Literature DB >> 22499423

Susceptibility of peritoneal macrophage from different species of neotropical primates to ex vivo Leishmania (L.) infantum chagasi-infection.

Liliane Almeida Carneiro1, Márcia Dalastra Laurenti, Marliane Batista Campos, Claudia Maria de Castro Gomes, Carlos Eduardo Pereira Corbett, Fernando Tobias Silveira.   

Abstract

This study examined the susceptibility of peritoneal macrophage (PM) from the Neotropical primates: Callithrix jacchus, Callithrix penicillata, Saimiri sciureus, Aotus azarae infulatus and Callimico goeldii to ex vivo Leishmania (L.) infantum chagasi-infection, the etiological agent of American visceral leishmaniasis (AVL), as a screening assay for evaluating the potential of these non-human primates as experimental models for studying AVL. The PM-susceptibility to infection was accessed by the PM-infection index (PMI) at 24, 72 h and by the mean of these rates (FPMI), as well as by the TNF-α, IL-12 (Capture ELISA) and Nitric oxide (NO) responses (Griess method). At 24h, the PMI of A. azarae infulatus (128) was higher than those of C. penicillata (83), C. goeldii (78), S. sciureus (77) and C. jacchus (55). At 72h, there was a significant PMI decrease in four monkeys: A. azarae infulatus (128/37), C. penicillata (83/38), S. sciureus (77/38) and C. jacchus (55/12), with exception of C. goeldii (78/54). The FPMI of A. azarae infulatus (82.5) and C. goeldii (66) were higher than C. jacchus (33.5), but not higher than those of C. penicillata (60.5) and S. sciureus (57.5). The TNF-a response was more regular in those four primates which decreased their PMI at 24/72 h: C. jacchus (145/122 pg/mL), C. penicillata (154/130 pg/mL), S. sciureus (164/104 pg/mL) and A. azarae infulatus (154/104 pg/mL), with exception of C. goeldii (38/83 pg/mL). The IL-12 response was mainly prominent in A. infulatus and C. goeldii which presented the highest FPMI and, the NO response was higher in C. goeldii, mainly at 72 h. These findings strongly suggest that these New World primates have developed a resistant innate immune response mechanism capable of controlling the macrophage intracellular growth of L. (L.) i. chagasi-infection, which do not encourage their use as animal model for studying AVL.

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Year:  2012        PMID: 22499423     DOI: 10.1590/s0036-46652012000200007

Source DB:  PubMed          Journal:  Rev Inst Med Trop Sao Paulo        ISSN: 0036-4665            Impact factor:   1.846


  3 in total

1.  Investigation of Leishmania (Viannia) braziliensis Infection in Wild Mammals in Brazil.

Authors:  Henrique Jordem Venial; Ana Montoya; Rocío Checa; Guadalupe Miró; Gabriel José Silva Uzai; Maria Aparecida da Silva; Louisiane de Carvalho Nunes; Renato Luiz Silveira; Eulógio C Queiroz de Carvalho
Journal:  Acta Parasitol       Date:  2022-01-06       Impact factor: 1.440

2.  Competence of non-human primates to transmit Leishmania infantum to the invertebrate vector Lutzomyia longipalpis.

Authors:  Ayisa Rodrigues de Oliveira; Guilherme Rafael Gomide Pinheiro; Herlandes P Tinoco; Maria Elvira Loyola; Carlyle Mendes Coelho; Edelberto Santos Dias; Érika Michalsky Monteiro; Fabiana de Oliveira Lara E Silva; Angela Tinoco Pessanha; Andreza Geisiane Maia Souza; Nathália Cristina Lima Pereira; Nelder F Gontijo; Ricardo T Fujiwara; Tatiane Alves da Paixão; Renato Lima Santos
Journal:  PLoS Negl Trop Dis       Date:  2019-04-17

3.  First report of Leishmania infantum infection in the endangered orangutan (Pongo pygmaeus pygmaeus) in Madrid, Spain.

Authors:  Guadalupe Miró; Amelia Troyano; Ana Montoya; Fernando Fariñas; Ma Luisa Fermín; Luís Flores; Carlos Rojo; Rocío Checa; Rosa Gálvez; Valentina Marino; Cristina Fragío; Eva Martínez-Nevado
Journal:  Parasit Vectors       Date:  2018-03-20       Impact factor: 3.876

  3 in total

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