| Literature DB >> 30114000 |
Ashley E Moore, Jessica R MacNeil, Xin Wang, Sandeep J Joseph, Lauren Lorentzson, Stepy Thomas, Amy Tunali, Tonia Parrott, Monica M Farley, Melissa Tobin-D'Angelo.
Abstract
Several countries in Europe and Australia are reporting an increasing incidence of Neisseria meningitidis serogroup W (NmW) as a consequence of the rapid expansion of a single NmW clone belonging to clonal complex 11 (1-5). Because this clone is reported to be associated with more severe disease, unusual clinical presentations, and a high case fatality ratio (CFR), it is considered a hypervirulent strain (1,6). In the United States, NmW accounts for approximately 5% of meningococcal disease reported each year, and this proportion has remained stable for several years (7). However, localized increases in NmW have been reported, most notably in Florida during 2008-2009 (8). In Georgia, NmW accounted for only 3% of meningococcal disease cases reported during 2006-2013; however, between January 2014 and December 2016, 42% of all reported cases were NmW. Surveillance data from Georgia were analyzed to describe the epidemiology and clinical characteristics of NmW cases, and whole-genome sequencing of NmW isolates was performed for comparison with NmW strains circulating in the United States and worldwide. These data indicate that the U.S. NmW strains might have evolved from the same ancestor as the hypervirulent strain that is circulating globally. Genetic analysis demonstrates that these strains are closely related, which would suggest that genetic variation led to the rise of different strains from the same ancestor. Given the recent global expansion of this potentially hypervirulent NmW lineage, clinicians and public health officials need to remain vigilant in obtaining isolates to monitor changes in circulating strains.Entities:
Mesh:
Year: 2018 PMID: 30114000 PMCID: PMC6095648 DOI: 10.15585/mmwr.mm6732a5
Source DB: PubMed Journal: MMWR Morb Mortal Wkly Rep ISSN: 0149-2195 Impact factor: 17.586
FIGURE 1Meningococcal disease cases, by serogroup type — Georgia, 2006–2016
Abbreviation: N. meningitidis = Neisseria meningitidis.
Selected characteristics of patients with meningococcal disease (N = 158), by serogroup type — Georgia, 2006–2016
| Characteristic* | ||
|---|---|---|
| NmW (n = 21) | Non-NmW (n = 137) | |
|
| ||
| Male | 14 (68) | 74 (54) |
| Female | 7 (32) | 63 (46) |
|
| ||
| Median, yrs (range) | 34 (9 mos–84 yrs) | 26 (13 days–91 yrs) |
| ≥18 | 19 (90) | 83 (61) |
| <18 | 2 (10) | 53 (39) |
|
| ||
| Black | 7 (35) | 51 (38) |
| White | 13 (65) | 80 (59) |
| Other | 0 | 4 (4) |
|
| ||
| Hispanic | 2 (10) | 8 (6) |
| Non-Hispanic | 19 (90) | 118 (94) |
|
| ||
| Bacteremia only | 11 (48) | 47 (35) |
| Meningitis | 5 (22) | 52 (38) |
| Other† | 7 (30) | 45 (33) |
|
| ||
| Yes | 10 (56) | 20 (54) |
| No | 8 (44) | 17 (46) |
|
| ||
| Survived | 16 (76) | 116 (85) |
| Died | 5 (24) | 21 (15) |
Abbreviations: ICU = intensive care unit; NmW = N. meningitidis serogroup W; Non-NmW = N. meningitidis nonserogroup W.
* Unknowns excluded from the table and the denominator calculations.
† Other infections not listed include pneumonia, septic arthritis, puerperal sepsis, cellulitis, epiglottitis, and supraglottitis. With the exception of bacteremia only, a patient might have multiple types of infections simultaneously.
§ This variable was not collected before 2010.
FIGURE 2Whole genome maximum likelihood phylogeny* of N. meningitidis serogroup W clonal complex 11 isolates from Georgia, other U.S. states, Europe, Africa, and South America, 2006–2016
* Branch length is related to the number of nucleotide substitutions. The more substitutions an isolate has, the longer its branch will be. More evolved strains will be further from their ancestor.