Volume 24, Number 10—October 2018
Dispatch
Rapid Spread of Pneumococcal Nonvaccine Serotype 7C Previously Associated with Vaccine Serotype 19F, England and Wales
, Shamez N. Ladhani, Georgia Kapatai, Ella Campion, Norman K. Fry, and Carmen Sheppard
Abstract
We observed a sudden and rapid increase in rare invasive pneumococcal disease serotype 7C, from an annual average of 3 cases during 2000–01 through 2015–16 to 29 cases in 2016–17. The increase was caused almost entirely by clonal expansion of sequence type 177, previously associated with vaccine serotype 19F.
The bacterium Streptococcus pneumoniae is a major global cause of meningitis, septicemia, and pneumonia and is associated with high rates of illness and death. In September 2006, the childhood immunization program in the United Kingdom introduced PCV7, a pneumococcal conjugate vaccine against the 7 most common serotypes causing invasive pneumococcal disease (IPD) in children; a 13-valent PCV replaced it in April 2010 (1). Both vaccines have been associated with rapid and widespread declines in IPD across all age groups and, despite an increase in other disease from non-PCV serotypes, overall IPD rates have dropped by 56% and have remained lower than prevaccine rates (1).
In England and Wales, Public Health England (PHE) conducts enhanced national surveillance for IPD (1). National Health Service laboratories routinely report clinically significant infections to PHE and submit invasive isolates to the PHE National Reference Laboratory for serotyping (2). We observed an unusual increase in invasive isolates serotyped as 7C early in 2017 that continued into the 2017–18 epidemiologic year. We analyzed the epidemiology, clinical characteristics, genetic epidemiology, and outcomes of serotype 7C IPD since 2000–01 in England and Wales.
We performed whole-genome sequencing (WGS) on 44 of 66 invasive 7C isolates collected during July 2005–June 2017, as well as 37 of 42 isolates collected during July 2017–January 31, 2018. We used previously published methods for WGS analysis (3,4). We used Bowtie version 2 (5) to map WGS reads to sequences for 1,689 antimicrobial-resistant genes in the ARG-ANNOT database (6). We used PBP typing to predict β-lactam resistance (7). Using MEGA7 (8), we drew a neighbor-joining tree (9) based on single-nucleotide polymorphism (SNP) alignments, as previously described (10). We included PHE data available on the European Nucleotide Archive (https://www.ebi.ac.uk/ena) (Technical Appendix Table) and used a non–sequence type (ST) 177 serotype 19F (Taiwan 19F-14; GenBank accession no. NC_012469.1) as a reference sequence. We did not identify and remove recombination events in the WGS alignment before constructing the phylogeny. Data on antimicrobial drug susceptibility testing performed according to British Society for Antimicrobial Chemotherapy guidelines (11) were available on a subset of isolates.
Figure 1
Figure 1. Cases of invasive pneumococcal disease (IPD) caused by serotype 7C between epidemiologic years 2000–01 and 2016–17 and an additional 42 cases reported July 1, 2017, through January 31, 2018, by (A)...
From epidemiologic year 2000–01 through 2015–16, a total of 84,305 laboratory-confirmed IPD episodes occurred in England and Wales, including 51 serotype 7C IPD cases; an annual average of 3 cases (range 1–6) were confirmed. In 2016–17, a total of 29 cases were confirmed, compared to 5, 4, and 4 in the previous 3 years (2013–14, 2014–15, and 2015–16, respectively); an additional 42 cases were confirmed during the first 7 months of the 2017–18 epidemiologic year (Figure 1, panel A). We found no evidence of geographic or temporal clustering of cases. Cases were diagnosed across all age groups and especially in those >65 years of age (84/122, 68.9%), including 38 cases in the 65–79 age group and 46 cases in persons >80 years of age. Of the 80 cases (93.8%) diagnosed from 2000–01 through 2016–17, a total of 75 included bacteremia and 5 meningitis (in patients ages 1 month, 5 months, 6 months, 30 years, and 48 years).
All isolates were cultured from blood or cerebrospinal fluid. Case-fatality ratio (CFR) was 25% (20/80) and increased with age: 12.5% (1/8) in children <15 years of age, 0 in the 15–44-year age group, 23% (3/13) in the 45–64-year age group, 25% (6/24) in the 65–79-year age group, and 37% (10/27) in the >80-year age group. CFR in the oldest 2 age groups was similar to the CFR for other serotypes in those age groups (23% for the 65–79-year age group and 40% for the >80-year age group).
The first serotype 7C isolate associated with ST177 appeared in 2012–13 and again in 2014–15, followed by all 4 cases in 2015–16 and 27/29 cases in 2016–17 (Figure 1, panel B). During July 2017–January 2018, a total of 35/37 sequenced 7C isolates were associated with ST177. A review of available PHE MLST data showed that ST177 was also associated with serotypes 19F (MLST derived for 25 isolates during 2002–2015) and 24F (MLST derived for 13 isolates during 2014–15).
Figure 2
Figure 2. Neighbor-joining tree following single-nucleotide polymorphism analyses on 59 pneumococcal isolates collected in England and Wales during July 2005–June 2017. The percentage of replicate trees in which the associated taxa clustered together...
We generated the neighbor-joining tree (Figure 2) following SNP analyses on 59 isolates, using MEGA7 using isolate Taiwan 19F-14. The tree shows that 7C-ST177 isolates had a more recent common ancestor with serotypes 19F and 24F belonging to ST177 than with non-ST177 7C isolates (except the single isolate belonging to ST11386, a single-locus variant [SLV] of ST177). The 7C-ST177 isolates were closely related, with <100 SNPs between them. We found >6,000 SNPs separating the 7C-ST177 and the non-ST177 serotype 7C (except 1 SLV of ST177 with <100 SNP distance from the ST177 isolates).
We did not detect any antimicrobial drug resistance determinants or PBP types suggesting β-lactam nonsusceptibility in the genomes of any ST177 7C isolates. MIC data were available on 13 serotype 7C isolates but only 2 were ST177; both were fully susceptible to all antimicrobial drugs tested.
In England and Wales, the recent increase in IPD due to the nonvaccine serotype 7C was associated with clonal expansion of ST177. Previously, this serotype was associated with vaccine serotype 19F, although we also observed serotype 24F isolates with this ST in later years. Nearly all the increase occurred in older adults, with no evidence of change in clinical presentation or CFR when compared with the other serotypes causing IPD in the same age groups. The age-related CFRs observed in our cohort are consistent with those from other industrialized countries with established PCV programs (12).
Additional WGS data from historical serotypes 19F and 24F isolates may help determine whether this 7C-ST177 arose from capsular switching, which appears likely given the rapid expansion of this clone. It is also possible that the increase in serotype 24F IPD after PCV13 replaced PCV7 may be attributable to ST177 (1), although we did not investigate this in our study. IPD cases due to serotype 24F have increased in children (from 3 to 28 cases), adults (from 7 to 71 cases), and older adults (from 14 to 84 cases) since PCV13 implementation (1).
ST177 has been associated with serotype 19F, with 39/42 isolates submitted to the PubMLST isolates database associated with this serotype (https://pubmlst.org/spneumoniae/). In England and Wales, ST177 was represented exclusively by serotype 19F in elderly patients before PCV7 introduction (13). Because serotypes 19F and 24F are common causes of IPD, we were unable to sequence all invasive isolates. The clonal expansion of 7C-ST177 could be a consequence of natural fluctuation of nonvaccine serotypes caused by negative frequency selection (14). Although ST177 is the ST of the globally disseminated Portugal 19F-21 Pneumococcal Molecular Epidemiology Network clone that is multidrug resistant (15), we did not identify resistance determinants in any of the 7C-ST177 isolates we studied.
In summary, serotype 7C remains a rare cause of IPD in England and Wales but is linked to a sudden, rapid increase in cases of IPD because of clonal expansion of ST177, previously associated with vaccine serotype 19F. We encourage other countries to monitor pneumococcal surveillance programs for evidence of similar increases.
Mr. Makwana is an epidemiologic analyst at Public Health England in London. He is involved in the enhanced national surveillance of invasive pneumococcal disease in England and Wales, with a particular interest in the direct and indirect population impact of conjugate vaccines on prevention of invasive bacterial infections.
Acknowledgments
We thank Mel Kephalas and Rashmi Malkani for the follow-up of unserotyped isolates; Pauline Waight, who managed pneumococcal surveillance before 2016; and Catrin Moore for reporting invasive pneumococcal disease cases in southern England serotyped by the John Radcliffe Hospital Oxford (Oxford, UK) laboratory. We also thank the staff at laboratories in England and Wales who referred isolates for serotyping and provided additional information on request.
Authors’ contributions: IPD surveillance: S.N.L., A.M. Laboratory surveillance: C.S., N.K.F., E.C. Bioinformatics: C.S., G.K. All authors jointly drafted, discussed, and revised the manuscript.
Disclaimers: C.S. and N.K.F. as employees of Public Health England’s Respiratory and Vaccine Preventable Bacteria Reference Unit, have received research funding from Pfizer and GlaxoSmithKline but receive no personal remuneration. The Immunisation, Hepatitis, and Blood Safety Department has provided vaccine manufacturers with postmarketing surveillance reports on vaccine-preventable diseases, including pneumococcal infections, which the companies are required to submit to the UK Licensing Authority in compliance with their Risk Management Strategy. A cost recovery charge is made for these reports. All other authors declare no competing interests.
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Cite This ArticleOriginal Publication Date: August 28, 2018
Table of Contents – Volume 24, Number 10—October 2018
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Ashley Makwana, Public Health England’s National Infection Service, Immunisation, Hepatitis, and Blood Safety Department, 61 Colindale Ave, London, NW9 5EQ, UK
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