Evidence map›Paper›PMID 29788965›Full record

ArticleBMC veterinary research2018

Diagnostic tools of caprine and ovine anaplasmosis: a direct comparative study.

I I Shabana, N M Alhadlag, H Zaraket

Abstract readComparative Study
In one paragraph

Article in BMC veterinary research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Emergence of NovelAnimals : an open access journal from MDPI · 2025
    Article
  7. Review
  8. Molecular detection of piroplasms,Frontiers in veterinary science · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Natural Co-Exposure toLife (Basel, Switzerland) · 2023
    Article
  15. Pathogens (Basel, Switzerland) · 2022
    Article
  16. Molecular Survey and Genetic Characterization ofAnimals : an open access journal from MDPI · 2022
    Article
  17. Article
  18. Multiple blood pathogen infections in apparently healthy sheltered dogs in southern Thailand.International journal of veterinary science and medicine · 2022
    Article
  19. Pathogens (Basel, Switzerland) · 2021
    Article
  20. Seroprevalence and Risk Factors ofAnimals : an open access journal from MDPI · 2021
    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

3 authors.

I I ShabanaBiology Department, Faculty of Science, Taibah University, Al- madinah Al-munawarah, Saudi Arabia. imanibrahim50@yahoo.com.ORCID http://orcid.org/0000-0001-6922-6356
N M AlhadlagBiology Department, Faculty of Science, Taibah University, Al- madinah Al-munawarah, Saudi Arabia.
H ZaraketDepartment of Experimental Pathology, Immunology & Microbiology, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe diagnosis of anaplasmosis is rather conflicting with other haemoprotozoans. Hence, the study aimed to compare and evaluate the efficiency of competitive ELISA (cELISA), indirect fluorescence antibody (IFA), and Polymerase chain reaction (PCR) for precise diagnosis of Anaplasma spp. and to assess their concordance with microscopic examination (ME).

resultsA total of 312 blood samples (189 sheep and 123 goats) were examined for Anaplasma infection during a 1 year period. Giemsa-stained blood smears were examined under the microscope. IFA and cELISA were used for the detection of Anaplasma spp. antibodies. PCR was used as a standard of truth and for the identification of Anaplasma species. Using cELISA assay, 47.4% (148) were positive (93 sheep and 55 goats) with a sensitivity and specificity of 91.9, and 86.9%, respectively. Using IFA, it was found that 57.4% (179)were positive (113 sheep and 66 goats) with a sensitivity and specificity of 100, and 93.3%, respectively. PCR assay identified A. ovis in 49 (25.3%) sheep and 30 (15.5%) goats, and A. phagocytophilumin 74 (38.1%) sheep and 41 (20.8%) goats.

conclusionsHigh sensitivity and specificity values of IFA and ELISA tests compared to microscopic examination strongly support their utility in the diagnosis of Anaplasma infection. PCR was a more specific diagnostic tool that allows to discriminate between Anaplasma subspecies, which makes it the method of choice for anaplasmosis diagnosis.

Indexed as

AnaplasmosisAnimalsEnzyme-Linked Immunosorbent AssayFemaleFluorescent Antibody Technique, IndirectGoat DiseasesGoatsMalePolymerase Chain ReactionProspective StudiesSensitivity and SpecificitySheepSheep Diseases

Identifiers

PMID29788965
PMCPMC5964659

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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.