A semi-automated cell tracking protocol for quantitative analyses of neutrophil swarming to sterile and S. aureus contaminated bone implants in a mouse femur model

• Published in: bioRxiv
• Main Authors: Lekkala, Sashank, Ren, Youliang, Weeks, Jason, Lee, Kevin, Jia Hui Tay, Allie, Liu, Bei, Xue, Thomas, Rainbolt, Joshua, Xie, Chao, Schwarz, Edward M, Yeh, Shu-Chi A
• Format: Journal Article Paper
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 08.12.2023
• Subjects: Automation; Bone imaging; Bone implants; Confocal microscopy; Drug resistance; Femur; Leukocyte migration; Leukocytes (neutrophilic); Methicillin; Microenvironments; Neutrophils; Osteomyelitis; Segmentation; Staphylococcus aureus; Staphylococcus infections; Swarming; Transplants & implants; Velocity; cell motility; bone infection; Trainable Weka Segmentation; cell tracking; Neutrophil swarming; TrackMate; bone marrow
• ISSN: 2692-8205; 2692-8205
• DOI: 10.1101/2023.12.07.570663

Implant-associated osteomyelitis remains a major orthopaedic problem. As neutrophil swarming to the surgical site is a critical host response to prevent infection, visualization and quantification of this dynamic behavior at the native microenvironment of infection will elucidate previously unrecognized mechanisms central to understanding the host response. We recently developed longitudinal intravital imaging of the bone marrow (LIMB) to visualize fluorescent on a contaminated transfemoral implant and host cells in live mice, which allows for direct visualization of bacteria colonization of the implant and host cellular responses using two-photon laser scanning microscopy. To the end of rigorous and reproducible quantitative outcomes of neutrophil swarming kinetics in this model, we developed a protocol for robust segmentation, tracking, and quantifications of neutrophil dynamics adapted from Trainable Weka Segmentation and TrackMate, two readily available Fiji/ImageJ plugins. In this work, mice with tdTomato expressing neutrophils received a transfemoral pin with or without ECFP-expressing USA300 methicillin-resistant (MRSA) to obtain 30-minute LIMB videos at 2-, 4-, and 6-hours post-implantation. The developed semi-automated neutrophil tracking protocol was executed independently by two users to quantify the distance, displacement, speed, velocity, and directionality of the target cells. The results revealed high inter-reader reliability for all outcomes (ICC > 0.98; p > 0.05). Consistent with the established paradigm on increased neutrophil swarming during active infection, the results also demonstrated increased neutrophil speed and velocity at all measured time points, and increased displacement at later time points (6 hours) in infected versus uninfected mice (p < 0.05). Neutrophils and bacteria also exhibit directionality during migration in the infected mice. The semi-automated cell tracking protocol provides a streamlined approach to robustly identify and track individual cells across diverse experimental settings and eliminates inter-observer variability.