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      Update on Vaccine-Derived Poliovirus Outbreaks — Worldwide, January 2020–June 2021

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          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 ). TABLE Circulating vaccine-derived polioviruses detected, by serotype, source, and other selected characteristics — worldwide, January 2020–June 2021 Country Outbreak/
Emergence designation* Years detected† Serotype No. of detections§ January 2020–June 2021 Capsid protein VP1 divergence from Sabin OPV strain**(%) Date of latest outbreak case, healthy child specimen, or environmental sample†† From AFP cases From other human sources (non-AFP)¶ From environmental surveillance Afghanistan PAK-GB-1 2020–2021 2 225 36 271 0.7–3.4 Jun 9, 2021 AFG-NGR-1 2020–2021 2 127 18 154 0.7–2.2 Jun 23, 2021 AFG-HLD-1 2020–2021 2 4 0 5 0.9–1.7 Jan 28, 2021 Angola ANG-HUI-1 2019–2020 2 2 0 0 1.3–1.5 Feb 9, 2020 ANG-LUA-1 2019–2020 2 1 0 0 1.5 Feb 9, 2020 Benin NIE-JIS-1 2019–2021 2 6 2 10 2.4–5.1 May 25, 2021 Burkina Faso NIE-JIS-1 2019–2021 2 61 13 0 3.1–5.5 Jun 9, 2021 TOG-SAV-1 2020 2 6 0 0 1.8–2.6 Oct 13, 2020 Cameroon CHA-NDJ-1 2019–2020 2 3 0 0 1.4–1.9 Sep 20, 2020 CAR-BER-1 2020 2 1 0 7 1.4–2.3 Sep 29, 2020 CAR-BNG-1 2020 2 3 4 3 1.7–2.8 Jun 2, 2020 Central African Republic CHA-NDJ-1 2020 2 3 1 0 1.4–1.7 Nov 4, 2020 CAR-BER-1 2019–2020 2 1 0 0 1.3 Feb 5, 2020 CAR-BNG-1 2019–2020 2 0 0 3 1.5–1.8 Feb 5, 2020 Chad NIE-JIS-1 2019–2020 2 8 3 1 3.1–4.5 Aug 10, 2020 CHA-NDJ-1 2019–2020 2 91 16 2 0.8–2.6 Dec 15, 2020 CAR-BIM-3 2020 2 1 0 0 1.4 Oct 18, 2020 China CHN-SHA-1 2020–2021 3 0 1 1 1.8–2.0 Jan 25, 2021 Côte d’Ivoire NIE-JIS-1 2019–2020 2 63 27 175 2.9–5.1 Dec 23, 2020 TOG-SAV-1 2020 2 1 0 0 2.0 Feb 10, 2020 Democratic Republic of the Congo DRC-KAS-3 2019–2021 2 82 82 2 1.7–3.1 Apr 30, 2021 DRC-MAN-2 2021 2 1 0 0 0.8 Jun 27, 2021 DRC-TPA-2 2020 2 0 6 0 0.7–0.8 May 14, 2020 DRC-EQT-1 2020 2 1 8 0 0.7–1.5 Sep 11, 2020 CAR-BNG-1 2020 2 0 2 0 2.3 Oct 27, 2020 ANG-LNO-2 2020 2 1 0 0 2.1 Feb 19, 2020 ANG-LUA-1 2019–2020 2 2 0 0 1.0–1.3 Jan 29, 2020 Egypt CHA-NDJ-1 2020–2021 2 0 0 11 2.1–2.5 Jun 8, 2021 Ethiopia ETH-ORO-1 2019–2021 2 22 6 4 1.4–4.3 Mar 27, 2021 ETH-ORO-2 2019–2020 2 2 0 0 1.3–1.5 Feb 18, 2020 ETH-ORO-3 2019–2020 2 1 2 0 2.0–2.8 Oct 11, 2020 ETH-ORO-4 2019–2020 2 1 0 0 2.9 Feb 23, 2020 ETH-SOU-1 2020–2021 2 9 0 0 1.1–2.4 Apr 13, 2021 ETH-SOU-2 2019–2021 2 5 0 0 2.1–3.0 Jun 24, 2021 SOM-AWL-1 2020 2 2 0 0 1.5–2.3 Dec 14, 2020 CHA-NDJ-1 2020 2 0 0 1 1.4 Dec 28, 2020 Ghana NIE-JIS-1 2019–2020 2 11 10 34 2.9–4.1 Jun 16, 2020 Guinea NIE-JIS-1 2020–2021 2 48 1 1 3.0–4.8 Apr 1, 2021 Guinea-Bissau NIE-JIS-1 2021 2 2 0 0 4.1–4.5 Jun 27, 2021 Iran PAK-GB-1 2020–2021 2 0 0 11 1.5–3.6 Feb 20, 2021 Kenya SOM-BAN-1 2018, 2020–2021 2 0 3 2 7.2–7.6 Jan 25, 2021 Liberia NIE-JIS-1 2020–2021 2 3 6 47 3.0–6.1 May 28, 2021 Madagascar MAD-SUE-1 2020–2021 1 6 9 18 3.0–3.6 Jun 29, 2021 MAD-SUO-1 2021 1 1 3 0 1.6–2.0 Feb 24, 2021 MAD-ANO-1 2021 1 0 0 5 1.3–1.6 May 17, 2021 Malaysia PHL-NCR-1 2019–2020 2 0 0 3 7.5 Feb 4, 2020 PHL-NCR-2 2019–2020 1 3 0 10 3.4–4.0 Mar 13, 2020 Mali NIE-SOS-7 2020 2 3 1 0 1.5–2.2 Jul 5, 2020 NIE-JIS-1 2020 2 47 2 10 3.1–4.6 Dec 23, 2020 Mauritania NIE-JIS-1 2021 2 0 0 2 3.9–4.0 Jun 30, 2021 Niger NIE-JIS-1 2018–2020 2 11 2 11 2.8–5.1 Dec 8, 2020 NIE-ZAS-1 2021 2 1 0 0 2.2 Jun 20, 2021 Nigeria NIE-JIS-1 2018–2021 2 15 3 19 2.8–4.6 Jun 29, 2021 NIE-SOS-8 2020 2 2 7 0 1.1–1.8 Sep 17, 2020 NIE-ZAS-1 2020–2021 2 69 13 83 1.8–3.5 Jun 30, 2021 NIE-SOS-7 2019, 2021 2 10 4 3 2.4–3.1 Jun 30, 2021 NIE-KGS-1 2019–2020 2 1 0 1 1.4–1.5 Jan 26, 2020 Pakistan PAK-GB-1 2019–2021 2 114 6 257 0.7–3.1 Apr 28, 2021 PAK-TOR-1 2019–2020 2 0 1 1 1.1–1.5 Mar 4, 2020 PAK-KHI-2 2020 2 0 0 4 0.7–1.0 Oct 14, 2020 PAK-FSD-1 2020 2 10 1 8 0.7–1.2 Oct 13, 2020 PAK-FSD-2 2020 2 2 0 0 0.8–1.4 Sep 29, 2020 PAK-ZHB-1 2020 2 0 0 5 0.7–1.1 Oct 16, 2020 AFG-NGR-1 2020–2021 2 12 2 59 0.7–2.3 May 18, 2021 AFG-HLD-1 2020 2 2 0 0 1.3–1.4 Aug 24, 2020 PAK-LKW-1 2020–2021 2 3 0 1 0.7–1.0 Jan 11, 2021 PAK-KAM-1 2020–2021 2 0 0 4 0.7–0.9 Feb 9, 2021 PAK-PWR-1 2021 2 0 0 2 0.8 Jun 14, 2021 Philippines PHL-NCR-1 2019–2020 2 1 0 4 7.1–7.6 Jan 24, 2020 Republic of the Congo ANG-HUI-1 2020 2 2 1 0 2.0–2.5 Nov 14, 2020 DRC-KAS-1 2021 2 1 0 0 2.2 Jan 31, 2021 CAR-BNG-1 2020–2021 2 0 0 4 2.3–2.6 Apr 14, 2021 CAR-BER-1 2021 2 0 0 1 3.3 Jun 1, 2021 ANG-LUA-1 2020 2 0 1 0 2.1 Oct 12, 2020 Senegal NIE-JIS-1 2020–2021 2 14 30 13 3.8–5.7 Jun 14, 2021 Sierra Leone NIE-JIS-1 2020–2021 2 15 16 10 3.4–4.6 Jun 29, 2021 Somalia SOM-BAN-1 2017–2021 2 14 9 37 5.5–8.3 May 23, 2021 SOM-AWL-1 2020 2 1 0 0 2.3 Aug 1, 2020 ETH-ORO-3 2020 2 0 5 0 2.8 Sep 22, 2020 South Sudan CHA-NDJ-1 2020–2021 2 56 24 11 1.3–3.0 Apr 8, 2021 ETH-SOU-1 2021 2 1 0 0 2.2 Jan 8, 2021 Sudan CHA-NDJ-1 2020 2 51 16 15 1.1–2.8 Dec 18, 2020 Tajikistan PAK-GB-1 2020–2021 2 26 11 51 2.2–3.8 Jun 26, 2021 The Gambia NIE-JIS-1 2021 2 0 0 14 4.0–4.6 Jun 24, 2021 Togo NIE-JIS-1 2019–2020 2 6 8 0 2.8–4.1 July 9, 2020 TOG-SAV-1 2019–2020 2 3 1 0 1.5–2.1 May 3, 2020 Uganda CHA-NDJ-1 2021 2 0 0 1 4.0 Jun 1, 2021 Yemen YEM-SAD-1 2019–2021 1 32 0 0 1.9–3.3 Jan 13, 2021 Total cVDPV —§§ —§§ —§§ 1,335 423 1,412 —§§ —§§ Abbreviations: AFP = acute flaccid paralysis; cVDPV = circulating vaccine-derived poliovirus; OPV = oral poliovirus; VDPV = vaccine-derived poliovirus; VP1 = viral protein 1. * In the column “Outbreaks/Emergences,” outbreaks list total cases clearly associated with cVDPVs, emergences indicate independent cVDPV outbreaks, and names of emergences designate the country and geographic subnational region of the emergence and the number of emergences in each subnational region. † Total years detected for previously reported cVDPV outbreaks. § During January 2020–June 2021 with data as of November 9, 2021. For AFP cases, the number of AFP cases with a VDPV-positive specimen or in which a direct contact of the case had a VDPV-positive specimen when the case did not; for other human sources, the number of contacts or healthy children with a VDPV-positive specimen; for detections from environmental surveillance, the total VDPVs detected from environmental (sewage) collections. ¶ Contacts and healthy child specimen sampling during January 2020–June 2021 with data as of November 9, 2021 for all emergences. ** Percentage of divergence is estimated from the number of nucleotide differences in the VP1 region from the corresponding parental OPV strain. †† For AFP cases, dates refer to date of paralysis onset; for contacts, healthy children, and environmental (sewage) samples, dates refer to date of collection during January 2020–June 2021 with data as of November 9, 2021. §§ Dashes indicate data were not cumulative. 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 is a map showing the global distribution of the ongoing circulating vaccine-derived poliovirus outbreaks during January 2020 through June 2021. 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 ). 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. Figure is a diagram that shows outbreak-associated cases of acute flaccid paralysis and environmental samples positive for circulating vaccine-derived poliovirus type 2 during October 2017-June 2021 and January 2019-June 2021 by outbreak and country. 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 ). Detection of cVDPV3 The most recent isolation of the CHN-SHA-1 cVDPV3 emergence, the only cVDPV3 in transmission during the reporting period, was through environmental surveillance in January 2021 in China (Table) (Figure 1). No paralytic cases were reported as of November 9, 2021. 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). Summary 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.

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          Update on Vaccine-Derived Poliovirus Outbreaks — Worldwide, July 2019–February 2020

          Circulating vaccine-derived polioviruses (cVDPVs) can emerge in areas with low poliovirus immunity and cause outbreaks* of paralytic polio ( 1 – 5 ). Among the three types of wild poliovirus, type 2 was declared eradicated in 2015 ( 1 , 2 ). The use of trivalent oral poliovirus vaccine (tOPV; types 1, 2, and 3 Sabin strains) ceased in April 2016 via a 1-month–long, global synchronized switch to bivalent OPV (bOPV; types 1 and 3 Sabin strains) in immunization activities ( 1 – 4 ). Monovalent type 2 OPV (mOPV2; type 2 Sabin strain) is available for cVDPV type 2 (cVDPV2) outbreak response immunization ( 1 – 5 ). The number and geographic breadth of post-switch cVDPV2 outbreaks have exceeded forecasts that trended toward zero outbreaks 4 years after the switch and assumed rapid and effective control of any that occurred ( 4 ). New cVDPV2 outbreaks have been seeded by mOPV2 use, by both suboptimal mOPV2 coverage within response zones and recently mOPV2-vaccinated children or contacts traveling outside of response zones, where children born after the global switch are fully susceptible to poliovirus type 2 transmission ( 2 – 4 ). In addition, new emergences can develop by inadvertent exposure to Sabin OPV2-containing vaccine (i.e., residual response mOPV2 or tOPV) ( 4 ). This report updates the January 2018–June 2019 report with information on global cVDPV outbreaks during July 2019–February 2020 (as of March 25, 2020) † ( 2 ). Among 33 cVDPV outbreaks reported during July 2019–February 2020, 31 (94%) were cVDPV2; 18 (58%) of these followed new emergences. In mid-2020, the Global Polio Eradication Initiative (GPEI) plans to introduce a genetically stabilized, novel OPV type 2 (nOPV2) that has a lower risk for generating VDPV2 than does Sabin mOPV2; if nOPV2 is successful in limiting new VDPV2 emergences, GPEI foresees the replacement of Sabin mOPV2 with nOPV2 for cVDPV2 outbreak responses during 2021 ( 2 , 4 , 6 ). Detection of cVDPV Type 1 No poliovirus genetically linked to the Papua New Guinea cVDPV type 1 (cVDPV1) emergence (PNG-MOR-1 § ) was detected after November 2018 ( 1 , 2 ). In Indonesia, the most recent cVDPV1 outbreak isolate was from February 2019 (IDN-PAP-1), and in Myanmar (Burma), the most recent were from August 2019 (MMR-KAY-1) ( 2 ) (Table) (Figure 1). During the reporting period, a new cVDPV1 emergence (PHL-NCR-2) was first detected in environmental surveillance (sewage) samples collected in July 2019 in the National Capital Region of the Philippines. Genetically linked virus was isolated from sewage samples collected in Sabah State, Malaysia, in June and November 2019; however, delays in sample processing resulted in findings not being released until December 2019. The most recent isolate linked to PHL-NCR-2 was detected in a specimen from a patient from Malaysia with acute flaccid paralysis (AFP) onset in January 2020. TABLE Circulating vaccine-derived polioviruses (cVDPVs) detected, by serotype, source and other selected characteristics — worldwide, July 2019–February 2020 Country Emergence designation* Years detected† Serotype No. of isolates§ July 2019–February 2020 Capsid protein VP1 divergence from Sabin OPV strain**(%) Date of latest outbreak case, healthy child specimen, or environmental sample†† From AFP cases From other human sources (non-AFP)¶ From environmental surveillance Afghanistan PAK-GB-1 2020 2 0 0 10 1.1–2.0 Feb 5, 2020 Angola ANG-HUI-1 2019–2020 2 76 2 13 0.7–1.8 Feb 9, 2020 Angola ANG-LNO-2 2019 2 14 1 0 1.1–2.2 Dec 25, 2019 Angola ANG-MOX-1 2019 2 12 2 0 0.8–1.6 Dec 18, 2019 Angola ANG-LUA-1 2019 2 34 3 14 0.7–1.5 Dec 27, 2019 Benin NIE-JIS-1 2019–2020 2 8 0 0 3.3 Jan 16, 2020 Burkina Faso NIE-JIS-1 2019–2020 2 1 3 0 3.7 Jan 11, 2020 Cameroon CHA-NDJ-1 2019 2 0 0 2 1.1 Dec 16, 2019 Cameroon NIE-JIS-1 2019 2 0 0 1 3.3 Dec 2, 2019 Cameroon CAR-BNG-1 2020 2 1 0 0 2.2 Jan 30, 2020 CAR CAR-BAM-1 2019 2 3 2 6 0.8–2.1 Nov 20, 2019 CAR CAR-BER-1 2019 2 3 3 1 0.8–1.2 Dec 8, 2019 CAR CAR-BIM-2 2019 2 0 0 3 1.3–2.2 Sep 11, 2019 CAR CAR-BIM-3 2019 2 2 7 0 0.8–1.6 Aug 23, 2019 CAR CAR-BNG-1 2019–2020 2 9 3 10 0.7–1.9 Feb 5, 2020 Chad NIE-JIS-1 2019–2020 2 5 7 2 2.6–4.5 Feb 5, 2020 Chad CHA-NDJ-1 2019–2020 2 8 3 10 0.7–2.5 Feb 5, 2020 China CHN-XIN-1 2018–2019 2 0 1 0 3.0 Aug 18, 2019 Côte d’Ivoire NIE-JIS-1 2019–2020 2 0 0 31 2.8–4.0 Feb 11, 2020 Côte d’Ivoire TOG-SAV-1 2020 2 1 0 0 2.0 Feb 10, 2020 DRC DRC-HLO-2 2019 2 13 5 0 1.0–1.7 Dec 13, 2019 DRC DRC-KAS-3 2019–2020 2 18 6 0 1.3–2.2 Feb 8, 2020 DRC DRC-SAN-1 2019 2 26 1 0 0.7–1.8 Nov 30, 2019 DRC ANG-LUA-1 2019–2020 2 12 3 0 0.7–1.3 Jan 22, 2020 Ethiopia SOM-BAN-1 2019 2 3 0 0 5.4–5.6 Aug 13, 2019 Ethiopia ETH-ORO-1 2019–2020 2 11 3 1 1.1–2.6 Feb 12, 2020 Ethiopia ETH-ORO-2 2019–2020 2 3 0 0 1.2–1.5 Jan 26, 2020 Ethiopia ETH-ORO-3 2019–2020 2 1 1 0 2.0–2.2 Feb 21, 2020 Ethiopia ETH-SOM-1 2019 2 0 1 2 1.5 Dec 30, 2019 Ghana NIE-JIS-1 2019–2020 2 24 29 50 1.8–4.0 Feb 15, 2020 Malaysia PHL-NCR-1 2019 2 0 0 2 6.8–7.1 Nov 19, 2019 Malaysia PHL-NCR-2 2019–2020 1 3 0 8 3.6–3.9 Jan 24, 2020 Myanmar§§ MMR-KAY-1 2019 1 2 5 0 3.4–3.6 Aug 21, 2019 Nigeria NIE-JIS-1 2018–2019 2 1 2 2 2.4–2.5 Oct 9, 2019 Nigeria NIE-KGS-1 2019–2020 2 2 1 5 0.9–1.5 Jan 26, 2020 Nigeria NIE-KGS-2 2019 2 1 3 0 0.7–0.8 Aug 8, 2019 Nigeria NIE-SOS-6 2019 2 0 0 1 1.1 Sep 11, 2019 Pakistan PAK-GB-1 2019–2020 2 41 18 65 0.7–2.0 Feb 10, 2020 Pakistan PAK-GB-2 2019 2 0 2 1 0.7–1.3 Aug 28, 2019 Pakistan PAK-GB-3 2019 2 1 1 0 0.9–1.0 Aug 22, 2019 Pakistan PAK-KOH-1 2019 2 1 1 2 0.7–1.3 Nov 12, 2019 Pakistan PAK-TOR-1 2019–2020 2 2 4 4 0.7–1.5 Jan 3, 2020 Philippines PHL-NCR-1 2019–2020 2 14 6 30 6.8–7.8 Jan 24, 2020 Philippines PHL-NCR-2 2019 1 1 1 22 3.3–4.4 Nov 28, 2019 Somalia SOM-BAN-1 2017–2020 2 0 0 10 5.7–6.4 Feb 4, 2020 Togo NIE-JIS-1 2019–2020 2 11 1 0 2.7–4.1 Jan 23, 2020 Togo TOG-SAV-1 2019–2020 2 3 2 0 1.4–1.9 Feb 1, 2020 Zambia ZAM-LUA-1 2019 2 1 2 0 1.0–1.1 Sep 25, 2019 Zambia ANG-MOX-1 2019 2 1 0 0 1.1 Nov 25, 2019 Total cVDPV —¶¶ —¶¶ —¶¶ 373 135 308 —¶¶ —¶¶ Abbreviations: AFP = acute flaccid paralysis; CAR = Central African Republic; DRC = Democratic Republic of the Congo; OPV = oral poliovirus vaccine. * Outbreaks list total cases clearly associated with cVDPVs; emergences indicate independent cVDPV outbreaks and designate the location of the emergence and the number of emergences in a geographic region. † Total years detected. § Total VDPV-positive specimens obtained from AFP patients and total VDPV-positive environmental (sewage) samples as of March 25 2020, for all emergences except the following: 1) ETH-ORO-1, ETH-ORO-2, ETH-ORO-3, ETH-SOM-1, and SOM-BAN-1 (as of March 24, 2020) and 2) CHA-NDJ-1, NIE-JIS-1, NIE-KGS-1, NIE-KGS-2, NIE-SOS-6, and TOG-SAV-1 (as of March 27, 2020). ¶ Contacts and healthy child sampling as of March 25, 2020, for all emergences except for the following: 1) ETH-ORO-1, ETH-ORO-3, and ETH-SOM-1 (as of March 24, 2020) and 2) CHA-NDJ-1, NIE-JIS-1, NIE-KGS-1, NIE-KGS-2, and TOG-SAV-1 (as of March 27, 2020). ** Percentage of divergence is estimated from the number of nucleotide differences in the VP1 region from the corresponding parental OPV strain. †† For AFP cases, dates refer to date of paralysis onset; for contacts, healthy children, and environmental (sewage) samples, dates refer to date of collection. §§ U.S. State Department country name is Burma. ¶¶ Not cumulative data. FIGURE 1 Ongoing circulating vaccine-derived poliovirus (cVDPV) outbreaks — worldwide, July 2019–February 2020* Abbreviations: cVDPV1 = cVDPV type 1; cVDPV2 = cVDPV type 2. * Data as of March 24–27, 2020. The figure consists of maps showing selected countries in Africa and Asia with ongoing circulating vaccine-derived poliovirus outbreaks during July 2019–February 2020. Detection of cVDPV2 During July 2019–February 2020, among 31 active cVDPV2 outbreaks, 18 (58%) followed new emergences; one outbreak in Malaysia and the Philippines (PHL-NCR-1) was detected during the reporting period, although genetic sequencing analyses indicate that the emergence occurred years earlier and genetically linked viruses circulated undetected by surveillance (Table) (Figure 1) ( 1 , 2 ). Twenty-four (77%) of the 31 active outbreaks affected African countries; seven of these (29%) resulted in international spread (Figure 2). FIGURE 2 Acute flaccid paralysis (AFP) cases and environmental samples positive for circulating vaccine-derived poliovirus type 2 associated with outbreaks ongoing during July 2019–February 2020 that involved international spread since emergence, by outbreak and country — Africa, October 2017–February 2020* ,† Abbreviation: CAR = Central African Republic; DRC = Democratic Republic of the Congo; ENV = environmental surveillance. * Dates (month/year) refer to the date of specimen collection. For samples collected on the same dates, symbols will overlap; thus, not all isolates are visible. † Data as of March 25, 2020, for all emergences except the following: 1) SOM-BAN-1 (as of March 24, 2020) and 2) CHA-NDJ-1, NIE-JIS-1, and TOG-SAV-1 (as of March 27, 2020). The figure is a diagram showing numbers and dates for acute flaccid paralysis cases and environmental samples positive for circulating vaccine-derived poliovirus type 2, which were associated with cVDPV2 outbreaks ongoing during July 2019–February 2020, that involved international spread since emergence, by outbreak and country, in Africa during October 2017–February 2020. Western Africa. The previously described cVDPV2 emergence in Nigeria (NIE-JIS-1) continued to circulate during the reporting period ( 1 , 2 ); the most recent NIE-JIS-1 isolations in Niger and Nigeria were detected among specimens from AFP patients in April and October 2019, respectively. Detection of genetically linked virus from AFP patients’ specimens and through environmental surveillance occurred in Benin, Burkina Faso, Cameroon, Chad, Côte d’Ivoire, Ghana, and Togo during the reporting period. Since its first detection in Nigeria in January 2018, NIE-JIS-1 emergence has resulted in 101 cases in seven countries ( 1 , 2 ). Ongoing transmission of previously reported cVDPV2 emergences (NIE-KGS-1 and NIE-KGS-2) and of a new cVDPV2 emergence (NIE-SOS-6) was detected in Nigeria ( 2 ). No polioviruses genetically linked to other previously described emergences (NIE-SOS-3, NIE-SOS-4, and NIE-SOS-5) ( 1 , 2 ) were detected during the reporting period. A new emergence (TOG-SAV-1) in Togo was first detected in November 2019, and a genetically linked virus was isolated from a specimen obtained from an AFP patient in Côte d’Ivoire in February 2020. Central Africa. Five Central African countries were affected by cVDPV2 outbreaks during July 2019–February 2020. Each country had a minimum of two cVDPV2 emergences circulating during the reporting period, with the Central African Republic (CAR) having five. In Angola, no poliovirus genetically linked to the previously described cVDPV2 emergence (ANG-LNO-1) was detected after May 2019 ( 2 ). However, polioviruses genetically linked to previously described emergences (ANG-HUI-1 and ANG-LNO-2) continued to circulate during the reporting period within Angola, resulting in 78 cases (ANG-HUI-1) and 15 cases (ANG-LNO-2) since first detection ( 2 ). In addition, two new emergences were detected in June (ANG-LUA-1) and September (ANG-MOX-1) 2019, resulting in a total of 46 cVDPV2 cases in Angola; the two emergences also circulated in the Democratic Republic of the Congo (DRC; ANG-LUA-1) and Zambia (ANG-MOX-1). The detection of concurrent and independent cVDPV2 emergences in Angola might be associated with mOPV2 response–related supplementary immunization activities (SIAs; vaccination campaigns) in neighboring DRC or related to other Sabin OPV2 inadvertent exposure in Angola; investigation is ongoing. In CAR, the previously described CAR-BAM-1 and CAR-BIM-2 emergences continued to circulate during the reporting period, resulting in three cases and six detections of CAR-BAM-1 and three detections of CAR-BIM-2 through environmental surveillance ( 2 ). No polioviruses genetically linked to the previously described CAR-BAM-2 or CAR-BIM-1 emergences were detected after June 2019 ( 2 ). Three new emergences (CAR-BER-1, CAR-BIM-3, and CAR-BNG-1) were detected during the reporting period and resulted in a total of 14 cases in CAR. Virus genetically linked to CAR-BNG-1 was isolated from a specimen obtained from an AFP patient in Cameroon with paralysis onset in January 2020. In Chad, circulation of a new emergence (CHA-NDJ-1) was first detected in October 2019. Genetically linked viruses were continually detected in specimens from AFP patients in Chad into 2020 and from environmental surveillance in Cameroon and Chad through the end of 2019. In DRC, the previously described emergences, DRC-HLO-2, DRC-KAS-3, and DRC-SAN-1, continued to circulate, resulting in 20, 21, and 32 cases, respectively, since detection ( 2 ). During the reporting period, cVDPV2 genetically linked to the Angola ANG-LUA-1 emergence was detected in specimens obtained from 12 AFP patients in DRC. No evidence of continued circulation of the other previously described emergences (DRC-HKA-1, DRC-HLO-1, DRC-KAS-1, DRC-KAS-2, DRC-MAN-1, DRC-MON-1, and DRC-TPA-1) was found ( 1 , 2 ). Southern Africa. In Zambia, the ZAM-LUA-1 emergence was detected in specimens obtained from an AFP patient and two contacts during July–September 2019. In addition, cVDPV2 linked to the ANG-MOX-1 emergence was detected in a specimen obtained from an AFP patient with paralysis onset in November 2019. In Mozambique, no transmission related to the previously described MOZ-ZAM-2 emergence has been detected since December 2018 ( 2 ). Horn of Africa. During July 2019–February 2020, cVDPV2 genetically related to the previously described SOM-BAN-1 emergence, which was first detected in October 2017 in Banadir Province, Somalia ( 1 – 3 ), continued to circulate. During this reporting period, genetically linked virus was detected from specimens from three AFP patients in Ethiopia and in 10 sewage samples from Banadir. In Ethiopia, four new cVDPV2 emergences (ETH-ORO-1, ETH-ORO-2, ETH-ORO-3, and ETH-SOM-1) were detected during this period among specimens from 15 AFP patients and through environmental surveillance in Addis Ababa and the Somali region. Pakistan and Afghanistan. The PAK-GB-1 emergence was the first of five total cVDPV2 emergences (PAK-GB-1, PAK-GB-2, PAK-GB-3, PAK-KOH-1, and PAK-TOR-1) detected in Pakistan during the reporting period. PAK-GB-1 has resulted in 41 AFP cases in Pakistan and has been isolated through environmental surveillance in Pakistan and Afghanistan as recently as February 2020. The last detections of the PAK-GB-2 and PAK-GB-3 cVDPV2s were in August 2019. PAK-KOH-1 and PAK-TOR-1 emergences were detected from specimens obtained from AFP patients and through environmental surveillance during September 2019–January 2020. Current genetic evidence indicates that the 2016 mOPV2 outbreak response SIAs in Pakistan did not initiate these cVDPV2 outbreaks. Possible origins include international importations from areas using mOPV2 or inadvertent use of residual tOPV or mOPV2 ( 4 ). China. The CHN-XIN-1 emergence was first isolated through environmental surveillance in Xinjiang province in April 2018; genetically linked virus was last detected in Sichuan province in August 2019 from the stool specimen of a community contact of an AFP patient who had paralysis onset in April 2019 ( 2 ). Malaysia and the Philippines. During the reporting period, the PHL-NCR-1 emergence was identified from a specimen obtained from an AFP patient with paralysis onset in June 2019 in Mindanao Province, the Philippines. Subsequently, genetically linked virus was detected among specimens from 13 additional AFP patients in the Philippines and through environmental surveillance in both Malaysia and the Philippines during July 2019–February 2020. Outbreak Control As of the end of February 2020, no transmission was detected for ≥13 months for previously reported outbreaks related to one cVDPV1 emergence in Papua New Guinea (PNG-MOR-1), one cVDPV3 emergence in Somalia (SOM-BAN-2), and six cVDPV2 emergences in DRC (DRC-HLO-1, DRC-MAN-1, DRC-MON-1, and DRC-HKA-1), Mozambique (MOZ-ZAM-2), and Syria (designation not assigned), indicating probable outbreak cessation ( 1 – 3 , 5 , 7 ). Emergences of cVDPV in Angola (ANG-LNO-1); CAR (CAR-BAM-2 and CAR-BIM-1); DRC (DRC-KAS-1, DRC-KAS-2, and DRC-TPA-1); Indonesia (IDN-PAP-1); and Nigeria (NIE-SOS-3, NIE-SOS-4, and NIE-SOS-5) have had no genetically linked isolations for 7–12 months, indicating possible outbreak cessation ( 1 , 2 , 5 , 7 ). Discussion After outbreak detection, prompt and effective mOPV2 vaccination of children will interrupt cVDPV2 transmission and limit emergence of new VDPV2 strains in outbreak response zones. Although many previously identified cVDPV2 outbreaks have been interrupted or controlled as forecasted ( 1 – 4 ), GPEI has been challenged by the increased number of outbreaks from newly seeded VDPV2 emergences during January 2018–February 2020, following mOPV2 SIAs that did not reach sufficient coverage; in addition, there are protracted cVDPV2 outbreaks from prior emergence that have not been successfully controlled for the same reason ( 1 – 4 ). In areas where no mOPV2 has yet been used, approximately four birth cohorts that are fully susceptible to mucosal poliovirus type 2 infection have accumulated since the April 2016 tOPV-to-bOPV switch ( 1 , 2 , 4 ). The utility of environmental surveillance to complement AFP surveillance has been demonstrated by detections of continued circulation after a long absence in detection of confirmed AFP cases (e.g., SOM-BAN-1 in Somalia) and of circulation before detection of confirmed AFP cases (e.g., NIE-JIS-1 in Ghana); some outbreak transmission has been detected only through environmental surveillance (e.g., NIE-SOS-6 in Nigeria) ( 8 ). To address these challenges, GPEI adopted the 2020–2021 Strategy for the Response to Type 2 Circulating Vaccine-Derived Poliovirus as an addendum to the Polio Endgame Strategy 2019–2023 ( 6 ). The response strategy aims to improve the quality of mOPV2 SIAs through enhanced technical support, enactment of full international health emergency procedures, and enhanced population protection from paralysis through periodic intensification of routine immunization with bOPV and injectable inactivated poliovirus vaccine. After accelerated development and clinical testing of nOPV2 ( 9 ), which has a substantially lower risk for reversion to neurovirulence ( 2 , 9 ), this vaccine is expected to be available in mid-2020 for initial outbreak responses under emergency use listing requirements ( 10 ). If wider outbreak response use is allowed and ample supplies are available by the end of 2020, nOPV2 will replace Sabin mOPV2 in outbreak response to prevent new VDPV2 emergences ( 6 ). This time line and the course of ongoing and newly emergent cVDPV outbreaks could be negatively affected during the coronavirus disease 2019 (COVID-19) pandemic because of changes in priorities for use of health care resources and decreased immunization activities. ¶ Cessation of all OPV use after certification of polio eradication will eliminate the risk of VDPV emergence ( 2 , 4 ). Summary What is already known about this topic? Circulating vaccine-derived polioviruses (cVDPVs) can emerge in settings with low poliovirus immunity and can cause paralysis. What is added by this report? Thirty-one ongoing and new cVDPV type 2 (cVDPV2) outbreaks were documented during July 2019–February 2020; nine outbreaks spread internationally. New cVDPV2 outbreaks were often linked to poor coverage with monovalent Sabin oral poliovirus vaccine (OPV) type 2 during outbreak response campaigns. What are the implications for public health practice? The Global Polio Eradication Initiative plans to introduce a genetically stabilized, novel OPV type 2 for outbreak response in mid-2020 and expand use in 2021. Cessation of all OPV use after certification of polio eradication will eliminate the risk of VDPV emergence.
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            Update on Vaccine-Derived Poliovirus Outbreaks — Worldwide, January 2018–June 2019

            Certification of global eradication of indigenous wild poliovirus type 2 occurred in 2015 and of type 3 in 2019. Since the launch of the Global Polio Eradication Initiative (GPEI) in 1988 and broad use of live, attenuated oral poliovirus vaccine (OPV), the number of wild poliovirus cases has declined >99.99% ( 1 ). Genetically divergent vaccine-derived poliovirus* (VDPV) strains can emerge during vaccine use and spread in underimmunized populations, becoming circulating VDPV (cVDPV) strains, and resulting in outbreaks of paralytic poliomyelitis.† In April 2016, all oral polio vaccination switched from trivalent OPV (tOPV; containing vaccine virus types 1, 2, and 3) to bivalent OPV (bOPV; containing types 1 and 3) ( 2 ). Monovalent type 2 OPV (mOPV2) is used in response campaigns to control type 2 cVDPV (cVDPV2) outbreaks. This report presents data on cVDPV outbreaks detected during January 2018–June 2019 (as of September 30, 2019). Compared with January 2017–June 2018 ( 3 ), the number of reported cVDPV outbreaks more than tripled, from nine to 29; 25 (86%) of the outbreaks were caused by cVDPV2. The increase in the number of outbreaks in 2019 resulted from VDPV2 both inside and outside of mOPV2 response areas. GPEI is planning future use of a novel type 2 OPV, stabilized to decrease the likelihood of reversion to neurovirulence. However, all countries must maintain high population immunity to decrease the risk for cVDPV emergence. Cessation of all OPV use after certification of polio eradication will eliminate the risk for VDPV emergence. Detection of cVDPV1 During January 2018–June 2019, cVDPV type 1 (cVDPV1) circulation was detected in three countries (Indonesia, Myanmar, and Papua New Guinea), compared with one country (Papua New Guinea) during the previous reporting period ( 3 ). cVDPV1 isolates from acute flaccid paralysis (AFP) cases and environmental surveillance (testing of sewage samples for poliovirus) continued to be detected from the previously reported Papua New Guinea outbreak ( 4 ) (Table); the AFP patient with the latest case had paralysis onset in October 2018. A new cVDPV1 outbreak was reported in Myanmar; the first patient had paralysis onset in May 2019, and the most recent case occurred in August 2019. A new cVDPV1 outbreak of one case was reported in Indonesia with paralysis onset in November 2018. TABLE Number of circulating vaccine-derived poliovirus (cVDPV) isolates detected, by serotype, source, and other selected characteristics — worldwide, January 2018–June 2019 Country Year(s) detected* Emergence designation† Serotype No. of isolates from AFP cases No. of isolates from other human sources (non-AFP)§ No. of isolates from environmental (sewage) surveillance Capsid protein VP1 divergence from Sabin OPV strain¶ (%) 2018 estimated national bOPV-3 coverage (%)** Date of latest outbreak case, healthy child sample, or environmental sample Angola 2019 HUI-1 2 2 12 0 0.7–1.2 56 Aug 13, 2019 Angola 2019 LNO-1 2 1 1 0 0.8–1.1 56 May 14, 2019 Angola 2019 LNO-2 2 1 0 0 1.1 56 Jul 29, 2019 Benin 2019 JIS-1 2 1 0 0 3.2 75 Jul 11, 2019 Cameroon 2019 JIS-1 2 0 0 1 2.8 78 Apr 20, 2019 CAR 2019 BAM-1 2 2 9 0 1.1–1.3 47 Jun 23, 2019 CAR 2019 BAM-2 2 0 3 0 0.7 47 May 27, 2019 CAR 2019 BIM-1 2 2 1 0 1.0–1.2 47 Jun 29, 2019 CAR 2019 BIM-2 2 0 13 0 1.0–2.0 47 Jun 28, 2019 China 2018–2019 XIN-1 2 1 2 1 1.4–3.7 99 Jun 27, 2019 DRC 2017–2018 HLO-1 2 7 3 0 2.2–3.2 79 Jun 8, 2018 DRC 2018 MON-1 2 11 10 0 2.0–2.9 79 Oct 29, 2018 DRC 2018 HKA-1 2 2 0 0 0.8–0.9 79 Oct 18, 2018 DRC 2019 HLO-2 2 7 1 0 0.9–1.3 79 Sept 9, 2019 DRC 2019 KAS-1 2 1 2 0 0.7–0.8 79 Mar 17, 2019 DRC 2019 KAS-2 2 4 1 0 0.7–1.2 79 Jun 22, 2019 DRC 2019 KAS-3 2 3 0 0 0.9–1.3 79 Jul 13, 2019 DRC 2019 SAN-1 2 6 2 0 0.7–1.4 79 Aug 30, 2019 DRC 2019 TPA-1 2 1 1 0 0.8 79 Aug 14, 2019 Ethiopia 2019 BAN-1 2 1 4 0 5.6 67 Aug 1, 2019 Ghana 2019 JIS-1 2 0 0 1 3.0 98 Sep 3, 2019 Indonesia 2018 PAP-1 1 1 2 0 6.4–6.6 80 Feb 13, 2019 Kenya 2018 BAN-1 2 0 0 2 5.0–5.2 81 Mar 21, 2018 Mozambique 2018 ZAM-2 2 1 2 0 0.7–1.1 80 Dec 17, 2018 Myanmar 2019 KAY-1 1 3 2 0 2.7–3.4 91 Aug 9, 2019 Nigeria 2018–2019 JIS-1 2 45 61 80 1.4–3.7 57 Aug 27, 2019 Nigeria 2019 KGS-1 2 1 0 0 0.9 57 Jul 22, 2019 Nigeria 2019 KGS-2 2 1 0 0 1.1 57 Aug 17, 2019 Nigeria 2018–2019 SOS-3 2 1 0 17 0.7–1.6 57 Mar 24, 2019 Nigeria 2019 SOS-4 2 0 0 3 1.8–2.2 57 Jun 10, 2019 Nigeria 2019 SOS-5 2 1 1 0 1.6–1.7 57 Jun 20, 2019 Niger 2018–2109 JIS-1 2 11 11 0 2.2–2.9 79 Apr 18, 2019 PNG 2018 MOR-1 1 26 8 7 1.4–2.7 67 Nov 4, 2018 Somalia 2017–2019 BAN-1 2 10 1 24 4.2–6.1 47 May 25, 2019 Somalia 2018 BAN-2 3 7 5 12 1.6–2.5 47 Sep 7, 2018 Total cVDPVs — — — 161 158 148 — — — Abbreviations: AFP = acute flaccid paralysis; bOPV = bivalent oral poliovirus vaccine; CAR = Central African Republic; DRC = Democratic Republic of the Congo; PNG = Papua New Guinea. * Total years detected for previously reported cVDPV outbreaks (DRC, Kenya, Nigeria, Papua New Guinea, and Somalia). † Outbreaks list total cases clearly associated with cVDPVs. Emergences indicate independent cVDPV outbreaks and designate the location of the emergence and the number of emergences in a geographic region. § Contacts and healthy child sampling. ¶ Percentage of divergence is estimated from the number of nucleotide differences in the VP1 region from the corresponding parental OPV strain. ** Coverage with 3 doses of OPV, based on 2018 data from the World Health Organization (WHO) Vaccine Preventable Diseases Monitoring System (2018 global summary) and WHO-United Nations Children’s Fund coverage estimates, https://www.who.int/gho/immunization/poliomyelitis/en/. National data might not reflect weaknesses at subnational levels. Detection of cVDPV2 During January 2018–June 2019, 25 cVDPV2 outbreaks were reported in 13 countries (Table). Twelve of the 13 countries were in Africa (Figure 1), and one outbreak occurred in China. During the reporting period, 124 (77%) of the 161 cVDPV cases were cVDPV2, a profile continuing the trend of type 2 dominance that has been observed for the past decade (Figure 2). FIGURE 1 Circulating vaccine-derived poliovirus (cVDPV) outbreaks* — worldwide, January 2018–June 2019 Abbreviation: cVDPV2 = circulating type 2 VDPV. * All cVDPV outbreaks were confirmed by genetic sequence data and evolutionary analyses. The figure is a map of the world indicating the location of circulating vaccine-derived poliovirus outbreaks during January 2018–June 2019. FIGURE 2 Number of circulating vaccine-derived poliovirus (cVDPV) cases detected, by serotype — worldwide, 2000–2019* Abbreviations: cVDPV1 = circulating type 1 VDPV; cVDPV2 = circulating type 2 VDPV; cVDPV3 = circulating type 3 VDPV. * Number of cases detected and reported as of September 10, 2019. The figure is a histogram showing the number of vaccine-derived poliovirus cases detected each year worldwide during 2000–2019. Western Africa. A single cVDPV2 emergence (designated JIS-1 § ) first detected by environmental surveillance in Jigawa State (Nigeria) in January 2018 was later detected in 12 other states in Nigeria and internationally throughout the reporting period. During the first half of 2019, isolates genetically linked to JIS-1 were detected from AFP cases and environmental surveillance samples initially in Niger, and subsequently in Benin, Cameroon, and Ghana ( 5 ). Five other independent cVDPV2 emergences were detected in Nigeria: two in Kogi State (KGS-1 and KGS-2) and three in Sokoto (SOS-3, SOS-4, and SOS-5) and Niger (SOS-3) states. During the reporting period, multiple mOPV2 outbreak response activities were conducted in Nigeria ( 5 ) and in neighboring countries where JIS-1 cVDPV2 was detected. Central Africa. During the reporting period, nine cVDPV2 emergences were detected among 42 AFP cases in five provinces in the Democratic Republic of the Congo (DRC); six of these emergences were detected during the first half of 2019. The previously reported cVDPV2 emergences first detected in Haut Lomami (HLO-1) and Mongala (MON-1) provinces ( 6 ) and a new 2018 emergence in Haut Katanga (HKA-1) were apparently interrupted (as of September 30, it has been 11–15 months since the latest detection). During January–June 2019, three additional independent cVDPV2 emergences were detected in Kasai (KAS-1–KAS-3) province, and three new cVDPV2 emergences were detected in Haut Lomami (HLO-2), Tshuapa (TPA-1), and Sankuru (SAN-1) provinces. During the reporting period, four new cVDPV2 emergences were detected in southern districts of Central African Republic (CAR); two were first reported in Bimbo District (BIM-1 and BIM-2) and two were first reported in Bambari District (BAM-1 and BAM-2). As of September 30, six AFP cases were associated with these four cVDPV2 emergences; the first patient had paralysis onset in May 2019. Estimated OPV coverage in CAR both before and after the tOPV-to-bOPV switch has been chronically low ( 3 years have passed since OPV2 cessation. International cVDPV2 spread of JIS-1 from Nigeria to Benin, Cameroon, Ghana, and Niger, and of BAN-1 from Somalia to Ethiopia suggests that multiple mOPV2 responses after detection in each of the countries were of insufficient quality, delayed, or too limited in scope to prevent further spread that, in some cases, led to international transmission. cVDPV1 and cVDPV3 outbreaks can emerge in countries with suboptimal routine and supplementary immunization coverage; at the subnational level, areas with very wide gaps in immunity carry a higher risk for VDPV emergence and circulation. bOPV campaigns in response to cVDPV1 and cVDPV3 emergences effectively controlled outbreaks in Papua New Guinea (cVDPV1) and Somalia (cVDPV3). cVDPV2 outbreak control requires the use of mOPV2, the release of which depends on the decision of the Director-General of the World Health Organization with the advice from the mOPV2 Advisory Group. Early cVDPV2 detection and timeliness of response are key in addressing circulating VDPV2s; a geographically limited scale mOPV2 campaign should be conducted within 14 days after laboratory cVDPV2 confirmation before larger scale rounds are implemented. Since April 2016, approximately 300 million mOPV2 doses have been administered in response to cVDPV2 outbreaks ( 7 ). Although the effective means to stop cVDPV2 outbreaks is mOPV2, the risks associated with its use include seeding of new VDPV2 emergences with the potential for further circulation. The increase in the frequency of new emergences of cVDPV2 outbreaks outside of mOPV2 response areas has led to enhanced surveillance activities and scaling the geographic distribution of mOPV2 campaigns to 1–4 million persons aged <5 years. GPEI partners are providing a surge in technical assistance staffing to outbreak countries to improve the timeliness and quality of mOPV2 responses to aid in more rapid control of outbreaks and limit new emergences. A novel OPV type 2 vaccine, stabilized to decrease the likelihood of reversion to neurovirulence during replication, is in clinical trials ( 8 ) and, if found to be safe and effective, could be available in limited supply for emergency use as early as mid-2020, and in larger supply at a later date. Expansion of environmental surveillance provides critical indicators for early VDPV detection ( 9 ); for example, environmental surveillance detection in Cameroon and Ghana in 2019 confirmed circulation of the cVDPV2 emergence of JIS-1 outside Nigeria in the absence of detection of AFP (Cameroon) or before detection (Ghana) of AFP cases. Since 2000, 1,085 cases of paralysis caused by cVDPV have been reported, 932 (86%) of which were type 2. During the same period, approximately 12 million cases of paralytic polio have been averted through polio eradication efforts. Vaccine-associated paralytic polio can occur in children who receive the vaccine, usually after the first dose, or in their susceptible close contacts, totaling about 2–4 cases per birth cohort of 1,000,000 children before the switch from tOPV to bOPV. Since the switch, an estimated 160–240 cases per year of type 2 vaccine-associated paralytic polio have been averted. In addition, there have been no new cases of VDPV2 excretion identified in persons with primary immunodeficiency (iVDPV) since the switch from tOPV-to-bOPV. Cessation of all OPV use after certification of polio eradication will eliminate the risk for VDPV emergence and spread. Summary What is already known about this topic? Circulating vaccine-derived polioviruses (cVDPVs) can emerge in settings with low population immunity and cause paralysis. What is added by this report? Following the synchronized switch from trivalent oral poliovirus vaccine (tOPV, types 1, 2, and 3) to bivalent oral poliovirus vaccine (bOPV, types 1 and 3 only) in 2016, transmission of type 2 cVDPVs was detected in 12 countries in Africa and also in China. Type 1 cVDPVs were identified in Indonesia, Myanmar, and Papua New Guinea, and type 3 cVDPVs were identified in Somalia. What are the implications for public health practice? All countries must maintain high population immunity. Cessation of all OPV use after certification of polio eradication will eliminate the risk for VDPV emergence.
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              Impact of COVID-19 Pandemic on Global Poliovirus Surveillance

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                Author and article information

                Journal
                MMWR Morb Mortal Wkly Rep
                MMWR Morb Mortal Wkly Rep
                WR
                Morbidity and Mortality Weekly Report
                Centers for Disease Control and Prevention
                0149-2195
                1545-861X
                10 December 2021
                10 December 2021
                : 70
                : 49
                : 1691-1699
                Affiliations
                Global Immunization Division, Center for Global Health, CDC; Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, CDC; Polio Eradication Department, World Health Organization, Geneva, Switzerland.
                Author notes
                Corresponding author: Mary M. Alleman; mea4@ 123456cdc.gov ; 404-639-8703.
                Article
                mm7049a1
                10.15585/mmwr.mm7049a1
                8659190
                34882653
                cf5e6a00-c8c5-4122-9bd9-dfe07063a9b7

                All material in the MMWR Series is in the public domain and may be used and reprinted without permission; citation as to source, however, is appreciated.

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