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. 2013 Oct 7;8(10):e75656. doi: 10.1371/journal.pone.0075656

Table 2. Evaluation of the progression of sporotrichosis caused by S. brasiliensis and S. schenckii in a subcutaneous murine model.

Strain Dissemination a , b
Secondary lesions Deathc Regression of the primary lesion Observations
Lung Spleen
Ss54 ++ ++ 1/5 1/5 2/5 Secondary open lesions along the tail; macroscopic lesions in the liver.
5110 ++ ++ 0/5 5/5 2/5 Inflammation in the paw and posterior leg joints (arthritis); macroscopic lesions in the liver; all mice died within 60 days post-infection.
HUPE 114158 ++ ++ 2/4 1/4 0/4 Persistent cutaneous lesions (more than 80 days)
UFTM 01 + +/- 3/5 1/5 1/5 Persistent cutaneous lesions (more than 80 days); inflammation in the paw and joints (arthritis); macroscopic lesions in the liver.
HUPE 114500 +/- + 1/5 0/5 0/5 Persistent cutaneous lesions (more than 80 days)
IPEC 17943 +/- +/- 0/5 0/5 4/5
1099-18 + + 0/5 0/5 4/5
IPEC 15383 +/- +/- 0/5 0/5 4/5 Secondary ulcerated lesions along the tail; inflammation in the posterior leg joints.
a

Dissemination was determined by CFU in lung and spleen specimens collected 40 days post-infection.

b

Relative CFU counts (+/-) 20 colonies; (+) 20 to 120 colonies and (++) >120 colonies per Petri dish (the tissue specimens were ressuspended in the same proportion g tissue/mL).

c

Mortality up to 60 days post-infection.