Page 337 - Resúmen - XXV Congreso Latinoamericano de Parasitología - FLAP
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                    The Longitudinal Cutaneous Microbiome in Cutaneous Leishmaniasis



               Gundacker,  Nathan ; Suárez,  José  Antonio ;  Sosa,  Néstor ;  Pascale,  Juan  Miguel ;
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                                                               2
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                                     1
               Ábrego, Leyda ; Weeden, Adriana ; Ortiz, Betsi ; Morrow, Casey
                                                    4
                               2
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                                              2
               1 Medical  College  of  Wisconsin;  Instituto  Conmemorativo  Gorgas,  SNI-Senacyt;  University  of  New
                                                                                           3
               Mexico;  Instituto Conmemorativo Gorgas;  University of Alabama at Birmingham
                       4
                                                     5

               Background: Leishmania is sandfly-borne neglected tropical parasite which affects over 12 million people
               worldwide  with  1.6  million  new  cases  annually.  In  Panama  there  are  over  3000  cases  of  Cutaneous
               Leishmaniasis (CL) every year, the majority caused by Leishmania panamensis. The pathogenesis in CL
               is typically localized to the skin and thought to be an imbalance in cell-mediated immunity. The cutaneous
               microbiome likely plays a role in priming the immune system, however the specific organisms associated
               with  this  activation  is  unknown  as  is  the  cutaneous  microbiome  associated  with  leishmaniasis.
               Methods: This prospective study enrolled adult patients with Cutaneous Leishmaniasis and then collected
               cutaneous samples from the leishmania lesions on day 0, 30 and 90 as well as a control microbiome sample
               from >2cm from the nearest leishmania border. 16S rRNA gene sequence data was generated by barcoding
               and  multiplexing  samples  onto  an  Illumina  MiSeq  platform.  Alpha  (within  sample)  and  Beta  (between
               samples, both lesion-perilesional and between patients) diversity were calculated.  Results: Preliminary
               descriptive  analysis  of  lesional  microbiome  revealed  a  predominance  of  several  phyla:
               Proteobacteria, Firmicutes and Bacteroidetes.  On  the  genus  level  Staphylococcus,  Corynebacterium,
               Acinetobacter were the most prominent organisms. The bioinformatics including Alpha and Beta diversity
               is  currently  being  calculated  on  a  longitudinal  basis.  Conclusions:  Patients  unexpectedly  had  a
               predominance of gram-negative organisms, an uncommon cutaneous organism. This is possibly due to the
               moist proteinaceous environment produced by the leishmania lesion. However, environmental conditions
               such as humidity and/or bathing conditions may also play a role in determining the cutaneous microbiome.
               The  presence  of Proteobacteria in  the  lesions  and  the  surrounding  skin  may  be  contributing  to  the
               imbalance in cell-mediated immunity. Future metabolomic studies need to be performed to identify potential
               therapeutic options to improve Leishmania healing.































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