Update on Vaccine-Derived Poliovirus Outbreaks — Worldwide, January 2020–June 2021
Weekly / December 10, 2021 / 70(49);1691–1699
Mary M. Alleman, PhD1; Jaume Jorba, PhD2; Elizabeth Henderson2; Ousmane M. Diop, PhD3; Shahzad Shaukat, PhD3; Mohamed A. Traoré3; Eric Wiesen, DrPH1; Steven G.F. Wassilak, MD1; Cara C. Burns, PhD2 (View author affiliations)
View suggested citationSummary
What is already known about this topic?
Circulating vaccine-derived polioviruses (cVDPVs) can emerge in settings with low poliovirus population immunity and cause paralysis.
What is added by this report?
During January 2020–June 2021, 44 cVDPV outbreaks were ongoing, resulting in 1,335 paralytic cases; 38 (86%) were cVDPV type 2 (cVDPV2). Initial use of novel type 2 oral poliovirus vaccine (OPV), modified to be more genetically stable than Sabin strain poliovirus, began in March 2021 for cVDPV2 outbreak responses; current supplies are limited.
What are the implications for public health practice?
A goal of the Global Polio Eradication Initiative’s 2022–2026 Strategic Plan is to better address the challenges to early cVDPV2 outbreak detection and initiate prompt and high coverage outbreak responses with available type 2 OPV to interrupt transmission by the end of 2023.
As of May 1, 2016, use of oral poliovirus vaccine (OPV) type 2 for routine and supplementary immunization activities ceased after a synchronized global switch from trivalent OPV (tOPV; containing Sabin strain types 1, 2, and 3) to bivalent OPV (bOPV; containing Sabin strain types 1 and 3) subsequent to the certified eradication of wild type poliovirus (WPV) type 2 in 2015 (1–3). Circulating vaccine-derived poliovirus (cVDPV) outbreaks* occur when transmission of Sabin strain poliovirus is prolonged in underimmunized populations, allowing viral genetic reversion to neurovirulence, resulting in cases of paralytic polio (1–3). Since the switch, monovalent OPV type 2 (mOPV2, containing Sabin strain type 2) has been used for response to cVDPV type 2 (cVDPV2) outbreaks; tOPV is used if cVDPV2 co-circulates with WPV type 1, and bOPV is used for cVDPV type 1 (cVDPV1) or type 3 (cVDPV3) outbreaks (1–4). In November 2020, the World Health Organization (WHO) Emergency Use Listing procedure authorized limited use of type 2 novel OPV (nOPV2), a vaccine modified to be more genetically stable than the Sabin strain, for cVDPV2 outbreak response (3,5). In October 2021, the Strategic Advisory Group of Experts on Immunization (WHO’s principal advisory group) permitted wider use of nOPV2; however, current nOPV2 supply is limited (6). This report updates that of July 2019–February 2020 to describe global cVDPV outbreaks during January 2020–June 2021 (as of November 9, 2021)† (3). During this period, there were 44 cVDPV outbreaks of the three serotypes affecting 37 countries. The number of cVDPV2 cases increased from 366 in 2019 to 1,078 in 2020 (7). A goal of the Global Polio Eradication Initiative’s (GPEI) 2022–2026 Strategic Plan is to better address the challenges to early CVDPV2 outbreak detection and initiate prompt and high coverage outbreak responses with available type 2 OPV to interrupt transmission by the end of 2023 (8).
Detection of cVDPV1
The most recently detected poliovirus genetically linked to the cVDPV1 emergence (PHL-NCR-2)§ circulating during the previous reporting period was found in environmental surveillance samples (sewage) in Malaysia during March 2020 (3) (Table) (Figure 1). During this reporting period, three new cVDPV1 emergences were detected in Madagascar (MAD-ANO-1, MAD-SUE-1, and MAD-SUO-1). The YEM-SAD-1 emergence was first isolated from specimens collected during July 2019 from contacts of an acute flaccid paralysis (AFP) patient in Yemen; circulation was confirmed after the previous global update (3).
Detection of cVDPV2
During January 2020–June 2021, there were 38 cVDPV2 emergences in active transmission in 34 countries; 28 (82%) of these countries are in Africa (Table) (Figure 1). Nineteen (50%) of the 38 emergences were previously detected during 2017–2019, three (8%) (ETH-ORO-4, ETH-SOU-2, and NIE-SOS-7) were newly detected in 2019 but were confirmed after the last global report, and 16 (42%) were newly detected during 2020–2021 (1,3). During the reporting period, fifteen (58%) of the 26 emergences in active transmission in African countries were detected, either in AFP patients or through environmental surveillance, outside of the country of first isolation of genetically linked virus (Figure 2). No polioviruses genetically linked to two previously described emergences (CHN-XIN-1 and ZAM-LUA-1) have been detected since 2019 (1,3).
Western Africa. The previously described cVDPV2 emergence (NIE-JIS-1) (1,3), first detected in Nigeria in 2018, continued to circulate during the reporting period. Since first detected, genetically linked virus has circulated in 17 west and central African countries, from Mauritania to Cameroon; during the reporting period; circulation was documented in 16 of the 17 countries (excluding Cameroon) resulting in 310 cases of cVDPV2 in 14 countries and detection through environmental surveillance in 13 countries (1,3). The most recent detection of the previously described NIE-KGS-1 emergence was through environmental surveillance in January 2020 (1,3).
During July–September 2019, the NIE-SOS-7 emergence was detected through environmental surveillance in Nigeria; circulation was confirmed after the previous global update (3). Virus genetically linked to the NIE-SOS-7 emergence was detected in specimens from AFP patients and from one healthy child in Mali during 2020. NIE-SOS-7 was not detected in Nigeria during 2020; however, genetically linked virus was isolated in 2021 from specimens obtained from AFP patients and healthy children, and through environmental surveillance. Two new cVDPV2 emergences (NIE-SOS-8 and NIE-ZAS-1) were detected and circulated in Nigeria during the reporting period, with the most recent detections in September 2020 and June 2021, respectively. During June 2021, NIE-ZAS-1 emergence was detected in Niger. There was no evidence of continued circulation of any other previously described emergences first detected in Nigeria (1,3). The previously reported TOG-SAV-1 cVDPV2 emergence circulated in Burkina Faso, Côte d’Ivoire, and Togo during the reporting period (3).
Central Africa. The most recent detection of the ANG-HUI-1 emergence in Angola was in February 2020; however, genetically linked virus was isolated from specimens collected from AFP patients and one healthy child during late 2020 in the Republic of the Congo (1,3). The ANG-LUA-1 emergence was most recently detected in the Democratic Republic of the Congo and Angola in specimens from AFP patients with paralysis onset in January and February 2020, respectively and in a healthy child in the Republic of the Congo in October 2020 (3). The ANG-LNO-2 emergence was last detected in Angola in December 2019; the most recent isolation of genetically linked virus was in the Democratic Republic of the Congo from specimens from an AFP patient with paralysis onset in February 2020 (1,3). No polioviruses genetically linked to two previously described emergences (ANG-LNO-1 and ANG-MOX-1) were detected during the reporting period (1,3).
The CHA-NDJ-1 emergence was first detected in Chad and then Cameroon during 2019; genetically linked virus was detected during the reporting period in Cameroon, the Central African Republic, Chad, Egypt, Ethiopia, South Sudan, Sudan, and Uganda (3). Genetically linked virus was most recently detected in Egypt and Uganda through environmental surveillance during June 2021. This emergence resulted in 204 paralytic cases in five of these eight countries during the reporting period.
Of the seven emergences first detected in the Central African Republic during 2019 (CAR-BAM-1, CAR-BAM-2, CAR-BER-1, CAR-BIM-1, CAR-BIM-2, CAR-BIM-3, and CAR-BNG-1), three (CAR-BER-1, CAR-BIM-3, and CAR-BNG-1) continued to circulate and spread internationally during the reporting period (1,3). Virus genetically linked to CAR-BER-1 was detected in Cameroon, the Central African Republic, and the Republic of the Congo; to CAR-BIM-3 was detected in Chad; and to CAR-BNG-1 was detected in Cameroon, the Central African Republic, the Republic of the Congo, and the Democratic Republic of the Congo.
Two previously described emergences (DRC-KAS-1 and DRC-KAS-3) detected in the Democratic Republic of the Congo in 2019 continued to circulate (1,3). After being first detected in 2019 in specimens from an AFP patient and healthy children (1), the DRC-KAS-1 emergence was not detected again until early 2021 in the Republic of the Congo in the specimens from an AFP patient. During the current reporting period, the DRC-KAS-3 emergence resulted in 82 paralytic cases in the Democratic Republic of the Congo, with the most recent paralysis onset in April 2021. Three new emergences (DRC-EQT-1, DRC-MAN-2, and DRC-TPA-2) were detected during the reporting period. There was no evidence of continued circulation of any other previously described emergences first detected in the Democratic Republic of the Congo (1,3).
Horn of Africa. The previously described SOM-BAN-1 emergence continued to circulate during the reporting period; genetically linked virus was detected each year during 2017–2021 in Somalia, and during 2018 and 2020–2021 in neighboring Kenya (1,3). During 2020, a new emergence (SOM-AWL-1) resulted in one case in Somalia and two cases in Ethiopia. Three previously described cVDPV2 emergences (ETH-ORO-1, ETH-ORO-2, and ETH-ORO-3) detected in Ethiopia in 2019 were detected during the reporting period in Ethiopia and Somalia (3). Two new emergences (ETH-ORO-4 and ETH-SOU-2) were confirmed after the previous global update (3) and subsequently resulted in six paralytic cases in Ethiopia. During 2020–2021, an additional new emergence (ETH-SOU-1) that circulated in Ethiopia and South Sudan resulted in ten paralytic cases. There have been no detections of the previously described ETH-SOM-1 emergence since 2019 (3).
Afghanistan, Iran, Pakistan, and Tajikistan. Among the five previously described cVDPV2 emergences detected in 2019 in Pakistan (PAK-GB-1, PAK-GB-2, PAK-GB-3, PAK-KOH-1, and PAK-TOR-1) only PAK-GB-1 and PAK-TOR-1 continued to be detected during the reporting period (3). The latest detection of PAK-TOR-1 was in a healthy child in Pakistan in early 2020. During the reporting period, PAK-GB-1 spread internationally resulting in a total of 251 cases in Afghanistan and Tajikistan, and 114 cases in Pakistan. There have been 11 environmental surveillance isolations of PAK-GB-1 in Iran, but no paralytic cases. During the reporting period, seven cVDPV2 emergences (PAK-FSD-1, PAK-FSD-2, PAK-KAM-1, PAK-KHI-2, PAK-LKW-1, PAK-PWR-1, and PAK-ZHB-1) were newly detected in Pakistan resulting in 15 paralytic cases; two cVDPV2 emergences (AFG-HLD-1 and AFG-NGR-1) were newly detected in Afghanistan during 2020 and spread to Pakistan. An additional cVDPV2 emergence (PAK-PB-1) was first and most recently detected through environmental surveillance in Pakistan in December 2019; confirmation of circulation occurred after the last global report (3).
Malaysia and the Philippines. The most recent detection of the PHL-NCR-1 cVDPV2 emergence in the Philippines was in January 2020 (3). The most recent detection of this emergence globally was through environmental surveillance during February 2020 in Malaysia (3).
Outbreak Control
As of October 31, 2021, no transmission was detected for >12 months for outbreaks in certain countries related to three cVDPV1 and 46 cVDPV2 emergences that circulated during 2018–2020, indicating probable interruption of transmission in those countries (>12 months since the most recent date of paralysis onset in an AFP patient, or of collection of environmental surveillance sample or other sample [e.g., healthy child], positive for genetically linked virus as of October 31, 2021) (1,3,9) (Table) (Supplementary Table; https://stacks.cdc.gov/view/cdc/112105). In addition, as of October 31, 2021, there have been no genetically linked isolations for 7 to 12 months, indicating possible outbreak cessation of AFG-HLD-1 in Afghanistan; TOG-SAV-1 in Burkina Faso; CHA-NDJ-1 in the Central African Republic, Chad, Ethiopia, and Sudan; CAR-BIM-3 in Chad; CHN-SHA-1 in China; NIE-JIS-1 in Côte d’Ivoire, Mali, and Niger; CAR-BNG-1 in the Democratic Republic of the Congo; ETH-ORO-1, ETH-ORO-3, and SOM-AWL-1 in Ethiopia; MAD-SUO-1 in Madagascar; PAK-FSD-1, PAK-KAM-1, PAK-KHI-2, PAK-LKW-1 and PAK-ZHB-1 in Pakistan; ANG-HUI-1, ANG-LUA-1, and DRC-KAS-1 in the Republic of the Congo; ETH-SOU-1 in South Sudan; PAK-GB-1 in Iran; SOM-BAN-1 in Kenya; and YEM-SAD-1 in Yemen (1,3).
Discussion
During January 2020–June 2021, GPEI continued to be challenged by cVDPV outbreaks, 86% of which were type 2 outbreaks affecting 28 African countries. The SOM-BAN-1, NIE-JIS-1, and CHA-NDJ-1 cVDPV2 emergences first detected in 2017, 2018, and 2019, respectively have continued to circulate well beyond the countries of first detection; these and numerous other old and new emergences have cumulatively resulted in 1,293 paralytic cVDPV2 cases during the reporting period (1,3).
Disruptions in AFP and environmental surveillance, partly because of the COVID-19 pandemic, might have resulted in case undercounts and delayed cVDPV2 outbreak detection during the reporting period (3,8,10). Outbreak response supplementary immunization activities were suspended during March–June 2020 (initial months of the COVID-19 pandemic) (8). Many outbreak response supplementary immunization activities conducted before and after the suspension have been of poor quality, and, in many countries, there have been delays of weeks to months in supplementary immunization activities implementation after outbreak confirmation, all leading to lingering and geographically expanding cVDPV2 transmission and seeding of new emergences (1,3,8).
A goal of the GPEI 2022–2026 Strategic Plan is to interrupt all cVDPV2 transmission by the end of 2023 by better addressing the challenges to early outbreak detection and effective outbreak responses (8). Initial nOPV2 outbreak response supplementary immunization activities, anticipated for late 2020 after the Emergency Use Listing was announced, were delayed until March 2021 (3,6,8); to date approximately 100 million nOPV2 doses have been administered in seven countries (Benin, Liberia, Niger, Nigeria, the Republic of the Congo, Sierra Leone, and Tajikistan) (6). The improved genetic stability of nOPV2 over that of the Sabin vaccine strain and its effectiveness in interrupting cVDPV2 transmission are being monitored because this vaccine is now authorized for wider use (6). In the interim, the initiative is confronted with multiple cVDPV2 outbreaks and limited nOPV2 supply because of manufacturing delays resulting from the COVID-19 pandemic and larger than anticipated nOPV2 consumption (6). Therefore, the recommendation from the Strategic Advisory Group of Experts on Immunization,¶ WHO Director-General’s Emergency Committee for the International Health Regulations regarding the spread of poliovirus as a Public Health Emergency of International Concern (9), and the GPEI Independent Monitoring Board** is that countries should initiate rapid outbreak response with available type 2 OPV, whether that is Sabin or the novel vaccine (6).
Acknowledgments
World Health Organization (WHO) Global Polio Laboratory Network (GPLN) sequencing laboratories; GPLN regional laboratory coordinators and field surveillance officers at the WHO-Eastern Mediterranean Regional Office, WHO-Regional Office for the Americas, WHO-European Regional Office, WHO-Western Pacific Regional Office, WHO-South-East Asian Regional Office, and WHO-African Regional Office; staff members of the Polio Eradication Branch, Global Immunization Division, Center for Global Health, CDC; staff members of the Polio and Picornavirus Laboratory Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, CDC; Geospatial Research, Analysis, and Services Program, Agency for Toxic Substances and Disease Registry; Emergency Operations Center, Center for Preparedness and Response, CDC.
Corresponding author: Mary M. Alleman; [email protected]; 404-639-8703.
1Global Immunization Division, Center for Global Health, CDC; 2Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, CDC; 3Polio Eradication Department, World Health Organization, Geneva, Switzerland.
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. No potential conflicts of interest were disclosed.
* In this report, a cVDPV outbreak is defined as two or more independent isolations of genetically linked VDPVs (through AFP or environmental surveillance, or from healthy community members among themselves or following confirmation of a VDPV-positive specimen from an AFP case in a person with whom they are associated). The number of outbreaks is equivalent to the number of cVDPV emergences. In summaries in this report, a given cVDPV emergence is counted once regardless of the number of countries affected after transmission beyond international borders. For the GPEI, an emergence detected in a country is considered an outbreak for that country.
† Data as of November 9, 2021 for all emergences.
§ Names designate the country and geographic subnational region of the emergence and the number of emergences in each subnational region.
¶ http://apps.who.int/iris/bitstream/handle/10665/341623/WER9622-eng-fre.pdf
** https://polioeradication.org/wp-content/uploads/2021/07/20th-IMB-report-20210631.pdf
References
- Jorba J, Diop OM, Iber J, et al. Update on vaccine-derived poliovirus outbreaks—worldwide, January 2018–June 2019. MMWR Morb Mortal Wkly Rep 2019;68:1024–8. https://doi.org/10.15585/mmwr.mm6845a4 PMID:31725706
- Global Polio Eradication Initiative. Standard operating procedures. Responding to a poliovirus event or outbreak. Geneva, Switzerland: World Health Organization; 2020. https://polioeradication.org/wp-content/uploads/2020/04/POL-SOP-V3.1-20200424.pdf
- Alleman MM, Jorba J, Greene SA, et al. Update on vaccine-derived poliovirus outbreaks—worldwide, July 2019–February 2020. MMWR Morb Mortal Wkly Rep 2020;69:489–95. https://doi.org/10.15585/mmwr.mm6916a1 PMID:32324719
- Moffett DB, Llewellyn A, Singh H, et al. Progress toward poliovirus containment implementation—worldwide, 2019–2020. MMWR Morb Mortal Wkly Rep 2020;69:1330–3. https://doi.org/10.15585/mmwr.mm6937a7 PMID:32941411
- World Health Organization. Polio vaccine—novel oral (nOPV) monovalent type 2. Geneva, Switzerland: World Health Organization; 2020. https://extranet.who.int/pqweb/vaccines/polio-vaccine-novel-oral-nopv-monovalent-type-2
- Global Polio Eradication Initiative. Independent experts advise move to next use phase for novel oral polio vaccine type 2. Geneva, Switzerland: World Health Organization; 2021. https://polioeradication.org/news-post/independent-experts-advise-transition-to-next-use-phase-for-novel-oral-polio-vaccine-type-2-nopv2/
- Global Polio Eradication Initiative. Circulating vaccine-derived poliovirus. Global circulating vaccine-derived poliovirus (cVDPV) as of 30 November 2021; Geneva, Switzerland: World Health Organization. Accessed November 30, 2021. https://polioeradication.org/polio-today/polio-now/this-week/circulating-vaccine-derived-poliovirus/
- Global Polio Eradication Initiative. Polio eradication strategy 2022–2026: delivering on a promise. Geneva, Switzerland: World Health Organization; 2021. https://polioeradication.org/gpei-strategy-2022-2026/
- World Health Organization. Statement of the twenty-ninth Polio IHR Emergency Committee. Geneva, Switzerland: World Health Organization; 2021. https://www.who.int/news/item/20-08-2021-statement-of-the-twenty-ninth-polio-ihr-emergency-committee
- Zomahoun DJ, Burman AL, Snider CJ, et al. Impact of COVID-19 pandemic on global poliovirus surveillance. MMWR Morb Mortal Wkly Rep 2021;69:1648–52. https://doi.org/10.15585/mmwr.mm695152a4 PMID:33382673
FIGURE 1. Ongoing circulating vaccine-derived poliovirus outbreaks — worldwide, January 2020–June 2021*
Abbreviations: cVDPV = circulating vaccine-derived poliovirus; cVDPV1 = cVDPV type 1; cVDPV2 = cVDPV type 2; cVDPV3 = cVDPV type 3.
* Data as of November 9, 2021.
FIGURE 2. Acute flaccid paralysis cases and environmental samples positive for circulating vaccine-derived poliovirus type 2 associated with outbreaks ongoing during January 2020–June 2021 that involved international spread since emergence, by outbreak and country — Africa, October 2017–June 2021 (A)*,†and January 2019–June 2021 (B)*,†
Abbreviations: AFP = acute flaccid paralysis; ENV = environmental samples.
* Dates (quarter and year) refer to the date of paralysis onset of AFP cases; ENV (sewage) dates refer to date of collection. When dates are the same, symbols will overlap; thus, not all isolates are visible. Outbreaks are illustrated for the country where the emergence was first detected and for countries where outbreaks with genetically linked virus were ongoing during January 2020–June 2021.
† Data as of November 9, 2021.
Suggested citation for this article: Alleman MM, Jorba J, Henderson E, et al. Update on Vaccine-Derived Poliovirus Outbreaks — Worldwide, January 2020–June 2021. MMWR Morb Mortal Wkly Rep 2021;70:1691–1699. DOI: http://dx.doi.org/10.15585/mmwr.mm7049a1.
MMWR and Morbidity and Mortality Weekly Report are service marks of the U.S. Department of Health and Human Services.
Use of trade names and commercial sources is for identification only and does not imply endorsement by the U.S. Department of
Health and Human Services.
References to non-CDC sites on the Internet are
provided as a service to MMWR readers and do not constitute or imply
endorsement of these organizations or their programs by CDC or the U.S.
Department of Health and Human Services. CDC is not responsible for the content
of pages found at these sites. URL addresses listed in MMWR were current as of
the date of publication.
All HTML versions of MMWR articles are generated from final proofs through an automated process. This conversion might result in character translation or format errors in the HTML version. Users are referred to the electronic PDF version (https://www.cdc.gov/mmwr) and/or the original MMWR paper copy for printable versions of official text, figures, and tables.
Questions or messages regarding errors in formatting should be addressed to [email protected].