Evidence map›Paper›PMID 31792802›Full record

ArticleIn vitro cellular & developmental biology. Animal2020

Establishment of two midgut cell lines from the fall armyworm, Spodoptera frugiperda (Lepidoptera: Noctuidae).

Kaile Zhou, Cynthia L Goodman, Joseph Ringbauer, Qisheng Song, Brenda Beerntsen, David Stanley

Abstract read
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In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. A database of crop pest cell lines.In vitro cellular & developmental biology. Animal · 2022
    Article
  8. Article
  9. RNA biology · 2021
    Article
  10. 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.

Kaile ZhouDivision of Plant Sciences, University of Missouri, Columbia, MO, 65211, USA.
Cynthia L GoodmanBiological Control of Insects Research Laboratory, USDA/Agricultural Research Service, 1503 S. Providence Road, Columbia, MO, 65203, USA. cindy.goodman@usda.gov.ORCID http://orcid.org/0000-0001-6631-9848
Joseph RingbauerBiological Control of Insects Research Laboratory, USDA/Agricultural Research Service, 1503 S. Providence Road, Columbia, MO, 65203, USA.
Qisheng SongDivision of Plant Sciences, University of Missouri, Columbia, MO, 65211, USA.
Brenda BeerntsenDepartment of Veterinary Pathobiology, University of Missouri, Columbia, MO, 65211, USA.
David StanleyBiological Control of Insects Research Laboratory, USDA/Agricultural Research Service, 1503 S. Providence Road, Columbia, MO, 65203, USA.

Funding

Center for Arthropod Management Technologies CRADA #58-3K95-4-1706
6 · The paper itself

Abstract

Two cell lines were generated from larval midguts of Spodoptera frugiperda and have been 26 passaged over 50 times. The CT/BCIRL-SfMG1-0611-KZ line was established from 27 trypsinized, minced whole midgut tissues: the CT/BCIRL-SfMG-0617-KZ line from isolated 28 midgut muscle tissue (containing some residual epithelial cells). Additional midgut cultures were 29 generated from isolated epithelial cells; some passaged not more than three times, which grew 30 very slowly and survived longer than 1 year. The continuously replicating cell lines contain 31 firmly adhering cells with different morphologies, including elongated, spherical, and/or 32 rectangular. The mean diameters of these cell lines are 9.3 ± 4.0 μm (SfMG1-0611) and 9.2 ± 3.9 33 μm (SfMG-0617). Growth curves for the two lines have relatively lengthy doubling times of 73.9 34 h and 50.4 h for SfMG1-0611 and SfMG-0617, respectively. We confirmed the identity of these 35 lines using DNA amplification fingerprinting (DAF-PCR) and noted that the DNA patterns for 36 each cell line were similar to their host tissues but distinctly different from other cell lines or 37 tissues from different insect species. Amplification of genomic DNA with species-specific 38 primers yielded DNA fragments of the expected sizes and with sequences nearly identical to 39 those from the S. frugiperda genome. Both cell lines were exposed to selected Bt Cry proteins 40 with minimal impact. These lines are currently available to researchers worldwide.

Indexed as

AnimalsBacillus thuringiensis ToxinsBacterial ProteinsCell CountCell LineDigestive SystemDNA FingerprintingEndotoxinsHemolysin ProteinsSpodopteraBacillus thuringiensis ToxinsBacterial ProteinsEndotoxinsHemolysin Proteinsinsecticidal crystal protein, Bacillus ThuringiensisBovine liver cell linesCytochrome P450HepatocytesLiver sinusoidal cellsmRNA expression

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.