Journal article
The relationship between invasive nontyphoidal salmonella disease, other bacterial bloodstream infections, and malaria in Sub-Saharan Africa
- Abstract:
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Background. Country-specific studies in Africa have indicated that Plasmodium falciparum is associated with invasive nontyphoidal Salmonella (iNTS) disease. We conducted a multicenter study in 13 sites in Burkina Faso, Ethiopia, Ghana, Guinea-Bissau, Kenya, Madagascar, Senegal, South Africa, Sudan, and Tanzania to investigate the relationship between the occurrence of iNTS disease, other systemic bacterial infections, and malaria.
Methods. Febrile patients received a blood culture and a malaria test. Isolated bacteria underwent antimicrobial susceptibility testing, and the association between iNTS disease and malaria was assessed.
Results. A positive correlation between frequency proportions of malaria and iNTS was observed (P = .01; r = 0.70). Areas with higher burden of malaria exhibited higher odds of iNTS disease compared to other bacterial infections (odds ratio [OR], 4.89; 95% CI, 1.61–14.90; P = .005) than areas with lower malaria burden. Malaria parasite positivity was associated with iNTS disease (OR, 2.44; P = .031) and gram-positive bacteremias, particularly Staphylococcus aureus , exhibited a high proportion of coinfection with Plasmodium malaria. Salmonella Typhimurium and Salmonella Enteritidis were the predominant NTS serovars (53/73; 73%). Both moderate (OR, 6.05; P = .0001) and severe (OR, 14.62; P < .0001) anemia were associated with iNTS disease.
Conclusions. A positive correlation between iNTS disease and malaria endemicity, and the association between Plasmodium parasite positivity and iNTS disease across sub-Saharan Africa, indicates the necessity to consider iNTS as a major cause of febrile illness in malaria-holoendemic areas. Prevention of iNTS disease through iNTS vaccines for areas of high malaria endemicity, targeting high-risk groups for Plasmodium parasitic infection, should be considered.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Publisher copy:
- 10.1093/cid/civ893
Authors
- Funder identifier:
- https://ror.org/029chgv08
- Funding agency for:
- Baker, S
- Grant:
- 100087/Z/12/Z
- Funder identifier:
- https://ror.org/0456r8d26
- Grant:
- OPPGH5231
- Publisher:
- Oxford University Press
- Journal:
- Clinical Infectious Diseases More from this journal
- Volume:
- 62
- Issue:
- S1
- Pages:
- S23-S31
- Publication date:
- 2016-03-01
- DOI:
- EISSN:
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1537-6591
- ISSN:
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1058-4838
- Language:
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English
- Keywords:
- Pubs id:
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pubs:609117
- UUID:
-
uuid:e8f9ed49-21f1-452c-8a60-5ad67dc750f3
- Local pid:
-
pubs:609117
- Source identifiers:
-
609117
- Deposit date:
-
2016-06-28
- ARK identifier:
Terms of use
- Copyright holder:
- Park et al.
- Copyright date:
- 2016
- Rights statement:
- © The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.
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