Evidence map›Paper›PMID 31814605›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Establishment of a Multiplex Real-Time TaqMan-MGB Polymerase Chain Reaction (PCR) Method for the Simultaneous Detection of Three Animal Chlamydia Species.

Fuping Nie, Qian Gong, Jun Yang, Cunxian Xi, Yu Wang, Guomin Wang, Lei Zhang, Xianliang Li, Danqun Huo, Changjun Hou

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 1 institution in 1 country.

Fuping NieCollege of Biomedical Engineering, Chongqing University, Chongqing, China (mainland).
Qian GongChongqing Customs Technology Center, Chongqing Engineering Technology Research Center of Import and Export Food Safety, Chongqing, China (mainland).
Jun YangChongqing Customs Technology Center, Chongqing Engineering Technology Research Center of Import and Export Food Safety, Chongqing, China (mainland).
Cunxian XiChongqing Customs Technology Center, Chongqing Engineering Technology Research Center of Import and Export Food Safety, Chongqing, China (mainland).
Yu WangChongqing Customs Technology Center, Chongqing Engineering Technology Research Center of Import and Export Food Safety, Chongqing, China (mainland).
Guomin WangChongqing Customs Technology Center, Chongqing Engineering Technology Research Center of Import and Export Food Safety, Chongqing, China (mainland).
Lei ZhangChongqing Customs Technology Center, Chongqing Engineering Technology Research Center of Import and Export Food Safety, Chongqing, China (mainland).
Xianliang LiChongqing Customs Technology Center, Chongqing Engineering Technology Research Center of Import and Export Food Safety, Chongqing, China (mainland).
Danqun HuoCollege of Biomedical Engineering, Chongqing University, Chongqing, China (mainland).
Changjun HouCollege of Biomedical Engineering, Chongqing University, Chongqing, China (mainland).
Chongqing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Chlamydiae are spread globally and cause infectious diseases in both humans and animals. The existing detection methods for this disease have numerous shortcomings, including low sensitivity, time consuming procedures, and high contamination vulnerability. MATERIAL AND METHODS To overcome shortcomings for detecting animal chlamydiosis, a multiplex quantitative polymerase chain reaction (PCR) assay was established for simultaneously detecting and differentiating 3 Chlamydia species (C. pecorum, C. abortus, and C. psittaci) by real time PCR based on TaqMan-MGB technology. RESULTS The limit of detection was 20.2 copies/µL for Chlamydophila (Cp.) abortus, 30.8 copies/µL for Cp. pecorum, and 16 copies/µL for Cp. psittaci. This method has good repeatability and stability as coefficients of variation range from 0.04% to 1.38%. Furthermore, compared with OIE (World Organization for Animal Health) recommended PCR assay and previously reported animal chlamydia shell PCR, this multiplex PCR assay demonstrated 99% concordance in detecting clinical samples of porcine nasal swabs and vaginal swabs. CONCLUSIONS The novel established method in this study was able to detect 3 types of Chlamydia species simultaneously, and had high sensitivity, strong specificity, and good stability. It provided a rapid, reliable, and convenient method for epidemiological and clinical diagnosis of chlamydiosis in animals.

Indexed as

AnimalsChlamydiaFemaleHumansMaleMultiplex Polymerase Chain ReactionReal-Time Polymerase Chain ReactionSensitivity and SpecificitySpecies SpecificitySwineZoonoses

Identifiers

PMID31814605
PMCPMC6921693
OpenAlexW2996329013

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.