However, M. catarrhalis O12E had no detectable inhibitory effect on the growth of these two strains (data not shown). The PRN1371 in vivo limited spectrum of killing activity for McbC also raises the possibility that it might serve to lyse other M. catarrhalis strains that lack

the mcbABCI locus, thereby making their DNA available for lateral gene transfer via transformation Stattic datasheet of the strain containing the mcbABCI operon. A similar mechanism has been described for how Streptococcus mutans might use its mutacin (bacteriocin) to acquire genes from closely related streptococcal species in vivo [48]. Conclusion Approximately 25% of the M. catarrhalis strains tested in this study produced a bacteriocin that could kill strains of this pathogen that lacked the mcbABCI locus. Expression of the gene products encoded by this locus conferred a competitive advantage in vitro over a strain that did not possess this set of genes. Whether this bacteriocin is expressed in vivo (i.e., in the human nasopharynx) remains to be determined, but production of this bacteriocin could facilitate lateral gene transfer among M. catarrhalis strains. Methods Bacterial strains, see more plasmids and growth conditions Bacterial strains and plasmids used in this study are listed in Table 1. Moraxella catarrhalis strains were routinely grown in brain

heart infusion (BHI) broth (Difco/Becton Dickinson, Sparks, MD) with aeration at 37°C, or on BHI solidified using 1.5% (wt/vol) agar. When appropriate, BHI was supplemented with kanamycin (15 μg/ml), streptomycin (100 μg/ml), or spectinomycin (15 μg/ml). BHI agar plates were incubated at 37°C in an atmosphere containing 95% air-5% CO2. old Mueller-Hinton (MH) broth (Difco/Becton Disckinson) was used for some growth experiments involving co-culture of two different M. catarrhalis strains. Streptococcus

mitis NS 51 (ATCC 49456) and the Streptococcus sanguinis type strain (ATCC 10556) were obtained from the American Type Culture Collection (Manassas, VA) and were grown on blood agar plates. Detection of bacteriocin production M. catarrhalis strains were tested for bacteriocin production by growing both the test strain (i.e., the putative bacteriocin-producing strain) and the indicator strain (i.e., the putative bacteriocin-sensitive strain) separately in BHI broth overnight at 37°C. The cells of the indicator strain were collected by centrifugation and resuspended in a 5 ml portion of BHI to an OD600 = 0.25. The cells of the test strain were collected by centrifugation and resuspended in a 1 ml volume of BHI. A 250-μl portion of the suspension of the indicator strain was used to inoculate a flask containing 25 ml of molten BHI agar [0.8% (wt/vol) agar] at a temperature of 45°C.