Evidence map›Paper›PMID 27847414›Full record

ArticleVeterinary world2016

Molecular identification of

Md Inkeyas Uddin, Md Harisul Abid, Md Shafiqul Islam, Tofazzal Md Rakib, Ashim Baran Sen, Shah Mohammed Ziqrul Haq Chowdhury, Md Nurul Anwar, Kazi Md Kamaruddin

Open access · goldAbstract read
In one paragraph

Article in Veterinary world, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Molecular identification ofVeterinary world · 2019
    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

8 authors at 3 institutions in 1 country.

Md Inkeyas UddinPoultry Research and Training Centre, Chittagong Veterinary and Animal Sciences University, Khulshi - 4225, Chittagong, Bangladesh.
Md Harisul AbidDepartment of Livestock Services, People's Republic of Bangladesh.
Md Shafiqul IslamDepartment of Pathology and Parasitology, Chittagong Veterinary and Animal Sciences University, Khulshi - 4225, Chittagong, Bangladesh.
Tofazzal Md RakibDepartment of Pathology and Parasitology, Chittagong Veterinary and Animal Sciences University, Khulshi - 4225, Chittagong, Bangladesh.
Ashim Baran SenDepartment of Livestock Services, People's Republic of Bangladesh.
Shah Mohammed Ziqrul Haq ChowdhuryLivestock Division, Bangladesh Agricultural Research Council, Dhaka - 1202, Bangladesh.
Md Nurul AnwarPort City International University, Chittagong, Bangladesh.
Kazi Md KamaruddinLivestock Division, Bangladesh Agricultural Research Council, Dhaka - 1202, Bangladesh.
Bangladesh Livestock Research Institute · BDChattogram Veterinary and Animal Sciences University · BDDhaka International University · BD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimWorldwide, MATERIALS AND

methodsA total of 365 serum samples were collected and tested for MS using serum plate agglutination (SPA) test for determination of MS seroprevalence. On the other hand, tracheal swabs were collected from each seropositive flocks for polymerase chain reaction (PCR) to determine the presence of MS organism.

resultsAmong the farms, the highest prevalence was found to be 69% and the lowest prevalence was 28% with the average 60%. The seroprevalence of MS infection in breeder farms was highest 70% with the flock size >10,000 birds, whereas it was lowest 57% in the flocks ranging from 4000 to 7000. According to age group, the prevalence was found highest 70% in >60 weeks age group of birds and lowest 42% in 10-19 weeks group. The seroprevalence of MS in winter season was found as highest as 64%, whereas it was found lowest 60% in the summer season. There was a statistically significant difference (p<0.01) among the seroprevalence of MS in different breeder farms, flock size, and age groups, but there was no significant (p>0.05) difference in the winter, summer, and rainy season. To confirm the presence of MS in the samples, PCR test was applied using specific primers to amplify a 214 bp region of the 16S rRNA gene of the organism. In PCR, all seropositive flocks showed a positive result for MS.

conclusionAs the plate agglutination test result showed 100% similar with PCR result, it can be suggested that agglutination test is better than molecular and culture techniques for MS detection and it is also cheaper and less time-consuming method.

Indexed as

breeder farmMycoplasma synoviaepolymerase chain reactionrespiratory infectionrisk factorsseroprevalence

Identifiers

PMID27847414
PMCPMC5104713
OpenAlexW2531733111

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.