Evidence map›Paper›PMID 29057765›Full record

ArticleThe Journal of veterinary medical science2017

Development of LAMP assays for the molecular detection of taeniid infection in canine in Tibetan rural area.

Kai Feng, Wei Li, Zhihong Guo, Hong Duo, Yong Fu, Xiuying Shen, Cheng Tie, Rijie E, Changqin Xiao, Yanhong Luo and 8 more

Abstract read
In one paragraph

Article in The Journal of veterinary medical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. LAMP Assay for the Detection ofPathogens (Basel, Switzerland) · 2021
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. 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

18 authors.

Kai FengLaboratory of Veterinary Parasitic Diseases, Graduate School of Medicine and Veterinary Medicine, University of Miyazaki, 1-1 Gakuen-Kibanadai-Nishi, Miyazaki, Miyazaki 889-2192, Japan.
Wei LiZoonosis Laboratory, Academy of Animal and Veterinary Medicine, Qinghai University, No. 1, Weier Road, Biological Industrial District, Xining, Qinghai, 810016, the People of Republic of China.
Zhihong GuoZoonosis Laboratory, Academy of Animal and Veterinary Medicine, Qinghai University, No. 1, Weier Road, Biological Industrial District, Xining, Qinghai, 810016, the People of Republic of China.
Hong DuoZoonosis Laboratory, Academy of Animal and Veterinary Medicine, Qinghai University, No. 1, Weier Road, Biological Industrial District, Xining, Qinghai, 810016, the People of Republic of China.
Yong FuZoonosis Laboratory, Academy of Animal and Veterinary Medicine, Qinghai University, No. 1, Weier Road, Biological Industrial District, Xining, Qinghai, 810016, the People of Republic of China.
Xiuying ShenZoonosis Laboratory, Academy of Animal and Veterinary Medicine, Qinghai University, No. 1, Weier Road, Biological Industrial District, Xining, Qinghai, 810016, the People of Republic of China.
Cheng TieVeterinary Department in Xinghai County, No. 4, Nongmu Road, Xinghai, Qinghai, 813300, the People of Republic of China.
Rijie EVeterinary Department in Xinghai County, No. 4, Nongmu Road, Xinghai, Qinghai, 813300, the People of Republic of China.
Changqin XiaoVeterinary Department in Xinghai County, No. 4, Nongmu Road, Xinghai, Qinghai, 813300, the People of Republic of China.
Yanhong LuoVeterinary Department in Haiyan County, No. 13, Qilian Road, Haiyan, Qinghai, 812299, the People of Republic of China.
Guo QiVeterinary Department in Haiyan County, No. 13, Qilian Road, Haiyan, Qinghai, 812299, the People of Republic of China.
Ma NiVeterinary Department in Haiyan County, No. 13, Qilian Road, Haiyan, Qinghai, 812299, the People of Republic of China.
Qingmei MaVeterinary Department in Haiyan County, No. 13, Qilian Road, Haiyan, Qinghai, 812299, the People of Republic of China.
Wataru YamazakiLaboratory of Veterinary Public Health, Department of Veterinary Sciences, Faculty of Agriculture, University of Miyazaki, 1-1 Gakuen-Kibanadai-Nishi, Miyazaki, Miyazaki 889-2192, Japan.
Ayako YoshidaLaboratory of Veterinary Parasitic Diseases, Graduate School of Medicine and Veterinary Medicine, University of Miyazaki, 1-1 Gakuen-Kibanadai-Nishi, Miyazaki, Miyazaki 889-2192, Japan.
Yoichiro HoriiLaboratory of Veterinary Parasitic Diseases, Graduate School of Medicine and Veterinary Medicine, University of Miyazaki, 1-1 Gakuen-Kibanadai-Nishi, Miyazaki, Miyazaki 889-2192, Japan.
Kinpei YagiMedical Zoology Group, Department of Infectious Diseases, Hokkaido Institute of Public Health, North 19, West 12, Kitaku, Sapporo, Hokkaido 060-0819, Japan.
Nariaki NonakaLaboratory of Veterinary Parasitic Diseases, Graduate School of Medicine and Veterinary Medicine, University of Miyazaki, 1-1 Gakuen-Kibanadai-Nishi, Miyazaki, Miyazaki 889-2192, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For field-identification of taeniid cestodes in canine animals in Tibetan area, loop-mediated isothermal amplification (LAMP) assays for Echinococcus multilocularis, E. shiquicus, Taenia hydatigena, T. multiceps, T. pisiformis and T. crassiceps were developed and evaluated along with the reported assay for E. granulosus. The LAMP assays showed specific reaction with their corresponding target species DNA with the detection limit of 1 to 10 pg. Moreover, the assays for E. granulosus, E. multilocularis, T. hydatigena and T. multiceps could detect DNA extracted from 3 or more eggs of their corresponding target species. Then, the LAMP assays were applied on samples containing 3 to 35 taeniid eggs obtained from 61 field-collected canine feces in Qinghai, and the result was compared with a reported multiplex PCR and sequence analysis. The LAMP assays and the PCR detected single species DNA of E. granulosus, E. shiquicus, T. hydatigena and T. multiceps in 5, 2, 44 and 2 samples, respectively. In the rest 8 samples, DNA of both E. granulosus and T. hydatigena were detected by the PCR but the LAMP assays detected those DNAs in 2 samples and only T. hydatigena DNA in 6 samples. It was assumed that less than 3 E. granulosus eggs were mixed in the samples although the samples contained 21 to 27 eggs in total. In conclusion, the LAMP assays were less sensitive than the multiplex PCR, but would have adequate sensitivity for field use in Tibetan area.

Indexed as

AnimalsDNA, HelminthDog DiseasesDogsEchinococcosisEchinococcusEchinococcus multilocularisMultiplex Polymerase Chain ReactionNucleic Acid Amplification TechniquesSensitivity and SpecificityTaeniaTaeniasisTibetDNA, HelminthcanineChinadiagnosistaeniid cestodeszoonosis

Identifiers

PMID29057765
PMCPMC5745177

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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.