Klebsiella pneumoniae, an important cause of bovine mastitis worldwide, is strongly pathogenic to bovine mammary epithelial cells (bMECs). Our objective was to determine the role of mitochondrial damage in the pathogenicity of K. pneumoniae on bMECs, by assessing several classical indicators of mitochondrial dysfunction, as well as differentially expressed genes (DEGs). Two K. pneumoniae strains (HLJ-D2 and HB-AF5), isolated from cows with clinical mastitis (CM), were used to infect bMECs (MAC-T line) cultured in vitro. In whole-transcriptome analysis of bMECs at 6 h post-infection (hpi), there were 3453 up-regulated and 3470 down-regulated genes for HLJ-D2, whereas for HB-AF5, there were 2891 up-regulated and 3278 down-regulated genes (P < 0.05). Based on GO term enrichment of differentially expressed genes (DEGs), relative to the controls, the primary categories altered in K. pneumoniae-infected bMECs included cellular macromolecule metabolism, metabolic process, binding, molecular function, etc. Infections increased (P < 0.05) malondialdehyde concentrations and formation of reactive oxygen species in bMECs. Additionally, both bacterial strains decreased (P < 0.05) total antioxidant capacity in bMECs at 6 and 12 hpi. Furthermore, infections decreased (P < 0.05) mitochondrial membrane potential and increased (P < 0.01) mitochondrial calcium concentrations. Finally, severe mitochondrial swelling and vacuolation, as well as mitochondrial rupture and cristae degeneration, were detected in infected bMECs. In conclusion, K. pneumoniae infections induced profound mitochondrial damage and dysfunction in bMECs; we inferred that this caused cellular damage and contributes to the pathogenesis of K. pneumoniae-induced CM in dairy cows.
Bovine mastitis caused by pathogenic microorganisms is an important economic threat to the dairy industry . Klebsiella pneumoniae, a major pathogen causing clinical mastitis (CM), induces a strong immune response, altering milk quality and causing inflammatory changes in the udder [2,3,4]. Furthermore, CM caused by K. pneumoniae is usually more severe than CM due to E. coli . Substantial damage of mammary tissue, specifically epithelial cells, occurs in CM caused by Klebsiella [5, 6].
Mitochondria are intracellular organelles with multiple features due to their bacterial ancestry . In addition to being a cell’s energy powerhouse, they are also a reservoir for cellular Ca2+, which is crucial for cell life and death . Furthermore, mitochondria have a role in the innate immune system by harboring innate sensors that can detect bacteria and trigger immune activation, making them an attractive target for pathogens [9, 10]. Indeed, during co-evolution of pathogens and hosts, the former have developed strategies to manipulate cellular machinery, particularly subverting mitochondrial function  and commonly causing damage to these organelles. Mitochondrial damage is usually characterized by increases in calcium and reactive oxygen species (ROS), a decrease in mitochondrial membrane potential (MMP), and morphological damage [12, 13]. In addition, a lower MMP and decreased activity of the respiratory chain with a simultaneous increase in ROS production, can lead to mitochondrial dysfunction .
In our previous study, K. pneumoniae isolated from bovine mastitis caused apoptosis and pro-inflammatory responses of bMECs cultured in vitro . K. pneumoniae isolates adhered to and invaded bMECs, causing ultrastructural damage, including swollen mitochondria and vesicle formation on the cell surface. In addition, in infected bMECs, there were increases in transcriptional expression of interleukin-1β (IL-1β), interleukin-6 (IL-6), interleukin-8 (IL-8) and tumor necrosis factor-α (TNF-α) genes and production of IL-1β, IL-8 and TNF-α . However, whether mitochondrial damage has a critical role in pathogenicity of K. pneumoniae on bMECs has not been well established. Therefore, our objective was to determine the role of mitochondrial damage in the pathogenicity of K. pneumoniae on bMECs by assessing several classical indicators of mitochondrial dysfunction, as well as differentially expressed genes (DEGs).
Materials and methods
Klebsiella pneumoniae strains
Two K. pneumoniae strains (HB-AF5 and HLJ-D2) isolated from cows with CM were used. Both of these strains belong to the K57 capsule serotype and have entB, ybtS, iutA, and mrkD genes. However, HLJ-D2 is a hypermucoviscous (HMV) strain, whereas HB-AF5 is a non-HMV strain [15, 16]. In our previous study, these two K. pneumoniae strains were cytopathogenic on bMECs and induced pro-inflammatory responses .
Cultured bovine mammary epithelial cells (bMECs)
A line of bMECs (MAC-T; Shanghai Jingma Biological Technology Co., Ltd., Shanghai, China) was cultured in cell culture plates (Corning Inc., Corning, NY, USA) in Dulbecco’s modification of Eagle’s medium (DMEM) with high glucose (Hyclone Laboratories, Logan City, UT, USA), supplemented with 10% heat-inactivated fetal bovine serum (FBS; Gibco, Grand Island, NY, USA) at 37 °C with 5% CO2. In all experiments, cells were allowed to grow and adhere for 24 h in culture medium prior to being infected with K. pneumoniae. At 70 to 80% confluence, bMECs were seeded in 6- or 96-well plates and incubated in 5% CO2 at 37 °C. Once bMECs reached 80 to 90% confluence, they were challenged with K. pneumoniae (three wells with bMECs + HB-AF5 and three wells with bMECs + HLJ-D2), whereas control cells were cultured only with culture medium (three wells with only bMECs).
Before infection, bMECs in a well were stained with 0.4% trypan blue (Beyotime Biotechnology, Beijing, China) and enumerated with a cell counter. The K. pneumoniae cultures were centrifuged for 15 min at 6000 g, washed once in sterile Phosphate Buffered Saline (PBS, Beijing Solarbio Science & Technology Co., Ltd., Beijing, China) at pH 7.2, and re-suspended in DMEM, with concentrations adjusted to achieve multiplicity of infection (MOI) = 5. The MOI was defined as the ratio of added K. pneumoniae to bMECs.
At 6 hpi, bMECs (plus non-infected controls) were collected and used for RNA sequencing analyses. Briefly, bMECs were washed with PBS and harvested with 1 mL of Trizol to extract total RNA, according to the manufacturer’s protocol (TransGen Biotech Co., Ltd, Beijing, China). Total RNA yield and purity were determined by absorbance at 260 and 280 nm, using a NanoDrop-2000 spectrophotometer (Thermo Fisher Scientific Inc., Waltham, MA, USA).
For RNA sequencing, 2 µg of RNA per sample was used. Sequencing libraries were generated using NEBNext UltraTM RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) following manufacturer’s recommendations, with index codes added to attribute sequences to each sample. Clustering of the index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v4-cBot-HS (Illumina, San Diego, CA, USA), according to the manufacturer’s instructions. After cluster generation, the library preparations were sequenced on an Illumina Hiseq 4000 platform and paired-end 150 bp reads were generated. Differential expression analysis of the two infected groups (HB-AF5 and HLJ-D2) and the control group was performed using the DESeq R package (Version 1.10.1), which provides statistical routines for determining differential expression in digital gene expression data, using a model based on the negative binomial distribution. The resulting P values were adjusted using Benjamini and Hochberg’s approach  for controlling the false discovery rate. Genes with an adjusted P-value < 0.05, as detected by DESeq, were designated as being differentially expressed. Gene Ontology (GO) enrichment analysis of differentially expressed genes (DEGs) was implemented by the GOseq R package-based Wallenius non-central hyper-geometric distribution  that adjusts for gene length bias in DEGs. MapMan software was used to analyze differential expression in metabolic pathways . Heat maps were generated using the gplots package in R . To identify genes that were significantly up- or down-regulated in infected bMECs compared to the corresponding non-infected control, DeSeq2 was used to generate log2 fold change values for each gene. Volcano plots were used to provide a global view of distribution of DEGs in each group. In addition, to characterize the functions and pathways of genes obtained from RNA-Seq, functional annotation and classification were performed by comparing sequences with Gene Ontology (GO) databases .
Malondialdehyde (MDA) and total antioxidant capacity (T-AOC)
To determine effects of K. pneumoniae on the antioxidant status of bMECs, malondialdehyde (MDA) concentrations and total antioxidant capacity (T-AOC) in supernatant fluid of cultured bMECs were determined using commercial kits, in accordance with the manufacturer’s instructions (Nanjing Jiancheng Technology Co. Ltd., Nanjing, China). The bMECs were cultured in six-well plates and challenged with HB-AF5 or HLJ-D2 K. pneumoniae (MOI = 5), with sampling after 1, 3, 6 and 12 h. Noninfected cells were similarly incubated as a control and sampled concurrent with infected bMECs.
Concentrations of MDA were determined using the thiobarbituric acid (TBA) method. The MDA detecting liquid (containing TBA) was prepared according to the manufacturer’s instructions. After infection with HB-AF5 and HLJ-D2 K. pneumoniae, 200 µL of bMECs supernatant was collected from each well, put into centrifuge tubes and centrifuged (8000 × g, 5 min). After centrifugation, 100 µL of supernatant was collected, 200 µL MDA detecting liquid added and the resulting solution thoroughly mixed. The tube was placed in boiling water for 15 min, then cooled to room temperature and centrifuged (1000 × g, 10 min). The supernatant was assessed at 532 nm (680 Multipurpose Microplate Reader, Biorad, Hercules, CA, USA). Assay results were normalized to the protein concentration in each sample and expressed as nmol/mg protein.
The T-AOC was determined using the 2, 2′-azino-bis (3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) method, using commercial kits. The ABTS detecting liquid and a standard curve were prepared according to the manufacturer’s instructions. At 1, 3, 6 and 12 hpi with HB-AF5 or HLJ-D2 K. pneumoniae (MOI = 5), bMECs were scraped off, washed with PBS three times, put into 200 µL cold PBS and ultrasound homogenization was done to disrupt cells and release antioxidants. After centrifugation (12 000 × g, 5 min, ~4 °C), 10 µL of supernatant was put into the wells of a 96-well plate, 200 µL ABTS detecting liquid added and after 5 min, absorbance was measured at 405 nm (680 Multipurpose Microplate Reader, Biorad).
Reactive oxygen species (ROS)
Generation of ROS was monitored with a Reactive Oxygen Species Assay Kit (Beyotime Institute of Biotechnology, Shanghai, China) using a 2′, 7′-Dichlorodihydrofluorescein diacetate (DCFH-DA) fluorescent probe. DCFH-DA changes into fluorescent dichlorofluorescein (DCF) when intracellular DCFH reacts with ROS. Cultured bMECs in six-well plates were challenged with HB-AF5 or HLJ-D2 K. pneumoniae (MOI = 5). Noninfected cells were similarly incubated as a control. At 1, 3, 6 and 12 hpi, bMECs were washed with PBS and stained with DCFH-DA. According to the instructions, the DCFH-DA was diluted to 10 μM in fresh DMEM medium and incubated with bMECs for 30 min at 37 °C in the dark. As a positive control, untreated bMECs were incubated with rosup (50 µg/µL) for 30 min and then stained with DCFH-DA, whereas for a negative control, untreated bMECs were stained with DCFH-DA. Within 1 h, DCFH-DA fluorescence was detected with an inverted fluorescence microscope at 488 nm excitation and 525 nm emission using a laser scanning confocal microscope (Olympus FV1200, Olympus Corporation, Tokyo, Japan).
Mitochondrial membrane potential (MMP)
A fluorescent carbocyanine dye JC-I assay kit (Beyotime Institute of Biotechnology, Shanghai, China) was used to determine MMP. Cultured bMECs in six-well plates were challenged with HB-AF5 or HLJ-D2 K. pneumoniae (MOI = 5), with noninfected cells similarly incubated as a control. At 1, 3, 6 and 12 hpi, bMECs were washed and re-suspended in PBS. Then, 0.5 mL of JC-I PBS buffer solution (10 µg/mL) was added to the suspension, which was kept in darkness at 37 °C for 30 min. After washing to remove excess probe, MMP was measured using flow cytometry (Becton Dickinson, Bergen City, NJ, USA) and presented as a relative ratio.
Cytoplasmic calcium concentration
Cytoplasmic calcium concentrations in bMECs were determined with a fluo-3 assay kit (Beyotime Institute of Biotechnology, Shanghai, China). Cultured bMECs in six-well plates were challenged with HB-AF5 or HLJ-D2 K. pneumoniae (MOI = 5), with noninfected cells similarly incubated as a control. At 1, 3, 6 and 12 hpi, bMECs were washed three times in PBS, detached with Trypsin–EDTA solution and re-suspended in DMEM (with 10% FBS). Then, bMECs were centrifuged at room temperature for 10 min at 1000 × g, washed with Ca2+-free Krebs Solution (with 4 mM EGTA in lieu of CaCl2) and stained with fluo-3 (final concentration, 10 μM) and incubated at 37 °C for 30 min in the dark. Fluorescence of the cell suspensions was analyzed with flow cytometry (BD FacsCalibur flow cytometer, Becton Dickinson) and Ca2+ concentration expressed as mean fluorescence of fluo-3.
Mitochondrial calcium concentration
Cultured bMECs in six-well plates were challenged with HB-AF5 or HLJ-D2 K. pneumoniae (MOI = 5), with noninfected cells similarly incubated as a control. At 1, 3, 6 and 12 hpi, bMECs were washed with PBS, detached with trypsin–EDTA solution and centrifuged at room temperature for 10 min at 1000 × g. Mitochondria were isolated from harvested cells using a mitochondria/cytosol Fractionation Kit (Beyotime Institute of Biotechnology, Shanghai, China). Calcium concentration in mitochondrial cytoplasm was determined with the calcium sensitive dye fluo-3; it was dissolved in dimethylsulfoxide to give a stock solution of 1 mg/mL and stored at -20 °C in the dark.
Transmission electron microscopy
Cultured bMECs in six-well plates were challenged with HB-AF5 or HLJ-D2 K. pneumoniae (MOI = 5), with noninfected bMECs similarly incubated as a control. At 6 hpi, bMECs were washed with PBS (pH 7.2), fixed with 2% glutaraldehyde and 1% paraformaldehyde (pH 7.2; Sinopharm Chemical Reagent Co., Shanghai, China) for 45 min at room temperature and processed for TEM . After washing with PBS, the fixed cells were harvested with a rubber scraper (Thermo Fisher Scientific). Then, cells were dehydrated using graded ethanol and acetone (three changes, 10 min each) and sequentially embedded in epoxy resin acetone mixtures (2:1) for 2 h and then in pure resin overnight at 37 °C. After resin had polymerized, ultra-thin sections were cut (Leica EM, Wetzlar, Germany), stained with 1% uranyl acetate followed by lead citrate, and viewed with a transmission electron microscope (Hitachi H-7650) at 80 kV. Imaging was performed using a 4 k CCD camera (Gatan Inc., Pleasanton, CA, USA) and iTEM software.
For assessment of MDA, T-AOC, ROS, MMP, cytoplasmic and mitochondrial Ca2+ concentrations, results were obtained from three independent experiments. Two-way ANOVA was used to determine effects of group and time, and their interaction, and Duncan’s multiple range test used to locate significant differences. A paired Student’s t-test with a 95% confidence interval was used to make contemporaneous comparisons between HLJ-D2 versus HB-AF5 groups. All statistical analyses were done with Statistical Product and Service Solutions 20.0 software (SPSS, Inc., Chicago, IL, USA) and P < 0.05 was considered significant. Results are expressed as mean ± standard deviation (SD). Data were displayed with Graphpad Prism V6.0 (Data Analysis and Graphing Software, San Diego, CA, USA). Data designated as independent variables in the model were as follows: treatments (time points or by isolates with HLJ-D2 or HB-AF5) in the MDA, T-AOC, ROS measurement assays, MMP assays, and cytoplasmic and mitochondrial Ca2+ concentration assays.
K. pneumoniae up- or down-regulated DEGs associated with mitochondrial damage in bMECs
GO enrichment analysis of DEGs
A total of 6923 and 6169 genes were differentially expressed with fold-change ≥ 2 or ≤ 0.5 (P-value < 0.05) after infection with HLJ-D2 or HB-AF5 K. pneumoniae (Figure 1A, B). The HLJ-D2 strain caused more changes at the transcriptional level in bMECs. There were 3453 genes up-regulated and 3470 down-regulated for the HLJ-D2 strain, whereas for the HB-AF5 strain, only 2891 genes were up-regulated and 3278 down-regulated. Based on cluster pattern analysis, DEGs from K. pneumonia-treated groups (HLJ-D2 and HB-AF5) had higher differential expression patterns compared to the control (Figure 1C).
In comparison to the control group, the top three enriched functional terms were cellular macromolecule metabolism, binding and molecular function in bMECs incubated with HB-AF5, whereas for HLJ-D2, they were primary metabolic process, binding and molecular function (Figure 2). Compared to the control, the most common up-regulated DEGs in bMECs after HLJ-D2 infection were associated with DNA (22), ADP (20), mitochondria (16) and interleukin (13), whereas mitochondria (100) and DNA (33) were also frequently detected as down-regulated DEGs (Figure 3A). For bMECs infected with the HB-AF5 strain, the most common up-regulated DEGs were DNA (21), ADP (17) and interleukin (12), whereas the most frequently down-regulated DEGs were mitochondria (88) and DNA (11) (Figure 3B).
K. pneumoniae induced oxidative damage in bMECs
Compared to control, the MDA concentration in bMECs incubated with K. pneumoniae was not significantly different at 1 hpi, but was higher at 3, 6 and 12 hpi (P < 0.05). However, there was no significant difference between the two strains for MDA concentrations (Figure 4A). Furthermore, compared to non-infected cells at 0 h, T-AOC concentrations in infected groups were not significantly different at 1 hpi, but lower than the control at 3, 6 and 12 hpi (P < 0.05), with no significant difference between the two strains (Figure 4B). Production of ROS in bMECs incubated with K. pneumoniae increased at 3, 6 and 12 hpi (P < 0.05; Figure 4D).
K. pneumoniae decreased MMP in bMECs
The ratio of MMP between the infection groups and control was calculated to determine MMP changes in bMECs. Compared to control, MMP was lower at 1, 3, 6 and 12 hpi (P < 0.05) in bMECs incubated with either K. pneumoniae strain (Figure 5). In addition, at 3 and 12 hpi, MMP was lower (P < 0.05) in bMECs infected with HLJ-D2 versus those infected with HB-AF5.
K. pneumoniae increased cytoplasmic and mitochondrial calcium concentrations
Compared to the control, cytoplasmic calcium concentrations in bMECs were generally higher after incubation with strains HLJ-D2 or HB-AF5 (P < 0.05), with differences between the two K. pneumoniae infection groups (P < 0.05), except for 12 hpi (Figure 6A). Meanwhile, there were huge increases in mitochondrial calcium concentrations in bMECs at 1, 3, 6 and 12 hpi, in both infection groups (Figure 6A). In addition, mitochondrial calcium concentrations were higher (P < 0.01) in bMECs infected with HLJ-D2 compared to HB-AF5 at 1 and 3 hpi, whereas at 6 and 12 hpi, mitochondrial calcium concentrations were higher (P < 0.01) in bMECs infected with HB-AF5 compared to HLJ-D2.
Mitochondrial morphology of bMECs
When viewed with TEM, mitochondria of non-infected bMECs had a normal structure, whereas bMECs infected with K. pneumoniae had apparent mitochondrial swelling (Figure 7). At 6 hpi, both strains had caused mitochondria to rupture and cristae to degenerate, followed by severe mitochondrial swelling and vacuolation, with damaged mitochondria becoming increasingly round. The mitochondrial matrix was compressed and dense, and the ridge was shortened, decreased or even disappeared. Additionally, matrix particles had disappeared and the matrix became lighter, whereas the gap in the mitochondrial ridge was wider and cavities of various sizes had formed.
In a previous study, we demonstrated that K. pneumoniae was cytopathogenic to bovine mammary epithelial cells, inducing cell damage and apoptosis . Mitochondrial damage has an important role in many kinds of cellular damage, particularly in apoptosis [22, 23]. In the present study, there were alterations in MMP, oxidative stress, and Ca2+ concentrations, all known markers of mitochondrial function or damage, consistent with a previous study that determined that cell damage was induced by stimulating mitochondrial dysfunction and calcium dysregulation . Furthermore, substantial morphological damage to mitochondria was confirmed with TEM. Therefore, the present findings provided further evidence that mitochondria may have a key role in damaging bMECs after K. pneumoniae infection. We inferred that cellular and molecular changes, including oxidative stress, dysregulation of Ca2+ and decreased MMP, were indicators of mitochondrial dysfunction and were involved in damage in bMECs caused by K. pneumoniae infection.
Transcriptome analysis, including GO enrichment analysis and pathway enrichment analysis, was done as a systemic screening of up or down-regulated genes in bMECs after infection with two strains of K. pneumoniae. Whole transcriptome analysis has been used to explore DEGs that may be involved in particular biological processes in bMECs infected by K. pneumoniae [25, 26]. In the present study, DEGs associated with mitochondria were the most common DEGs enriched in bMECs after infection with K. pneumoniae, indicating that K. pneumoniae had appreciable impacts on mitochondrial functions. Among DEGs associated with ADP, apoptosis, autophagy, DNA, endoplasmic reticulum, interleukin, oxidative stress and mitochondria, changes were greatest in mitochondrial DEGs.
Under various pathological conditions, mitochondria often undergo several morphological changes, including swelling, hyperplasia, hypertrophy and increased density of the mitochondrial matrix . In this study, there was severe mitochondrial swelling and vacuolation, as well as mitochondrial rupture and degenerate cristae after K. pneumoniae infection, consistent with a previous study  and providing morphological evidence of mitochondrial damage.
Mitochondria are major sources of cellular ROS and key players in oxidative stress, as they are major regulators of cellular energy metabolism [29,30,31]. When ROS exceed antioxidant capacity of cells, total antioxidative capacity decreases and MDA formation increases, which can accelerate mitochondrial damage [29, 32]. Consistent with a previous study on Prototheca zopfii , ROS formation increased significantly after K. pneumoniae infection, manifested as increased MDA and decreased T-AOC. Therefore, we concluded that K. pneumoniae provoked ROS production and oxidative stress generation in bMECs. It was suggested that bovine mastitis caused oxidative stress of mammary tissue, manifested as increases in ROS, MDA and decreased T-AOC, resulting in mitochondria-mediated apoptosis and inflammation [33, 34].
The significant decrease in MMP at 1, 3, 6 and 12 hpi indicated that K. pneumoniae rapidly and profoundly suppressed MMP. It is noteworthy that MMP is reflective of the functional metabolic status of mitochondria, and a normal MMP is a prerequisite for maintaining mitochondrial metabolism . Therefore, it arguably is a reliable indicator of mitochondrial function. A change in mitochondrial membrane potential can reflect the permeability of mitochondrial inner membrane, an indicator of mitochondrial function and damage. Furthermore, a decreased mitochondrial inner membrane potential can induce apoptosis . Perhaps the reduction in MMP was due to a primary effect of an unknown Klebsiella virulence factor.
It is well established that Ca2+ has a fundamental role in several cellular functions, regulating or inducing many processes, including proliferation, differentiation, secretion, metabolism, cell death and survival, migration, and gene expression . In this study, infection with K. pneumoniae increased (P < 0.05) Ca2+ concentrations in mitochondria of bMECs compared to Ca2+ concentrations in mitochondria of non-infected bMECs. Therefore, we concluded that K. pneumoniae stimulated excessive calcium transfer in bMECs. Excessive cytoplasmic calcium concentrations caused calcium overload in mitochondria, as mitochondria are cytosolic Ca2+ buffers . Our results were consistent with a previous study that disruption of Ca2+ homeostasis or mitochondrial signaling leads to cell damage . For cytoplasmic Ca2+, there was a significant decrease at 3 hpi with HLJ-D2, whereas a significant decrease occurred at 6 hpi with HB-AF5. Subsequently, cytoplasmic Ca2+ concentrations increased significantly for both HLJ-D2 and HB-AF5 infected bMECs. Dysregulated Ca2+ release from intracellular reservoirs, combined with an influx from the extracellular domain, cause a sustained increase in intracellular Ca2+ over time . Perhaps K. pneumoniae infection increased membrane permeability in bMECs, leading to a decrease in the Ca2+ exchange in the cytoplasm and therefore, a temporary decrease of Ca2+ in the cytoplasm. Cytoplasmic Ca2+ concentrations are a dynamic system in determining both cell survival and death . A further investigation of the exact mechanisms explaining how K. pneumoniae contributes to the dysregulation of Ca2+ homeostasis is warranted.
The two K. pneumoniae strains (non-HMV and HMV) were also used in our previous study . Compared to the non-HMV strain (HB-AF5), the HMV strain (HLJ-D2) had more up- or down-regulated DEGs, and a significantly greater effect on mitochondrial calcium concentrations. However, the non-HMV strain caused a bigger change in MMP. Therefore, we assumed that there were differences among K. pneumoniae strains in their ability to damage mitochondria. However, the HMV phenotype of K. pneumoniae did not have a key role in causing mitochondrial damage. We emphasize that the results of our in vitro study cannot be generalized to represent in vivo pathology induced by K. pneumoniae in the bovine udder.
There were many DEGs associated with mitochondria in bMECs after infection with K. pneumoniae. Furthermore, K. pneumoniae infection significantly decreased MMP and increased ROS generation, whereas cytoplasmic and mitochondrial Ca2+ in bMECs were significantly increased. Therefore, based on multiple end points, K. pneumoniae induced profound mitochondrial damage and dysfunction in bMECs. Furthermore, we inferred that this contributed to the pathogenicity of cellular damage in CM in dairy cows induced by K. pneumoniae.
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
2,2′-Azino-bis (3-ethylbenzthiazoline-6-sulfonic acid)
Bovine mammary epithelial cells;
Differentially expressed genes
Fetal bovine serum
Multiplicity of infection
Mitochondrial membrane potential
Phosphate Buffered Saline
Reactive oxygen species
Statistical Product and Service Solutions
Total antioxidant capacity
Transmission electron microscopy
Tumor necrosis factor-α
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The authors thank our laboratory members who helped us to improve the research and the manuscript with their skillful technical assistance, invaluable comments and suggestions.
This study was financially supported by Beijing Municipal Natural Science Foundation (No. 6192013), National Key Research and Development Project (2018YFD0501601-01, 2016YFD0501203), National Natural Science Foundation of China (No. 31772813), Hebei Key Research and Development Project (19226607D) and Ningxia Key R&D Project (No. 2019BBF02027).
Ethics approval and consent to participate
Approval was granted by the Ethical Committee of the College of Veterinary Medicine, China Agricultural University (CAU), Beijing and the study was conducted according to standard ethical guidelines implemented at CAU (SYXK, 2016–0008).
The authors declare that they have no competing interests.
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Cheng, J., Zhang, J., Yang, J. et al. Klebsiella pneumoniae infection causes mitochondrial damage and dysfunction in bovine mammary epithelial cells. Vet Res 52, 17 (2021). https://doi.org/10.1186/s13567-021-00898-x
- Klebsiella pneumoniae
- Mitochondrial damage