Enterovirus A71 capsid coloured by chains
Enterovirus A71 capsid
coloured by chains
Virus classification Edit this classification
(unranked): Virus
Realm: Riboviria
Kingdom: Orthornavirae
Phylum: Pisuviricota
Class: Pisoniviricetes
Order: Picornavirales
Family: Picornaviridae
Genus: Enterovirus

See text

Enterovirus is a genus of positive-sense single-stranded RNA viruses associated with several human and mammalian diseases. Enteroviruses are named by their transmission-route through the intestine ('enteric' meaning intestinal).[1]

Serologic studies have distinguished 71 human enterovirus serotypes on the basis of antibody neutralization tests. Additional antigenic variants have been defined within several of the serotypes on the basis of reduced or nonreciprocal cross-neutralization between variant strains. On the basis of their pathogenesis in humans and animals, the enteroviruses were originally classified into four groups, polioviruses, Coxsackie A viruses (CA), Coxsackie B viruses (CB), and echoviruses, but it was quickly realized that there were significant overlaps in the biological properties of viruses in the different groups. Enteroviruses isolated more recently are named with a system of consecutive numbers: EV-D68, EV-B69, EV-D70, EV-A71, etc., where genotyping is based on the VP1 capsid region.[2]

Enteroviruses affect millions of people worldwide each year and are often found in the respiratory secretions (e.g., saliva, sputum, or nasal mucus) and stool of an infected person. Historically, poliomyelitis was the most significant disease caused by an enterovirus, namely poliovirus. There are 81 non-polio and 3 polio enteroviruses that can cause disease in humans. Of the 81 non-polio types, there are 22 Coxsackie A viruses, 6 Coxsackie B viruses, 28 echoviruses, and 25 other enteroviruses.[3]

Poliovirus, as well as coxsackie and echovirus, is spread through the fecal–oral route. Infection can result in a wide variety of symptoms, including those of: mild respiratory illness (the common cold), hand, foot and mouth disease, acute hemorrhagic conjunctivitis, aseptic meningitis, myocarditis, severe neonatal sepsis-like disease, acute flaccid paralysis, and the related acute flaccid myelitis.[3]


Enterovirus genome, polyprotein processing cascade, and architecture of enterovirus capsid

Enteroviruses are members of the picornavirus family, a large and diverse group of small RNA viruses characterized by a single positive-strand genomic RNA. All enteroviruses contain a genome of approximately 7,500 bases and are known to have a high mutation rate due to low-fidelity replication and frequent recombination.[4] After infection of the host cell, the genome is translated in a cap-independent manner into a single polyprotein, which is subsequently processed by virus-encoded proteases into the structural capsid proteins and the nonstructural proteins, which are mainly involved in the replication of the virus.[5]

RNA recombination appears to be a major driving force in the evolution of enteroviruses as well as in the shaping of their genetic architecture.[6] The mechanism of recombination of the RNA genome likely involves template strand switching during RNA replication, a process known as copy choice recombination.[6] RNA recombination is considered to be an adaptation for dealing with RNA genome damage and a source of genetic diversity.[7] It is also a source of concern for vaccination strategies, because live attenuated/mutated strains used for vaccination could potentially recombine with wild-type related strains, as has been the case with circulating vaccine derived polio viruses (cVDPDs).[8][9] The capsid region and especially VP1 is a recombination coldspot, and this is one of the main reasons to use this region for genotyping.[2] However, the 5'UTR - capsid junction and the beginning of the P2 region have been observed to recombine very frequently, although recombinations do occur in the rest of the genome as well. Interestingly, the enterovirus species EV-A, EV-B, EV-C, EV-D have not been observed so far to exchange genomic regions among them, with the exception of the 5'UTR.[10]

Member viruses

Enterovirus A–L

Main articles: Coxsackie A virus, Coxsackie B virus, and Echovirus

Enteroviruses are a group of ubiquitous viruses that cause a number of infections which are usually mild. The genus enterovirus includes enteroviruses and rhinoviruses. Enterovirus A include coxsackievirus A2, A3, A4, A5, A6, A7, A8, A10, A12, A14, A16 and enterovirus A71, A76, A89, A90, A91, A92, A144, A119, A120, A121, A122 (simian virus 19), A123 (simian virus 43), A124 (simian virus 46), A125 (baboon enterovirus A13).[11] Some viruses initially reported as novel have been found to be misidentified. Thus, coxsackievirus A23 is the same serotype as echovirus 9, and coxsackievirus A15 is the same serotype as coxsackievirus A11 and coxsackievirus A18 is the same serotype as coxsackievirus A13.[citation needed]

Life cycle of an enterovirus

Coxsackie A16 virus causes human hand, foot and mouth disease.[citation needed]

Enterovirus B includes coxsackievirus B1,2,3,4,5,6; coxsackievirus A9; echovirus 1–33 and enterovirus B69–113.[11] Coxsackie B viruses are found worldwide and can cause myocarditis (inflammation of the heart); pericarditis (inflammation of the sac surrounding the heart); meningitis (inflammation of the membranes that line the brain and spinal cord); and pancreatitis (inflammation of the pancreas). The Coxsackie B viruses are also reported to cause a spastic paralysis due to the degeneration of neuronal tissue and muscle injury. Infections usually occur during warm summer months with symptoms including exanthema, pleurodynia, flu-like illness consisting of fever, fatigue, malaise, myalgia, nausea, abdominal pain and vomiting.[12] Echoviruses are a cause of many of the nonspecific viral infections that can range from minor illness to severe, potentially fatal conditions such as aseptic meningitis, encephalitis, paralysis and myocarditis.[13] It is mainly found in the intestine, and can cause nervous disorders.[14] Type B enteroviruses are responsible for a vast number of mild and acute infections. They have been reported to remain in the body causing persistent infections contributing to chronic diseases such as type I diabetes.[15]

Enterovirus C consists of polioviruses 1,2 and 3; coxsackieviruses A1, A11, A13, A18, A17, 20, A21, A22, A24 and enterovirus C95, C96, C99, C102, C104, C105, C109, C113, C118. The three serotypes of poliovirus, PV-1, PV-2, and PV-3 each have a slightly different capsid protein. Capsid proteins define cellular receptor specificity and virus antigenicity. PV-1 is the most common type to cause infection in humans; however, all three forms are extremely contagious spreading through person-to-person contact. Poliovirus causes Polio, or Poliomyelitis, which is a disabling and life-threatening disease that causes paresthesia, meningitis and permanent paralysis.[16] Symptoms can include sore throat, fever, tiredness, nausea, headache and stomach pain although 72% of those that get infected will not display visible symptoms.[16] There are two types of vaccines available to prevent polio: inactivated poliovirus vaccine given as an injection in the leg (IPV) or arm and oral poliovirus vaccine (OPV). The polio vaccine is highly efficacious giving protection to 99 out of 100 children vaccinated.[16]

Persistent non-cytolytic enterovirus

Enteroviruses are capable of producing acute infections that are rapidly cleared by the adaptive immune response.[17][18] However, genomic mutations which enterovirus B serotypes (such as coxsackievirus B and echovirus) may acquire in the host during the acute phase of the infection can transform these viruses into the non-cytolytic form (also known as non-cytopathic or defective enterovirus), a form which is capable of causing persistent low-level infections in human tissues that can last indefinitely.[19]

This persistent non-cytolytic enterovirus is a mutated quasispecies,[17] and such non-cytolytic infections have been found in the pancreas in type 1 diabetes,[20][21] in chronic myocarditis and dilated cardiomyopathy,[22][17][23] in valvular heart disease,[24] in the muscles, intestines and brain in myalgic encephalomyelitis,[25][26] and in Sjögren's syndrome.[27] In these persistent infections, enteroviral RNA is present at low levels in the tissues (both as single-stranded viral RNA, and in the more immune resistant doubled-stranded RNA form). Some researchers believe this enteroviral RNA is just a remnant of the acute infection,[18] although other scientists believe these persistent intracellular viral RNA infections may have pathological effects, playing a causal role their associated diseases.[28]

Enterovirus D68

Main article: Enterovirus D68

EV-D68 first was identified in California in 1962. Compared with other enteroviruses, it has been rarely reported in the U.S. in the past 40 years. Most people who get infected are infants, children, and teens. EV-D68 usually causes mild to severe respiratory illness; however, the full spectrum of EV-D68 illness is not well-defined. Most start with common cold symptoms of runny nose and cough. Some, but not all, may also have fever. For more severe cases, difficulty breathing, wheezing or problems catching your breath may occur. As of October 4, 2014, there has been one death in New Jersey directly linked to EV-D68,[29] as well as one death in Rhode Island[citation needed] attributed to a combination of EV-D68 and sepsis caused by an infection of staphylococcus aureus.[30][31]

Enterovirus A71

Main article: Enterovirus A71

Enterovirus A71 (EV-A71) is notable as one of the major causative agents for hand, foot and mouth disease (HFMD), and is sometimes associated with severe central nervous system diseases.[32] EV-A71 was first isolated and characterized from cases of neurological disease in California in 1969.[33][34] To date, little is known about the molecular mechanisms of host response to EV-A71 infection, but increases in the level of mRNAs encoding chemokines, proteins involved in protein degradation, complement proteins, and proapoptotis proteins have been implicated.[35]


Main article: Poliovirus

There are three serotypes of poliovirus, PV-1, PV-2, and PV-3; each with a slightly different capsid protein. Capsid proteins define cellular receptor specificity and virus antigenicity. PV-1 is the most common form encountered in nature; however, all three forms are extremely infectious.[36] Poliovirus can affect the spinal cord and cause poliomyelitis.

Polioviruses were formerly classified as a species belonging to the genus Enterovirus in the family Picornaviridae. The Poliovirus species has been eliminated from the genus Enterovirus. The following serotypes, Human poliovirus 1, Human poliovirus 2, and Human poliovirus 3, were assigned to the species Human enterovirus C, in the genus Enterovirus in the family Picornaviridae. The type species of the genus Enterovirus was changed from Poliovirus to Human enterovirus C. This has been ratified in April 2008.[37] The 39th Executive Committee (EC39) of the International Committee on Taxonomy of Viruses (ICTV) met in Canada during June 2007 with new taxonomic proposals.[38]

Two of the proposals with three changes were:

Proposals approved at the (EC39) meeting of 2007, were sent to members of ICTV via email for ratification and have become official taxonomy. There have been a total of 215 taxonomic proposals, which have been approved and ratified since the 8th ICTV Report of 2005.[41]

The ratification process was performed by email. The proposals were sent electronically via email on March 18, 2008, to ICTV members with a request to vote on whether to ratify the taxonomic proposals, with a 1-month deadline. The following are two of the taxonomic proposals with three changes that were ratified by ICTV members in April 2008:


Diseases caused by enterovirus infection

Enteroviruses generally infect by the fecal–oral route and target the gastrointestinal epithelium early during their life cycle. They can also infect by the respiratory tract as in the case of enterovirus D68 and rhinoviruses.[42]

Enteroviruses cause a wide range of symptoms, and while their long list of signs and symptoms should put them on the differential diagnosis list of many illnesses, they often go unnoticed. Enteroviruses can cause anything from rashes in small children, to summer colds, to encephalitis, to blurred vision, to pericarditis. Enteroviral infections have a great range in presentation and seriousness. Non polio enteroviruses cause 10–15 million infections and tens of thousands of hospitalizations in the US each year.[43] Enteroviruses can be identified through cell culture or PCR assay, collected from fecal or respiratory specimens.[44] Below are common enterovirus related diseases, including poliomyelitis.

Suspected diseases

Encephalitis lethargica, the 1917–1926 "sleeping sickness".[52]

Possible correlations being studied

Enterovirus has been speculated to be connected with Type 1 diabetes.[53][54][55][56] It has been proposed that type 1 diabetes is a virus-triggered autoimmune response in which the immune system attacks virus-infected cells along with the insulin-producing beta cells in the pancreas.[57] A team working at University of Tampere, Finland identified the enterovirus Coxsackievirus B1 as possibly linked to type 1 diabetes (which is an autoimmune disease).[58][59]

Enteroviruses, including polioviruses, may be a cause of myalgic encephalomyelitis/chronic fatigue syndrome (CFS/ME).[60]


Most people who contract enterovirus have mild symptoms lasting about a week. Those with higher risk may have more complications, sometimes becoming fatal.[61] The most common sign of enterovirus is a common cold. More intense symptoms of enterovirus include hypoxia, aseptic meningitis, conjunctivitis, hand, foot and mouth disease, and paralysis.


Treatment for enteroviral infection is mainly supportive. In cases of pleurodynia, treatment consists of analgesics to relieve the severe pain that occurs in patients with the disease; in some severe cases, opiates may be needed. Treatment for aseptic meningitis caused by enteroviruses is also mainly symptomatic. In patients with enteroviral carditis, treatment consists of the prevention and treatment of complications such as arrhythmias, pericardial effusion, and cardiac failure. Other treatments that have been investigated for enteroviral carditis include intravenous immunoglobulin.[62]


Maximum likelihood phylogenetic trees of enterovirus species A, B, C, D and rhinovirus A, B, C isolates from Latin America. The 5'UTR region is much more affected by recombination events than the VP4/VP2 coding sequence.[63]

The enterovirus genus includes the following fifteen species:[64]

These fifteen species' serotype include:

See also


  1. ^ "Genus: Enterovirus". International Committee on Taxonomy of Viruses (ICTV). Retrieved 5 February 2019. Derivation of names Entero: from Greek enteron, 'intestine'[dead link]
  2. ^ a b Oberste MS, Maher K, Kilpatrick DR, Pallansch MA (March 1999). "Molecular evolution of the human enteroviruses: correlation of serotype with VP1 sequence and application to picornavirus classification". Journal of Virology. 73 (3): 1941–8. doi:10.1128/JVI.73.3.1941-1948.1999. PMC 104435. PMID 9971773.
  3. ^ a b "Overview of Enterovirus Infections". Merck & Co. February 2018. Retrieved 2019-07-17.
  4. ^ Li L, He Y, Yang H, Zhu J, Xu X, Dong J, Zhu Y, Jin Q (August 2005). "Genetic characteristics of human enterovirus 71 and coxsackievirus A16 circulating from 1999 to 2004 in Shenzhen, People's Republic of China". Journal of Clinical Microbiology. 43 (8): 3835–9. doi:10.1128/JCM.43.8.3835-3839.2005. PMC 1233905. PMID 16081920.
  5. ^ Merkle I, van Ooij MJ, van Kuppeveld FJ, Glaudemans DH, Galama JM, Henke A, Zell R, Melchers WJ (October 2002). "Biological significance of a human enterovirus B-specific RNA element in the 3' nontranslated region". Journal of Virology. 76 (19): 9900–9. doi:10.1128/JVI.76.19.9900-9909.2002. PMC 136489. PMID 12208967.
  6. ^ a b Muslin C, Mac Kain A, Bessaud M, Blondel B, Delpeyroux F. Recombination in Enteroviruses, a Multi-Step Modular Evolutionary Process. Viruses. 2019 Sep 14;11(9):859. doi: 10.3390/v11090859. PMID 31540135 Review.
  7. ^ Barr JN, Fearns R. How RNA viruses maintain their genome integrity. J Gen Virol. 2010 Jun;91(Pt 6):1373–87. doi: 10.1099/vir.0.020818-0. Epub 2010 Mar 24. PMID 20335491 Review
  8. ^ Rakoto-Andrianarivelo, Mala; Guillot, Sophie; Iber, Jane; Balanant, Jean; Blondel, Bruno; Riquet, Franck; Martin, Javier; Kew, Olen; Randriamanalina, Bakolalao; Razafinimpiasa, Lalatiana; Rousset, Dominique (2007-12-14). Holmes, Edward C (ed.). "Co-Circulation and Evolution of Polioviruses and Species C Enteroviruses in a District of Madagascar". PLOS Pathogens. 3 (12): e191. doi:10.1371/journal.ppat.0030191. ISSN 1553-7374. PMC 2134956. PMID 18085822.
  9. ^ Joffret, Marie-Line; Jégouic, Sophie; Bessaud, Maël; Balanant, Jean; Tran, Coralie; Caro, Valerie; Holmblat, Barbara; Razafindratsimandresy, Richter; Reynes, Jean-Marc; Rakoto-Andrianarivelo, Mala; Delpeyroux, Francis (2012-05-01). "Common and Diverse Features of Cocirculating Type 2 and 3 Recombinant Vaccine-Derived Polioviruses Isolated From Patients With Poliomyelitis and Healthy Children". The Journal of Infectious Diseases. 205 (9): 1363–1373. doi:10.1093/infdis/jis204. ISSN 1537-6613. PMID 22457288.
  10. ^ Muslin, Claire; Joffret, Marie-Line; Pelletier, Isabelle; Blondel, Bruno; Delpeyroux, Francis (2015-11-12). Lauring, Adam (ed.). "Evolution and Emergence of Enteroviruses through Intra- and Inter-species Recombination: Plasticity and Phenotypic Impact of Modular Genetic Exchanges in the 5' Untranslated Region". PLOS Pathogens. 11 (11): e1005266. doi:10.1371/journal.ppat.1005266. ISSN 1553-7374. PMC 4643034. PMID 26562151.
  11. ^ a b "Enterovirus A". ICTV. Retrieved 2020-11-21.
  12. ^ Tariq, Naveen; Kyriakopoulos, Chris (2020), "Group B Coxsackie Virus", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32809618, retrieved 2020-11-21
  13. ^ "Echovirus Infection: Background, Pathophysiology, Epidemiology". 2020-03-22. Retrieved 21 November 2020.
  14. ^ Huang HI, Shih SR (24 Nov 2015). "Neurotropic Enterovirus Infections in the Central Nervous System". Viruses. 7 (11): 6051–6066. doi:10.3390/v7112920. PMC 4664993. PMID 26610549.
  15. ^ Marjomäki, Varpu; Turkki, Paula; Huttunen, Moona (2015-12-07). "Infectious Entry Pathway of Enterovirus B Species". Viruses. 7 (12): 6387–6399. doi:10.3390/v7122945. ISSN 1999-4915. PMC 4690868. PMID 26690201.
  16. ^ a b c "What is Polio?". www.cdc.gov. 2020-06-17. Retrieved 2020-11-21.
  17. ^ a b c Kim KS, Tracy S, Tapprich W, Bailey J, Lee CK, Kim K, Barry WH, Chapman NM (June 2005). "5'-Terminal deletions occur in coxsackievirus B3 during replication in murine hearts and cardiac myocyte cultures and correlate with encapsidation of negative-strand viral RNA". Journal of Virology. 79 (11): 7024–41. doi:10.1128/JVI.79.11.7024-7041.2005. PMC 1112132. PMID 15890942.
  18. ^ a b Flynn CT, Kimura T, Frimpong-Boateng K, Harkins S, Whitton JL (December 2017). "Immunological and pathological consequences of coxsackievirus RNA persistence in the heart". Virology. 512: 104–112. doi:10.1016/j.virol.2017.09.017. PMC 5653433. PMID 28950225.
  19. ^ Chapman, Nora M. (2022-05-12). "Persistent Enterovirus Infection: Little Deletions, Long Infections". Vaccines. 10 (5): 770. doi:10.3390/vaccines10050770. ISSN 2076-393X. PMC 9143164. PMID 35632526.
  20. ^ Krogvold, Lars; Edwin, Bjørn; Buanes, Trond; Frisk, Gun; Skog, Oskar; Anagandula, Mahesh; Korsgren, Olle; Undlien, Dag; Eike, Morten C.; Richardson, Sarah J.; Leete, Pia; Morgan, Noel G.; Oikarinen, Sami; Oikarinen, Maarit; Laiho, Jutta E. (May 2015). "Detection of a low-grade enteroviral infection in the islets of langerhans of living patients newly diagnosed with type 1 diabetes". Diabetes. 64 (5): 1682–1687. doi:10.2337/db14-1370. hdl:10871/17927. ISSN 1939-327X. PMID 25422108. S2CID 40883074.
  21. ^ Chehadeh, W.; Kerr-Conte, J.; Pattou, F.; Alm, G.; Lefebvre, J.; Wattré, P.; Hober, D. (November 2000). "Persistent infection of human pancreatic islets by coxsackievirus B is associated with alpha interferon synthesis in beta cells". Journal of Virology. 74 (21): 10153–10164. doi:10.1128/jvi.74.21.10153-10164.2000. ISSN 0022-538X. PMC 102054. PMID 11024144.
  22. ^ Chapman, N. M.; Kim, K. S. (2008). "Persistent Coxsackievirus Infection: Enterovirus Persistence in Chronic Myocarditis and Dilated Cardiomyopathy". Group B Coxsackieviruses. Current Topics in Microbiology and Immunology. Vol. 323. pp. 275–292. doi:10.1007/978-3-540-75546-3_13. ISBN 978-3-540-75545-6. ISSN 0070-217X. PMID 18357775.
  23. ^ "Persistent Coxsackievirus Infection: Enterovirus Persistence in Chronic Myocarditis and Dilated Cardiomyopathy". Group B coxsackieviruses. Tracy, S. (Steven), Oberste, M. Steven., Drescher, Kristen M. Berlin: Springer. 2008. pp. 275–286. ISBN 9783540755463. OCLC 233973571.((cite book)): CS1 maint: others (link)
  24. ^ "Enterovirus replication in valvular tissue from patients with chronic rheumatic heart disease". academic.oup.com. Retrieved 2023-10-11.
  25. ^ O'Neal, Adam J.; Hanson, Maureen R. (2021-06-18). "The Enterovirus Theory of Disease Etiology in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Critical Review". Frontiers in Medicine. 8: 688486. doi:10.3389/fmed.2021.688486. ISSN 2296-858X. PMC 8253308. PMID 34222292.
  26. ^ Hanson, Maureen R. (2023-08-17). "The viral origin of myalgic encephalomyelitis/chronic fatigue syndrome". PLOS Pathogens. 19 (8): e1011523. doi:10.1371/journal.ppat.1011523. ISSN 1553-7366. PMC 10434940. PMID 37590180.
  27. ^ Triantafyllopoulou, Antigoni; Tapinos, Nikos; Moutsopoulos, Haralampos M. (September 2004). "Evidence for coxsackievirus infection in primary Sjögren's syndrome". Arthritis and Rheumatism. 50 (9): 2897–2902. doi:10.1002/art.20463. ISSN 0004-3591. PMID 15457458.
  28. ^ Zhang, Hongyi; Li, Yanwen; McClean, Dougal R; Richardson, Peter J; Latif, Najma; Dunn, Michael J; Archard, Leonard C; Florio, Richard; Sheppard, Mary; Morrison, Karen (2004). "Detection of enterovirus capsid protein VP1 in myocardium from cases of myocarditis or dilated cardiomyopathy by immunohistochemistry: Further evidence of enterovirus persistence in myocytes". Medical Microbiology and Immunology. 193 (2–3): 109–114. doi:10.1007/s00430-003-0208-8. PMID 14634804. S2CID 20457715.
  29. ^ Mohney G (4 October 2014). "Medical Examiner Finds NJ Preschooler Died Due to Enterovirus 68". ABCNews. Retrieved 6 October 2014.
  30. ^ "The facts about enterovirus D68". Childrensmn.org. Children's Hospitals and Clinics of Minnesota. Archived from the original on 2014-10-06. Retrieved 2014-02-25.
  31. ^ Malone S (1 October 2014). "Rhode Island child with Enterovirus dies after infection: officials". Reuters. Archived from the original on October 1, 2014. Retrieved 6 October 2014.
  32. ^ Lin TY, Chu C, Chiu CH (October 2002). "Lactoferrin inhibits enterovirus 71 infection of human embryonal rhabdomyosarcoma cells in vitro". The Journal of Infectious Diseases. 186 (8): 1161–1164. doi:10.1086/343809. PMID 12355368.
  33. ^ Wang JR, Tuan YC, Tsai HP, Yan JJ, Liu CC, Su IJ (January 2002). "Change of major genotype of enterovirus 71 in outbreaks of hand-foot-and-mouth disease in Taiwan between 1998 and 2000". Journal of Clinical Microbiology. 40 (1): 10–15. doi:10.1128/JCM.40.1.10-15.2002. PMC 120096. PMID 11773085.
  34. ^ Laboratory Investigation of a Suspected Enterovirus 71 Outbreak Archived 2008-05-28 at the Wayback Machine
  35. ^ Shih SR, Stollar V, Lin JY, Chang SC, Chen GW, Li ML (October 2004). "Identification of genes involved in the host response to enterovirus 71 infection". Journal of Neurovirology. 10 (5): 293–304. doi:10.1080/13550280490499551. PMID 15385252. S2CID 13074639.
  36. ^ Paul JR (1971). A History of Poliomyelitis. (Yale studies in the history of science and medicine). New Haven, Conn: Yale University Press. ISBN 978-0-300-01324-5.
  37. ^ "ICTV Newsletter #6 2008" (PDF). ICTV. February 2008. p. 1. Archived from the original (PDF) on July 23, 2011.
  38. ^ "2005.261-262V.04.Polio.pdf – Vertebrate (through 2014) – Approved Proposals since the 8th Report – ICTV Collaboration". Talk.ictvonline.org. 2008-03-05. Archived from the original on July 26, 2011. Retrieved 2016-04-14.
  39. ^ "2005.263V.04.TypeSpEntero.pdf – Vertebrate (through 2014) – Approved Proposals since the 8th Report – ICTV Collaboration". Talk.ictvonline.org. 2008-03-05. Retrieved 2016-04-14.[dead link]
  40. ^ "ICTV Newsletter #7 2009" (PDF). ICTV. October 2009. p. 1.
  41. ^ Wells, Alexandra I.; Coyne, Carolyn B. (May 2019). "Enteroviruses: A Gut-Wrenching Game of Entry, Detection, and Evasion". Viruses. 11 (5): 460. doi:10.3390/v11050460. PMC 6563291. PMID 31117206.
  42. ^ "Non-Polio Enterovirus | Home | Picornavirus | CDC". www.cdc.gov. Retrieved 2017-03-22.
  43. ^ "Non-Polio Enterovirus | For Health Care Professionals | Picornavirus | CDC". www.cdc.gov. Retrieved 2017-03-22.
  44. ^ Seroka, Rachel (23 February 2014). "Mysterious polio-like illness found in 5 California children". American Academy of Neurology. Retrieved 24 February 2014.
  45. ^ "Mysterious Polio-Like Illness Found in California Children". Voice of America. February 24, 2014. Retrieved 24 February 2014.
  46. ^ "Pediatric Enteroviral Infections Clinical Presentation: History, Physical, Causes". emedicine.medscape.com. Retrieved 2018-07-21.
  47. ^ "Non-Polio Enterovirus Infections". CDC. 8 September 2014. Retrieved 9 September 2014.
  48. ^ Grammatikos, A., Bright, P., Pearson, J. et al. Chronic Enteroviral Meningoencephalitis in a Patient with Good's Syndrome Treated with Pocapavir. J Clin Immunol (2022). https://doi.org/10.1007/s10875-022-01321-6
  49. ^ a b Schultz JC, Hilliard AA, Cooper LT, Rihal CS (November 2009). "Diagnosis and treatment of viral myocarditis". Mayo Clinic Proceedings. 84 (11): 1001–9. doi:10.1016/S0025-6196(11)60670-8. PMC 2770911. PMID 19880690.
  50. ^ Chia JK, Chia AY (January 2008). "Chronic fatigue syndrome is associated with chronic enterovirus infection of the stomach". Journal of Clinical Pathology. 61 (1): 43–8. doi:10.1136/jcp.2007.050054. PMID 17872383. S2CID 15705222.
  51. ^ "Mystery of the forgotten plague". 27 July 2004 – via news.bbc.co.uk.
  52. ^ Oikarinen, M.; Tauriainen, S.; Oikarinen, S.; Honkanen, T.; Collin, P.; Rantala, I.; Maki, M.; Kaukinen, K.; Hyoty, H. (2012). "Type 1 Diabetes is Associated with Enterovirus Infection in Gut Mucosa". Diabetes. 61 (3): 687–691. doi:10.2337/db11-1157. PMC 3282798. PMID 22315304.
  53. ^ Richardson, S. J.; Morgan, N. G. (2018). "Enteroviral infections in the pathogenesis of type 1 diabetes: New insights for therapeutic intervention". Current Opinion in Pharmacology. 43: 11–19. doi:10.1016/j.coph.2018.07.006. PMC 6294842. PMID 30064099.
  54. ^ Bergamin, C. S.; Dib, S. A. (2015). "Enterovirus and type 1 diabetes: What is the matter?". World Journal of Diabetes. 6 (6): 828–839. doi:10.4239/wjd.v6.i6.828. PMC 4478578. PMID 26131324.
  55. ^ "Type 1 diabetes belongs to autoimmune diseases, which are when the body incorrectly identifies its own useful cells as an attacking organism". 15 January 2019.
  56. ^ Fairweather D, Rose NR (April 2002). "Type 1 diabetes: virus infection or autoimmune disease?". Nature Immunology. 3 (4): 338–40. doi:10.1038/ni0402-338. PMID 11919574. S2CID 12672403.
  57. ^ "Finnish team makes diabetes vaccine breakthrough | Yle Uutiset". Yle.fi. 21 October 2013. Retrieved 2016-04-14.
  58. ^ 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 (February 2014). "Coxsackievirus B1 is associated with induction of β-cell autoimmunity that portends type 1 diabetes". Diabetes. 63 (2): 446–55. doi:10.2337/db13-0619. PMID 23974921.
  59. ^ Hanson, Maureen R. (August 2023). "The viral origin of myalgic encephalomyelitis/chronic fatigue syndrome". PLOS Pathogens. 19 (8): e1011523. doi:10.1371/journal.ppat.1011523. PMC 10434940. PMID 37590180.
  60. ^ Enterovirus Foundation (2018). "SYMPTOMS AND SIGNS OF AN ENTEROVIRUS INFECTION". Enterovirus Foundation.
  61. ^ Schwartz RA (2018-10-05). "Enteroviruses Treatment & Management". Medscape.
  62. ^ Garcia J, Espejo V, Nelson M, Sovero M, Villaran MV, Gomez J, Barrantes M, Sanchez F, Comach G, Arango AE, Aguayo N, de Rivera IL, Chicaiza W, Jimenez M, Aleman W, Rodriguez F, Gonzales MS, Kochel TJ, Halsey ES (October 2013). "Human rhinoviruses and enteroviruses in influenza-like illness in Latin America". Virology Journal. 10: 305. doi:10.1186/1743-422x-10-305. PMC 3854537. PMID 24119298.
  63. ^ "ICTV Master Species List 2018 – (10th Report) – Master Species Lists – Master Species Lists – ICTV Collaboration". ictvonline.org. 2018-07-01. Retrieved 2019-02-19.[dead link]
  64. ^ "ICTV Master Species List 2017 – (10th Report) – Master Species Lists – Master Species Lists – ICTV Collaboration". ictvonline.org. 2017-07-01. Retrieved 2018-07-29.[dead link]