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Background MBLs, which require Zn for catalytic activity, are a major contributor to high-level β-lactam resistance when tested using conventional CAMHB. We have previously reported marked reductions in meropenem (MEM) MICs in Zn-depleted media (Chelex-CAMHB and EDTA-CAMHB; Zn [C] <0.002 mg/L) compared with conventional CAMHB (Zn [C] 0.959 mg/L) against a variety of MBL-producing isolates, whereas Zn-depletion had no impact on levofloxacin (LVX) MICs (ASM Microbe 2019, San Francisco. Abstract P508). To explore in vivo implications, we evaluated the efficacy of MEM human simulated regimen (HSR) against MBL-producing isolates in a murine pneumonia model. In addition, LVX HSR was examined for model validation. Methods Nine MBL-producing isolates (NDM, n = 5; VIM, n = 2; IMP, n = 2) were utilized. CAMHB, Chelex-CAMHB, and EDTA-CAMHB MEM MICs ranged from 16 to > 64, ≤0.0625 to 0.5, and ≤ 0.0625 to 0.5 mg/L, respectively. LVX MICs ranged from ≤ 0.0625 – > 64 mg/L. Neutropenic lung-infected ICR mice received a MEM HSR of 2g q8h [1.5 hours infusion], 2 lower MEM exposures or LVX 750 mg q24h HSR. Zn [C] were determined in the epithelial lining fluid (ELF) of infected mice. Results LVX displayed predictable in vivo efficacy consistent with its phenotypic profile irrespective of the media utilized for MIC testing (figure). Despite attaining zero %T> MIC using values generated in CAMHB, MEM HSR produced marked bacterial reductions against all MBL-producing isolates (figure). Reductions in MEM exposures produced bacterial killing concordant with its pharmacodynamic profile using Zn-depleted CAMHB MIC values. Zn [C] in infected murine ELF were undetectable, i.e., <0.002 mg/L. Conclusion Our results indicate that MEM in vivo efficacy is best represented by the pharmacodynamic profile generated using MICs determined in Zn-depleted media for MBL-producing Enterobacteriaceae. These observations are consistent with the case reports describing positive outcomes in MBL-infected patients following treatment with carbapenems (Infection 2018;46:1–13). Our translational data suggest that the use of conventional CAMHB for MBL susceptibility testing is inappropriate in distinguishing meaningful in vivo resistance given that Zn [C] are supraphysiologic in conventional CAMHB and negligible at infection sites. Disclosures All authors: No reported disclosures.

open forum infectious diseases

1533. Is Cation-Adjusted Mueller–Hinton Broth (CAMHB) Appropriate for Metallo-β-lactamase (MBL) Susceptibility Testing? Novel Insights in In Vitro–In Vivo Discordance Among MBL-Producing Enterobacteriaceae