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O: Public Health
Oral Abstract Submission
Ron Dagan, MD
Professor of Pediatrics and Infectious Disease
Ben-Gurion University of the Negev
Beer Sheva, HaDarom, Israel
Disclosure: Memed, MSD, Pfizer: Consultant, Grant/Research Support, Advisor or Review Panel member, Speaker's Bureau
Shalom Ben-Shimol, MD
Senior Consultant PID
Soroka University Med Ctr and Ben-Gurion University
Beer Sheva, HaDarom, Israel
Disclosure: Pfizer: Grant/Research Support, Speaker's Bureau
Rachel Benisty, PhD
Pediatric Infectious Disease Laboratory Head
Soroka University Med Ctr and Ben-Gurion University
Beer Sheva, HaDarom, Israel
Disclosure: Nothing to disclose
Gili Regev-Yochay, MD
Senior infectious disease consultant
Sheba Medical Center
Ramat Gan, HaMerkaz, Israel
Disclosure: Pfizer: Advisor or Review Panel member
Merav Ron, PhD
Head of Streptococcus Reference Center
Ministry of Health
Jerusalem, Yerushalayim, Israel
Disclosure: Nothing to disclose
Noga Givon-Lavi, PhD
Epidemiologist
Soroka Univ Med Ctr and Ben-Gurion Univ
Beer Sheva, HaDarom, Israel
Disclosure: Nothing to disclose
Assaf Rokney, PhD
Head of National Reference Centers
Ministry of Health
Jerusalem, Yerushalayim, Israel
Disclosure: Nothing to disclose
Background : IPD caused by Sp2 (non-PCV13 serotype) is relatively rare. However, Sp2 has a high potential for causing IPD including meningitis. Large scale outbreaks of Sp2 IPD are rare and were not reported post-PCV implementation. We describe Sp2 IPD outbreak in Israel, in the PCV13 era, caused by a novel clone. Additionally, we analyzed the population structure and evolutionary dynamics of Sp2 during 2006-2018.
Methods : An ongoing, population-based, nationwide active surveillance, conducted since July 2009. PCV7/PCV13 were implemented in Israel in Jul-2009 and Nov-2010, respectively. All isolates were tested for antimicrobial susceptibility, PFGE, MLST and whole genome sequencing (WGS).
Results :
Overall, 173 Sp2 IPD cases were identified; all isolates were analyzed by MLST (Figure 1). During 2016-2017, Sp2 caused 7.6% of all-IPD, a 7-fold increase compared with 2006-2015, and ranked second (after serotype 12F causing 12%) among IPD isolates.
During 2006-2015, 98% (40/41) Sp2 IPD were caused by the previously reported global ST-1504 clone. The outbreak was caused by a novel clone ST-13578, not previously reported (Figure 2). WGS analysis confirmed that ST-13578 was related, but genetically distinct from ST-1504, observed exclusively before the outbreak. A single strain of clone ST-74 previously globally reported was identified in 2017-2018.
An additional case was identified in an adult in the UK, following a family visit from Israel. The ST-13578 clone was identified only in the Jewish population and was mainly distributed in 3 of the 7 Israeli districts. All tested strains were penicillin-susceptible (MIC < 0.06 μg/mL).
To the best of our knowledge, this is the first widespread Sp2 outbreak since PCV13 introduction worldwide, caused by a novel clone ST-13578. The outbreak is still ongoing, although a declining trend was noted since 2017.