Title
Distribution of Capsular Types of Campylobacter jejuni Isolates from Symptomatic and Asymptomatic Children in Peru
Date Issued
01 January 2019
Access level
open access
Resource Type
journal article
Author(s)
Rojas J.D.
Reynolds N.D.
Pike B.L.
Espinoza N.M.
Kuroiwa J.
Jani V.
RÃos P.A.
Nunez R.G.
Yori P.P.
Bernal M.
Meza R.A.
McCoy A.J.
Simons M.P.
Gregory M.J.
Guerry P.
Poly F.M.
Publisher(s)
American Society of Tropical Medicine and Hygiene
Abstract
Campylobacter jejuni is the leading bacterial cause of diarrhea worldwide. A capsular polysaccharide (CPS) conjugate vaccine is under development and requires determination of the valency. However, distribution of CPS types circulating globally is presently poorly described. We aimed to determine whether CPS type distribution in Peru differs from that in other endemic regions. We used a multiplex polymerase chain reaction (PCR) assay for the detection of CPS encoding genes capable of distinguishing all 35 CPS types on Campylobacter isolates in two prospective communities based studies conducted in cohorts of children less than 59 months of age in Peru. Results showed that CPS type HS4 complex was the most prevalent, followed by HS3 complex and HS15. Differences in CPS type for symptomatology were not statistically significant. Most subjects demonstrated repeated infections over time with different CPS types, suggesting that CPS types may confer of a level of homologous protective immunity. In this dataset, some differences in CPS type distribution were observed in comparison to other low-middle income countries. Further studies need to be conducted in endemic areas to increase our knowledge of CPS type distribution and guide vaccine development.
Start page
541
End page
548
Volume
101
Issue
3
Language
English
OCDE Knowledge area
GastroenterologÃa, HepatologÃa
Scopus EID
2-s2.0-85071897549
PubMed ID
Source
American Journal of Tropical Medicine and Hygiene
ISSN of the container
00029637
Sponsor(s)
Financial support: This work was supported by U.S. Naval Medical Research and Development Command Work Unit 6000.RAD1. DA3.A0308. Additional funding was obtained in part by NIH award K01-TW005717 (M. N. K.) and the Fisher Center Discovery Award at the Johns Hopkins School of Medicine.
Sources of information:
Directorio de Producción CientÃfica
Scopus