Camilla Santos

Dr. Camilla Santos

University of São Paulo (USP)
orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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1 January 2021 in Aquaculture
Verified
Journal Article
Closed access
Camilla SantosCamilla Santos
Camilla Santos
SASónia C.S. Andrade
Sónia C.S. Andrade
ATAna K. Teixeira
Ana K. Teixeira
FFFlávio Farias
Flávio Farias
AGAna C. Guerrelhas
Ana C. Guerrelhas
PFPatrícia D. Freitas
Patrícia D. Freitas

28 August 2014 in Frontiers in Genetics
Verified
Journal Article
Open access
PDF file
Camilla SantosCamilla Santos
Camilla Santos
DBDanielly V. Blanck
Danielly V. Blanck
PFPatrícia Domingues de Freitas
Patrícia Domingues de Freitas
The sequences of all different RNA transcripts present in a cell or tissue that are related to the gene expression and its functional control represent what it is called a transcriptome. The transcripts vary between cells, tissues, ontogenetic and environmental conditions and the knowledge that can be gained through them is of a solid relevance for genetic applications in aquaculture. Some of the techniques used in transcriptome studies, such as microarrays, are being replaced for next-generation sequencing approaches. RNA-seq emerges as a new possibility for the transcriptome complexity analysis as well as for the candidate genes and polymorphisms identification of penaeid species. Thus, it may also help to understand the determination of complex traits mechanisms and genetic improvement of stocks. In this review, it is first introduced an overview of transcriptome analysis by RNA-seq, followed by a discussion of how this approach may be applied in genetic progress within penaeid stocks.

10 April 2018 in Frontiers in Genetics
Verified
Journal Article
Open access
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Camilla SantosCamilla Santos
Camilla Santos
SASónia Cristina Da Silva Andrade
Sónia Cristina Da Silva Andrade
ATAna K. Teixeira
Ana K. Teixeira
FFFlávio Farias
Flávio Farias
KKKarin Kurkjian
Karin Kurkjian
PFPatrícia Domingues de Freitas
Patrícia Domingues de Freitas
Litopenaeus vannamei Transcriptome Profile of Populations Evaluated for Growth Performance and Exposed to White Spot Syndrome Virus (WSSV)

16 July 2020 in Genes
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Journal Article
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Camilla SantosCamilla Santos
Camilla Santos
SASónia Cristina Da Silva Andrade
Sónia Cristina Da Silva Andrade
Jorge FernandesJorge Fernandes
Jorge Fernandes
PFPatrícia Domingues de Freitas
Patrícia Domingues de Freitas
White Spot Syndrome Virus (WSSV) is one of the main threats to farming Litopenaeus vannamei, the most important crustacean commercialized in aquaculture worldwide. Here, we performed RNA-seq analyses in hepatopancreas and muscle from WSSV-negative (healthy) and WSSV-positive (unhealthy) L. vannamei, previously exposed to the virus, to obtain new insights about the molecular basis of resistance to WSSV. We detected 71% of our reads mapped against the recently described L. vannamei genome. This is the first report mapping RNA-seq transcripts from shrimps exposed to WSSV against the species reference genome. Differentially expressed gene (DEG) analyses were performed for four independent comparisons, and 13,338 DEGs were identified. When the redundancies and isoforms were disregarded, we observed 8351 and 6514 DEGs, respectively. Interestingly, after crossing the data, we detected a common set of DEGs for hepatopancreas and healthy shrimps, as well as another one for muscle and unhealthy shrimps. Our findings indicate that genes related to apoptosis, melanization, and the Imd pathway are likely to be involved in response to WSSV, offering knowledge about WSSV defense in shrimps exposed to the virus but not infected. These data present potential to be applied in further genetic studies in penaeids and other farmed shrimp species.

26 June 2026 in bioRxiv
Verified
Preprint
Open access
GFGiulio Formenti
Giulio Formenti
DADominic E. Absolon
Dominic E. Absolon
LALinelle Ann L. Abueg
Linelle Ann L. Abueg
FAFrancine Ackerman
Francine Ackerman
FAFarooq Omar Al-Ajli
Farooq Omar Al-Ajli
EJErich D Jarvis
Erich D Jarvis
The Vertebrate Genomes Project (VGP) aims to produce complete and near-error-free reference genomes for all ∼70,000 extant vertebrate species. Organized in four phases, it progressively targets all vertebrate orders, families, genera, and eventually all species. Here we present the completion of VGP Phase I, delivering reference genomes for ∼97% of vertebrate orders, along with additional lineages within those orders, totaling 815 species and 1.6 trillion base pairs of main haplotype sequence. These genomes were assembled and annotated over an 8-year period (2018-2026) of rapid advances in genome sequencing, assembly, and annotation methods, alongside the growth of associated consortium initiatives and international collaborations. They represent some of the highest-quality vertebrate genomes currently available, and most have become the primary reference for their respective species in public databases. Comparative analyses across a subset of 579 species when we reached a threshold of 85% of orders allowed us to reconstruct the genome of the last common ancestor of all vertebrates 500 million years ago, identify diverse modes of sex chromosome evolution, reveal clade-specific three-dimensional genome architecture, discover methylated epigenetic landscapes across vertebrates, and provide a framework for studying gene and pseudogene evolution, immune loci, cancer-associated genes, and other trait-associated loci. Approximately a quarter of this subset are listed as Vulnerable to Critically Endangered by the IUCN Red List of Threatened Species, and have enabled more advanced genomic investigations of extinction risk. VGP Phase I delivers the reference backbone for vertebrate genomics, enabling discoveries that would otherwise remain out of reach across evolution, conservation, and medicine.

4 July 2018 in PeerJ
Verified
Journal Article
Open access
PDF file
Camilla SantosCamilla Santos
Camilla Santos
SASónia Cristina Da Silva Andrade
Sónia Cristina Da Silva Andrade
PFPatrícia Domingues de Freitas
Patrícia Domingues de Freitas
Litopenaeus vannameiis one of the most important shrimp species for worldwide aquaculture. Despite this, little genomic information is available for this penaeid and other closely related taxonomic crustaceans. Consequently, genes, proteins and their respective polymorphisms are poorly known for these species. In this work, we used the RNA sequencing technology (RNA-seq) inL. vannameishrimp evaluated for growth performance, and exposed to the White Spot Syndrome Virus (WSSV), in order to investigate the presence of Single Nucleotide Polymorphisms (SNPs) within genes related to innate immunity and growth, both features of great interest for aquaculture activity. We analyzed individuals with higher and lower growth rates; and infected (unhealthy) and non-infected (healthy), after exposure to WSSV. Approximately 7,000 SNPs were detected in the samples evaluated for growth, being 3,186 and 3,978 exclusive for individuals with higher and lower growth rates, respectively. In the animals exposed to WSSV we found about 16,300 unique SNPs, in which 9,338 were specific to non-infected shrimp, and 7,008 were exclusive to individuals infected with WSSV and symptomatic. In total, we describe 4,312 unigenes containing SNPs. About 60% of these unigenes returned GO blastX hits for Biological Process, Molecular Function and Cellular Component ontologies. We identified 512 KEGG unique KOs distributed among 275 pathways, elucidating the majority of metabolism roles related to high protein metabolism, growth and immunity. These polymorphisms are all located in coding regions, and certainly can be applied in further studies involving phenotype expression of complex traits, such as growth and immunity. Overall, the set of variants raised herein enriches the genomic databases available for shrimp, given that SNPs originated from nextgen are still rare for this relevant crustacean group, despite their huge potential of use in genomic selection approaches.