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. Author manuscript; available in PMC: 2018 Nov 27.
Published in final edited form as: J Infect Dis. 2017 Nov 27;216(9):1130–1140. doi: 10.1093/infdis/jix446

Table 2.

Overall and serogroup-specific meningococcal carriage among carriage evaluation participants at an Oregon university, March 2015–February 2016

Round 1: March 2015, N (%) Round 2: May 2015, N (%) Round 3: October 2015, N (%) Round 4: February 2016, N (%) TotalN (%)
N. meningitidis carriage 167 (14) 183 (17) 110 (11) 163 (17) 622 (15)
Serogroup
 Genotypic (rt-PCR)1
  B 14 (1.2) 23 (2.3) 20 (1.9) 22 (2.4) 78 (1.8)
  C 3 (0.26) 1 (0.09) 3 (0.29) 1 (0.11) 8 (0.19)
  W 2 (0.17) 0 (0) 0 (0) 1 (0.11) 3 (0.07)
  X 1 (0.09) 1 (0.09) 0 (0) 0 (0) 2 (0.05)
  Y 3 (0.26) 2 (0.19) 3 (0.29) 5 (0.53) 13 (0.31)
  Nongroupable 144 (12) 156 (15) 84 (8.0) 134 (14) 510 (12)
 Phenotypic (SASG)1
  B 3 (0.26) 5 (0.47) 3 (0.29) 5 (0.53) 16 (0.38)
  W 1 (0.09) 0 (0) 0 (0) 1 (0.11) 2 (0.05)
  X 0 (0) 1 (0.09) 0 (0) 0 (0) 3 (0.07)
  Y 1 (0.09) 0 (0) 0 (0) 3 (0.32) 5 (0.12)
  Other 162 (14) 177 (17) 107 (10) 154 (16) 577 (14)
Total participants 1173 1069 1045 938 4225
1

Real time PCR (rt-PCR) and slide agglutination (SASG) both tested for serogroups A, B, C, W, X, and Y. For SASG, isolates were classified as “Other” if serogroup A, B, C, W, X, and Y capsule antigens were not detected; this classification includes phenotypically nongroupable bacteria as well as serogroups E and Z, which are rarely associated with disease. For rt-PCR, isolates were classified as nongroupable if serogroup A, B, C, W, X, and Y biosynthesis genes were not detected.