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Int J Med Sci 2019; 16(8):1078-1088. doi:10.7150/ijms.33723 This issue Cite

Research Paper

Yunnan Baiyao reduces hospital-acquired pressure ulcers via suppressing virulence gene expression and biofilm formation of Staphylococcus aureus

Jun Liu^1,2, Mufa Cai³, Huimin Yan², Jiawu Fu⁴, Guocai Wu⁵, Zuguo Zhao¹, Yi Zhao¹, Yan Wang¹, Yuanming Sun⁶, Yongke You⁷, Liyao Lin⁸, Juan Huang², Riming Huang⁶ , Jincheng Zeng²

1. Laboratory of Pathogenic Biology, Guangdong Medical University, Zhanjiang 524023, China;
2. Dongguan Key Laboratory of Medical Bioactive Molecular Developmental and Translational Research, Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Guangdong Medical University, Dongguan 523808, China;
3. Department of Clinical Laboratory, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong 524001, China;
4. Department of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China.
5. Department of Blood Internal Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China;
6. Guangdong Provincial Key Laboratory of Food Quality and Safety, College of Food Science, South China Agricultural University, Guangzhou 510642, China;
7. School of Chinese Medicine, The University of Hongkong, Pokfulam, Hongkong;
8. Department of Cardiothoracic Surgery, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong 524001, China.

✉ Corresponding author: Dr. Jincheng Zeng, E-mail: zengjcedu.cn Dongguan Key Laboratory of Medical Bioactive Molecular Developmental and Translational Research, Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Guangdong Medical University, Dongguan 523808, China, Phone: +86 769 22896440; Dr. Riming Huang, E-mail: huangrimingedu.cn College of Marine Science, South China Agricultural University, Guangzhou 510642, China, Phone: +86 20 8528 3448. More

Abstract

Yunnan Baiyao (YB) as a kind of famous Chinese herbal medicine, possessed hemostatic, invigorating the circulation of blood, and anti-inflammatory effects. Identifying strategies to protect patients at risk for hospital-acquired pressure ulcers (HAPU) is essential. Herein, our results showed that YB treatment can effectively reduce the acne wound area and improve efficacy in a comparative study of 60 cases HAPU patients with S. aureus positive of acne wound pathogens. Furthermore, YB inhibited HIa expression and suppressed accessory gene regulator (agr) system controlled by regulatory RNA II and RNA III molecule using pALC1740, pALC1742 and pALC1743 S. aureus strain linked to gfp_uvr reporter gene. Moreover, YB downregulated cao mRNA expression and inhibited coagulase activity by RT-PCR, slide and tube coagulase test. Additionally, YB downregulated seb, sec, sed, and tsst-1 mRNA expression to suppress enterotoxin and tsst-1 secretion and adhesion function related genes sarA, icaA, and cidA mRNA expression. Taken together, the data suggest that YB may reduce HAPU via suppressing virulence gene expression and biofilm formation of S. aureus.

Keywords: Yannan Baiyao, hospital-acquired pressure ulcers, Staphylococcus aureus, agr system, virulence factors, biofilms

Introduction

Hospital-acquired pressure ulcers (HAPUs)-induced skin and soft-tissue injuries are the most common problems encountered in hospitalized patients and those in long-term institutional care and threat to patients health [1]. HAPUs may prolong the hospital stay and lead to increased medical costs. The Healthcare Cost and Utilization Project (HCUP) report estimated that the average cost of treating pressure injuries is $37,800 per patient [2]. Additionally, the main infectious complications that can develop from HAPUs are cellulitis, abscess, osteomyelitis, and bacteremia [3]. Therefore, reduction and prevention of pressure ulcers is one of the greatest healthcare challenges to reducing patient harm.

Staphylococcus aureus (S. aureus), known as one of the most frequent strain usually causes food poisoning and widespread infection, and is a risk factor for exacerbating HAPUs. It comes from superficial skin and other soft tissue infections to life threatening toxic shock, skeletal system, circulatory system, respiratory system, implantable medical devices, and the blood stream [4-6]. At present, S. aureus-associated HAPUs have been increasing year by year. However, due to the abuse of antibiotics, S. aureus is seriously resistant to drugs and the therapeutic effect of HAPUs is limited [7]. Therefore, there is an urgent need for a novel strategy that does not cause microbial resistance.

In Asia, traditional Chinese medicine for treatment of infection has a long history [8]. Yunnan Baiyao (YB) as a kind of famous Chinese herbal medicine, possessed hemostatic, invigorating the circulation of blood, and anti-inflammatory effects [9, 10]. It has been used for more than 100 years and has not caused any infection, indicating that YB may be a promising drug-resistant drug.

Our previous study proposed for the first time that sub-MIC value of the aqueous extract of YB could efficiently inhibit secretion of toxins, movement of flagellum and pili, and the formation of biofilms of gram-negative bacterium Pseudomonas aeruginosa [11]. This prompted us to pay considerable attention to understand whether YB has its potential influence on S. aureus and HAPUs patients. This study was designed to investigate the effect of YB on HAPUs patients and sub-MICs of YB active ingredients on the expression of S. aureus agr system, virulence factors and biofilms. Combined with our previous reported, herein, we found that YB treatment can effectively reduce the acne wound area and improve efficacy in a comparative study of 60 cases HAPU patients with S. aureus positive of acne wound pathogens. Furthermore, antibacterial effect of YB on S. aureus also showed that YB may reduce HAPU via suppressing virulence gene expression and biofilm formation of S. aureus.

Materials and methods

Patients

60 cases of hospital-acquired pressure ulcers (HAPU) patients who were hospitalized at Affiliated Hospital of Guangdong Medical University were enrolled in this study. Subjects with missing at least one item from the following: admission method, consciousness status, pain, and Braden subscales were excluded. The demographic and clinical characteristics for all study subjects are described in Table 1. This study was approved by the Internal Review and the Ethics Boards of Guangdong Medical University. Informed written consent was obtained from all study subjects.

Patient treatment with Yunnan Baiyao (YB)

The patient performed routine debridement of the wound to completely remove the necrotic tissue from the wound, and then cleaned the wound with hydrogen peroxide and sterile saline until the fluid that was discharged was clean. The wound surface is exposed and the appropriate infrared irradiation parameters are selected according to the area and location of the wound surface for 20~30 min, the distance is 30~50 cm, and the intensity is based on the patient's feeling of warmth. The treatment group was prepared into a paste by adding appropriate amount of Yunnan Baiyao (YB group Co, Ltd) according to the size of the wound surface, and then applied to the wound surface with a sterile cotton swab, covered with sterile Vaseline gauze and covered with sterile gauze. The control group was filled with Vaseline oil yarn to fill the pressure wound, and then covered with sterile gauze, and changed once a day. The effects of the two groups were evaluated after 20 days of treatment, and divided into four categories according to the treatment effect. (1) Effective: wound healing, scarring and shedding. (2) Markedly effective: no secretions, shrinkage of the wound, granulation tissue growth. (3) Improvement: the exudate is reduced and the wound is not enlarged. (4) Ineffective: wound does not heal, there is still exudate.

Bacteria strains

S. aureus strain pALC1740 (hla promoter fused to a gfp_uvr reporter gene), pALC1742 (containing an RNAII promoter linked to gfp_uvr reporter gene) and pALC1743 (containing an RNAIII promoter linked to gfp_uvr reporter gene) were a kind gifted by Professor Ambrose L. Cheung at Dartmouth College. coa⁺ S. aureus, icaA⁺ S. aureus, sarA⁺ S. aureus, cidA⁺ S. aureus, sea⁺ S. aureus, seb⁺ S. aureus, sec⁺ S. aureus, sed⁺ S. aureus, see⁺ S. aureus and tsst-1⁺ S. aureus strains were collected from Affiliated Hospital of Guangdong Medical University, from April 2013 to February 2017. S. aureus ATCC29213 was purchased from National Institutes for Food and Drug Control (China).

Preparation of drug extract

According to the reported method [12], 100 g YB powder purchase from YB group Co, Ltd. was extracted with 500 mL ultrapure water at 50 ^oC for 24 h. The aqueous extract was centrifuged twice at 25000 rpm for 60 min. The supernatant liquor of the extract was concentrated in vacuo to 100 mL aqueous extract, then lyophilized (YO0230, Thermo). The lyophilized powder was stored at -50 ^oC before it was used.

Determination of MIC and sub-MIC

Based on the reported method [13], the MIC and sub-MIC of active components in YB were determined by tube dilution method. The MIC value of YB for S. aureus was determined by two-old macro-dilutions in Mueller-Hinton broth with an inoculum of 5×10⁵ colony forming unit (CFU)/mL. The final concentration of active components in YB was 512 mg/mL to 0.125 mg/mL. The MIC value was defined as the lowest concentration of YB allowing no visible growth, and the sub-MIC was defined as the highest concentration of YB that did not inhibit growth by measuring cell density. For other experiments, S. aureus was cultured in a 20-mL conical flask with shaking at 37 ^oC in LB broth containing appropriate concentrations of YB. Bacterial cultures were sampled at intervals of 1 h. Cell density was determined by measuring absorbance at 600 nm.

RNA extraction

S. aureus carrying genes tsst-1, coa, sarA, icaA, cidA, sea, seb, sec, sed, and see, were cultured by experimental group with sub-MIC value of the aqueous extract of YB and control group without aqueous extract of YB, respectively. These bacteria were collected at their exponential growth phase. Total bacterial mRNA was isolated using Kit RNA_fast200 (TaKaRa Biotechnology, China). The mRNA was qualified using ND-2000 ultra-micro nucleic acid protein analyzer (Nanodrop, USA), then was stored at -80 ^oC before it was used.

Confocal Laser Scanning Microscope

The 1.5×10⁸ CFU/mL pALC1742 and pALC1743 were prepared. The active ingredients of YB were diluted with TSB broth and configuration of bacteria fluid. Finally, the concentration of YB active ingredient and bacterial fluid were sub-MIC and 5×10⁵ CFU/mL. The biofilm of pALC1740, pALC1742 and pALC1743 were cultivated in laser confocal culture dishes (Shanghai Jingan Biotechnology Co. LTD) at 37 ^oC for 7 days. The inhibitory effects of YB at different concentrations on hla expression, RNA II and RNA III expression, and the effects on the growth of biofilms were observed by a laser confocal scanning microscope TCSSP5II (Leica, Germany) and a fluorescence microscope TE2000-U (Nikon) from the second day. Each reported strain was cultured with TSB broth without YB as the control. Each experiment was repeated three times.

Rabbit blood plate test

The rabbit blood plate with sub-MIC YB and the normal rabbit blood plate were prepared. 10 μL 1.5×10⁸ CFU/ml ATCC29213 was added to the rabbit blood plate with sub-MIC YB and the normal rabbit blood plate then observed the hemolytic ring after 24 hours.

Slide and tube coagulase tests

According to the reported method [14, 15], the effects of YB with sub-MIC on bound coagulases were carried out using slide coagulase tests ATCC29213 was cultured in the rabbit blood plate with YB. A drop of EDTA anticoagulant rabbit plasma and some bacterial colony were mixed in clean glass slide, and ATCC29213 with normal rabbit blood plate was cultured as control, both of which were observed within 10 s. The effects of YB with sub-MIC on free coagulases were carried out using tube coagulase tests. ATCC29213 was cultured in the rabbit blood plate with sub-MIC YB. A 1/4 of fresh rabbit plasma 1 ml and six colonies were mixed in 2 mL EP tubes, and ATCC29213 with normal rabbit blood plate was cultured as control, both of which were in water bath at 37 ^oC for 3 h before they were observed.

Reverse Transcription-Polymerase Chain Reaction (RT-PCR)

According to the gene sequence in Genebank, using the oligo7 software design RT-PCR primers of reference (16SrRNA) and cao, sarA, icaA, cidA, tsst-1, sea, seb, sec, sed, see, and seg gene. The mRNA relative expressions of genes were detected using RT-PCR (ROCHE, LightCycler480 II). The primers were synthesized by Shanghai Jingan Biotechnology Co. LTD. The kits for RT-PCR and kits RNA_fast200 (RR820A) were purchased from TaKaRa Biotechnology, China. The RT-PCR primers shown in Table 2.

Statistical analysis

Statistical analyses were performed as previously described using SPSS 20 statistical software [16-18]. Measured data are expressed as mean ± standard deviation and analyzed using the t-test, χ²-test and variations considered significant at p < 0.05.

Results

Characteristics of the subjects included in the study

Among all prospectively enrolled subjects, 45 cases were stage III HAPU patients, 15 cases were stage IV HAPU patients. The ulcer site of 32 patients was sacrococcygeal region (SR), 17 patients was ischial tuberosity (IT) and 11 patients was greater trochanter (GT). Bacterial culture of wound pathogens in all patients showed S. aureus positive. The demographic and clinical characteristics for YB treatment and control subjects were shown in Table 1. No significant difference in terms of age, gender, stage and course of disease were noted between YB treatment and control subjects.

YB treatment reduces HAPU

To assess the role of YB in the treatment of HAPU patients, 60 cases of HAPU patients were divided into two groups, YB treatment and control group. After 20 days of YB treatment, our results showed that YB treatment can effectively reduce the acne wound area (p < 0.05) and improve efficacy (p < 0.05), seen in Table 3. These results showed that YB treatment can effectively reduce HAPU.

Antibacterial effect of YB

Above results showed YB treatment reduce acne wound area of HAPU patients with S. aureus positive in wound pathogens detecting (Table 1). At present, a number of research reports that S. aureus associated with pressure ulcers [19, 20]. Therefore, the antibacterial effects of YB on S. aureus were evaluated. First, the MIC and sub-MIC values of YB for S. aureus pALC1743, pALC1742, pALC1740, and ATCC29213 were 16 mg/mL and 1 mg/mL, respectively. While the MIC value of YB for S. aureus carrying genes coa, sarA, icaA, cidA, sea, seb, sec, sed, see, and tsst-1 ranged from 16 mg/mL to 32 mg/mL, and its sub-MIC value ranged from 1 mg/mL to 2 mg/mL. The effects of different concentrations of YB on the growth of pALC1740, pALC1742, pALC1743, ATCC29213, coa⁺ S. aureus, icaA⁺ S. aureus, sarA⁺ S. aureus, cidA⁺ S. aureus, sea⁺ S. aureus, seb⁺ S. aureus, sec⁺ S. aureus, sed⁺ S. aureus, see⁺ S. aureus and tsst-1⁺ S. aureus were shown in Figure 1.

YB inhibits HIa expression in S. aureus

α-hemolysin (Hla) toxin is the most emphasized and characterized virulence factor in S. aureus [21]. Herein, to study the role of YB on virulence gene Hla expression, a standard S. aureus strain pALC1740, which hla promoter fused to a gfp_uvr reporter gene was used. Results showed that the GFP-mediated fluorescence attributable to the hla promoter activity was lower in YB-treated pALC1740 than in the parental un-treated strain (Figure 2A). GFP fluorescence intensity, used to indicate HIa expression was increased in pALC1740 strain after culturing for 4 days to reach a top, and then decreased after culturing for 7 days (Figure 2B, 2C). However, after YB treatment, overall fluorescence intensity (Figure 2B) and fluorescence intensity of the largest biofilm (Figure 2C) were significantly lower than that in the parental un-treated strain. Additionally, the area of the largest biofilm in YB-treated pALC1740 strain was significantly smaller than that in un-treated strain (Figure 2D). These results suggested YB inhibited HIa expression.

 Figure 1 

The role of YB on the growth of S. aureus. S. aureus strain pALC1740 (A), pALC1742 (B), pALC1743 (C), ATCC29213 (D), coa⁺ S. aureus (E), icaA⁺ S. aureus (F), sarA⁺ S. aureus (G), cidA⁺ S. aureus (H), sea⁺ S. aureus (I), seb⁺ S. aureus (J), sec⁺ S. aureus (K), sed⁺ S. aureus (L), see⁺ S. aureus (M) and tsst-1⁺ S. aureus (N) were cultured for 12 h with different concentrations of YB. The effect of YB on the growth of SA was evaluated by measuring OD600.

 Figure 2 

The role of YB on HIa expression of S. aureus strain pALC1740. GFP fluorescence intensity was used to indicate HIa expression in YB-treated pALC1740. (A) hla promoter activity was evaluated by GFP-mediated fluorescence in YB-treated pALC1740. (B) Overall fluorescence intensity in YB-treated pALC1740. (C) Fluorescence intensity of the largest biofilm in YB-treated pALC1740. (D) The area of the largest biofilm in YB-treated pALC1740. WL: White light.

YB inhibits agr system in S. aureus

Recent studies have shown that most of the virulence factors in S. aureus are regulated by accessory gene regulator (agr) system [22], which comprises two divergent transcripts, RNAII and RNAIII [23, 24]. Herein, we want to detect whether the RNAII and RNAIII expression is reduced in YB-treated S. aureus. To verify this possibility, we also used two standard S. aureus strain pALC1742 or pALC1743, containing an RNAII or RNAIII promoter linked to gfp_uvr reporter gene, respectively. Results showed that the GFP fluorescence intensity and the area of the largest biofilm both on YB-treated pALC1742 strain (Figure 3) and pALC1743 strains (Figure 4) were decreased. These results suggested YB inhibited RNAII and RNAIII expression.

YB inhibits coagulase activity in S. aureus

ATCC29213 strain was used to detect coagulase activity in S. aureus by slide coagulase test and tube coagulase test. Results showed that ATCC29213 strain was negative in YB-treated blood plates (Figure 5A).Both slide coagulase test (Figure 5B) and tube coagulase test (Figure 5C) showed ATCC29213 strain has low coagulase activity after YB treatment. Moreover, the relative expression of cao gene in YB-treated ATCC29213 strain was significantly lowers than that in control group (Figure 5D). These results suggested YB inhibited coagulase activity.

YB inhibits enterotoxin and tsst-1

To further evaluate the role of YB on enterotoxin and tsst-1 secretion, sea, seb, sec, sed, see, and tsst-1 positive SA were used to enterotoxin and tsst-1 expression using RT-PCR. Results showed that the mRNA expression of seb, sec, sed, and tsst-1 were significantly reduced after YB treatment (Figure 6). These results suggested YB inhibited enterotoxin and tsst-1 secretion.

YB inhibits adhesion function related genes expression

In addition, YB inhibits adhesion function related genes sarA, icaA, and cidA mRNA expression in icaA⁺ S. aureus, sarA⁺ S. aureus, cidA⁺ S. aureus, respectively (Figure 7).

 Figure 3 

The role of YB on agr system of S. aureus strain pALC1742. GFP fluorescence intensity was used to indicate agr system RNAII or RNAIII promoter in YB-treated pALC1742. (A) RNAII or RNAIII promoter activity was evaluated by GFP-mediated fluorescence in YB-treated pALC1742. (B) Overall fluorescence intensity in YB-treated pALC1742. (C) Fluorescence intensity of the largest biofilm in YB-treated pALC1742. (D) The area of the largest biofilm in YB-treated pALC1742. WL: White light.

 Figure 4 

The role of YB on agr system of S. aureus strain pALC1743. GFP fluorescence intensity was used to indicate agr system RNAII or RNAIII promoter in YB-treated pALC1743. (A) RNAII or RNAIII promoter activity was evaluated by GFP-mediated fluorescence in YB-treated pALC1743. (B) Overall fluorescence intensity in YB-treated pALC1743. (C) Fluorescence intensity of the largest biofilm in YB-treated pALC1743. (D) The area of the largest biofilm in YB-treated pALC1743. WL: White light.

 Figure 5 

The role of YB on coagulase activity of S. aureus strain ATCC29213. ATCC29213 strain was used to detect coagulase activity in S. aureus by slide coagulase test, tube coagulase test and RT-PCR. (A) Blood plates.(B) Slide coagulase test. (C) Tube coagulase test. (D) The relative expression of cao gene in YB-treated ATCC29213 strain was detected by RT-PCR.

 Figure 6 

The role of YB on enterotoxin and tsst-1 expression of S. aureus. To further evaluate the role of YB on enterotoxin and tsst-1 secretion, sea (A), seb (B), sec (C), sed (D), see (E), and tsst-1 (F) positive S. aureus were used to enterotoxin and tsst-1 expression using RT-PCR.

 Figure 7 

The role of YB on adhesion function related genes expression of S. aureus. YB inhibits adhesion function related genes sarA (A), icaA (B), and cidA (C) mRNA expression in icaA, sarA, cidA positive S. aureus.

Discussion

YB is a secret herbal medicinal formula developed in 1902 by Qu Huangzhang and widely used by Traditional Chinese Medicine (TCM) practitioners to stop bleeding caused by traumatic injury and surgery, haemoptysis, hematochezia, hemorrhoid haemorrhage, metrorrhagia, metrostaxis and ulcer (ulcerative colitis, peptic ulcer, oral ulcer and skin ulcer) in China. Herein, we found that YB treatment can effectively reduce the acne wound area and improve efficacy on HAPU patients with S. aureus positive of acne wound pathogens. Further in-depth research showed that the sub-MIC of YB has an inhibitory effects on the expression of S. aureus agr system, which may be related to YB containing complex medical plant ingredients. These ingredients can act directly or indirectly on bioactive molecules of the agr system through complex mechanisms, and different from some sub-MICs of antibiotics (such as oxacillin, etc.), which can enhance the expression of agr system [25]. In view of the fact that sub-MIC is unavoidable in the course of antibiotic treatment, YB can be used as an adjunct therapy for antibiotics and is of great promise in reducing the side effects of antibiotics on HAPU patients.

Recent studies have shown that most of the virulence factors in S. aureus are regulated by accessory gene regulator (agr) system, which contains two RNA transcription units RNA II and RNA III [22]. The transcription of RNA II and RNA III is controlled by the transcriptional promoters P2 and P3. When the synthesis of RNA II and RNA III increases, the secretion of virulence factors from S. aureus increases [22, 26]. The virulence factors of S. aureus mainly include α-hemolysin (regulated by hla), coagulase (regulated by cao), enterotoxin and toxic shock syndrome toxin-1 (tsst-1) and so on [27-29]. The virulence factor is closely related to the pathogenicity of S. aureus, because in most cases, virulence is a pathogenic prerequisite for bacteria, but it is not necessary for bacterial growth. The reason for microbial infection is that the site of infection is coordinated by a certain number of pathogenic bacteria [30, 31]. That is to say, as long as the virulence of the bacteria is completely inhibited, even if the bacteria survive, it will not cause the occurrence of infectious diseases. Therefore, the therapeutic regimen of inhibiting virulence not only achieves the purpose of treating the infection but also does not destroy the integrity of the original host flora. Due to the imbalance of bacteria, a series of changes in host immune function and infection can be avoided, which greatly reduces the pressure of antibiotic selection and reduces the probability of occurrence of drug-resistant bacteria [32, 33]. Herein, our results showed that the active ingredients of sub-MIC of YB significantly inhibited α-hemolysin, coagulase, enterotoxin B, enterotoxin C, enterotoxin D and tsst-1.

Possible contributions to these results are as follows: (1) α-hemolysin, coagulase and some enterotoxins regulated by the agr system [34]. When the sub-MIC of YB significantly inhibited the expression of RNAII and RNAIII, the expression of the relevant virulence factors regulated by the agr system was significantly decreased. (2) YB is composed of complex molecules derived from medicinal plants and it can reasonably be concluded that its mechanism or mechanism of action is also complex. These molecules may directly affect the corresponding virulence factors to reduce the production of the related virulence factors. Currently, it has been clearly demonstrated that agr-encoded proteins cannot explain all steps in the core autoinduction circuit [35]. There was no difference in sea and see mRNA expression between the experimental and control groups, as the expression of sea and see mRNA was not regulated by the agr system [36]. The above analysis shows that the regulatory mechanisms of the virulence factors such as S. aureus toxins are complex, and more efforts should be made to deal with the increasingly severe S. aureus infection.

Biofilm is closely related to the pathogenicity of S. aureus [37]. Our research results showed that YB with sub-MIC could significantly inhibited sarA, icaA and cidA mRNA expression. And the area of the largest area of the biofilm of pALC1740, pALC1742 and pALC1743 in the experimental group was significantly smaller than those in the control group when it was cultured for five days. This further confirms that YB can inhibit the formation of biofilms of S. aureus. At the initial stage of bacterial adhesion and aggregation, α-hemolysin is required for cell-to-cell interactions during biofilm formation, and the hla mutant is unable to fully colonize plastic surfaces under both static and flow conditions [38]. Therefore, the sub-MIC of YB could obviously inhibit the biofilm formation when it could obviously inhibit the gene hla. The biofilm formed in the observation group was obviously loose than that in the control group, probably because of sub-MIC of YB activity significantly inhibited extracellular DNA (eDNA) regulatory gene cidA. eDNA plays an important role in the initial stage of biofilm formation, and is the basis for the construction of mature biofilm [39].

It is worth noting that, in general, inhibition of the agr system affects the formation of S. aureus biofilm. These results suggest that YB affects S. aureus biofilm formation through multiple pathways. To sum up, YB may significantly reduce HAPU via suppressing virulence gene expression and biofilm formation of S. aureus.

Herbal therapies exert their therapeutic benefit via various mechanisms, including immune regulation, anti-oxidant activity, inhibition of leukotriene B4 and NF-κB, and antiplatelet activity [40]. HAPU is a dysregulated chronic inflammation and may be associated with S. aureus infection. Herein, we found the Chinese herbal medicine YB may be a potential antimicrobial agent with promising pharmaceutical prospect in resisting S. aureus infection on HAPU patients.

Acknowledgements

We thank Professor Ambrose L. Cheung for providing us with the pALC1740, pALC1742 and pALC1743 strains.

Fund Information

This work was supported by Traditional Chinese Medicine Bureau of Guangdong Province (20151261), Natural Science Foundation of Guangdong (2016A030313151, 2016A030313674, 2015A030310046), Science and Technology Planning Project of Guangdong Province (2017A020217002, 2016A020215224), Finance Special Project of Zhanjiang City (2013A01007, 2015A01036), and the General Projects of Guangdong Medical College (M2015007).

Competing Interests

The authors have declared that no competing interest exists.

References

1. Systematic Reviews on Preventing Pressure Ulcers: A Systematic Review. Oslo, Norway: Knowledge Centre for the Health Services at The Norwegian Institute of Public Health (NIPH). 2016

2. Healthcare Cost and Utilization Project (HCUP) Statistical Briefs. Rockville (MD): Agency for Healthcare Research and Quality (US). 2006

3. Livesley NJ, Chow AW. Infected pressure ulcers in elderly individuals. Clin Infect Dis. 2002;35(11):1390-1396

4. McNeil JC, Hultén KG, Mason EO. et al. Impact of Health Care Exposure on Genotypic Antiseptic Tolerance in Staphylococcus aureus Infections in a Pediatric Population. Antimicrob Agents Chemother. 2017;61(7):e00223-17

5. Song KH, Kim M, Kim CJ. et al. Impact of Vancomycin MIC on Treatment Outcomes in Invasive Staphylococcus aureus Infections. Antimicrob Agents Chemother. 2017;61(3):e01845-16

6. Álvarez O, Plaza-Plaza JC, Ramirez M. et al. Pharmacokinetic Assessment of Vancomycin Loading Dose in Critically Ill Patients. Antimicrob Agents Chemother. 2017;61(8):e00280-17

7. Chen F, Di H, Wang Y. et al. Small-molecule targeting of a diapophytoene desaturase inhibits S. aureus virulence. Nat Chem Biol. 2016;12(3):174-179

8. Li J, Li J, Zhang F. The immunoregulatory effects of Chinese herbal medicine on the maturation and function of dendritic cells. J Ethnopharmacol. 2015;171:184-195

9. Liu X, Guan X, Chen R. et al. Repurposing of yunnan baiyao as an alternative therapy for minor recurrent aphthous stomatitis. Evid Based Complement Alternat Med. 2012;2012:284620

10. Yang B, Xu ZQ, Zhang H. et al. The efficacy of Yunnan Baiyao on haemostasis and antiulcer: a systematic review and meta-analysis of randomized controlled trials. Int J Clin Exp Med. 2014;7(3):461-482

11. Zhao ZG, Yan SS, Yu YM. et al. An aqueous extract of Yunnan Baiyao inhibits the quorum-sensing-related virulence of Pseudomonas aeruginosa. J Microbiol. 2013;51(2):207-212

12. Chen Y, Liu T, Wang K. et al. Baicalein Inhibits Staphylococcus aureus Biofilm Formation and the Quorum Sensing System In Vitro. PLoS One. 2016;11(4):e0153468

13. Bala A, Kumar R, Harjai K. Inhibition of quorum sensing in Pseudomonas aeruginosa by azithromycin and its effectiveness in urinary tract infections. J Med Microbiol. 2011;60(Pt 3):300-306

14. Doern GV. Evaluation of a commercial latex agglutination test for identification of Staphylococcus aureus. J Clin Microbiol. 1982;15(3):416-418

15. Jungkind DL, Torhan NJ, Corman KE. et al. Comparison of two commercially available test methods with conventional coagulase tests for identification of Staphylococcus aureus. J Clin Microbiol. 1984;19(2):191-193

16. Chen G, Liang Y, Guan X. et al. Circulating low IL-23: IL-35 cytokine ratio promotes progression associated with poor prognosisin breast cancer. Am J Transl Res. 2016;8(5):2255-2264

17. Ren D, Lin B, Zhang X. et al. Maintenance of cancer stemness by miR-196b-5p contributes to chemoresistance of colorectal cancer cells via activating STAT3 signaling pathway. Oncotarget. 2017;8(30):49807-49823

18. Zhang X, Zhang L, Lin B. et al. Phospholipid Phosphatase 4 promotes proliferation and tumorigenesis, and activates Ca2+-permeable Cationic Channel in lung carcinoma cells. Mol Cancer. 2017;16(1):147

19. Espejo E, Andrés M, Borrallo RM. et al. Bacteremia associated with pressure ulcers: a prospective cohort study. Eur J Clin Microbiol Infect Dis. 2018;37(5):969-975

20. Gandra S, Barysauskas CM, Mack DA. et al. Impact of contact precautions on falls, pressure ulcers and transmission of MRSA and VRE in hospitalized patients. J Hosp Infect. 2014;88(3):170-176

21. Arroliga AC, Velazco JF, Midturi JK. et al. Back to the future: α-hemolysin activity on blood agar to predict ventilator-associated pneumonia caused by Staphylococcus aureus. Am J Respir Crit Care Med. 2014;190(10):1086-1088

22. Painter KL, Krishna A, Wigneshweraraj S. et al. What role does the quorum-sensing accessory gene regulator system play during Staphylococcus aureus bacteremia. Trends Microbiol. 2014;22(12):676-685

23. Morfeldt E, Tegmark K, Arvidson S. Transcriptional control of the agr-dependent virulence gene regulator, RNAIII, in Staphylococcus aureus. Mol Microbiol. 1996;21(6):1227-1237

24. Novick RP, Ross HF, Projan SJ. et al. Synthesis of staphylococcal virulence factors is controlled by a regulatory RNA molecule. EMBO J. 1993;12(10):3967-3975

25. Rudkin JK, Laabei M, Edwards AM. et al. Oxacillin alters the toxin expression profile of community-associated methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 2014;58(2):1100-1107

26. Vasquez JK, Tal-Gan Y, Cornilescu G. et al. Simplified AIP-II Peptidomimetics Are Potent Inhibitors of Staphylococcus aureus AgrC Quorum Sensing Receptors. Chembiochem. 2017;18(4):413-423

27. Pollitt EJ, West SA, Crusz SA. et al. Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus. Infect Immun. 2014;82(3):1045-1051

28. Wiemels RE, Cech SM, Meyer NM. et al. An Intracellular Peptidyl-Prolyl cis/trans Isomerase Is Required for Folding and Activity of the Staphylococcus aureus Secreted Virulence Factor Nuclease. J Bacteriol. 2017:199 (1)

29. Yanagihara K, Tashiro M, Fukuda Y. et al. Effects of short interfering RNA against methicillin-resistant Staphylococcus aureus coagulase in vitro and in vivo. J Antimicrob Chemother. 2006;57(1):122-126

30. Cardona PJ, Asensio JG, Arbués A. et al. Extended safety studies of the attenuated live tuberculosis vaccine SO2 based on phoP mutant. Vaccine. 2009;27(18):2499-2505

31. Wu T, Grassel C, Levine MM. et al. Live attenuated Shigella dysenteriae type 1 vaccine strains overexpressing shiga toxin B subunit. Infect Immun. 2011;79(12):4912-4922

32. Maisuria VB, Los SYL, Tufenkji N. et al. Cranberry-derived proanthocyanidins impair virulence and inhibit quorum sensing of Pseudomonas aeruginosa. Sci Rep. 2016;6:30169

33. Tsou LK, Dossa PD, Hang HC. Small molecules aimed at type III secretion systems to inhibit bacterial virulence. Medchemcomm. 2013;4(1):68-79

34. Castillo-Juárez I, Maeda T, Mandujano-Tinoco EA. et al. Role of quorum sensing in bacterial infections. World J Clin Cases. 2015;3(7):575-598

35. Wang B, Muir TW. Regulation of Virulence in Staphylococcus aureus: Molecular Mechanisms and Remaining Puzzles. Cell Chem Biol. 2016;23(2):214-224

36. Tseng CW, Zhang S, Stewart GC. Accessory gene regulator control of staphyloccoccal enterotoxin d gene expression. J Bacteriol. 2004;186(6):1793-1801

37. Tan X, Yang D, Yang G. et al. The investigation of inhibiting quorum sensing and methicillin-resistant Staphylococcus aureus biofilm formation from Liriodendron hybrid. Pak J Pharm Sci. 2015;28(3):903-908

38. Caiazza NC, O'Toole GA. Alpha-toxin is required for biofilm formation by Staphylococcus aureus. J Bacteriol. 2003;185(10):3214-3217

39. Thomas VC, Thurlow LR, Boyle D. et al. Regulation of autolysis-dependent extracellular DNA release by Enterococcus faecalis extracellular proteases influences biofilm development. J Bacteriol. 2008;190(16):5690-5698

40. Triantafillidis JK, Triantafyllidi A, Vagianos C. et al. Favorable results from the use of herbal and plant products in inflammatory bowel disease: evidence from experimental animal studies. Ann Gastroenterol. 2016;29(3):268-281

Author Biography

Dr. Jincheng Zeng is an assoicate professor of medical technology at Guangdong Medical University, a director of Dongguang key Laboratory of Medical Bioactive Molecular Development and Translational Research, an assistant director of Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, and a visiting scholar at University of Pennsylvania School of Dental Medicine. The current research interests in the Dr. Zeng's group is to reveal the role of cellular polyamine metabolism on tumor and infection immunity, as well as the development of medical bioactive molecular against polyamine metabolism.

Riming Huang gained his Ph.D. degree from South China Sea Institute of Oceanology, Chinese Academy of Sciences, majoring in Marine Chemistry (mainly in marine natural products), in 2010. After graduation, he became an Assistant Professor and Associated Professor at South China Botanical Garden, Chinese Academy of Sciences in Guangzhou, China. He was academic visitor at University of Bath (UK) during 2014 to 2015. Since 2016, he becomes a Professor at South China Agricultural University. His current research focuses on the isolation, structure elucidation and biological characterization of polysaccharides or oligosaccharides from marine algae.

Corresponding author: Dr. Jincheng Zeng, E-mail: zengjcedu.cn Dongguan Key Laboratory of Medical Bioactive Molecular Developmental and Translational Research, Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Guangdong Medical University, Dongguan 523808, China, Phone: +86 769 22896440; Dr. Riming Huang, E-mail: huangrimingedu.cn College of Marine Science, South China Agricultural University, Guangzhou 510642, China, Phone: +86 20 8528 3448.

Received 2019-1-31
Accepted 2019-5-17
Published 2019-7-21

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