The JAK-STAT pathway controls Plasmodium vivax load in early stages of Anopheles aquasalis infection

Autor: Wanderli Pedro Tadei, Helena R. C. Araújo, Antonio Jorge Tempone, Nágila Francinete Costa Secundino, Yeon Soo Han, Paulo F. P. Pimenta, Yara M. Traub-Cseko, Carolina Barillas-Mury, Claudia María Ríos-Velásquez, Ana C. Bahia, Bruno A. M. Guedes, Marina S. Kubota, Alessandra S Orfanó
Rok vydání: 2010
Předmět:
Male
Plasmodium vivax
Protein Expression
Stat Gene
Gene
Mosquitoes
Parasite Load
Oocyst
Pias Gene
RNA interference
Plasmodium Vivax
Isolation And Purification
Stat Transcription Factors
lcsh:Public aspects of medicine
JAK-STAT signaling pathway
Immunohistochemistry
Protein Inhibitors of Activated STAT
Nos Gene
STAT Transcription Factors
Protein Inhibitor Of Activated Stat
Infectious Diseases
Gene Knockdown Techniques
Medicine
Female
Immunocytochemistry
Brazil
Human
Research Article
Dna Sequence
Gene Sequence
lcsh:Arctic medicine. Tropical medicine
lcsh:RC955-962
Immunology
Molecular Sequence Data
Anopheles Aquasalis
Biology
Biosynthesis
Microbiology
stat
Vector Biology
Molecular Genetics
Immune system
Stat Protein
parasitic diseases
Anopheles
medicine
Parasitic Diseases
Animals
Controlled Study
Gene Silencing
Transcription factor
Epithelium Cell
Rna Interference
Protein Inhibitors Of Activated Stat
Protozoal Genetics
Animal
Brasil
Gene Expression Profiling
fungi
Public Health
Environmental and Occupational Health

Immunity
Nucleotide Sequence
lcsh:RA1-1270
Sequence Analysis
Dna

Sequence Analysis
DNA

biology.organism_classification
medicine.disease
Nonhuman
Virology
Malaria
Organismal Interaction
STAT protein
Janus Kinase
Parasitology
Nitric Oxide Synthase
Zdroj: PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases, Vol 5, Iss 11, p e1317 (2011)
Repositório Institucional do INPA
Instituto Nacional de Pesquisas da Amazônia (INPA)
instacron:INPA
ISSN: 1935-2735
Popis: Malaria affects 300 million people worldwide every year and 450,000 in Brazil. In coastal areas of Brazil, the main malaria vector is Anopheles aquasalis, and Plasmodium vivax is responsible for the majority of malaria cases in the Americas. Insects possess a powerful immune system to combat infections. Three pathways control the insect immune response: Toll, IMD, and JAK-STAT. Here we analyze the immune role of the A. aquasalis JAK-STAT pathway after P. vivax infection. Three genes, the transcription factor Signal Transducers and Activators of Transcription (STAT), the regulatory Protein Inhibitors of Activated STAT (PIAS) and the Nitric Oxide Synthase enzyme (NOS) were characterized. Expression of STAT and PIAS was higher in males than females and in eggs and first instar larvae when compared to larvae and pupae. RNA levels for STAT and PIAS increased 24 and 36 hours (h) after P. vivax challenge. NOS transcription increased 36 h post infection (hpi) while this protein was already detected in some midgut epithelial cells 24 hpi. Imunocytochemistry experiments using specific antibodies showed that in non-infected insects STAT and PIAS were found mostly in the fat body, while in infected mosquitoes the proteins were found in other body tissues. The knockdown of STAT by RNAi increased the number of oocysts in the midgut of A. aquasalis. This is the first clear evidence for the involvement of a specific immune pathway in the interaction of the Brazilian malaria vector A. aquasalis with P. vivax, delineating a potential target for the future development of disease controlling strategies.
Author Summary Malaria is endemic in 22 countries in the Americas where the Anopheles aquasalis mosquito is an important malaria vector and the Plasmodium vivax parasite is responsible for most malaria cases. This natural vector-parasite pair is difficult to study due to the lack of cultivating system for P. vivax, and to the lack of genome data for A. aquasalis. Moreover, almost all previous studies are based on African and Asian anopheline species. Understanding the interaction mechanisms between mosquito vectors and plasmodia is important for the development of malaria control strategies. Our results showed that the JAK-STAT immune pathway is activated in A. aquasalis after P. vivax challenge and is important to maintain the low levels of P. vivax load observed in this vector. Our results add to the understanding of the A. aquasalis interaction with P. vivax and lead to possible explanations for this vector competence in P. vivax transmission. All information generated here may be used to direct the development of new or specific strategies to block malaria transmission by A. aquasalis in some parts of the Americas.
Databáze: OpenAIRE