Cathelicidins are antimicrobial peptides, stored by mammalian leukocytes, showing an antimicrobial activity against bacteria, fungi, protozoa and enveloped viruses. In accordance with other authors, we reported in a previous study that the protegrin-1 (PG-1), at 80 microg mL(-1), inhibited the in vitro growth of Chlamydia trachomatis serovars D, H and L2; however, we observed an increased infectivity of some animal chlamydial species after their treatment with the same PG-1 concentration. In this study, the treatment of LLC-MK2 cells with PG-1 before chlamydial infection resulted in an increased infectivity of Chlamydophila abortus probably due to their easier entry into the host cells, whereas no increase in S26/3 infectivity was detected in LLC-MK2 cells treated with PG-1 postchlamydial infection.

Increasing effect of a high dose of PG-1 peptide on the infectivity of Chlamydophila abortus / Donati, M.; Di Francesco, A.; Gennaro, Renato; Benincasa, Monica; Di Paolo, M.; Shurdhi, A.; Ostanello, F.; Baldelli, R.; Cevenini, R.. - In: FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY. - ISSN 0928-8244. - STAMPA. - 59/2010:(2010), pp. 221-222. [10.1111/j.1574-695X.2010.00679.x]

Increasing effect of a high dose of PG-1 peptide on the infectivity of Chlamydophila abortus.

GENNARO, RENATO;BENINCASA, MONICA;
2010-01-01

Abstract

Cathelicidins are antimicrobial peptides, stored by mammalian leukocytes, showing an antimicrobial activity against bacteria, fungi, protozoa and enveloped viruses. In accordance with other authors, we reported in a previous study that the protegrin-1 (PG-1), at 80 microg mL(-1), inhibited the in vitro growth of Chlamydia trachomatis serovars D, H and L2; however, we observed an increased infectivity of some animal chlamydial species after their treatment with the same PG-1 concentration. In this study, the treatment of LLC-MK2 cells with PG-1 before chlamydial infection resulted in an increased infectivity of Chlamydophila abortus probably due to their easier entry into the host cells, whereas no increase in S26/3 infectivity was detected in LLC-MK2 cells treated with PG-1 postchlamydial infection.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2302388
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