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Further studies on clinical isolates are necessary to validate our findings.
Further studies using the same panel of isolates are necessary to allow a formal comparison of both methods.
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Further investigation of these isolates is necessary to determine their relatedness to DUGV.
Analysis of a larger number of group C SDSE isolates is necessary to determine whether the absence of CRISPR interference is common to these isolates (table 3).
Accurate susceptibility testing of all isolates is necessary to insure optimal care of both the index patients and any culture-positive household contacts.
Obtaining tissue samples or abscess fluid for culture and molecular epidemiologic studies of C. botulinum isolates is necessary to facilitate identification of the source of the contaminated heroin.
A full-scale validation of the oCelloScope system including more isolates is necessary to assess the impact of using it for antimicrobial susceptibility testing (AST).
A full-scale validation of the oCelloScope system including more isolates is necessary to assess the impact of using it for AST.
Although these data suggest that, in our limited sampling, the MAT1-1 matype type is found more frequently on Myotis myotis (18 out of 23), more sampling of European fungal isolates is necessary to understand the prevalence of mating types in P. destructans.
Our data demonstrate that the optimization of AMT for each isolate is necessary to establish efficient AMT methods.
However, assigning a designation to the IS 6110 pattern for each isolate was necessary to allow entry of the result into the epidemiologic database.
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