Gram-negative bacteria produce outer membrane vesicles(OMVs)that play a critical role in cell−cell communication and virulence.OMVs have emerged as promising therapeutic agents for various biological applications such...Gram-negative bacteria produce outer membrane vesicles(OMVs)that play a critical role in cell−cell communication and virulence.OMVs have emerged as promising therapeutic agents for various biological applications such as vaccines and targeted drug delivery.However,the full potential of OMVs is currently constrained by inherent heterogeneities,such as size and cargo differences,and traditional ensemble assays are limited in their ability to reveal OMV heterogeneity.To overcome this issue,we devised an innovative approach enabling the identification of various characteristics of individual OMVs.This method,employing fluorescence microscopy,facilitates the detection of variations in size and surface markers.To demonstrate our method,we utilize the oral bacterium Aggregatibacter actinomycetemcomitans(A.actinomycetemcomitans)which produces OMVs with a bimodal size distribution.As part of its virulence,A.actinomycetemcomitans secretes leukotoxin(LtxA)in two forms:soluble and surface associated with the OMVs.We observed a correlation between the size and toxin presence where larger OMVs were much more likely to possess LtxA compared to the smaller OMVs.In addition,we noted that,among the smallest OMVs(<100 nm diameter),the fractions that are toxin positive range from 0 to 30%,while the largest OMVs(>200 nm diameter)are between 70 and 100%toxin positive.展开更多
基金supported by grants from the National Institutes of Health to N.J.W.(R21GM134414,R15GM152918)and A.C.B.(R21DE027769,R21DE032153).
文摘Gram-negative bacteria produce outer membrane vesicles(OMVs)that play a critical role in cell−cell communication and virulence.OMVs have emerged as promising therapeutic agents for various biological applications such as vaccines and targeted drug delivery.However,the full potential of OMVs is currently constrained by inherent heterogeneities,such as size and cargo differences,and traditional ensemble assays are limited in their ability to reveal OMV heterogeneity.To overcome this issue,we devised an innovative approach enabling the identification of various characteristics of individual OMVs.This method,employing fluorescence microscopy,facilitates the detection of variations in size and surface markers.To demonstrate our method,we utilize the oral bacterium Aggregatibacter actinomycetemcomitans(A.actinomycetemcomitans)which produces OMVs with a bimodal size distribution.As part of its virulence,A.actinomycetemcomitans secretes leukotoxin(LtxA)in two forms:soluble and surface associated with the OMVs.We observed a correlation between the size and toxin presence where larger OMVs were much more likely to possess LtxA compared to the smaller OMVs.In addition,we noted that,among the smallest OMVs(<100 nm diameter),the fractions that are toxin positive range from 0 to 30%,while the largest OMVs(>200 nm diameter)are between 70 and 100%toxin positive.
