Evidence map›Paper›PMID 33339514›Full record

ArticleBMC genetics2020

Geographic distribution of sex chromosome polymorphism in Anastrepha fraterculus sp. 1 from Argentina.

María Cecilia Giardini, Mariela Nieves, Alejandra Carla Scannapieco, Claudia Alejandra Conte, Fabián Horacio Milla, María Elena Schapovaloff, Maria Soledad Frissolo, María Isabel Remis, Jorge Luis Cladera, Silvia Beatriz Lanzavecchia

Abstract read
In one paragraph

Article in BMC genetics, 2020. 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.

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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

10 authors.

María Cecilia GiardiniLaboratorio de Insectos de Importancia Agronómica, Instituto de Genética (IGEAF), Instituto de Agrobiotecnología y Biología Molecular (IABIMO), INTA- CONICET, Hurlingham, Buenos Aires, Argentina.
Mariela NievesGrupo de Investigación en Biología Evolutiva, Departamento de Ecología, Genética y Evolución, IEGEBA (CONICET), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.
Alejandra Carla ScannapiecoLaboratorio de Insectos de Importancia Agronómica, Instituto de Genética (IGEAF), Instituto de Agrobiotecnología y Biología Molecular (IABIMO), INTA- CONICET, Hurlingham, Buenos Aires, Argentina.
Claudia Alejandra ConteLaboratorio de Insectos de Importancia Agronómica, Instituto de Genética (IGEAF), Instituto de Agrobiotecnología y Biología Molecular (IABIMO), INTA- CONICET, Hurlingham, Buenos Aires, Argentina.
Fabián Horacio MillaLaboratorio de Insectos de Importancia Agronómica, Instituto de Genética (IGEAF), Instituto de Agrobiotecnología y Biología Molecular (IABIMO), INTA- CONICET, Hurlingham, Buenos Aires, Argentina.
María Elena SchapovaloffConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.
Maria Soledad FrissoloSubprograma La Rioja, Programa Nacional de Control y Erradicación de Moscas de los Frutos (PROCEM), La Rioja, Argentina.
María Isabel RemisConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.
Jorge Luis CladeraLaboratorio de Insectos de Importancia Agronómica, Instituto de Genética (IGEAF), Instituto de Agrobiotecnología y Biología Molecular (IABIMO), INTA- CONICET, Hurlingham, Buenos Aires, Argentina.
Silvia Beatriz LanzavecchiaLaboratorio de Insectos de Importancia Agronómica, Instituto de Genética (IGEAF), Instituto de Agrobiotecnología y Biología Molecular (IABIMO), INTA- CONICET, Hurlingham, Buenos Aires, Argentina. lanzvecchia.silvia@inta.gob.ar.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnastrepha fraterculus is recognized as a quarantine pest in several American countries. This fruit fly species is native to the American continent and distributed throughout tropical and subtropical regions. It has been reported as a complex of cryptic species, and at least eight morphotypes have been described. Only one entity of this complex, formerly named Anastrepha fraterculus sp. 1, is present in Argentina. Previous cytogenetic studies on this morphotype described the presence of sex chromosome variation identified by chromosomal size and staining patterns. In this work, we expanded the cytological study of this morphotype by analyzing laboratory strains and wild populations to provide information about the frequency and geographic distribution of these sex chromosome variants. We analyzed the mitotic metaphases of individuals from four laboratory strains and five wild populations from the main fruit-producing areas of Argentina, including the northwest (Tucumán and La Rioja), northeast (Entre Ríos and Misiones), and center (Buenos Aires) of the country.

resultsIn wild samples, we observed a high frequency of X

conclusionsWe discuss the importance of cytogenetics to understand the possible route of invasion and dispersion of this pest in Argentina and the evolutionary forces acting under laboratory conditions, possibly driving changes in the chromosomal frequencies. Our findings provide deep and integral genetic knowledge of this species, which has become of relevance to the characterization and selection of valuable A. fraterculus sp. 1 strains for mass rearing production and SIT implementation.

Indexed as

Genetics, PopulationPolymorphism, GeneticAnimalsArgentinaChromosomes, InsectFemaleGeographyKaryotypingMaleSex ChromosomesTephritidaeDispersion patternsFruit fly pestKaryomorphsKaryotypic polymorphismMorphotypesSIT

Identifiers

PMID33339514
PMCPMC7747450

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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.