TY - JOUR
T1 - Preclinical Testing of Vaccines and Therapeutics for Gonorrhea in Female Mouse Models of Lower and Upper Reproductive Tract Infection
AU - Connolly, Kristie L.
AU - Pilligua-Lucas, Michelle
AU - Gomez, Carolina
AU - Costenoble-Caherty, Allison C.
AU - Soc, Anthony
AU - Underwood, Knashka
AU - MacIntyre, Andrew N.
AU - Sempowski, Gregory D.
AU - Jerse, Ann E.
N1 - Publisher Copyright:
© 2021 Published by Oxford University Press for the Infectious Diseases Society of America 2021.
PY - 2021/8/15
Y1 - 2021/8/15
N2 - Murine models of Neisseria gonorrhoeae lower reproductive tract infection are valuable systems for studying N. gonorrhoeae adaptation to the female host and immune responses to infection. These models have also accelerated preclinical testing of candidate therapeutic and prophylactic products against gonorrhea. However, because N. gonorrhoeae infection is restricted to the murine cervicovaginal region, there is a need for an in vivo system for translational work on N. gonorrhoeae pelvic inflammatory disease (PID). Here we discuss the need for well-characterized preclinical upper reproductive tract infection models for developing candidate products against N. gonorrhoeae PID, and report a refinement of the gonorrhea mouse model that supports sustained upper reproductive tract infection. To establish this new model for vaccine testing, we also tested the licensed meningococcal 4CMenB vaccine, which cross-protects against murine N. gonorrhoeae lower reproductive tract infection, for efficacy against N. gonorrhoeae in the endometrium and oviducts following transcervical or vaginal challenge.
AB - Murine models of Neisseria gonorrhoeae lower reproductive tract infection are valuable systems for studying N. gonorrhoeae adaptation to the female host and immune responses to infection. These models have also accelerated preclinical testing of candidate therapeutic and prophylactic products against gonorrhea. However, because N. gonorrhoeae infection is restricted to the murine cervicovaginal region, there is a need for an in vivo system for translational work on N. gonorrhoeae pelvic inflammatory disease (PID). Here we discuss the need for well-characterized preclinical upper reproductive tract infection models for developing candidate products against N. gonorrhoeae PID, and report a refinement of the gonorrhea mouse model that supports sustained upper reproductive tract infection. To establish this new model for vaccine testing, we also tested the licensed meningococcal 4CMenB vaccine, which cross-protects against murine N. gonorrhoeae lower reproductive tract infection, for efficacy against N. gonorrhoeae in the endometrium and oviducts following transcervical or vaginal challenge.
KW - antibiotics
KW - gonorrhea
KW - mouse
KW - PID
KW - reproductive tract
KW - vaccine
KW - vaginal microbicides
UR - http://www.scopus.com/inward/record.url?scp=85114225011&partnerID=8YFLogxK
U2 - 10.1093/infdis/jiab211
DO - 10.1093/infdis/jiab211
M3 - Article
C2 - 34396408
AN - SCOPUS:85114225011
SN - 0022-1899
VL - 224
SP - S152-S160
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
ER -