The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana 11 Medical and Health Sciences 1108 Medical Microbiology 11 Medical and Health Sciences 1117 Public Health and Health Services

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The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana 11 Medical and Health Sciences 1108 Medical Microbiology 11 Medical and Health Sciences 1117 Public Health and Health Services. / Lamptey, Helena; Ofori, Michael Fokuo; Kusi, Kwadwo Asamoah; Adu, Bright; Owusu-Yeboa, Eunice; Kyei-Baafour, Eric; Arku, Andrea Twumwaa; Bosomprah, Samuel; Alifrangis, Michael; Quakyi, Isabella A.

In: Malaria Journal, Vol. 17, 331, 2018.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Lamptey, H, Ofori, MF, Kusi, KA, Adu, B, Owusu-Yeboa, E, Kyei-Baafour, E, Arku, AT, Bosomprah, S, Alifrangis, M & Quakyi, IA 2018, 'The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana 11 Medical and Health Sciences 1108 Medical Microbiology 11 Medical and Health Sciences 1117 Public Health and Health Services', Malaria Journal, vol. 17, 331. https://doi.org/10.1186/s12936-018-2479-y

APA

Lamptey, H., Ofori, M. F., Kusi, K. A., Adu, B., Owusu-Yeboa, E., Kyei-Baafour, E., Arku, A. T., Bosomprah, S., Alifrangis, M., & Quakyi, I. A. (2018). The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana 11 Medical and Health Sciences 1108 Medical Microbiology 11 Medical and Health Sciences 1117 Public Health and Health Services. Malaria Journal, 17, [331]. https://doi.org/10.1186/s12936-018-2479-y

Vancouver

Lamptey H, Ofori MF, Kusi KA, Adu B, Owusu-Yeboa E, Kyei-Baafour E et al. The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana 11 Medical and Health Sciences 1108 Medical Microbiology 11 Medical and Health Sciences 1117 Public Health and Health Services. Malaria Journal. 2018;17. 331. https://doi.org/10.1186/s12936-018-2479-y

Author

Lamptey, Helena ; Ofori, Michael Fokuo ; Kusi, Kwadwo Asamoah ; Adu, Bright ; Owusu-Yeboa, Eunice ; Kyei-Baafour, Eric ; Arku, Andrea Twumwaa ; Bosomprah, Samuel ; Alifrangis, Michael ; Quakyi, Isabella A. / The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana 11 Medical and Health Sciences 1108 Medical Microbiology 11 Medical and Health Sciences 1117 Public Health and Health Services. In: Malaria Journal. 2018 ; Vol. 17.

Bibtex

@article{9caa5d244be1445aa9ed1bcec36b00ba,
title = "The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana 11 Medical and Health Sciences 1108 Medical Microbiology 11 Medical and Health Sciences 1117 Public Health and Health Services",
abstract = "Background: The gametocyte stage of Plasmodium falciparum is considered an important target for disrupting malaria transmission. Indications are that various demographic groups, such as children and pregnant women may differ in risk of harbouring gametocytes, which may be crucial for targeted control. In this study, the relationship between the prevalence and multiplicity of P. falciparum, asexual parasite infections and gametocytaemia was assessed in three different demographic groups in an area of southern Ghana with low malaria endemicity. Levels of antibody responses to Pfs230 were also assessed as a proxy for the presence of gametocytes. Methods: The study involved multiple cross-sectional sampling of children (N = 184, aged 2-15 years), male and non-pregnant female adults (N = 154, aged 16-65 years) and pregnant women (N = 125, aged 18-45 years) from Asutsuare in the Shai Osudoku District of Greater Accra Region in Ghana. Asexual parasitaemia was detected by microscopy and PCR, and gametocytaemia was assessed by Pfs25-real time PCR. Multiclonal P. falciparum infections were estimated by msp2 genotyping and an indirect ELISA was used to measure plasma IgG antibodies to Pfs230 antigen. Results: Overall, children and pregnant women had higher prevalence of submicroscopic gametocytes (39.5% and 29.7%, respectively) compared to adults (17.4%). Multiplicity of infection observed amongst children (3.1) and pregnant women (3.9) were found to be significantly higher (P = 0.006) compared with adults (2.7). Risk of gametocyte carriage was higher in individuals infected with P. falciparum having both Pfmsp2 3D7 and FC27 parasite types (OR = 5.92, 95% CI 1.56-22.54, P = 0.009) compared with those infected with only 3D7 or FC27 parasite types. In agreement with the parasite prevalence data, anti-Pfs230 antibody levels were lower in gametocyte positive adults (β = - 0.57, 95% CI - 0.81, - 0.34, P < 0.001) compared to children. Conclusions: These findings suggest that children and pregnant women are particularly important as P. falciparum submicroscopic gametocyte reservoirs and represent important focus groups for control interventions. The number of clones increased in individuals carrying gametocytes compared to those who did not carry gametocytes. The higher anti-gametocyte antibody levels in children suggests recent exposure and may be a marker of gametocyte carriage.",
keywords = "Gametocyte prevalence, Ghana, Multiplicity of infection, Pfs230, Plasmodium falciparum, Seroprevalence, Submicroscopic infections",
author = "Helena Lamptey and Ofori, {Michael Fokuo} and Kusi, {Kwadwo Asamoah} and Bright Adu and Eunice Owusu-Yeboa and Eric Kyei-Baafour and Arku, {Andrea Twumwaa} and Samuel Bosomprah and Michael Alifrangis and Quakyi, {Isabella A.}",
year = "2018",
doi = "10.1186/s12936-018-2479-y",
language = "English",
volume = "17",
journal = "Malaria Journal",
issn = "1475-2875",
publisher = "BioMed Central",

}

RIS

TY - JOUR

T1 - The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana 11 Medical and Health Sciences 1108 Medical Microbiology 11 Medical and Health Sciences 1117 Public Health and Health Services

AU - Lamptey, Helena

AU - Ofori, Michael Fokuo

AU - Kusi, Kwadwo Asamoah

AU - Adu, Bright

AU - Owusu-Yeboa, Eunice

AU - Kyei-Baafour, Eric

AU - Arku, Andrea Twumwaa

AU - Bosomprah, Samuel

AU - Alifrangis, Michael

AU - Quakyi, Isabella A.

PY - 2018

Y1 - 2018

N2 - Background: The gametocyte stage of Plasmodium falciparum is considered an important target for disrupting malaria transmission. Indications are that various demographic groups, such as children and pregnant women may differ in risk of harbouring gametocytes, which may be crucial for targeted control. In this study, the relationship between the prevalence and multiplicity of P. falciparum, asexual parasite infections and gametocytaemia was assessed in three different demographic groups in an area of southern Ghana with low malaria endemicity. Levels of antibody responses to Pfs230 were also assessed as a proxy for the presence of gametocytes. Methods: The study involved multiple cross-sectional sampling of children (N = 184, aged 2-15 years), male and non-pregnant female adults (N = 154, aged 16-65 years) and pregnant women (N = 125, aged 18-45 years) from Asutsuare in the Shai Osudoku District of Greater Accra Region in Ghana. Asexual parasitaemia was detected by microscopy and PCR, and gametocytaemia was assessed by Pfs25-real time PCR. Multiclonal P. falciparum infections were estimated by msp2 genotyping and an indirect ELISA was used to measure plasma IgG antibodies to Pfs230 antigen. Results: Overall, children and pregnant women had higher prevalence of submicroscopic gametocytes (39.5% and 29.7%, respectively) compared to adults (17.4%). Multiplicity of infection observed amongst children (3.1) and pregnant women (3.9) were found to be significantly higher (P = 0.006) compared with adults (2.7). Risk of gametocyte carriage was higher in individuals infected with P. falciparum having both Pfmsp2 3D7 and FC27 parasite types (OR = 5.92, 95% CI 1.56-22.54, P = 0.009) compared with those infected with only 3D7 or FC27 parasite types. In agreement with the parasite prevalence data, anti-Pfs230 antibody levels were lower in gametocyte positive adults (β = - 0.57, 95% CI - 0.81, - 0.34, P < 0.001) compared to children. Conclusions: These findings suggest that children and pregnant women are particularly important as P. falciparum submicroscopic gametocyte reservoirs and represent important focus groups for control interventions. The number of clones increased in individuals carrying gametocytes compared to those who did not carry gametocytes. The higher anti-gametocyte antibody levels in children suggests recent exposure and may be a marker of gametocyte carriage.

AB - Background: The gametocyte stage of Plasmodium falciparum is considered an important target for disrupting malaria transmission. Indications are that various demographic groups, such as children and pregnant women may differ in risk of harbouring gametocytes, which may be crucial for targeted control. In this study, the relationship between the prevalence and multiplicity of P. falciparum, asexual parasite infections and gametocytaemia was assessed in three different demographic groups in an area of southern Ghana with low malaria endemicity. Levels of antibody responses to Pfs230 were also assessed as a proxy for the presence of gametocytes. Methods: The study involved multiple cross-sectional sampling of children (N = 184, aged 2-15 years), male and non-pregnant female adults (N = 154, aged 16-65 years) and pregnant women (N = 125, aged 18-45 years) from Asutsuare in the Shai Osudoku District of Greater Accra Region in Ghana. Asexual parasitaemia was detected by microscopy and PCR, and gametocytaemia was assessed by Pfs25-real time PCR. Multiclonal P. falciparum infections were estimated by msp2 genotyping and an indirect ELISA was used to measure plasma IgG antibodies to Pfs230 antigen. Results: Overall, children and pregnant women had higher prevalence of submicroscopic gametocytes (39.5% and 29.7%, respectively) compared to adults (17.4%). Multiplicity of infection observed amongst children (3.1) and pregnant women (3.9) were found to be significantly higher (P = 0.006) compared with adults (2.7). Risk of gametocyte carriage was higher in individuals infected with P. falciparum having both Pfmsp2 3D7 and FC27 parasite types (OR = 5.92, 95% CI 1.56-22.54, P = 0.009) compared with those infected with only 3D7 or FC27 parasite types. In agreement with the parasite prevalence data, anti-Pfs230 antibody levels were lower in gametocyte positive adults (β = - 0.57, 95% CI - 0.81, - 0.34, P < 0.001) compared to children. Conclusions: These findings suggest that children and pregnant women are particularly important as P. falciparum submicroscopic gametocyte reservoirs and represent important focus groups for control interventions. The number of clones increased in individuals carrying gametocytes compared to those who did not carry gametocytes. The higher anti-gametocyte antibody levels in children suggests recent exposure and may be a marker of gametocyte carriage.

KW - Gametocyte prevalence

KW - Ghana

KW - Multiplicity of infection

KW - Pfs230

KW - Plasmodium falciparum

KW - Seroprevalence

KW - Submicroscopic infections

U2 - 10.1186/s12936-018-2479-y

DO - 10.1186/s12936-018-2479-y

M3 - Journal article

C2 - 30223841

AN - SCOPUS:85053544314

VL - 17

JO - Malaria Journal

JF - Malaria Journal

SN - 1475-2875

M1 - 331

ER -

ID: 208874930