Compositions and methods for pathogen transport
View Patent ↗This disclosure provides a method for transporting a pathogen under ambient conditions, by culturing the pathogen with an amoeba under conditions that favor the incorporation of the pathogen into a trophozoite, starving the amoeba until it encysts, then culturing under conditions that favor conversion of the amoeba back to a trophozoite. In one aspect, the conditions that favor incorporation of the pathogen into the cyst of the amoeba comprises contacting the pathogen with the amoeba in an iron rich environment. Virus and/or bacteria are pathogens that can be transported by the disclosed method. Amoeba that are useful in the disclosed methods include, without limitation Acanthamoeba castellanii, Hartmannella vermiformis and Naegleria gruberi . The disclosed methods have utility in: transporting pathogens from military field hospitals and clinics to the laboratory; transporting pathogens from global satellite laboratories to clinical laboratories; long term storage of pathogens; enriching contaminated patient samples for pathogens of interest; biosurveillance and detection efforts.
1. A transport population or culture of amoeba capable of encysting a pathogen, in a two compartment container, the container comprising:
a) a first compartment that has at one end a removable cap with a locking device to which is attached an elongated sampling device or swab member and wherein the first compartment comprises iron rich media,
b) a second compartment comprising the amoeba in a buffer,
c) a pathogen sample, and
d) a permeable membrane that separates the container into the two compartments that is ruptured by the elongated member when the locking device is activated allowing the mixing of the iron rich media, the pathogen sample and the amoeba.
2. The population or culture of claim 1 , wherein the pathogen is selected from the group consisting of a virus or a bacterium.
3. The population or culture of claim 1 , wherein the pathogen is selected from the group consisting of Legionella, Mycobacterium, Francisella, Yersinia, Coxiella, Klebsiella, Pseudomonas, Burkeholderia and Acinetobacer.
4. The population or culture of claim 1 , wherein the amoeba is selected from the group consisting of Acanthamoeba castellanii, Hartmannella vermiformis and Naegleria gruberi.
5. A culture transport device comprising a housing having a first compartment and a second compartment, the first and second compartments being separated by a permeable membrane, wherein the first compartment comprises an iron rich media and the second compartment comprising a population of amoeba in a buffer, a removable cap comprising a sampling elongated member and a locking device, wherein when the locking device is activated, the permeable membrane is ruptured by the elongated member.
6. The device of claim 5 , wherein the housing of the device is comprised of an impermeable material.
7. The device of claim 6 , wherein the impermeable material is polyethylene.
8. The culture transport device of claim 5 , wherein the housing of the device is comprised of an impermeable material.
9. The population or culture of claim 8 , wherein the impermeable material is polyethylene.
10. The culture transport device of claim 5 , wherein iron-rich media comprises media comprising at least 2× concentration of iron.
11. The culture transport device of claim 5 , wherein the amoeba is selected from the group consisting of Acanthamoeba castellanii, Hartmannella vermiformis and Naegleria gruberi.
12. A method for transporting a pathogen, comprising
Contacting a pathogen with the elongate swabbing member of the device of claim 5 and inserting the swab and the pathogen into the second compartment of the device by rupturing the permeable membrane and closing the cap and engaging the locking member.