Bacteriophages isolated from dairy farm mitigated Klebsiella pneumoniae-induced inflammation in bovine mammary epithelial cells cultured in vitro
BMC Veterinary Research volume 17, Article number: 37 (2021)
Klebsiella pneumoniae, an environmental pathogen causing mastitis in dairy cattle, is often resistant to antibiotics. K. pneumoniae was used as the host bacteria to support bacteriophage replication; 2 bacteriophages, CM8-1 and SJT-2 were isolated and considered to have therapeutic potential. In the present study, we determined the ability of these 2 bacteriophages to mitigate cytotoxicity, pathomorphological changes, inflammatory responses and apoptosis induced by K. pneumoniae (bacteriophage to K. pneumoniae MOI 1:10) in bovine mammary epithelial cells (bMECs) cultured in vitro.
Bacteriophages reduced bacterial adhesion and invasion and cytotoxicity (lactate dehydrogenase release). Morphological changes in bMECs, including swelling, shrinkage, necrosis and hematoxylin and eosin staining of cytoplasm, were apparent 4 to 8 h after infection with K. pneumoniae, but each bacteriophage significantly suppressed damage and decreased TNF-α and IL-1β concentrations. K. pneumoniae enhanced mRNA expression of TLR4, NF-κB, TNF-α, IL-1β, IL-6, IL-8, caspase-3, caspase-9 and cyt-c in bMECs and increased apoptosis of bMECs, although these effects were mitigated by treatment with either bacteriophage for 8 h.
Bacteriophages CM8-1 and SJT-2 mitigated K. pneumoniae-induced inflammation in bMECs cultured in vitro. Therefore, the potential of these bacteriophages for treating mastitis in cows should be determined in clinical trials.
Bovine mastitis caused by infection with pathogenic microorganisms reduces milk production and quality, inflicting huge economic losses in the dairy industry [1, 2]. Klebsiella pneumoniae, a common environmental pathogen, causes mastitis in dairy cows [3, 4], accounting for 10 to 13% clinical mastitis, second to E. coli [5, 6]. Although antimicrobials are the most common therapy for bovine mastitis caused by K. pneumoniae, it often has single or multidrug resistance , with increasing risk of recurrence after treatment.
Bovine mammary epithelial cells (bMECs) are the first line of defense against invading pathogens that enter the udder through the streak canal, at the distal end of the bovine teat [4, 7]. Thus, bMECs have critical roles in both nonspecific and specific immune defenses against infection by pathogenic microorganisms ; furthermore, they can be infected by a variety of pathogenic microorganisms that damage these cells, leading to mastitis [8, 9]. Toll-like Receptor 4 (TLR4) and the NF-κB pathway are classic regulators of inflammation . Lipopolysaccharides (LPS), the main component of the cell wall of gram-negative bacteria, can activate the TLR4-mediated NF-κB pathway to induce an inflammatory response . Inhibiting or knocking out TLR4 down-regulated expression of inflammatory factors in cells, thereby suppressing inflammation [11, 12]. Although a timely and appropriate inflammatory response can effectively contain invading pathogens, an excessive inflammatory response can cause various degrees of cellular damage, including apoptosis, necrosis or pyroptosis [13, 14]. K. pneumoniae can multiply rapidly in bovine mammary tissues, causing a severe inflammatory response and tissue damage [4, 15]. In bovine mastitis induced by K. pneumoniae, infection of bMECs is an important component. Antibiotics are commonly used to treat bovine mastitis and consequently, drug resistance in gram-negative bacteria, including K. pneumoniae, is rapidly increasing [3, 16, 17]. Therefore, it is important to identify alternatives to antibiotics for treating bacterial infections, especially for bovine mastitis caused by K. pneumoniae.
Bacteriophages are small viruses, nearly ubiquitous in the natural environment . Bacteriophage can lyse pathogens in vivo and in vitro without harmful effects on host cells and have been widely used in various fields [19, 20]. For example, 3 Myoviridae bacteriophages were used as adjunctive therapy and were safe and effective with severe Staphylococcus aureus infections . Furthermore, a bacteriophage “cocktail” was very successful in controlling bacterial wilt in tomatoes . However, use of a bacteriophage for treatment of bovine mastitis caused by K. pneumoniae has apparently not been reported. Therefore, our objective was to investigate the role of bacteriophages for controlling K. pneumoniae in an in vitro infection model of bMECs.
Transmission electron microscopy (TEM) of bacteriophages
Ultrastructures of K. pneumoniae bacteriophages CM8-1 and SJT-2 are shown (Fig. 1). Bacteriophages CM8-1 and SJT-2 were comprised of a head, neck and tail wire (Fig. 1A2, B2). Bacteriophages CM8-1 and SJT-2 had a polyhedral head, approximately 100 and 103 nm, respectively, whereas their tails were 103 and 116 nm and contained obvious tail filaments (Fig. 1A2, B2).
Effect of bacteriophages on adhesion and invasion of K. pneumoniae
Adhesion of K. pneumoniae to bMECs in the K. pneumoniae, K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups were significantly increased in comparison to the Control (Fig. 2a). Starting soon after K. pneumoniae infection and as interval after infection increased, bacteriophages CM8-1 and SJT-2 reduced adhesion (P < 0.01) of K. pneumoniae to bMECs in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups as compared to the K. pneumoniae group at 1.5, 2, 2.5 and 3 h post infection (hpi) (Fig. 2a).
Adhesion of K. pneumoniae to bMECs in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups was similar to that in the K. pneumoniae group, without significant changes at 0.5 hpi (Fig. 2B). However, as duration of infection increased, adhesion of K. pneumoniae to bMECs in the K. pneumoniae, K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups increased (P < 0.01) compared to the Control group (Fig. 2B). Furthermore, adhesion of K. pneumoniae to bMECs in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups was lower (P < 0.01) than that of the K. pneumoniae group at 2, 2.5 and 3 hpi (Fig. 2B).
Effect of bacteriophages on K. pneumoniae-induced cytotoxicity in bMECs
There was no difference in LDH release among the Control, CM8-1 and SJT-2 groups (Fig. 3). At 2 hpi with K. pneumoniae, LDH release in the K. pneumoniae group was higher (P < 0.01) than in the Control group (Fig. 3), whereas at 4, 6 and 8 hpi, LDH release in the K. pneumoniae, K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups was greater (P < 0.01) than in the Control group (Fig. 3). At 2, 4, 6 and 8 hpi, LDH release in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups was significantly decreased compared to the K. pneumoniae group (Fig. 3).
Morphological changes in bMECs
At 2 hpi with K. pneumoniae, morphological appearance was similar in the K. pneumoniae and Control groups. At 4 and 6 hpi with K. pneumoniae, there was no significant changes compared to the Control group (Fig. 4A1-C1, A2-C2). However, at 8 hpi with K. pneumoniae, damage to bMECs in K. pneumoniae group included cell swelling, nuclear hyperchromatism and necrosis, as well as reductions in number of bMECs, compared to the Control group (Fig. 4D1-D2). Furthermore, the extent of damage to bMECs gradually increased with interval after infection. However, morphology of bMECs in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups was similar compared to the K. pneumoniae and Control groups at 2 hpi. Swelling and necrosis of bMECs in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups were less severe compared to the K. pneumoniae group at 4, 6 and 8 hpi (Fig. 4A3-D3, A4-D4).
Effect of bacteriophages on concentrations of inflammatory factors and inflammatory responses in K. pneumoniae-infected bMECs
Concentrations of IL-1β and TNF-α proteins were increased (P < 0.01) at 4, 6 and 8 hpi with K. pneumoniae (Fig. 5a and b). However, TNF-α and IL-1β concentrations in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups were significantly decreased in comparison to the K. pneumoniae group at 4, 6 and 8 hpi (Fig. 5a and b).
Expression levels of TLR4, NF-κB and inflammatory factors (TNF-α, IL-1β, IL-6 and IL-8) in bMECs were determined by real-time PCR. At 2 hpi, mRNA expression levels of TLR4, NF-κB, TNF-α, IL-1β, IL-6 and IL-8 in bMECs were significantly higher in the K. pneumoniae versus Control groups (Fig. 6a-f). Furthermore, at 4, 6 and 8 hpi, mRNA expression levels of TLR4, NF-κB and inflammatory factors in the K. pneumoniae, K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups were significantly up-regulated compared to the Control group (Fig. 6a-f). In contrast, after treatment with bacteriophages CM8-1 and SJT-2, at 4, 6 and 8 hpi, mRNA expression levels of TLR4, NF-κB and inflammatory factors in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups were significantly down-regulated as compared to the K. pneumoniae group (Fig. 6a-f).
Effect of bacteriophages on apoptosis in infected bMECs
At 2 hpi of bMECs with K. pneumoniae, mRNA expression levels of apoptosis factors caspase-3 and caspase-9 were higher (P < 0.05) in the K. pneumoniae groups than in the Control group (Fig. 7a, b). At 4, 6 and 8 hpi, mRNA expression levels of apoptosis factors in the K. pneumoniae, K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups were significantly up-regulated compared to Controls (Fig. 7a-c). When compared to the K. pneumoniae group, at 4, 6 and 8 hpi, bacteriophages CM8-1 and SJT-2 significantly down-regulated mRNA expression levels of apoptosis factors in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups (Fig. 7a-c).
Apoptosis of bMECs in the K. pneumoniae group was higher (P < 0.05) than in the Control group at 2 hpi (Fig. 8). Furthermore, apoptosis rate of bMECs in the K. pneumoniae + CM8-1 and K. pneumoniae + SJT-2 groups was lower (P < 0.01) compared to the K. pneumoniae group at 4, 6 and 8 hpi (Fig. 8), although apoptosis was significantly higher in each of these groups compared to the Control group at all of these time points (Fig. 8).
This was apparently the first report that bacteriophages CM8-1 and SJT-2 isolated from mastitic bovine milk mitigated inflammatory responses and apoptosis in bMECs induced by K. pneumoniae by decreasing bacterial adhesion and invasion and suppressing expression of inflammatory factors. We concluded that bacteriophages CM8-1 and SJT-2 were protective in K. pneumoniae-infected bMECs and therefore have potential therapeutic value against bovine mastitis caused by K. pneumoniae.
K. pneumoniae can infect a variety of cells and tissues, inducing inflammatory responses and cell damage [23,24,25]. In addition, it also infects bMECs in development of mastitis in dairy cows . When bacteria infect cells, bacterial adhesion and invasion are critical determinants of virulence ; therefore, the absence of genes related to synthesis of adhesion proteins reduce adhesion rates and cell toxicity. Furthermore, pathogens with high rates of adhesion and invasion have potential to cause serious damage to cells. In this study, adhesion and invasion of K. pneumoniae to bMECs increased significantly with interval after infection, although this was mitigated by bacteriophages CM8-1 and SJT-2. Bacteriophages can specifically lyse pathogens and therefore reduce adhesion and invasion. In the current study, bacteriophages CM8-1 and SJT-2 reduced ability of K. pneumoniae to infect and bMECs by mitigating adhesion and invasion.
Lactate dehydrogenase (LDH) is an important marker of bacterial cytotoxicity [28, 29]. Infection of bMECs with gram-negative bacteria, including K. pneumoniae and E. coli, increases LDH release and is accompanied by substantial cell damage [4, 30]. In this study, LDH significantly increased after bMECs were infected by K. pneumoniae, with increasing concentrations over time. Therefore, K. pneumoniae had toxic effects on bMECs, consistent with cell swelling and necrosis and decreasing numbers of bMECs.
A lack of toxic effects on host cells is characteristic of bacteriophages [19, 31]. Treatment of bMECs with either CM8-1 or SJT-2 bacteriophage did not increase release of LDH relative to the Control group, indicating that these bacteriophages were not toxic to bMECs. However, they can lyse and kill K. pneumoniae, reducing its virulence and mitigating damage to bMECs, manifested by less morphological damage and lower LDH concentrations.
Infection of bMECs by pathogens in development of bovine mastitis is usually accompanied by a severe inflammatory response . Various pathogenic bacteria, including K. pneumoniae, E. coli, S. aureus and S. agalactiae, cause inflammation by producing inflammatory factors [4, 33,34,35]. In this study, concentrations of IL-1β and TNF-α in bMECs culture medium increased significantly after bMECs were infected with K. pneumoniae; furthermore, there was a positive association with duration of infection time, confirming K. pneumoniae-induced inflammation of bMECs. Gram negative bacteria such as K. pneumoniae and E. coli can activate TLR4 mediated NF-κB pathway to induce inflammation of bMECs [4, 11, 36, 37]. In this study, after exposing bMECs to K. pneumoniae, mRNA levels of TLR4 and NF-κB, in the pathway of regulating inflammatory response in bMECs, were significantly up-regulated and positively associated with duration of infection. In addition, downstream genes in TLR4 and NF-κB pathways, namely mRNA expression levels of TNF-α, IL-1β, IL-6 and IL-8 in bMECs were also up-regulated, confirming that K. pneumoniae induced an inflammatory response in bMECs. However, bacteriophages CM8-1 and SJT-2 were able to lyse K. pneumoniae and mitigate the inflammatory response induced by K. pneumoniae, manifested by decreased concentrations of IL-1β and TNF-α in bMECs culture medium, as well as reduced mRNA expression levels of TLR4, NF-κB, TNF-α, IL-1β, IL-6 and IL-8.
In this study, K. pneumoniae induced apoptosis of bMECs. Mitochondria are involved in the common apoptotic pathway, which mainly depends on the caspase families and cyt-c for regulation [38,39,40]. In the current study, K. pneumoniae infection of bMECs presumably enhanced release of cyt-c from mitochondria, triggered the caspase-9 and caspase-3 cascade reaction and accelerated cell apoptosis. The mRNA expression of caspase-3, caspase-9 and cyt-c in bMECs significantly increased with duration of infection time, implying apoptosis was triggered by K. pneumoniae. Based on flow cytometry, the apoptosis rate of bMECs increased gradually after K. pneumoniae treatment, which further confirmed that K. pneumoniae induced apoptosis of bMECs. However, bacteriophages CM8-1 and SJT-2 decreased expression of caspase-3, caspase-9 and cyt-c, as well as apoptosis rate of bMECs. Therefore, bacteriophages CM8-1 and SJT-2 mitigated apoptosis of bMECs induced by K. pneumoniae.
Bacteriophages CM8-1 and SJT-2 mitigated K. pneumoniae-induced inflammation in bovine mammary epithelial cells cultured in vitro. Therefore, the potential of these bacteriophages for treating mastitis in cows should be determined in clinical trials.
The bacterial strain used in this study, isolated from clinical mastitis in a dairy cow, was K. pneumoniae (CM-KP8) with K57 capsule serotype . This isolate was stored at the mastitis diagnostic laboratory, College of Veterinary Medicine, China Agricultural University. Prior to each experiment, fresh bacterial suspensions were prepared from frozen stocks by culture on LB nutrient agar medium and incubated at 37 oC for 18 h. Thereafter, bacteria were sub-cultured on brain heart infusion broth for 18 h to mid-log phase and bacterial concentration was determined by the plate counting method for the following experiments.
Bacteriophages CM8-1 and SJT-2 were isolated from dairy farm wastewater. Prior to each experiment, a bacterial solution in mid-log phase was mixed with bacteriophage stock solution and spread over a double-layer plate (96.6% LB liquid medium and 3.4% agar powder), with sodium magnesium (SM) buffer added after the bacteriophage had grown on the entire plate. Thereafter, this plate was placed on a shaker at 120 rpm/min for 2 h to liberate the bacteriophage from the plate and into the SM solution. The latter was collected and passed through a 0.22 µm filter to obtain the bacteriophage stock solution. Thereafter, PEG8000 (10%) was add into the bacteriophage suspension and left overnight at 4 oC. Then, the bacteriophage suspension was centrifuged at 10,000 × g for 10 min to obtain bacteriophage precipitation. The above process was repeated twice to obtain pure bacteriophage. The bacteriophage precipitation was resuspended with DMEM for the following experiments.
Cell culture and treatment
Bovine mammary epithelial cells (bMECs), line MAC-T (Shanghai Jingma Biological Technology Co., Ltd. China), were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% (v/v) Gibco® fetal bovine serum at 37 oC in a humidified atmosphere of 5% CO2. Cells from 3 to 8 passages were used for experiments, with the same passages of cells used in each experiment. The bMECs were treated with or without K. pneumoniae (MOI, ratio of K. pneumoniae to bMECs was 10:1) and bacteriophages CM8-1 or SJT-2 (MOI, ratio of bacteriophage to K. pneumoniae was 1:10), to form the following groups: Control; K. pneumoniae infection group (K. pneumoniae), K. pneumoniae plus bacteriophage CM8-1 group (K. pneumoniae + CM8-1) and K. pneumoniae plus bacteriophage SJT-2 group (K. pneumoniae + SJT-2).
Transmission electron microscopy (TEM)
A suspension (20 µL) of bacteriophages (titer = 109 PFU/mL) was dropped on a copper mesh and precipitated for 2 min at room temperature, with excess liquid absorbed by filter paper. Bacteriophages were then stained with 2% uranium acetate for 1 min, excess liquid absorbed, naturally dried for 15 min at room temperature and then observed under a transmission electron microscope (H-7650, Hitachi, Tokyo, Japan) at 80 kV.
Adhesion and invasion
Adhesion and invasion were measured as described . The bMECs were inoculated into a 6-well cell culture plate and grown to 80% confluence, washed with phosphate buffer saline (PBS) and then DMEM supplemented with 1% (v/v) Gibco® Fetal Bovine Serum was added. At a multiplicity of infection (MOI, ratio of K. pneumoniae to cells) of 10:1, the bMECs were cultured at 37 °C in a humidified atmosphere of 5% CO2 for 0.5 h, and then with addition of bacteriophages CM8-1 or SJT-2 (MOI, ratio of bacteriophages to K. pneumoniae) of 1:10 for 0.5, 1, 1.5, 2 and 2.5 h. After incubation, cells were washed with PBS (to remove non-adherent bacteria), and the cell suspension was 10-fold diluted and cultured on LB liquid medium plate for counting colony forming units. Meanwhile, after incubation, cells were washed with PBS and treated with 1 mL of DMEM containing kanamycin (100 µg/mL) and then cultured at 37 °C in a humidified atmosphere of 5% CO2 for 2 h. The culture medium was removed, cells were lysed with 0.5% TritonX-100 and the lysate diluted and cultured on LB liquid medium plate as described above. Colonies were counted and invasion rate of K. pneumoniae into bMECs was calculated.
Lactate dehydrogenase (LDH) assay
The bMECs were seeded in 96-well plates (density of 1 × 105 cells/well), grown to 80% confluence, then DMEM supplemented with 1% (v/v) Gibco® Fetal Bovine Serum was added. Cells were then treated with K. pneumoniae and bacteriophages CM8-1 or SJT-2, as described above. After culture for 1, 2, 4, 6 or 8 h, supernatants were collected, centrifuged at 11,586 × g for 15 min at 4 oC and LDH release measured by cytotoxicity (LDH Assay Kit-WST®, Dojingdo Laboratories, Kumamoto, Japan), according to manufacturer’s instructions. Absorbance of optical density was determined at 492 nm with a microplate reader (Bio-Rad, Hercules, CA, USA).
Morphological observation of bMECs
The bMECs were seeded in 6-well plates with glass slides and grown to 80% confluence. Cells were then treated with K. pneumoniae and bacteriophages CM8-1 or SJT-2, as described above. Cells were cultured at 37 °C in a humidified atmosphere of 5% CO2 for 2, 4, 6 or 8 h. Then, cells were collected, fixed in 4% paraformaldehyde for 30 min, washed 3 times with PBS and dried naturally for 5 min. Hematoxylin-eosin (HE) staining was performed according to manufacturer’s instructions. An increasing alcohol gradient (75, 85, 95 and 100%) was used to dehydrate cells, which were subsequently observed under a light microscope at 40×.
Detection of cytokine concentrations
Culture medium was collected, centrifuged at 11,586 × g for 10 min at 4 oC and supernatant removed. Concentrations of inflammatory cytokines TNF-α and IL-1β in supernatant were measured using ELISA kits (Shanghai Zhenke Biotechnology Co., Ltd, Shanghai, China), used in accordance with manufacturer’s instructions.
Quantifying cytokine mRNA with real‐time PCR
The bMECs were treated with K. pneumoniae and bacteriophages CM8-1 or SJT-2, and cells collected for total RNA extraction. Trizol Reagent (1 mL) was pre-chilled on ice and added to cell samples for 5 min to lyse cells. Mixed liquid was centrifuged at 11,586 × g for 15 min at 4 oC and supernatant collected. Total mRNA of bMECs was extracted with mRNA extraction kit (TransGen Biotech Co., Ltd. Beijing, China), used according to manufacturer’s instructions. Primers for GAPDH (housekeeping gene), TLR4, NF-κB, TNF-α, IL-1β, IL-6, IL-8, caspase-3, caspase-9 and cyt-c were designed using primer 5.0 software (Table 1). Relative expression levels of TLR4, NF-κB, TNF-α, IL-1β, IL-6, IL-8, caspase-3, caspase-9 and cyt-c mRNA were determined using the Mx3000P™ RT-PCR system (Stratagene, USA) real-time PCR RG-3000A and the SYBR® Premix Ex Taq™ (Perfect Real Time) Kit (Takara, Japan).
Detection of apoptosis by flow cytometry
After bMECs were treated with K. pneumoniae and bacteriophages CM8-1 and SJT-2, apoptosis was assessed with an Annexin V-FITC apoptosis detection kit (Beyotime Biotechnology Co., Ltd, Shanghai, China). Cell culture fluid and washing fluid were collected. Then, cells were harvested with trypsin without EDTA and washed with PBS. Cells were centrifuged at 965 × g for 10 min, supernatant removed and cells re-suspended in 195 µL Annexin V-FITC binding solution and then transferred to a sterile flow cytometry glass tube. Annexin V-FITC (5 µL) was add to the cell suspension, followed by 10 µL propidium iodide staining solution. After 20 min at room temperature in dark conditions, apoptotic cells were detected using flow cytometry.
Data were expressed as mean ± standard deviation (SD), followed by post hoc Tukey’s tests using SPSS 22.0 (SPSS Inc., Chicago, IL, USA). All measurements were replicated three times and P < 0.05 was considered significant.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
- K. pneumoniae :
bovine mammary epithelial cells
Multiplicity of infection
Dulbecco’s modified Eagle’s medium
Transmission electron microscopy
Polymerase chain reaction
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This study was financially supported by Beijing Municipal Natural Science Foundation (No. 6192013), the National Natural Science Foundation of China (No. 31772813 and 31572587), the National Key R&D Project (No. 2016YFD0501203), Hebei Key R&D Project (19226607D) and the High-end Foreign Experts Recruitment Program (No. GDT20171100013). The above “Funding Organizations” provided financial support, and they had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Ethics approval and consent to participate
The current work was carried out according to ethical guidelines of China Agricultural University (CAU), Beijing, and approved by China Agricultural University Animal Ethics Committee (protocol CAUAEC-2010–0603). There were no vulnerable populations involved and no endangered species used in the experiment.
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Shi, Y., Zhao, W., Liu, G. et al. Bacteriophages isolated from dairy farm mitigated Klebsiella pneumoniae-induced inflammation in bovine mammary epithelial cells cultured in vitro. BMC Vet Res 17, 37 (2021). https://doi.org/10.1186/s12917-020-02738-0
- Klebsiella pneumoniae
- Bovine mastitis