Cooperation between apoptotic and viable metacyclics enhances the pathogenesis of leishmaniasis

João Luis Mendes Wanderley, Lucia Helena Pinto da Silva, Poliana Deolindo, Lynn Soong, Valéria Matos Borges, Deboraci Brito Prates, Ana Paula Almeida de Souza, Aldina Barral, José Mario de Freitas Balanco, Michelle Tanny Cunha do Nascimento, Elvira Maria Saraiva, Marcello André Barcinski

Research output: Contribution to journalArticle

60 Citations (Scopus)

Abstract

Mimicking mammalian apoptotic cells by exposing phosphatidylserine (PS) is a strategy used by virus and parasitic protozoa to escape host protective inflammatory responses. With Leishmania amazonensis (La), apoptotic mimicry is a prerogative of the intramacrophagic amastigote form of the parasite and is modulated by the host. Now we show that differently from what happens with amastigotes, promastigotes exposing PS are non-viable, non-infective cells, undergoing apoptotic death. As part of the normal metacyclogenic process occurring in axenic cultures and in the gut of sand fly vectors, a subpopulation of metacyclic promastigotes exposes PS. Apoptotic death of the purified PS-positive (PSPOS) sub-population was confirmed by TUNEL staining and DNA laddering. Transmission electron microscopy revealed morphological alterations in PSPOS metacyclics such as DNA condensation, cytoplasm degradation and mitochondrion and kinetoplast destruction, both in in vitro cultures and in sand fly guts. TUNELPOS promastigotes were detected only in the anterior midgut to foregut boundary of infected sand flies. Interestingly, caspase inhibitors modulated parasite death and PS exposure, when added to parasite cultures in a specific time window. Efficient in vitro macrophage infections and in vivo lesions only occur when PSPOS and PS-negative (PSNEG) parasites were simultaneously added to the cell culture or inoculated in the mammalian host. The viable PSNEG promastigote was the infective form, as shown by following the fate of fluorescently labeled parasites, while the PSPOS apoptotic sub-population inhibited host macrophage inflammatory response. PS exposure and macrophage inhibition by a subpopulation of promastigotes is a different mechanism than the one previously described with amastigotes, where the entire population exposes PS. Both mechanisms co-exist and play a role in the transmission and development of the disease in case of infection by La. Since both processes confer selective advantages to the infective microorganism they justify the occurrence of apoptotic features in a unicellular pathogen.

Original languageEnglish (US)
Article numbere5733
JournalPLoS One
Volume4
Issue number5
DOIs
StatePublished - May 29 2009

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phosphatidylserines
Leishmaniasis
leishmaniasis
Phosphatidylserines
promastigotes
pathogenesis
Parasites
amastigotes
Psychodidae
Phlebotominae
Macrophages
parasites
Leishmania amazonensis
macrophages
Sand
Leishmania
death
Cell culture
digestive system
inflammation

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Wanderley, J. L. M., da Silva, L. H. P., Deolindo, P., Soong, L., Borges, V. M., Prates, D. B., ... Barcinski, M. A. (2009). Cooperation between apoptotic and viable metacyclics enhances the pathogenesis of leishmaniasis. PLoS One, 4(5), [e5733]. https://doi.org/10.1371/journal.pone.0005733

Cooperation between apoptotic and viable metacyclics enhances the pathogenesis of leishmaniasis. / Wanderley, João Luis Mendes; da Silva, Lucia Helena Pinto; Deolindo, Poliana; Soong, Lynn; Borges, Valéria Matos; Prates, Deboraci Brito; de Souza, Ana Paula Almeida; Barral, Aldina; de Freitas Balanco, José Mario; do Nascimento, Michelle Tanny Cunha; Saraiva, Elvira Maria; Barcinski, Marcello André.

In: PLoS One, Vol. 4, No. 5, e5733, 29.05.2009.

Research output: Contribution to journalArticle

Wanderley, JLM, da Silva, LHP, Deolindo, P, Soong, L, Borges, VM, Prates, DB, de Souza, APA, Barral, A, de Freitas Balanco, JM, do Nascimento, MTC, Saraiva, EM & Barcinski, MA 2009, 'Cooperation between apoptotic and viable metacyclics enhances the pathogenesis of leishmaniasis', PLoS One, vol. 4, no. 5, e5733. https://doi.org/10.1371/journal.pone.0005733
Wanderley, João Luis Mendes ; da Silva, Lucia Helena Pinto ; Deolindo, Poliana ; Soong, Lynn ; Borges, Valéria Matos ; Prates, Deboraci Brito ; de Souza, Ana Paula Almeida ; Barral, Aldina ; de Freitas Balanco, José Mario ; do Nascimento, Michelle Tanny Cunha ; Saraiva, Elvira Maria ; Barcinski, Marcello André. / Cooperation between apoptotic and viable metacyclics enhances the pathogenesis of leishmaniasis. In: PLoS One. 2009 ; Vol. 4, No. 5.
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