# Sex-dependent vulnerability for Wistar rats model following intranasal instillation with Klebsiella pneumoniae ATCC 43816 causing lobar pneumonia

**Authors:** Patrick Hervé Diboue Betote, Esther Del Florence Ndedi Moni, Sonia Raïssa Gayap Matchuenkam, Sandrine Suzanne Bayengue Beack, Rodrigue Fifen, Raogo Ouedraogo, Gabriel A. Agbor, Rasmané Semde, Nga Nnanga, Maximilienne Ascension Nyegue

PMC · DOI: 10.1186/s41479-024-00126-y · Pneumonia · 2024-03-25

## TL;DR

This study shows that female Wistar rats are more vulnerable to pneumonia caused by Klebsiella pneumoniae compared to males, highlighting sex differences in disease progression.

## Contribution

The study reveals sex-dependent differences in the physiopathogenesis of K. pneumoniae-induced lobar pneumonia in Wistar rats.

## Key findings

- Female rats showed higher susceptibility to K. pneumoniae-induced lobar pneumonia compared to males.
- The disease peaked on day 15 post-inoculation with more severe effects in females.
- Sex differences were observed in LD50, bacterial load, weight loss, and lung tissue damage.

## Abstract

Klebsiella pneumoniae has become one of the major threats to public health as it causes nosocomial and community-acquired infections like lobar pneumonia. This infection causes acute inflammation in the lung, characterized by the recruitment of polymorphonuclear cells, generating free radicals, and decreasing the endogenous antioxidant balance system. Many experimental studies have focused on the induction, progression and resolution of infection up to its peak, but these documented processes remain highly random and their sex dependence un-elicited. These fluctuations of physiopathological parameters would impact disease progression depending on the animal’s model and bacterial strain used. The present study investigated the sex-dependent vulnerability of Wistar rats to K. pneumoniae ATCC 43816 lobar pneumonia induced by the intranasal instillation method.

Experimental pneumonia was induced by K. pneumoniae ATCC 43816 in male and female Wistar rats following intranasal instillation. The physiopathogenesis of the disease was studied by bacteriological and histopathological exams, histomorphometric analysis of the blood and/or lung tissue, and body weight loss in infected animals. In addition, the overall severity of lesions was determined by the total score obtained by averaging the individual scores from the same group of animals.

The K. pneumoniae ATCC 43816 strain showed inoculation dose-, incubation time of the disease- and sex-dependent- differences in its ability to induce lobar pneumonia. Evaluation of different parameters showed that the disease peaked on day 15 post-inoculation, with more pathogenic effects on female rats. This observed sex-dependence difference in Wistar rats was mainly highlighted by the determined lethal dose 50 (LD50), bacterial load count in whole blood and lung tissues, body weight loss, inflammatory granulomas forming and diffuse alveolar damages. The pathogenicity was confirmed by scoring the severity of pathologic lesions of lung tissues.

The results obtained highlighted the gender-dependency in the physiopathogenesis processes of K. pneumoniae ATCC 43816 induced-lobar pneumonia, in Wistar rats. Female Wistar rats’ susceptibility is useful in studying pathology and in preclinical trial investigations of new treatments for infectious pneumonia.

## Linked entities

- **Species:** Klebsiella pneumoniae (taxon 573)

## Full-text entities

- **Diseases:** infection (MESH:D007239), pathologic lesions (MESH:D013568), inflammatory granulomas (MESH:D006099), inflammation (MESH:D007249), weight loss (MESH:D015431), nosocomial (MESH:D003428), infectious pneumonia (MESH:D011014), alveolar damages (MESH:D055370)
- **Chemicals:** free radicals (MESH:D005609)
- **Species:** Klebsiella pneumoniae ATCC 43816 (strain) [taxon 1316582], Rattus norvegicus (brown rat, species) [taxon 10116], Klebsiella pneumoniae (species) [taxon 573]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC10962189/full.md

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Source: https://tomesphere.com/paper/PMC10962189