Characterizationharacterization of Extremophilic Actinomycetes Strains as Sources of Antimicrobial Agents

Extremophilic actinomycetes strains can survive extreme saline and alkaline environments and produce antimicrobial agents. In this chapter, we discuss laboratory methods that can be used to isolate and characterize actinomycetes strains capable of potentially producing novel antimicrobial agent(s) when cultured in conditions that mimic the environments from which they were isolated. Methods used to screen for antibacterial and antiviral activities from these producer strains, and microbiological and molecular approaches used to identify these strains are described. Here we describe three methods. Method 1 focuses on the strategy to select optimal conditions to synthesize and accumulate the antibiotics from the studied actinomycetes strains by preparing crude extracts. In Method 2, we describe the screening strategies used to test the actinomycetes strains against gram-negative and gram-positive bacteria, antifungal agents, multidrug-resistant pathogens (MDR), and viral pathogens. Thus, the specific techniques to test for MDR pathogens such as the disk diffusion assay and wells assay are outlined. We also describe the antiviral activity screening of the selected actinomycetes extracts in Method 2 of this chapter. Specifically, we concentrate on methods used to test for antiviral activities such as primary hemolytic, hemagglutination, neuraminidase, and specific virus-inhibitory activities. Finally, the Method 3 section reveals the microbiological techniques used to morphologically characterize the actinomycetes strains that depend on the culture medium utilized for growth. Additionally, the method used to perform a detailed characterization of the morphology that actinomycetes strains possess is specified by the protocol for sample preparation and visualization using the scanning electron microscopy (SEM). Finally, we summarize the molecular approaches used to characterize actinomycetes strains, focusing specifically on the PCR and sequencing techniques.