Evidence map›Paper›PMID 26700867›Full record

ArticleBMC veterinary research2015

Comparative clinico-pathological observations in young Zebu (Bos indicus) cattle experimentally infected with Trypanosoma vivax isolates from tsetse infested and non-tsetse areas of Northwest Ethiopia.

Shimelis Dagnachew, Getachew Terefe, Getachew Abebe, Asegedech Sirak, Enrico Bollo, Dave Barry, Bruno Goddeeris

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 18% of its field
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 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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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

7 authors at 6 institutions in 4 countries.

Shimelis DagnachewAddis Ababa University, College of Veterinary Medicine and Agriculture, Debre Zeit, Ethiopia. dagne2121@gmail.com.
Getachew TerefeAddis Ababa University, College of Veterinary Medicine and Agriculture, Debre Zeit, Ethiopia. getachew_terefe@yahoo.com.
Getachew AbebeFood and Agriculture Organization of the United Nations, Addis Ababa, Ethiopia. Getachew.Abebe@fao.org.
Asegedech SirakNational Animal Health and Disease Investigation Center, Sebeta, Ethiopia. ejigua@yahoo.com.
Enrico BolloUniversity of Turin, DSV, Turin, Italy. enrico.bollo@unito.it.
Dave BarryUniversity of Glasgow, CMVLS, Glasgow, UK. Dave.Barry@glasgow.ac.uk.
Bruno GoddeerisCatholic University of Leuven, Faculty of Bioscience Engineering, Leuven, Belgium. Bruno.Goddeeris@kuleuven.be.
Addis Ababa University · ETAmhara Regional Health Bureau · ETKU Leuven · BEUnited Nations Economic Commission for Africa · ETUniversity of Glasgow · GBUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Northwest region of Ethiopia is affected by both tsetse and non-tsetse transmitted trypanosomosis with a huge impact on livestock productivity. The objective of this experimental study was to determine clinical and pathological findings in young Zebu cattle experimentally infected with Trypanosoma vivax isolates from tsetse infested and non-tsetse infested areas of Northwest Ethiopia. A total of 18 cattle (Bos indicus) aged between 6 and 12 months, purchased from a trypanosome-free and confirmed to be trypanosome negative divided into three groups of six animals were used. Animals in the first two groups (Group TT: tsetse infested isolate infected and Group NT: non-tsetse infested isolate infected) received 2 mL of infected blood from donor animals at 10(6) trypanosomes/mL, and the remaining group was non-infected control (NIC). Each group was observed for a period of eight consecutive weeks, daily for clinical signs and once per week for parasitaemia. Postmortem examinations were done on euthanized animals, and tissue samples were taken for histopathological analysis.

resultsThe prepatent period of the disease was earlier in the NT group 6 days post infection (dpi) than TT group 12 dpi. The infection was characterized by reduced feed intake, intermittent pyrexia and parasitaemia, enlarged lymph nodes, lacrimation, reduced feed intake and emaciation. Less frequently diarrhea, oedema and nervous signs were observed in both groups of infected animals. At necropsy, infected animals showed enlarged spleen, enlarged lymph nodes, pneumonic and emphysematous lung, enlarged liver, and haemorrhages on the brain and intestine. Histopathological analysis revealed lymphoid hyperplasia of the spleen, necrosis of the liver, encephalitis and hyperplasia of lymph nodes.

conclusionTrpanosoma vivax isolates from both tsetse infested and non-tsetse areas showed a variety of virulence factors leading to the development of acute clinical signs, gross and histopathological lesions. However, the parasitaemia and clinical signs appeared earlier in the NT compared to TT infected groups.

Indexed as

Trypanosoma vivaxTsetse FliesAnimalsCattleCattle DiseasesEthiopiaTrypanosomiasis, African

Identifiers

PMID26700867
PMCPMC4690226
OpenAlexW2200420514

What OpenQuestion holds

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LicenceCC BY
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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.