Evidence map›Paper›PMID 39160482›Full record

ArticleBMC infectious diseases2024

Detection of male genital schistosomiasis (MGS) associated with human, zoonotic and hybrid schistosomes in Southern Malawi.

Sekeleghe Kayuni, Lucas Cunningham, Bright Mainga, Dingase Kumwenda, David Lally Jnr, Priscilla Chammudzi, Donales Kapira, Gladys Namacha, Alice Chisale, Tereza Nchembe and 17 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Sekeleghe KayuniMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi. sekekayuni@live.com.
Lucas CunninghamDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, CTID Building, Pembroke Place, Liverpool, Merseyside, L3 5QA, UK.
Bright MaingaMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Dingase KumwendaMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
David Lally JnrMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Priscilla ChammudziMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Donales KapiraMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Gladys NamachaMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Alice ChisaleMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Tereza NchembeMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Louis KinleyMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Ephraim ChibwanaMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Bessie NtabaMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
Gilbert ChapwetekaNsanje District Hospital, Ministry of Health, Nsanje, Malawi.
Waleke KhumaloNsanje District Hospital, Ministry of Health, Nsanje, Malawi.
Henry ChibowaMangochi District Hospital, Ministry of Health, Mangochi, Malawi.
Victor KumfundaMangochi District Hospital, Ministry of Health, Mangochi, Malawi.
Alexandra JuhaszDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, CTID Building, Pembroke Place, Liverpool, Merseyside, L3 5QA, UK.
Sam JonesDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, CTID Building, Pembroke Place, Liverpool, Merseyside, L3 5QA, UK.
John ArcherDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, CTID Building, Pembroke Place, Liverpool, Merseyside, L3 5QA, UK.
Angus M O'FerrallDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, CTID Building, Pembroke Place, Liverpool, Merseyside, L3 5QA, UK.
Sarah RollasonSchool of Biosciences, The Sir Martin Evans Building, Cardiff University, Cardiff, CF10 3AX, UK.
John ChiphwanyaCommunity Health Sciences Unit (CHSU), National Schistosomiasis and Soil-Transmitted Helminths Control Programme, Ministry of Health, Area 3, Off Mtunthama Drive, Private Bag 65, Lilongwe, Malawi.
Peter MakaulaMalawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
E James LaCourseDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, CTID Building, Pembroke Place, Liverpool, Merseyside, L3 5QA, UK.
Janelisa Musaya *Malawi Liverpool Wellcome Programme, Kamuzu University of Health Sciences, Queen Elizabeth Central Hospital, campus, 1 Chipatala Avenue, Private Bag 360, Blantyre 3, Chichiri, Malawi.
J Russell Stothard *Department of Tropical Disease Biology, Liverpool School of Tropical Medicine, CTID Building, Pembroke Place, Liverpool, Merseyside, L3 5QA, UK.

Funding

Wellcome TrustWellcome Trust WT 220818/Z/20/Z
6 · The paper itself

Abstract

backgroundMale Genital Schistosomiasis (MGS) remains an often-overlooked chronic sequela of urogenital schistosomiasis in endemic areas of sub-Saharan Africa. As part of a 2-year longitudinal study on Hybridization of UroGenital Schistosomiasis (HUGS) in Malawi, a MGS sub-study was conducted to assess whether hybrid schistosomes were incriminated.

methodsDuring recruitment, demographic, health and socio-economic data were collected through individual questionnaire interviews in Mthawira community from Nsanje District along Shire River and Samama community from Mangochi District along Lake Malawi shoreline. Urine and semen samples were collected and analysed to determine the identity of schistosome infection. Urine filtration and microscopy, direct microscopy of semen and its sediments (after centrifugation) were performed. Thereafter, the sediments were examined by molecular DNA analysis with a novel two-tube real-time PCR assay. The participants were also screened for Human papilloma virus (HPV) and other sexually transmitted infections (STIs).

resultsTwenty-two men were recruited for the sub-study, 8 in Nsanje District and 14 in Mangochi District, with a median age of 22.0 years. By microscopy, ten (45.7%) participants had Schistosoma ova in their urine, 11 (50.0%) in semen while 16 (72.7%) were positive by real-time PCR. One participant had both S. haematobium and S. mattheei ova in his semen, three showed symptoms, and one had a mixed infection of S. mansoni and possible S. haematobium-S. mattheei hybrid. Twelve men had detectable high-risk HPV serotypes 16, 18 and others while six had Trichomonas vaginalis and other STIs.

conclusionZoonotic and hybrid schistosomes can cause MGS similar to human schistosomes, which can be co-infected with HPV and STIs, thereby posing a new challenge in diagnosis, management and control measures in resource poor settings. Increased awareness of these infections among local communities and primary healthcare workers and improvement of disease management are needed and advocated.

Indexed as

Schistosomiasis haematobiaAdolescentAdultAnimalsHumansLongitudinal StudiesMalawiMaleMiddle AgedSchistosomaSchistosoma haematobiumSemenYoung AdultZoonosesLake MalawiSchistosoma haematobiumSchistosoma mattheeiSemenShire RiverUrogenital schistosomiasis

Identifiers

PMID39160482
PMCPMC11331596

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.