Evidence map›Paper›PMID 31870298›Full record

ArticleBMC microbiology2019

Detection and characterization of bacterial endosymbionts in Southeast Asian tephritid fruit fly populations.

Elias D Asimakis, Vangelis Doudoumis, Ashok B Hadapad, Ramesh S Hire, Costas Batargias, Changying Niu, Mahfuza Khan, Kostas Bourtzis, George Tsiamis

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Frontiers in insect science · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Detection ofInsects · 2020
    Article
  8. Frontiers in microbiology · 2020
    Review
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 at 6 institutions in 5 countries.

Elias D AsimakisDepartment of Environmental Engineering, University of Patras, 2 Seferi St., 30100, Agrinio, Greece.
Vangelis DoudoumisDepartment of Environmental Engineering, University of Patras, 2 Seferi St., 30100, Agrinio, Greece.
Ashok B HadapadNuclear Agriculture & Biotechnology Division, Bhabha Atomic Research Centre (BARC), Trombay, Mumbai, Maharashtra, 400 085, India.
Ramesh S HireNuclear Agriculture & Biotechnology Division, Bhabha Atomic Research Centre (BARC), Trombay, Mumbai, Maharashtra, 400 085, India.
Costas BatargiasDepartment of Fisheries & Aquaculture Management, Technological Educational Institute of Western Greece, 30200, Messolonghi, Greece.
Changying NiuHuazhong Agricultural University, Wuhan, 430070, Hubei, China.
Mahfuza KhanInsect Biotechnology Division, Institute of Food and Radiation Biology (IFRB), Atomic Energy Research Establishment (AERE), Ganakbari, Savar, Dhaka, 1349, Bangladesh.
Kostas BourtzisInsect Pest Control Laboratory, Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture, Vienna International Centre, P.O. Box 100, 1400, Vienna, Austria.
George TsiamisDepartment of Environmental Engineering, University of Patras, 2 Seferi St., 30100, Agrinio, Greece. gtsiamis@upatras.gr.
Bhabha Atomic Research Centre · INTechnological Educational Institute of Western Greece · GRUniversity of Patras · GRBangladesh Atomic Energy Commission · BDHuazhong Agricultural University · CNInternational Atomic Energy Agency · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVarious endosymbiotic bacteria, including Wolbachia of the Alphaproteobacteria, infect a wide range of insects and are capable of inducing reproductive abnormalities to their hosts such as cytoplasmic incompatibility (CI), parthenogenesis, feminization and male-killing. These extended phenotypes can be potentially exploited in enhancing environmentally friendly methods, such as the sterile insect technique (SIT), for controlling natural populations of agricultural pests. The goal of the present study is to investigate the presence of Wolbachia, Spiroplasma, Arsenophonus and Cardinium among Bactrocera, Dacus and Zeugodacus flies of Southeast Asian populations, and to genotype any detected Wolbachia strains.

resultsA specific 16S rRNA PCR assay was used to investigate the presence of reproductive parasites in natural populations of nine different tephritid species originating from three Asian countries, Bangladesh, China and India. Wolbachia infections were identified in Bactrocera dorsalis, B. correcta, B. scutellaris and B. zonata, with 12.2-42.9% occurrence, Entomoplasmatales in B. dorsalis, B. correcta, B. scutellaris, B. zonata, Zeugodacus cucurbitae and Z. tau (0.8-14.3%) and Cardinium in B. dorsalis and Z. tau (0.9-5.8%), while none of the species tested, harbored infections with Arsenophonus. Infected populations showed a medium (between 10 and 90%) or low (< 10%) prevalence, ranging from 3 to 80% for Wolbachia, 2 to 33% for Entomoplasmatales and 5 to 45% for Cardinium. Wolbachia and Entomoplasmatales infections were found both in tropical and subtropical populations, the former mostly in India and the latter in various regions of India and Bangladesh. Cardinium infections were identified in both countries but only in subtropical populations. Phylogenetic analysis revealed the presence of Wolbachia with some strains belonging either to supergroup B or supergroup A. Sequence analysis revealed deletions of variable length and nucleotide variation in three Wolbachia genes. Spiroplasma strains were characterized as citri-chrysopicola-mirum and ixodetis strains while the remaining Entomoplasmatales to the Mycoides-Entomoplasmataceae clade. Cardinium strains were characterized as group A, similar to strains infecting Encarsia pergandiella.

conclusionsOur results indicated that in the Southeast natural populations examined, supergroup A Wolbachia strain infections were the most common, followed by Entomoplasmatales and Cardinium. In terms of diversity, most strains of each bacterial genus detected clustered in a common group. Interestingly, the deletions detected in three Wolbachia genes were either new or similar to those of previously identified pseudogenes that were integrated in the host genome indicating putative horizontal gene transfer events in B. dorsalis, B. correcta and B. zonata.

Indexed as

AnimalsBacteriaDNA, BacterialDNA, RibosomalGene Transfer, HorizontalPest Control, BiologicalPhylogenyRNA, Ribosomal, 16SSymbiosisTephritidaeDNA, BacterialDNA, RibosomalRNA, Ribosomal, 16S16S rRNAArsenophonusBactroceraCardiniumHorizontal gene transferMulti locus sequence typingSpiroplasmaWolbachiaZeugodacus

Identifiers

PMID31870298
PMCPMC7050614
OpenAlexW2995583534

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.