf R, Cleator GM, Van Loon AM (1998) Molecular typing of enteroviruses: current status and future requirements. Clin Microbiol Rev 11(1):202–227PubMedCentralPubMed
12.
go back to reference Oberste MS, Maher K, Flemister MR (2000) Comparison of classic and molecular approaches for the identification of untypeable enteroviruses. J Clin Microbiol 38:1170–1174PubMedCentralPubMed Oberste MS, Maher K, Flemister MR (2000) Comparison of classic and molecular approaches for the identification of untypeable enteroviruses. J Clin Microbiol 38:1170–1174PubMedCentralPubMed
13.
go back to reference Ishiko H, Takeda N, Miyamura K, Kato N, Tanimura M, Lin KH, Yin-Murphy M, Tam JS, Mu GF, Yamazaki S (1992) Phylogenetic analysis of a coxsackievirus A24 variant: the most recent worldwide pandemic was caused by progenies of a virus prevalent around 1981. Virology 187:748–759CrossRefPubMed Ishiko H, Takeda N, Miyamura K, Kato N, Tanimura M, Lin KH, Yin-Murphy M, Tam JS, Mu GF, Yamazaki S (1992) Phylogenetic analysis of a coxsackievirus A24 variant: the most recent worldwide pandemic was caused by progenies of a virus prevalent around 1981. Virology 187:748–759CrossRefPubMed
14.
go back to reference Hughes MS, Hoey EM, Coyle PV (1993) A nucleotide sequence comparison of coxsackievirus B4 isolates from aquatic samples and clinical specimens. Epidemiol Infect 110:389–398PubMedCentralCrossRefPubMed Hughes MS, Hoey EM, Coyle PV (1993) A nucleotide sequence comparison of coxsackievirus B4 isolates from aquatic samples and clinical specimens. Epidemiol Infect 110:389–398PubMedCentralCrossRefPubMed
15.
go back to reference Takeda N, Tanimura M, Miyamura K (1994) Molecular evolution of the major capsid protein VP1 of enterovirus 70. J Virol 68:854–862PubMedCentralPubMed Takeda N, Tanimura M, Miyamura K (1994) Molecular evolution of the major capsid protein VP1 of enterovirus 70. J Virol 68:854–862PubMedCentralPubMed
16.
go back to reference Brown BA, Oberste MS, Alexander JP Jr, Kennett ML, Pallansch MA (1999) Molecular epidemiology and evolution of enterovirus 71 strains isolated from 1970 to 1998. J Virol 73:9969–9975PubMedCentralPubMed Brown BA, Oberste MS, Alexander JP Jr, Kennett ML, Pallansch MA (1999) Molecular epidemiology and evolution of enterovirus 71 strains isolated from 1970 to 1998. J Virol 73:9969–9975PubMedCentralPubMed
17.
go back to reference Santti J, Harvala H, Kinnunen L, Hyypia T (2000) Molecular epidemiology and evolution of coxsackievirus A9. J Gen Virol 81:1361–1372CrossRefPubMed Santti J, Harvala H, Kinnunen L, Hyypia T (2000) Molecular epidemiology and evolution of coxsackievirus A9. J Gen Virol 81:1361–1372CrossRefPubMed
18.
go back to reference Wang JR, Tsai HP, Huang SW, Kuo PH, Kiang D, Liu CC (2002) Laboratory diagnosis and genetic analysis of an echovirus 30- associated outbreak of aseptic meningitis in Taiwan in 2001. J Clin Microbiol 40:4439–4444PubMedCentralCrossRefPubMed Wang JR, Tsai HP, Huang SW, Kuo PH, Kiang D, Liu CC (2002) Laboratory diagnosis and genetic analysis of an echovirus 30- associated outbreak of aseptic meningitis in Taiwan in 2001. J Clin Microbiol 40:4439–4444PubMedCentralCrossRefPubMed
19.
go back to reference Bailly JL, Brosson D, Archimbaud C, Chambon M, Henquell C, Peigue-Lafeuille H (2002) Genetic diversity of echovirus 30 during a meningitis outbreak, demonstrated by direct molecular typing from cerebrospinal fluid. J Med Virol 68(4):558–567CrossRefPubMed Bailly JL, Brosson D, Archimbaud C, Chambon M, Henquell C, Peigue-Lafeuille H (2002) Genetic diversity of echovirus 30 during a meningitis outbreak, demonstrated by direct molecular typing from cerebrospinal fluid. J Med Virol 68(4):558–567CrossRefPubMed
20.
22.
go back to reference Mulders MN, Salminen M, Kalkkinen N, Hovi T (2000) Molecular epidemiology of coxsackievirus B4 and disclosure of the correct VP1/2A (pro) cleavage site: evidence for high genomic diversity and long-term endemicity of distinct genotypes. J Gen Virol 81(Pt3):803–812CrossRefPubMed Mulders MN, Salminen M, Kalkkinen N, Hovi T (2000) Molecular epidemiology of coxsackievirus B4 and disclosure of the correct VP1/2A (pro) cleavage site: evidence for high genomic diversity and long-term endemicity of distinct genotypes. J Gen Virol 81(Pt3):803–812CrossRefPubMed
23.
go back to reference McWilliam Leitch EC, Cabrerizo M, Cardos J, Harvala H, Ivanova OE, Kroes AC, Lukashev A, Muir P, Odoom J et al (2010) Evolutionary dynamics and temporal/geographical correlates of recombination in the human enterovirus echovirus types 9, 11, and 30. J Virol 84:9292–9300. doi:10.1128/JVI.00783-10 PubMedCentralCrossRefPubMed McWilliam Leitch EC, Cabrerizo M, Cardos J, Harvala H, Ivanova OE, Kroes AC, Lukashev A, Muir P, Odoom J et al (2010) Evolutionary dynamics and temporal/geographical correlates of recombination in the human enterovirus echovirus types 9, 11, and 30. J Virol 84:9292–9300. doi:10.​1128/​JVI.​00783-10 PubMedCentralCrossRefPubMed
24.
go back to reference Oberste MS, Maher K, Kennett ML, Campbell JJ, Carpenter MS, Schnurr D, Pallansch MA (1999) Molecular epidemiology and genetic diversity of echovirus type 30 (E30): genotypes correlate with temporal dynamics of E30 isolation. J Clin Microbiol 37:3928–3933PubMedCentralPubMed Oberste MS, Maher K, Kennett ML, Campbell JJ, Carpenter MS, Schnurr D, Pallansch MA (1999) Molecular epidemiology and genetic diversity of echovirus type 30 (E30): genotypes correlate with temporal dynamics of E30 isolation. J Clin Microbiol 37:3928–3933PubMedCentralPubMed
25.
go back to reference Oberste MS, Nix WA, Kilpatrick DR, Flemister MR, Pallansch MA (2003) Molecular epidemiology and type-specific detection of echovirus 11 isolates from the Americas, Europe, Africa, Australia, southern Asia and the Middle East. Virus Res 91:241–248CrossRefPubMed Oberste MS, Nix WA, Kilpatrick DR, Flemister MR, Pallansch MA (2003) Molecular epidemiology and type-specific detection of echovirus 11 isolates from the Americas, Europe, Africa, Australia, southern Asia and the Middle East. Virus Res 91:241–248CrossRefPubMed
26.
go back to reference Fares W, Rezig D, Seghier M, Ben Yahia A, Touzi H, Triki H (2011) Phylogenetic analysis of complete VP1 sequences of echoviruses 11 and 6: high genetic diversity and circulation of genotypes with a wide geographical and temporal range. J Med Microbiol 60(Pt7):1017–1025. doi:10.1099/jmm.0.028795-0 CrossRefPubMed Fares W, Rezig D, Seghier M, Ben Yahia A, Touzi H, Triki H (2011) Phylogenetic analysis of complete VP1 sequences of echoviruses 11 and 6: high genetic diversity and circulation of genotypes with a wide geographical and temporal range. J Med Microbiol 60(Pt7):1017–1025. doi:10.​1099/​jmm.​0.​028795-0 CrossRefPubMed
27.
32.
go back to reference Bahri O, Rezig D, Nejma-Oueslati BB, Yahia AB, Sassi JB, Hogga N, Sadraoui A, Triki H (2005) Enteroviruses in Tunisia: virological surveillance over 12 years (1992–2003). J Med Microbiol 54(Pt1):63–69CrossRefPubMed Bahri O, Rezig D, Nejma-Oueslati BB, Yahia AB, Sassi JB, Hogga N, Sadraoui A, Triki H (2005) Enteroviruses in Tunisia: virological surveillance over 12 years (1992–2003). J Med Microbiol 54(Pt1):63–69CrossRefPubMed
33.
go back to reference McWilliam Leitch EC, Cabrerizo M, Cardosa J, Harvala H, Ivanova OE, Koike S, Kroes AC, Lukashev A, Perera D, Roivainen M, Susi P, Trallero G, Evans DJ, Simmonds P (2012) The association of recombination events in the founding and emergence of subgenogroup evolutionary lineages of human enterovirus 71. J Virol 86(5):2676–2685. doi:10.1128/JVI.06065-11 PubMedCentralCrossRefPubMed McWilliam Leitch EC, Cabrerizo M, Cardosa J, Harvala H, Ivanova OE, Koike S, Kroes AC, Lukashev A, Perera D, Roivainen M, Susi P, Trallero G, Evans DJ, Simmonds P (2012) The association of recombination events in the founding and emergence of subgenogroup evolutionary lineages of human enterovirus 71. J Virol 86(5):2676–2685. doi:10.​1128/​JVI.​06065-11 PubMedCentralCrossRefPubMed
34.
go back to reference Bailly JL, Mirand A, Henquell C, Archimbaud C, Chambon M, Regagnon C, Charbonné F, Peigue-Lafeuille H (2011) Repeated genomic transfers from echovirus 30 to echovirus 6 lineages indicate co-divergence between co-circulating populations of the two human enterovirus serotypes. Infect Genet Evol 11(2):276–289. doi:10.1016/j.meegid.2010.06.019 CrossRefPubMed Bailly JL, Mirand A, Henquell C, Archimbaud C, Chambon M, Regagnon C, Charbonné F, Peigue-Lafeuille H (2011) Repeated genomic transfers from echovirus 30 to echovirus 6 lineages indicate co-divergence between co-circulating populations of the two human enterovirus serotypes. Infect Genet Evol 11(2):276–289. doi:10.​1016/​j.​meegid.​2010.​06.​019 CrossRefPubMed
35.
go back to reference Tao Z, Wang H, Li Y, Xu A, Zhang Y, Song L, Yoshida H, Xu Q, Yang J, Zhang Y, Liu Y, Feng L, Xu W (2011) Cocirculation of two transmission lineages of echovirus 6 in Jinan, China, as revealed by environmental surveillance and sequence analysis. Appl Environ Microbiol 77(11):3786–3792. doi:10.1128/AEM.03044-10 PubMedCentralCrossRefPubMed Tao Z, Wang H, Li Y, Xu A, Zhang Y, Song L, Yoshida H, Xu Q, Yang J, Zhang Y, Liu Y, Feng L, Xu W (2011) Cocirculation of two transmission lineages of echovirus 6 in Jinan, China, as revealed by environmental surveillance and sequence analysis. Appl Environ Microbiol 77(11):3786–3792. doi:10.​1128/​AEM.​03044-10 PubMedCentralCrossRefPubMed
39.
Metadata
Title
Molecular epidemiology of coxsackievirus type B1
Authors
Ichrak Abdelkhalek
Mohamed Seghier
Ahlem Ben Yahia
Henda Touzi
Zina Meddeb
Henda Triki
Dorra Rezig
Publication date
01-11-2015
Publisher
Springer Vienna
Published in
Archives of Virology / Issue 11/2015
Print ISSN: 0304-8608
Electronic ISSN: 1432-8798
DOI
https://doi.org/10.1007/s00705-015-2561-5

Other articles of this Issue 11/2015

Archives of Virology 11/2015 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.