Evidence map›Paper›PMID 28527138›Full record

ArticleEnvironmental science and pollution research international2017

Application of hyper-branched rolling circle amplification (HRCA) and HRCA-based strip test for the detection of Chattonella marina.

Xiaoli Nie, Chunyun Zhang, Yuanyuan Wang, Changlu Guo, Jin Zhou, Guofu Chen

Abstract read
PubMed Publisher
In one paragraph

Article in Environmental science and pollution research international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

6 authors.

Xiaoli NieCollege of Oceanology, School of Marine Science and Technology, Harbin Institute of Technology at Weihai, Wenhua West Road, 2#, Weihai, 264209, Shandong Province, People's Republic of China.
Chunyun ZhangCollege of Oceanology, School of Marine Science and Technology, Harbin Institute of Technology at Weihai, Wenhua West Road, 2#, Weihai, 264209, Shandong Province, People's Republic of China. zhangchunyun@hitwh.edu.cn.
Yuanyuan WangCollege of Oceanology, School of Marine Science and Technology, Harbin Institute of Technology at Weihai, Wenhua West Road, 2#, Weihai, 264209, Shandong Province, People's Republic of China.
Changlu GuoCollege of Oceanology, School of Marine Science and Technology, Harbin Institute of Technology at Weihai, Wenhua West Road, 2#, Weihai, 264209, Shandong Province, People's Republic of China.
Jin ZhouDivision of Ocean Science and Technology, Graduate School at Shenzhen, Tsinghua University, Shenzhen University Town, Xili Town, Shenzhen City, 518055, Guangdong Province, People's Republic of China.
Guofu ChenCollege of Oceanology, School of Marine Science and Technology, Harbin Institute of Technology at Weihai, Wenhua West Road, 2#, Weihai, 264209, Shandong Province, People's Republic of China. chenguofu@hitwh.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Harmful algal blooms (HABs) are global threats to marine ecosystems, fisheries, and human health. Therefore, developing effective and accurate methods for identifying causative algae and monitoring seawater quality is urgent. However, traditional, microscopy-based methods are complex, inaccurate, and time-consuming. Here, we present a novel method for effective and sensitive detection of Chattonella marina using hyper-branched rolling circle amplification (HRCA) and HRCA-based strip test (HBST). The large subunit (LSU) ribosomal DNA (rDNA) D1-D2 region of C. marina was firstly sequenced to design a species-specific padlock probe (PLP). The HRCA reaction with two amplification primers and further HBST for C. marina was established. The optimized reaction conditions for HRCA were PLP concentration, 20 pM; ligation temperature, 65 °C; ligation time, 60 min; amplification temperature, 61 °C; and amplification time, 60 min. The developed HBST detection procedure involved HRCA reaction, test strip preparation, hybridization, coloration, and judgment of hybridization by the naked eye. Specificity and sensitivity of the established methods were validated. Moreover, the results showed that the established detection methods were specific and sensitive to C. marina. The detection limits of HRCA and HBST assays were 10 copies and 1 copy μL

Indexed as

Harmful Algal BloomNucleic Acid HybridizationPolymerase Chain ReactionBase SequenceDNA, RibosomalEnvironmental MonitoringEukaryotaHumansPlasmidsDNA, RibosomalChattonella marinaDetectionHyper-branched rolling circle amplificationTest strip

Identifiers

What OpenQuestion holds

Textmetadata
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.