Evidence map›Paper›PMID 28220445›Full record

ArticleAMB Express2017

In vitro and in vivo antibacterial effect of NZ2114 against Streptococcus suis type 2 infection in mice peritonitis models.

Jian Jiao, Ruoyu Mao, Da Teng, Xiumin Wang, Ya Hao, Na Yang, Xiao Wang, Xingjun Feng, Jianhua Wang

Abstract read
In one paragraph

Article in AMB Express, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Effect of NZ2114 againstFrontiers in microbiology · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Frontiers in cellular and infection microbiology · 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

9 authors.

Jian JiaoKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Ruoyu MaoKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Da TengKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Xiumin WangKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Ya HaoKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Na YangKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Xiao WangKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Xingjun FengInstitute of Animal Nutrition, Northeast Agricultural University, Harbin, 150030, People's Republic of China.
Jianhua WangKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China. wangjianhua@caas.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NZ2114 is a promising candidate for therapeutic application owing to potent activity to gram-positive bacterium such as Streptococcus pneumoniae and Staphylococcus aureus. This work is the first report to describe the in vitro and in vivo antibacterial characteristics of NZ2114 against Streptococcus suis. It exhibited strong antimicrobial activity against S. suis type 2 strains CVCC 606, CVCC 3309, and CVCC 3928 at a low minimal inhibitory concentration (MIC) of 0.03-0.06 μM. The NZ2114 killed over 99.9% of tested S. suis CVCC 606 in Mueller-Hinton medium within 4 h when treated with 4 × MIC. It caused only less than 0.25% hemolytic activity in the concentration of 256 μg/ml. Additionally, NZ2114 exhibited potent in vivo activity to S. suis. All mice were survival when the dosage was low to 0.2 mg/kg. Over 99% of S. suis cells were killed within 4 h in blood, lung, liver and spleen with dosage of 10, 20, and 40 mg/kg in mice peritonitis models and no pathogen were detected after 24 h of treatment. Further, no pathological phenomenon in lung and low level of inflammatory cytokines in blood were detected. These results indicate that NZ2114 has the potential to be a new antimicrobial agent candidate for the clinical treatment of infection caused by S. suis type 2.

Indexed as

Antimicrobial peptidesAnti-S. suis in vivoNZ2114Streptococcus suis

Identifiers

PMID28220445
PMCPMC5318318

What OpenQuestion holds

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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.