TY - JOUR
T1 - Generation of Mature Toxoplasma gondii Bradyzoites in Human Immortalized Myogenic KD3 Cells
AU - Maus, Deborah
AU - Curtis, Blake
AU - Warschkau, David
AU - Betancourt, Estefanía Delgado
AU - Seeber, Frank
AU - Blume, Martin
N1 - Publisher Copyright:
© 2024 The Authors; exclusive licensee Bio-protocol LLC.
PY - 2024/1/5
Y1 - 2024/1/5
N2 - Toxoplasma gondii is a zoonotic protozoan parasite and one of the most successful foodborne pathogens. Upon infection and dissemination, the parasites convert into the persisting, chronic form called bradyzoites, which reside within cysts in muscle and brain tissue. Despite their importance, bradyzoites remain difficult to investigate directly, owing to limited in vitro models. In addition, the need for new drugs targeting the chronic stage, which is underlined by the lack of eradicating treatment options, remains difficult to address since in vitro access to drug-tolerant bradyzoites remains limited. We recently published the use of a human myotube-based bradyzoite cell culture system and demonstrated its applicability to investigate the biology of T. gondii bradyzoites. Encysted parasites can be functionally matured during long-term cultivation in these immortalized cells and possess many in vivo–like features, including pepsin resistance, oral infectivity, and antifolate resistance. In addition, the system is scalable, enabling experimental approaches that rely on large numbers, such as metabolomics. In short, we detail the cultivation of terminally differentiated human myotubes and their subsequent infection with tachyzoites, which then mature to encysted bradyzoites within four weeks at ambient CO2 levels. We also discuss critical aspects of the procedure and suggest improvements.
AB - Toxoplasma gondii is a zoonotic protozoan parasite and one of the most successful foodborne pathogens. Upon infection and dissemination, the parasites convert into the persisting, chronic form called bradyzoites, which reside within cysts in muscle and brain tissue. Despite their importance, bradyzoites remain difficult to investigate directly, owing to limited in vitro models. In addition, the need for new drugs targeting the chronic stage, which is underlined by the lack of eradicating treatment options, remains difficult to address since in vitro access to drug-tolerant bradyzoites remains limited. We recently published the use of a human myotube-based bradyzoite cell culture system and demonstrated its applicability to investigate the biology of T. gondii bradyzoites. Encysted parasites can be functionally matured during long-term cultivation in these immortalized cells and possess many in vivo–like features, including pepsin resistance, oral infectivity, and antifolate resistance. In addition, the system is scalable, enabling experimental approaches that rely on large numbers, such as metabolomics. In short, we detail the cultivation of terminally differentiated human myotubes and their subsequent infection with tachyzoites, which then mature to encysted bradyzoites within four weeks at ambient CO2 levels. We also discuss critical aspects of the procedure and suggest improvements.
KW - Bradyzoites
KW - Cell culture
KW - Human myotubes
KW - Tissue cysts
KW - Toxoplasma gondii
UR - http://www.scopus.com/inward/record.url?scp=85183434645&partnerID=8YFLogxK
U2 - 10.21769/BioProtoc.4916
DO - 10.21769/BioProtoc.4916
M3 - Article
SN - 2331-8325
VL - 14
JO - Bio-protocol
JF - Bio-protocol
IS - 1
M1 - e4916
ER -