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Spatial-temporal and phylogenetic analyses of epidemiologic data to help understand the modes of transmission of endemic typhoid fever in Samoa.
Sikorski, Michael J; Ma, Jianguo; Hazen, Tracy H; Desai, Sachin N; Tupua, Siaosi; Nimarota-Brown, Susana; Sialeipata, Michelle; Rambocus, Savitra; Ballard, Susan A; Valcanis, Mary; Thomsen, Robert E; Robins-Browne, Roy M; Howden, Benjamin P; Naseri, Take K; Levine, Myron M; Rasko, David A.
Afiliação
  • Sikorski MJ; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
  • Ma J; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
  • Hazen TH; Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
  • Desai SN; Department of Geographical Sciences, University of Maryland, College Park, Maryland, United States of America.
  • Tupua S; Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
  • Nimarota-Brown S; Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
  • Sialeipata M; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
  • Rambocus S; Ministry of Health, Government of Samoa, Apia, Samoa.
  • Ballard SA; Ministry of Health, Government of Samoa, Apia, Samoa.
  • Valcanis M; Ministry of Health, Government of Samoa, Apia, Samoa.
  • Thomsen RE; Microbiological Diagnostic Unit Public Health Laboratory, Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
  • Robins-Browne RM; Microbiological Diagnostic Unit Public Health Laboratory, Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
  • Howden BP; Microbiological Diagnostic Unit Public Health Laboratory, Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
  • Naseri TK; Ministry of Health, Government of Samoa, Apia, Samoa.
  • Levine MM; Microbiological Diagnostic Unit Public Health Laboratory, Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
  • Rasko DA; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
PLoS Negl Trop Dis ; 16(10): e0010348, 2022 10.
Article em En | MEDLINE | ID: mdl-36251704
ABSTRACT
Salmonella enterica serovar Typhi (S. Typhi) is either widely distributed or proximally transmitted via fecally-contaminated food or water to cause typhoid fever. In Samoa, where endemic typhoid fever has persisted over decades despite water quality and sanitation improvements, the local patterns of S. Typhi circulation remain unclear. From April 2018-June 2020, epidemiologic data and GPS coordinates were collected during household investigations of 260 acute cases of typhoid fever, and 27 asymptomatic shedders of S. Typhi were detected among household contacts. Spatial and temporal distributions of cases were examined using Average Nearest Neighbor and space-time hotspot analyses. In rural regions, infections occurred in sporadic, focal clusters contrasting with persistent, less clustered cases in the Apia Urban Area. Restrictions to population movement during nationwide lockdowns in 2019-2020 were associated with marked reductions of cases. Phylogenetic analyses of isolates with whole genome sequences (n = 186) revealed one dominant genotype 3.5.4 (n = 181/186) that contains three Samoa-exclusive sub-lineages 3.5.4.1, 3.5.4.2, and 3.5.4.3. Variables of patient sex, age, and geographic region were examined by phylogenetic groupings, and significant differences (p<0.05) associated genetically-similar isolates in urban areas with working ages (20-49 year olds), and in rural areas with age groups typically at home (<5, 50+). Isolates from asymptomatic shedders were among all three sub-lineages. Whole genome sequencing provided evidence of bacterial genetic similarity, which corroborated 10/12 putative epidemiologic linkages among cases and asymptomatic shedders, as well as 3/3 repeat positives (presumed relapses), with a median of one single nucleotide polymorphism difference. These findings highlight various patterns of typhoid transmission in Samoa that differ between urban and rural regions as well as genomic subtypes. Asymptomatic shedders, detectable only through household investigations, are likely an important reservoir and mobile agent of infection. This study advances a "Samoan S. Typhi framework" that supports current and future typhoid surveillance and control efforts in Samoa.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Febre Tifoide Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Febre Tifoide Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article