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DOI 10.1097/inf.0000000000001237

Медицинская библиотека · The Pediatric infectious disease journal · 2016

Density Distribution of Pharyngeal Carriage of Meningococcus in Healthy Young Adults: New Approaches to Studying the Epidemiology of Colonization and Vaccine Indirect Effects.

Finn Adam, Morales-Aza Begonia, Sikora Paulina, Giles Jessica, Lethem Ryan, Marlais Matko, Thors Valtyr, Pollard Andrew J, Faust Saul, Heath Paul, Vipond Ian, Ferreira Muriel, Muir Peter, Januário Luís, Rodrigues Fernanda

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Аннотация

BACKGROUND

Improved understanding of Neisseria meningitidis (Nm) carriage biology and better methods for detection and quantification would facilitate studies of potential impact of new vaccines on colonization and transmission in adolescents.

METHODS

We performed plate cultures on 107 oropharyngeal swabs stored frozen in skim milk tryptone glucose glycerol (STGG) broth and previously positive for Nm. We compared quantitative polymerase chain reaction (qPCR) detection of Nm in 601 STGG-swabs with culture. Using qPCR (n = 87), a log-phase broth culture standard curve and semiquantitative plate cultures (n = 68), we measured density of carriage. We compared qPCR genogrouping of DNA extracts from STGG-swabs and from plate culture lawns (n = 110) with purified isolates (n = 80).

RESULTS

Swab storage resulted in only 10% loss of culture sensitivity. Direct sodC qPCR Nm detection yielded more positives (87/601, 14.5%) than culture (80/601, 13.3%). Most samples (57/110) positive by culture were also positive by qPCR and vice versa, but discrepancies (single positives) were frequent among low-density samples. sodC qPCR was positive in 79/80 isolates but in only 65 by ctrA qPCR. Density both by culture and qPCR varied across 4 orders of magnitude with the majority being low (<50 bacteria-gene copies/mL) and a minority being high (>1000). Genogrouping qPCRs yielded more positive results when performed on DNA extracts from lawn cultures.

CONCLUSIONS

We provide the first description of the distribution of Nm carriage density. This could be important for understanding transmission dynamics and population-level effectiveness of adolescent vaccine programs. Storage of swabs frozen in STGG for batched laboratory analysis facilitates carriage studies and direct sodC qPCR for Nm combined with qPCR genogrouping of lawn culture extracts provides accurate, detailed description of colonization.

Для цитирования: Finn Adam, Morales-Aza Begonia, Sikora Paulina, Giles Jessica, Lethem Ryan, Marlais Matko, Thors Valtyr, Pollard Andrew J, Faust Saul, Heath Paul, Vipond Ian, Ferreira Muriel, Muir Peter, Januário Luís, Rodrigues Fernanda. Density Distribution of Pharyngeal Carriage of Meningococcus in Healthy Young Adults: New Approaches to Studying the Epidemiology of Colonization and Vaccine Indirect Effects.. The Pediatric infectious disease journal. 2016. DOI: 10.1097/inf.0000000000001237.

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