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March 21, 2026Advanced Intelligent Discovery3 citationsOpen Access

Automated Bacterial Identification and Morphological Feature Analysis in Low‐Dose Cryo‐EM Using YOLOv11

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SMSita Sirisha MadugulaLMLynnicia N. MassenburgSBSpenser R. Brown

Key Points

  • The aim is to develop an automated workflow for identifying bacteria and analyzing morphological features in low-dose cryo-EM images.
  • Combined low-dose cryo-TEM imaging with YOLOv11 for instance segmentation.
  • Automated bacterial localization from low-magnification images.
  • Measured cell-envelope thickness and anisotropy from higher-magnification images.
  • Quantified bacteria-flagella interactions, including overlap and curvature metrics.
  • Automated measurements aligned with manual annotations.
  • Substantial reduction in analysis time compared to manual methods.
  • Enabled scalable bacterial identification and phenotyping.

Abstract

Bacteria rapidly adapt to environmental cues through morphological and ultrastructural changes that correlate with physiology and behavior. Cryogenic transmission electron microscopy (cryo‐TEM) can capture these phenotypic changes in near‐native, vitrified states, but manual analysis of low‐dose micrographs is labor intensive and limits throughput. Here, we present an end‐to‐end workflow that combines low‐dose cryo‐TEM imaging with a YOLOv11‐based instance‐segmentation model to automatically identify bacteria and quantify key structural features directly from the micrographs. This workflow enables (i) robust bacterial localization and counting from low‐magnification atlas/montage images, (ii) automated measurements of cell‐envelope (outer–inner membrane) thickness and anisotropy from higher‐magnification views, and (iii) detection and quantification of bacteria–flagella interactions, including overlap length and curvature metrics for interacting versus noninteracting flagella. Using Pantoea sp. YR343 grown under distinct media conditions, we show that the automated measurements agree with manual annotations while substantially reducing analysis time. Together, these tools provide a practical framework for scalable bacterial identification and quantitative phenotyping in low‐dose cryo‐TEM datasets and establish a foundation for extending cryo‐TEM image analysis toward higher‐throughput studies of microbial heterogeneity and biointerfaces.

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Cite This Study

Madugula et al. (2026) studied this question.

synapsesocial.com/papers/69be36bf6e48c4981c675e83https://doi.org/10.1002/aidi.202500241
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