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  1. AU="Baikova, Olga Y"
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  1. Article ; Online: Non-Polio Enteroviruses Isolated by Acute Flaccid Paralysis Surveillance Laboratories in the Russian Federation in 1998-2021: Distinct Epidemiological Features of Types.

    Ivanova, Olga E / Eremeeva, Tatiana P / Morozova, Nadezhda S / Mikhailova, Yulia M / Kozlovskaya, Liubov I / Baikova, Olga Y / Shakaryan, Armen K / Krasota, Alexandr Y / Korotkova, Ekaterina A / Yakovchuk, Elizaveta V / Shustova, Elena Y / Lukashev, Alexander N

    Viruses

    2024  Volume 16, Issue 1

    Abstract: More than 100 types of non-polio enteroviruses (NPEVs) are ubiquitous in the human population and cause a variety of symptoms ranging from very mild to meningitis and acute flaccid paralysis (AFP). Much of the information regarding diverse pathogenic ... ...

    Abstract More than 100 types of non-polio enteroviruses (NPEVs) are ubiquitous in the human population and cause a variety of symptoms ranging from very mild to meningitis and acute flaccid paralysis (AFP). Much of the information regarding diverse pathogenic properties of NPEVs comes from the surveillance of poliovirus, which also yields NPEV. The analysis of 265 NPEV isolations from 10,433 AFP cases over 24 years of surveillance and more than 2500 NPEV findings in patients without severe neurological lesions suggests that types EV-A71, E13, and E25 were significantly associated with AFP. EV-A71 was also significantly more common among AFP patients who had fever at the onset and residual paralysis compared to all AFP cases. In addition, a significant disparity was noticed between types that were common in humans (CV-A2, CVA9, EV-A71, E9, and E30) or in sewage (CVA7, E3, E7, E11, E12, and E19). Therefore, there is significant evidence of non-polio viruses being implicated in severe neurological lesions, but further multicenter studies using uniform methodology are needed for a definitive conclusion.
    MeSH term(s) Humans ; Laboratories ; alpha-Fetoproteins ; Poliomyelitis/epidemiology ; Enterovirus Infections/epidemiology ; Enterovirus A, Human ; Poliovirus ; Russia ; Antigens, Viral ; Myelitis ; Neuromuscular Diseases ; Central Nervous System Viral Diseases
    Chemical Substances alpha-Fetoproteins ; Antigens, Viral
    Language English
    Publishing date 2024-01-18
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v16010135
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Case of Poliomyelitis Caused by Significantly Diverged Derivative of the Poliovirus Type 3 Vaccine Sabin Strain Circulating in the Orphanage

    Korotkova, Ekaterina A / Prostova, Maria A / Gmyl, Anatoly P / Kozlovskaya, Liubov I / Eremeeva, Tatiana P / Baikova, Olga Y / Krasota, Alexandr Y / Morozova, Nadezhda S / Ivanova, Olga E

    Viruses. 2020 Sept. 01, v. 12, no. 9

    2020  

    Abstract: Significantly divergent polioviruses (VDPV) derived from the oral poliovirus vaccine (OPV) from Sabin strains, like wild polioviruses, are capable of prolonged transmission and neuropathology. This is mainly shown for VDPV type 2. Here we describe a ... ...

    Abstract Significantly divergent polioviruses (VDPV) derived from the oral poliovirus vaccine (OPV) from Sabin strains, like wild polioviruses, are capable of prolonged transmission and neuropathology. This is mainly shown for VDPV type 2. Here we describe a molecular-epidemiological investigation of a case of VDPV type 3 circulation leading to paralytic poliomyelitis in a child in an orphanage, where OPV has not been used. Samples of feces and blood serum from the patient and 52 contacts from the same orphanage were collected twice and investigated. The complete genome sequencing was performed for five polioviruses isolated from the patient and three contact children. The level of divergence of the genomes of the isolates corresponded to approximately 9–10 months of evolution. The presence of 61 common substitutions in all isolates indicated a common intermediate progenitor. The possibility of VDPV3 transmission from the excretor to susceptible recipients (unvaccinated against polio or vaccinated with inactivated poliovirus vaccine, IPV) with subsequent circulation in a closed children’s group was demonstrated. The study of the blood sera of orphanage residents at least twice vaccinated with IPV revealed the absence of neutralizing antibodies against at least two poliovirus serotypes in almost 20% of children. Therefore, a complete rejection of OPV vaccination can lead to a critical decrease in collective immunity level. The development of new poliovirus vaccines that create mucosal immunity for the adequate replacement of OPV from Sabin strains is necessary.
    Keywords Enterovirus C ; blood serum ; children ; evolution ; feces ; genome ; mucosal immunity ; neuropathology ; neutralizing antibodies ; patients ; sequence analysis ; serotypes ; vaccination ; vaccines
    Language English
    Dates of publication 2020-0901
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    ZDB-ID 2516098-9
    ISSN 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v12090970
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: Case of Poliomyelitis Caused by Significantly Diverged Derivative of the Poliovirus Type 3 Vaccine Sabin Strain Circulating in the Orphanage.

    Korotkova, Ekaterina A / Prostova, Maria A / Gmyl, Anatoly P / Kozlovskaya, Liubov I / Eremeeva, Tatiana P / Baikova, Olga Y / Krasota, Alexandr Y / Morozova, Nadezhda S / Ivanova, Olga E

    Viruses

    2020  Volume 12, Issue 9

    Abstract: Significantly divergent polioviruses (VDPV) derived from the oral poliovirus vaccine (OPV) from Sabin strains, like wild polioviruses, are capable of prolonged transmission and neuropathology. This is mainly shown for VDPV type 2. Here we describe a ... ...

    Abstract Significantly divergent polioviruses (VDPV) derived from the oral poliovirus vaccine (OPV) from Sabin strains, like wild polioviruses, are capable of prolonged transmission and neuropathology. This is mainly shown for VDPV type 2. Here we describe a molecular-epidemiological investigation of a case of VDPV type 3 circulation leading to paralytic poliomyelitis in a child in an orphanage, where OPV has not been used. Samples of feces and blood serum from the patient and 52 contacts from the same orphanage were collected twice and investigated. The complete genome sequencing was performed for five polioviruses isolated from the patient and three contact children. The level of divergence of the genomes of the isolates corresponded to approximately 9-10 months of evolution. The presence of 61 common substitutions in all isolates indicated a common intermediate progenitor. The possibility of VDPV3 transmission from the excretor to susceptible recipients (unvaccinated against polio or vaccinated with inactivated poliovirus vaccine, IPV) with subsequent circulation in a closed children's group was demonstrated. The study of the blood sera of orphanage residents at least twice vaccinated with IPV revealed the absence of neutralizing antibodies against at least two poliovirus serotypes in almost 20% of children. Therefore, a complete rejection of OPV vaccination can lead to a critical decrease in collective immunity level. The development of new poliovirus vaccines that create mucosal immunity for the adequate replacement of OPV from Sabin strains is necessary.
    MeSH term(s) Antibodies, Viral/blood ; Child, Preschool ; Female ; Humans ; Infant ; Male ; Orphanages/statistics & numerical data ; Poliomyelitis/blood ; Poliomyelitis/epidemiology ; Poliomyelitis/transmission ; Poliomyelitis/virology ; Poliovirus/genetics ; Poliovirus/isolation & purification ; Poliovirus/physiology ; Poliovirus Vaccine, Oral/administration & dosage ; Poliovirus Vaccine, Oral/genetics ; Poliovirus Vaccine, Oral/immunology ; Russia/epidemiology
    Chemical Substances Antibodies, Viral ; Poliovirus Vaccine, Oral
    Language English
    Publishing date 2020-09-01
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v12090970
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

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