Evidence map›Paper›PMID 28697609›Full record

ArticleThe Onderstepoort journal of veterinary research2017

Differential virulence and tsetse fly transmissibility of

Purity K Gitonga, Kariuki Ndung'u, Grace A Murilla, Paul C Thande, Florence N Wamwiri, Joanna E Auma, Geoffrey N Ngae, James K Kibugu, Richard Kurgat, John K Thuita

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Article in The Onderstepoort journal of veterinary research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
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  3. Article
  4. Transcriptional Studies onFrontiers in cellular and infection microbiology · 2021
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4 · The record

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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

10 authors.

Purity K Gitonga
Kariuki Ndung'uKenya Agricultural and Livestock Research Organization - Biotechnology Research Institute (KALROBioRI), Kikuyu. kariukindungu36@yahoo.com.
Grace A Murilla
Paul C Thande
Florence N Wamwiri
Joanna E Auma
Geoffrey N Ngae
James K Kibugu
Richard Kurgat
John K Thuita

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

African animal trypanosomiasis causes significant economic losses in sub-Saharan African countries because of livestock mortalities and reduced productivity. Trypanosomes, the causative agents, are transmitted by tsetse flies (Glossina spp.). In the current study, we compared and contrasted the virulence characteristics of five Trypanosoma congolense and Trypanosoma brucei isolates using groups of Swiss white mice (n = 6). We further determined the vectorial capacity of Glossina pallidipes, for each of the trypanosome isolates. Results showed that the overall pre-patent (PP) periods were 8.4 ± 0.9 (range, 4-11) and 4.5 ± 0.2 (range, 4-6) for T. congolense and T. brucei isolates, respectively (p < 0.01). Despite the longer mean PP, T. congolense-infected mice exhibited a significantly (p < 0.05) shorter survival time than T. brucei-infected mice, indicating greater virulence. Differences were also noted among the individual isolates with T. congolense KETRI 2909 causing the most acute infection of the entire group with a mean ± standard error survival time of 9 ± 2.1 days. Survival time of infected tsetse flies and the proportion with mature infections at 30 days post-exposure to the infective blood meals varied among isolates, with subacute infection-causing T. congolense EATRO 1829 and chronic infection-causing T. brucei EATRO 2267 isolates showing the highest mature infection rates of 38.5% and 23.1%, respectively. Therefore, our study provides further evidence of occurrence of differences in virulence and transmissibility of eastern African trypanosome strains and has identified two, T. congolense EATRO 1829 and T. brucei EATRO 2267, as suitable for tsetse infectivity and transmissibility experiments.

Indexed as

AfricaAnimalsInsect VectorsMiceTrypanosoma brucei bruceiTrypanosoma congolenseTrypanosomiasis, AfricanTsetse FliesVirulence

Identifiers

PMID28697609
PMCPMC6238703

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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.