Christian C. Figueroa

Prof. Dr. Christian C. Figueroa

Biological Sciences, University of Talca, Talca, Maule, Chile
orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 June 2012 in PLOS ONE
Verified
Journal Article
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ASAndrea X. Ximena Silva Silva
Andrea X. Ximena Silva Silva
GJGeorg Jander
Georg Jander
HSHoracio Samaniego
Horacio Samaniego
JRJohn S Ramsey
John S Ramsey
Christian C. FigueroaChristian C. Figueroa
Christian C. Figueroa
Insecticide resistance is one of the best examples of rapid micro-evolution found in nature. Since the development of the first synthetic insecticide in 1939, humans have invested considerable effort to stay ahead of resistance phenotypes that repeatedly develop in insects. Aphids are a group of insects that have become global pests in agriculture and frequently exhibit insecticide resistance. The green peach aphid, Myzus persicae, has developed resistance to at least seventy different synthetic compounds, and different insecticide resistance mechanisms have been reported worldwide. To further characterize this resistance, we analyzed genome-wide transcriptional responses in three genotypes of M. persicae, each exhibiting different resistance mechanisms, in response to an anti-cholinesterase insecticide. The sensitive genotype (exhibiting no resistance mechanism) responded to the insecticide by up-regulating 183 genes primarily ones related to energy metabolism, detoxifying enzymes, proteins of extracellular transport, peptidases and cuticular proteins. The second genotype (resistant through a kdr sodium channel mutation), up-regulated 17 genes coding for detoxifying enzymes, peptidase and cuticular proteins. Finally, a multiply resistant genotype (carrying kdr and a modified acetylcholinesterase), up-regulated only 7 genes, appears not to require induced insecticide detoxification, and instead down-regulated many genes. This study suggests strongly that insecticide resistance in M. persicae is more complex that has been described, with the participation of a broad array of resistance mechanisms. The sensitive genotype exhibited the highest transcriptional plasticity, accounting for the wide range of potential adaptations to insecticides that this species can evolve. In contrast, the multiply resistant genotype exhibited a low transcriptional plasticity, even for the expression of genes encoding enzymes involved in insecticide detoxification. Our results emphasize the value of microarray studies to search for regulated genes in insects, but also highlights the many ways those different genotypes can assemble resistant phenotypes depending on the environmental pressure.

7 July 2021 in Communications Biology
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Journal Article
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KSKumar Saurabh Singh
Kumar Saurabh Singh
ECErick M. G. Cordeiro
Erick M. G. Cordeiro
BTBartlomiej J. Troczka
Bartlomiej J. Troczka
APAdam Pym
Adam Pym
JMJoanna Mackisack
Joanna Mackisack
CBChris Bass
Chris Bass
The aphid Myzus persicae is a destructive agricultural pest that displays an exceptional ability to develop resistance to both natural and synthetic insecticides. To investigate the evolution of resistance in this species we generated a chromosome-scale genome assembly and living panel of >110 fully sequenced globally sampled clonal lines. Our analyses reveal a remarkable diversity of resistance mutations segregating in global populations of M. persicae. We show that the emergence and spread of these mechanisms is influenced by host–plant associations, uncovering the widespread co‐option of a host-plant adaptation that also offers resistance against synthetic insecticides. We identify both the repeated evolution of independent resistance mutations at the same locus, and multiple instances of the evolution of novel resistance mechanisms against key insecticides. Our findings provide fundamental insights into the genomic responses of global insect populations to strong selective forces, and hold practical relevance for the control of pests and parasites.

27 January 2004 in Molecular Ecology Notes
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AWAlex C. C. Wilson
Alex C. C. Wilson
BMBlandine Massonnet
Blandine Massonnet
JSJean‐Christophe Simon
Jean‐Christophe Simon
NPNathalie Prunier‐Leterme
Nathalie Prunier‐Leterme
LDLotfali Dolatti
Lotfali Dolatti
PSPaul Sunnucks
Paul Sunnucks

24 October 2008 in Molecular Ecology
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Journal Article
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JPJ. Peccoud
J. Peccoud
Christian C. FigueroaChristian C. Figueroa
Christian C. Figueroa
ASA. X. Silva
A. X. Silva
CRClaudio C. Ramirez
Claudio C. Ramirez
LML. Mieuzet
L. Mieuzet
JSJ.‐C. Simon
J.‐C. Simon

20 April 2005 in Heredity
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Journal Article
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Christian C. FigueroaChristian C. Figueroa
Christian C. Figueroa
JSJ-C Simon
J-C Simon
JGJ-F Le Gallic
J-F Le Gallic
NPN Prunier-Leterme
N Prunier-Leterme
LBL M Briones
L M Briones
HNH M Niemeyer
H M Niemeyer
In Chile, the aphid Sitobion avenae is of recent introduction, lives on cultivated and wild Poaceae, and is thought to reproduce by permanent parthenogenesis. In order to study the genetic variability and population structure of this species, five microsatellite loci were typed from individual aphids collected from different cultivated and wild host plants, from different geographical zones, and years. Chilean populations showed a high degree of heterozygosity and a low genetic variability across regions and years, with four predominant genotypes representing nearly 90% of the sample. This pattern of low clonal diversity and high heterozygosity was interpreted as the result of recent founder events from a few asexually reproducing genotypes. Most geographical and temporal variation observed in the genetic composition resulted from fluctuations of a few predominant clones. In addition, comparisons of the genotypes found in Chile with those described in earlier surveys of S. avenae populations in Western Europe led us to identify ‘superclones’ with large geographical distribution and high ecological success, and to make a preliminary exploration of the putative origin(s) of S. avenae individuals introduced to Chile.

1 August 2011 in Trends in Ecology & Evolution
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Journal Article
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RNRoberto Nespolo
Roberto Nespolo
LBLeonardo D. Bacigalupe
Leonardo D. Bacigalupe
Christian C. FigueroaChristian C. Figueroa
Christian C. Figueroa
PKPawel Koteja
Pawel Koteja
JOJuan C. Opazo
Juan C. Opazo