Effect of a Multispecies Probiotic on Intestinal and Skin Colonization by Multidrug-Resistant Gram-Negative Bacteria in Patients in a Long-Term Care Facility: A Pilot Study
by
,
Ines Zollner-Schwetz
1,*, 
Monika Scarpatetti
2,
Gerald Pichler
2,
Christian Pux
2,
Ingeborg Klymiuk
3,
Slave Trajanoski
3 and
Robert Krause
1 
1
Section of Infectious Diseases and Tropical Medicine, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, 8036 Graz, Austria
2
Geriatric Health Centres of the City of Graz, Albert-Schweitzer-Gasse 36, 8020 Graz, Austria
3
Core Facility Molecular Biology, Centre for Medical Research, Medical University of Graz, Stiftingtalstraße 24/1, 8010 Graz, Austria
*
Author to whom correspondence should be addressed.
Nutrients 2020, 12(6), 1586; https://0-doi-org.brum.beds.ac.uk/10.3390/nu12061586
Submission received: 23 April 2020
/
Revised: 20 May 2020
/
Accepted: 27 May 2020
/
Published: 28 May 2020
(This article belongs to the Special Issue Role of Prebiotics and Probiotics in Health and Disease)
Abstract
:Residents in long-term care facilities (LTCFs) are frequently colonized by multidrug-resistant Gram-negative bacteria, putting them at risk for subsequent infections. We aimed to evaluate the effect of the multispecies probiotic Omnibiotic10AAD® on the intestinal and inguinal skin colonization of patients by multidrug-resistant Gram-negative bacteria in LTCFs. Patients colonized by multidrug-resistant Gram-negative bacteria received a 12 week oral course of Omnibiotic10AAD®. Inguinal swabs and stool samples were collected during and after treatment for microbiological and microbiome analysis. The median age of patients was 76 years. Twelve patients completed the pilot study. Intestinal colonization was reduced to 42% of patients 8 weeks after the end of treatment, but increased to 66% 24 weeks after the end of probiotic treatment. Colonization of inguinal skin was lowest during probiotic treatment and increased thereafter. Fecal microbiome analysis revealed statistically significant increases of the genus Enterococcus comparing start and end of probiotic treatment. In conclusion, a 12 week course of a multispecies probiotic led to a transient reduction of intestinal colonization 8 weeks after the end of treatment. The findings of our pilot study warrant further research in the area of probiotics and intestinal colonization by multidrug-resistant bacteria.
1. Introduction
Infections due to multidrug-resistant Gram-negative bacteria have become a serious health concern worldwide and lead to elevated health care costs and increased mortality [1,2]. These organisms are capable of colonizing the human gastrointestinal tract, which then constitutes a reservoir in hospitals and in the community [3,4]. Asymptomatic carriage of these organisms carries the risk of subsequent infection, but also implies a potential source of transmission to others, in particular in hospital settings [5,6]. Factors such as fecal incontinence and diarrhea contribute to the subsequent dissemination of pathogens into health care environments. The risk of transmission renders colonization by multidrug-resistant Gram-negative bacteria an important issue in infection control. Several studies have demonstrated that residents in long-term care facilities (LTCFs) are frequently colonized by multidrug-resistant Gram-negative bacteria with rates varying from 4.7% to 64% [6,7,8,9,10].
Efforts to curb gastrointestinal carriage of multidrug-resistant Gram-negatives have included oral administration of nonabsorbable antimicrobial agents such as neomycin and polymyxin E with very limited long-term effects [11,12]. Furthermore, this approach has led to the development of additional antimicrobial resistance in colonizing bacteria [13]. As a consequence, decolonization using antimicrobial agents is not recommended by international societies [14]. Fecal microbiota transplantation (FMT), that is, administration of healthy donor stool into a patient’s gut, has also been studied as a possibility to eradicate multidrug-resistant bacteria from the intestinal tract with varying degrees of success [15,16,17]. However, FMT may not be feasible for all patients affected by intestinal colonization by multidrug-resistant bacteria.
Probiotics are defined as live microbial food supplements with health-promoting attributes when administered in adequate amounts [18]. They have been suggested as a possibility to counteract intestinal colonization by multidrug-resistant bacteria [19]. Several mechanisms of action of probiotics have been proposed, such as (1) colonization of the intestinal tract, preventing colonization by pathogens, a mechanism termed “colonization resistance”; (2) production of toxins and acids to inhibit growth of pathogens; (3) improvement of intestinal barrier function, hence reducing adherence of pathogens to the mucosa; (4) modulation of the host immune system [19,20,21,22].
The aims of our pilot study were to evaluate the effect of the multispecies probiotic Omnibiotic10 AAD® (Institut Allergosan, Graz, Austria) on the intestinal and inguinal skin colonization of patients by multidrug-resistant Gram-negative bacteria in LTCFs in the Geriatric Health Centers Graz, Austria and to evaluate effects of the probiotic on stool and skin microbiome. We chose this particular probiotic formula on the basis of its in vitro characteristics to inhibit growth of intestinal bacteria and to survive a low pH as well as bile [23]. In a study in healthy volunteers taking amoxicillin, intake of this multispecies probiotic led to a significant increase in the mean number of enterococci in stool [23]. Furthermore, clinical observations by one of the authors (M.S.) suggested efficacy of Omnibiotic10 AAD® in eliminating colonization by multidrug-resistant Acinteobacter baumannii isolates following an outbreak [24].
2. Materials and Methods
2.1. Setting
The Geriatric Health Centers Graz is a local institution comprising, among others, an apallic care unit (ACU) caring long term for patients with disorders of consciousness and three long-term geriatric wards. Patients who are treated at the long-term geriatric wards (total of 90 beds) are chronically ill, elderly patients who need constant medical attention.
Upon admission to the ACU and the geriatric wards, all patients are routinely screened for colonization by multidrug-resistant bacteria, including multidrug-resistant Gram-negative bacteria (Pseudomonas aeruginosa, Acinetobacter baumannii, enterobacteriaceae including extendend sprectrum betalactamase (ESBL)-producers). This initial screening is part of the local infection control strategy. All patients who were colonized by multidrug-resistant Gram-negative (MRGN) bacteria as defined by the Robert Koch Institute, Germany, in the gastrointestinal tract were eligible for the study [25]. Patients were excluded if they had a history of solid organ transplantation or allogeneic hematopoietic stem cell transplantation, an active hematooncological malignancy or neutropenia, acute pancreatitis, or an ongoing immunosuppressive therapy [26]. Demographic data were obtained at study initiation. Collected variables included age, sex, functional status (bedridden or mobile, incontinence), presence of an enteral feeding tube, urinary catheter, comorbidities, and current medication including proton pump inhibitors and any immunosuppressive agents. Informed written consent was obtained from the patients or their legal representatives. The study was approved by the local ethics committee (votum number: 29-569 ex 16/17, Medical University of Graz).
2.2. Study Design
All patients received Omnibiotic AAD 10® (Institut Allergosan, Graz, Austria) twice daily orally or via the enteral feeding tube for 3 months. It consists of 10 different bacterial strains: Enterococcus faecium W54, Lactobacillus acidophilus W55 and W37, L. paracasei W72, L. rhamnosus W71, L. salivarius W24, L. plantarum W62, Bifidobacterium bifidum W23, B. lactis W18, und B. longum W51. Patients were screened for side effects during the study by measuring body temperature daily and daily visits by treating physicians looking for signs and symptoms (including nausea, diarrhea, discomfort, loss of appetite, etc.).
Inguinal skin swabs were collected by local nursing staff following a standardized procedure. Screening was scheduled in the morning ward round before bathing and dressing the patients. Stool samples were collected by local nursing staff. Both inguinal swabs and stool samples were collected at the start of the study before probiotic treatment was initiated, followed by samples at weeks 4, 8, 12, 16, 20, 24, and 36 (Figure 1). The primary endpoint was successful intestinal decolonization, defined as two consecutive MRGN-negative stool samples at weeks 24 and 36. The secondary endpoint was successful decolonization from skin, defined as two consecutive MRGN-negative skin samples at weeks 24 and 36.
2.3. Microbiological Methods
The swabs (Transystem, Copan, Brescia, Italy) and stool samples were transported immediately to the microbiological laboratory of the Section of Infectious Diseases and Tropical Medicine at the Medical University of Graz. Samples were plated on ChromID ESBL® and McConkey agars (bioMerieux, Marcy l’Etoile, France). The plates were incubated under aerobic conditions at 36 °C and were evaluated for growth after 24 and 48 h. Suspected colonies were identified to species level using MALDI-TOF (Bruker, Billerica, MA, USA), and antimicrobial susceptibility was tested by disk diffusion according to European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoints. Extended betalactamase (ESBL) production was determined with Clinical and Laboratory Standards Institute (CLSI) confirmatory test using Etest strips (bioMerieux, Marcy l’Etoile, France). Isolates were classified as 3MRGN or 4MRGN according to the Robert Koch Institute guidance document [25]. In brief, isolates resistant to three out of four relevant antimicrobial classes (acylureidopenicillin, third/fourth-generation cephalosporins, carbapenems, fluoroquinolones) were classified as 3MRGN. Enterobacteriaceae resistant to carbapenems were classified as 4MRGN even if the isolate remained susceptible to one other antibiotic class. Isolates resistant to all four classes were classified as 4MRGN. All isolates were stored at −70 °C for analysis of genetic relatedness by whole-genome sequencing at the end of the study. Swabs for skin microbiome analysis (FLOQ Swabs, Copan, Brescia, Italy) and stool samples for microbiome analysis were taken at the same time as microbiological samples and were stored at −70 °C for analysis at the end of the study.
2.4. Whole-Genome Sequencing
From each patient, the isolates with identical phenotypes in terms of antimicrobial susceptibility were selected as follows: one isolate from stool at the start of the study, one isolate from stool during the study, and at least one isolate from skin. Table A2 shows all isolates that were selected with their susceptibility patterns. For E. coli isolates, genomic DNA isolation, genome library preparation using Nextera XT chemistry (Illumina Inc., San Diego, CA, USA), and whole-genome sequencing using an Illumina MiSeq instrument (Illumina Inc., San Diego, CA, USA) were performed as described previously [27]. Assessment of the core genome multilocus sequence typing (cgMLST) was done using the Enterobase cgMLST scheme (Enterobase.warwick.ac.uk. Available at: http://enterobase.warwick.ac.uk). Assembled genomes were compared using the Enterobase core genome (cg)MLST scheme (http://enterobase.warwick.ac.uk) using SeqSphere+ with a cluster type threshold (CT) of ten allelic differences. For K. pneumoniae isolates, extraction of genomic DNA, genomic library preparation, and whole-genome sequencing was performed as described [28]. For phylogenetic analysis, the classical multilocus sequence type (MLST) and the cgMLST were extracted from the whole-genome sequence data [29]. Based on the defined K. pneumoniae sensu lato cgMLST in SeqSphere+, comprising 2358 target genes, a gene-by-gene approach was used to compare genomes. Isolates were visualized as minimum spanning trees (MST), and genotypically related isolates were identified with a Complex Type Distance of 15 alleles (https://www.cgmlst.org/ncs/schema/2187931/).
2.5. DNA Isolation for Microbiome Analysis, 16S rRNA Gene PCR Amplification and Sequencing
Total DNA was isolated from stool samples as well as dermal swab samples by mechanic and enzymatic lysis according to standard procedures as published in Klymiuk et al. [30]. Briefly, dermal swabs were put into 250 µL PBS (Roth, Karlsruhe, Germany) with 250 µL bacterial lysis buffer (Roche, Mannheim, Germany) and vortexed vigorously. Of the solution, 250 µL was transferred to MagnaLyser tubes (Roche, Mannheim, Germany) and homogenized at 6500 rpm for 30 s, two times each in a MagnaLyser instrument (Roche, Mannheim, Germany). After adding 25 µL lysozyme (100 mg/mL, Roth), samples were incubated at 37 °C for 30 min, treated with proteinase K (20 mg/mL) at 65 °C for 60 min, and incubated at 95 °C for 10 min for inactivation. Total DNA was extracted from 250 µL lysed supernatant on a MagNA Pure LC 2.0 (Roche, Mannheim, Germany) according to manufacturer’s instructions with the MagNA Pure LC DNA Isolation Kit III (Bacteria, Fungi) (Roche, Mannheim, Germany). Similarly, 175 mg of stool sample was homogenized in 500 µL PBS, and 250 µL of the suspensions was used with 250 µ bacterial lysis buffer for DNA isolation as described above. Empty tubes as negative controls were run with each isolation batch. Of total DNA, 2 µL (for stool samples) to 5 µL (for dermal samples) was used in a 25 µL PCR reaction in triplicate using a FastStart High Fidelity PCR system (Roche, Mannheim, Germany) according to Klymiuk et al. with the target specific primers F27-AGAGTTTGATCCTGGCTCAG and R357- CTGCTGCCTYCCGTA [30,31]. The 6 pM library was sequenced on an Illumina MiSeq desktop sequencer (Eindhoven, Netherlands) with 20% PhiX control DNA (Illumina, Eindhoven, Netherlands) and v3 chemistry for 600 cycles in paired-end mode according to manufacturer’s instructions. FastQ raw reads were used for subsequent data analysis. A total of 3,847,966 (stool) and 3,201,263 (dermal swabs) MiSeq paired-end raw sequence forward and reverse reads were quality-filtered, denoised, dereplicated, merged, and checked for chimeras using DADA2 pipeline [32] with standard settings as implemented in QIIME2 2018.7 microbiome bioinformatics platform [33]. Taxonomic assignment of the DADA2 representative sequence set was provided with the QIIME2 sklearn-based classifier against SILVA rRNA database Release 132 at 99% identity [34]. Phylogenetic tree was created with FastTree on Mafft-aligned representative sequences [35,36]. Finally, the DADA2-generated feature table was reduced by removing all features present in only one sample with less than 10 reads (singletons). Further downstream statistical data analysis including alpha and beta diversity was conducted with the R 3.5.1 program for statistical computing (https://www.R-project.org). To calculate the size factors for the normalization of the feature table we used GMPR method, and for the differential taxa analysis between investigated groups count-based regression model DESeq2 was applied [37,38].
3. Results
3.1. Patients’ Characteristics
Stool samples of 132 patients at the Geriatric Health Centers Graz were screened for multidrug-resistant Gram-negative bacteria. Thirty-two samples were positive. Eleven patients or their legal representatives did not give their consent to participate in the study. Therefore, twenty-one patients were included in the study (median age 76 years, range 19–100; 8/21 female). The mean duration of stay at the wards was 55 ± 55 months, range 1–191. Clinical characteristics are summarized in Table 1. During the study, one patient was transferred to a different long-term care facility and was lost to follow-up. Eight patients died (five after cessation of probiotic treatment). Causes of death were pneumonia (n = 2), aspiration pneumonia (n = 3), heart failure (n = 2), stroke (n = 1). Patient charts were reviewed by two independent investigators. There was no evidence suggestive of a causal relationship between probiotic treatment and death. One patient suffered from loss of appetite as a side effect of probiotic treatment. Twelve patients completed the study. Of those, seven were treated with proton pump inhibitors throughout the study. Of the patients who completed the study, 5/12 received antibiotic treatment (4 with amoxicillin/clavulanate, 1 with cefuroxime; 3 during probiotic treatment, 2 after probiotic treatment). In supplement B, Table 1, patients who received antibiotics are marked.
3.2. Prevalence of Colonization by MRGN Bacteria During and after Probiotic Treatment
3.1.1. Stool
At the beginning of the study, all patients (n = 12, those who completed the study) were colonized by multidrug-resistant Gram negatives: 8/12 by E. coli, 3 by Klebsiella spp., and 1 by Pseudomonas aeruginosa. At the end of the probiotic treatment (week 12), 9/12 patients were still colonized (per protocol analysis, omitting those lost to follow-up). At weeks 20 and 24, only 42% of patients (5/12) were colonized. At week 36, 66% (8/12) were colonized (Figure 2). The primary endpoint (two consecutive MRGN-negative stool samples at weeks 24 and 36) was met by 4/12 patients (4/9 patients from ACU and 0/3 patients from the geriatric wards). A detailed summary of all MRGN isolates of all patients who completed the study is given in Appendix B, Table A1.
3.1.2. Skin
At the beginning of the study, 7 of 12 patients who completed the study were colonized by multidrug-resistant Gram negatives on their inguinal skin: 2 by E. coli, 3 by Klebsiella spp., 1 by Pseudomonas aeruginosa, and 1 by Acinetobacter baumannii. Colonization of the skin in the inguinal regions decreased during probiotic treatment (to 14% at week 4, 28% at weeks 8 and 12). After the end of the treatment period, there was an increase up to 71% at week 20 in the per protocol analysis including the 7 patients who were initially colonized and completed the study (Figure 3). The secondary endpoint (two consecutive MRGN-negative skin samples at week 24 and 36) was met by 3/7 patients (1/5 patients from ACU and 2/2 patients from the geriatric wards).
3.3. Genetic Relatedness of E. coli and K. pneumoniae Isolates
A total of 18 E. coli isolates from 6 patients were analyzed by core genome multilocus sequence typing. E. coli isolates of four patients were all found to be ST 131. However, isolates from different patients differed in complex type. Isolates from patients 16 and 18 were found to be ST 354 and ST 38, respectively (Appendix A, Figure A1). Each patient was colonized by the same ST and complex type throughout the study period. A total of 7 K. pneumoniae isolates from 2 patients were analyzed. K. pneumoniae core genome multilocus sequence typing of 7 isolates from 2 patients revealed ST 15 for all isolates. The differences in alleles were below the threshold of 15 alleles (i.e., the isolates were identical). Both patients stayed at the same ward (Appendix A, Figure A2).
3.4. Microbiome Analysis
3.4.1. Stool
The stool microbiome of five randomly selected patients was analyzed at four different time points (start before probiotic treatment, week 12 = end of probiotic treatment, week 24, and week 36). There was no significant difference in alpha-diversity (Shannon Diversity Index) and beta-diversity (Weighted UniFrac distances) comparing different time points (i.e., start, end of treatment, weeks 24 and 36). In-depth analysis revealed statistically significant increases of the genera Enterococcus and Tyzzerella (Figure 4) comparing start and week 12 (p = 0.006 and p = 0.0008, respectively). There was a statistically significant increase of the genus Ruminococcus comparing start with week 24 (adjusted p = 0.02) and of the family Actinomycetaceae comparing start with week 36 (adjusted p = 0.02).
3.4.2. Skin
Swabs were taken from the inguinal region of the skin. The skin microbiome of the same randomly selected five patients was analyzed at four different time points (start before probiotic treatment, week 12 = end of probiotic treatment, week 24, und week 36). There was no significant difference in alpha-diversity (Shannon Diversity Index) and beta-diversity (Weighted UniFrac distances) comparing different time points. In-depth analysis revealed statistically significant increases of the genera Aerococcus and Actinotignum (Figure 4) comparing start and week 12 (adjusted p = 0.005 and p = 0.002, respectively). In addition, there were significant increases of the order Actinomycetales and the family Actinomycetacae of which Actinotignum is a part (adjusted p = 0.006 and p = 0.004) comparing start and week 12.
4. Discussion
This pilot study aimed to assess the effect of the multispecies probiotic Omnibiotic AAD 10® on colonization by multidrug-resistant Gram-negative bacteria in patients in LTCFs. Notable findings were (1) intestinal colonization was reduced to 42% of patients 8 weeks after the end of treatment (week 20); (2) fecal microbiome analysis revealed statistically significant increases of the genus Enterococcus comparing start and week 12 (end of probiotic treatment); (3) colonization of inguinal skin was lowest during probiotic treatment.
We expected a decrease in the intestinal colonization during probiotic treatment. However, the prevalence of intestinal colonization by multidrug-resistant Gram-negative bacteria decreased only to 75% at the end of probiotic treatment at week 12, followed by a marked reduction to 42% 8 and 12 weeks after the end of treatment (i.e., weeks 20 and 24). Fecal microbiome analysis revealed a significant increase in the genus Ruminococcaceae at week 24. In contrast, the genus Enterococcus significantly increased at the end probiotic treatment (week 12) but not later on. Enterococcus faecium was a component of the multispecies probiotic used in the study. Our findings suggest that even the transient changes of the fecal microbiome may influence colonization by MRGN bacteria. Even though the probiotic strains Lactobacillus rhamnosus and L. paracasei inhibited the growth of various Gram-negative bacteria, including E.coli, Klebsiella spp. and P. aeruginosa, in vitro [39], direct antimicrobial activity of probiotic strains, such as production of toxins or acids to inhibit the growth of other bacteria, are less likely to have played a role in our study.
At week 36, two patients who were negative for MRGN bacteria at weeks 20 and 24 were positive for MRGN bacteria that had not been detected before in these patients. This finding suggests a new colonization from the environment of the LTCF. One could speculate that a combination of repeated probiotic treatment and enforced infection control could be a successful strategy for maintaining a decolonized status.
Ljungquist et al. recently published a placebo-controlled clinical trial using a different multispecies probiotic (Vivomixx®) in patients with intestinal colonization by ESBL-producing enterobacteria [40]. Successful intestinal decolonization was achieved only in 12.5% in the probiotics group compared with 5% in the control group, a difference that was not statistically significant. The probiotic used in the study consisted of Lactobacillus spp., Bifidobacterium spp., and Streptococcus thermophiles, according to the producers. The probiotic used in our study also contained Lactobacillus spp. and Bifidobacterium spp. but in addition, E. faecium, a species that was found to have increased significantly in numbers at the end of the treatment (week 12) in the microbiome analysis. Results on the potential for intestinal decolonization cannot be generalized between different probiotics.
We chose to study inguinal swabs as inguinal colonization is thought to have a high impact on cross-transmission in health care settings and is of importance in terms of infection control [6]. Inguinal skin is assumed to be colonized by MRGN bacteria from the intestinal tract, particularly in patients suffering from fecal incontinence. This assumption is supported by the detection of genetically identical E. coli and K. pneumoniae isolates from stool and inguinal skin of the same patient in our study. A possibly favorable effect of oral probiotics on skin colonization could unfold by similar mechanisms. However, recent evidence suggests that the intestinal microbiota and their metabolites also impact cutaneous physiology and immune response in a complex fashion via the “gut–skin axis” [41].
Probiotics have been demonstrated to exert beneficial effects on skin health [42,43,44]. For example, a two month supplementation of Lactobacillus paracasei decreased skin sensitivity and increased the rate of barrier function recovery in a placebo-controlled trial [43]. In our study, the prevalence of inguinal colonization by MRGN bacteria was lowest during probiotic treatment and increased steadily thereafter. As most patients were colonized by various different bacteria in the inguinal region that were not found in their intestinal tract, recolonization from the environment is likely to have occurred in addition to colonization from the intestinal tract. Significant increases of the taxa Aerococcus and Actinotignum were detected in skin microbiome at the end of probiotic treatment (week 12) but not later on. This could suggest that probiotic strains led to a transient change in skin microbiome which, in turn, reduced colonization by MRGN Gram-negative bacteria.
Intestinal and skin colonization by MRGN K. pneumoniae and E. coli persisted throughout the study period in serval patients. For example, patient 16 was colonized by genetically identical E. coli isolates at the start of the study and at week 36. This is in line with data from a meta-analysis from 2016 which found that a significant proportion of carriers of ESBL-producing enterobacteria remained colonized for up to one year in health care settings [45]. Two patients (6 and 20) staying at the same ward were colonized by genetically identical K. pneumoniae isolates. This finding could indicate cross-contamination between patients by staff may have taken place, as has been described before [24]. Due to financial constraints, not all isolates could be analyzed by whole genome sequencing. Selection of the isolates was based on susceptibility testing patterns, which may have led to selection bias.
In our study, the probiotic was safe and tolerated. Side effects (loss of appetite) occurred only in one patient. This is in accordance to a recent meta-analysis that found probiotics to be safe in the elderly [46]. However, it should be kept in mind that patients with active hematooncological malignancy, neutropenia, acute pancreatitis, or an ongoing immunosuppressive therapy were excluded from the study.
This study has several strengths. Adherence to the interventional product was very high because all patients stayed at a LTCF during the study period. Microbiological testing was performed frequently, that is, once a month until week 24, followed by a final examination at week 36. The major limitations of the study are the lack of a placebo-controlled design and the limited number of participants, which are limitations owing to the design as a pilot study. However, our findings justify future research on the effects of the multispecies probiotic Omnibiotic AAD 10® on intestinal colonization. In addition, we only included patients from LTFCs in our study. These patients are likely to be different in many physiologic aspects compared with elderly persons living at home. Our findings may not be generalizable to other groups of patients. Furthermore, none of the patients who finished the trial experienced infections due to multidrug-resistant Gram-negative bacteria. In conclusion, a 12 week course of the multispecies probiotic Omnibiotic AAD 10® led to a reduction of intestinal colonization 8 weeks after the end of treatment. Our findings warrant further research in the area of probiotics and intestinal colonization by MRGN bacteria.
Author Contributions
Conceptualization, I.Z.-S. and M.S.; methodology, C.P. and I.K.; software, S.T.; formal analysis, S.T.; writing—original draft preparation, I.Z.-S.; writing—review and editing, G.P. and R.K.; data curation, M.S. and C.P.; supervision, C.P.; grant acquisition, I.Z.-S. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by an investigator-initiated research grant by Institut Allergosan, Graz, Austria.
Conflicts of Interest
The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
Appendix A
Figure A1.
Results of core genome multilocus sequence typing in 18 E. coli isolates (cluster distance threshold 10).
Figure A1.
Results of core genome multilocus sequence typing in 18 E. coli isolates (cluster distance threshold 10).
Figure A2.
Results of core genome multilocus sequence typing in 7 K. pneumoniae isolates (cluster distance threshold 15).
Figure A2.
Results of core genome multilocus sequence typing in 7 K. pneumoniae isolates (cluster distance threshold 15).
Appendix B
Table A1.
Antimicrobial susceptibility of MRGN isolates that were selected for whole genome sequencing
Table A1.
Antimicrobial susceptibility of MRGN isolates that were selected for whole genome sequencing
| Isolate | Amox/clav | Pip | Pip/Taz | CAZ | Cefepim | Mero | Imi | Cipro | Azt | Genta | ESBL |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Patient 6 | |||||||||||
| K. pneumoniae (week 0, stool) | R | R | S | R | R | S | S | R | R | R | + |
| K. pneumoniae (week 24, stool) | R | R | S | R | R | S | S | R | R | R | + |
| K. pneumoniae (week 8, skin) | R | R | S | R | R | S | S | R | R | R | + |
| Patient 20 | |||||||||||
| K. pneumoniae (week 0, stool) | R | R | S | R | R | S | S | R | R | R | + |
| K. pneumoniae (week 12, stool) | R | R | S | R | R | S | S | R | R | R | + |
| K. pneumoniae (week 4, skin) | R | R | S | R | R | S | S | R | R | R | + |
| K. pneumoniae (week 36, skin) | R | R | S | R | R | S | S | R | R | R | + |
| Patient 15 | |||||||||||
| E. coli (week 0, stool) | R | R | S | R | R | S | S | R | R | S | + |
| E. coli (week 36, stool) | R | R | S | R | R | S | S | R | R | S | + |
| E. coli (week 12, skin) | R | R | S | R | R | S | S | R | R | S | + |
| Patient 19 | |||||||||||
| E. coli (week 0, stool) | R | R | S | R | R | S | S | R | R | S | + |
| E. coli (week 8, stool) | R | R | S | R | R | S | S | R | R | S | + |
| E. coli (week 0, skin) | R | R | S | R | R | S | S | R | R | S | + |
| Patient 13 | |||||||||||
| E. coli (week 0, stool) | R | R | S | R | R | S | S | R | R | R | + |
| E. coli (week 36, stool) | R | R | S | R | R | S | S | R | R | R | + |
| E. coli (week 4, skin) | R | R | S | R | R | S | S | R | R | R | + |
| Patient 16 | |||||||||||
| E. coli (week 0, stool) | R | R | S | R | R | S | S | R | R | R | + |
| E. coli (week 36, stool) | R | R | S | R | R | S | S | R | R | R | + |
| E. coli (week 20, skin) | R | R | S | R | R | S | S | R | R | R | + |
| Patient 18 | |||||||||||
| E. coli (week 0, stool) | R | R | S | R | R | S | S | R | R | R | + |
| E. coli (week 12, stool) | R | R | S | R | R | S | S | R | R | R | + |
| E. coli (week 8, skin) | R | R | S | R | R | S | S | R | R | R | + |
| Patient 21 | |||||||||||
| E. coli (week 4, stool) | R | R | S | R | R | S | S | R | R | R | + |
| E. coli (week 16, stool) | R | R | S | R | R | S | S | R | R | R | + |
| E. coli (week 24, skin) | R | R | S | R | R | S | S | R | R | R | + |
E. coli = Escherichia coli; K. pneumoniae = Klebsiella pneumonia, S = susceptible, R= resistant according to EUCAST. Amox/clav = amoxicillin/clavulanate; Pip = piperacillin, Pip/Taz = piperacillin/tazobactam; CAZ = ceftazidime; Mero = meropenem; Imi = imipenem; Cipro = ciprofloxacin; Azt = aztreonam; Genta = gentamicin, ESBL = extended betalactamase.
Table A2.
Colonization by 3MRGN or 4MRGN bacteria in stool and inguinal skin of 12 patients who completed the study.
Table A2.
Colonization by 3MRGN or 4MRGN bacteria in stool and inguinal skin of 12 patients who completed the study.
| Patient | Start | Week 4 | Week 8 | Week 12 | Week 16 | Week 20 | Week 24 | Week 36 | |
|---|---|---|---|---|---|---|---|---|---|
| 1 | Stool | E. coli | - | - | - | - | - | - | - |
| Skin | A. baumannii | - | - | - | - | A. baumannii | A. baumannii | A. baumannii | |
| 2 | Stool | K. oxytoca | - | K. oxytocaAC | K. oxytoca | - | - | - | - |
| Skin | - | - | K. oxytoca | K. oxytoca | - | - | - | A. baumanni | |
| 5 | Stool | E. coli | E. coli/ K. aerog. | E. coli | E. coli | E. coli | - | E. coli | E. coli |
| Skin | E. cloacae | - | - | - | E. coli | E. coli | - | - | |
| 6 | Stool | K. pneumoniae# | K. pneumoniae | K. pneumoniaeC | - | K. pneumoniae | K. pneumoniae | K. pneumoniae# | K. pneumoniae |
| Skin | - | K. pneumoniae | K. pneumoniae# | K. pneumoniae | K. pneumoniae | - | - | - | |
| 12 | Stool | P. aeruginosa | P. aeruginosa | P. aeruginosa | P. aeruginosa | P. aeruginosa | - | - | - |
| Skin | - | - | - | - | - | - | - | - | |
| 13 | Stool | E. coli * | E. coli | - | E. coli | E. coli | - | E. coli | E. coli* |
| Skin | - | E. coli * | E. coli | E. coli | - | E. coli | E. coli | - | |
| 15 | Stool | E. coli§ | - | E. coli | E. coli | E. coli | E. coli | E. coli | E. coli§ |
| Skin | E. coli | - | - | E. coli§ | - | E. coli | - | - | |
| 16 | Stool | E. coli& | E. coli | E. coli | E. coli | E. coli | E. coli | E. coli | E. coli& |
| Skin | K. pneumoniae | - | K. pneumoniae | K. pneumoniae | K. pneumoniae | E.coli&/K. pn. | - | K. pneumoniae | |
| 18 | Stool | E. coli$ | E. coliAC | - | E. coli$ | A. baumannii | - | - | M. morganii |
| Skin | P. aeruginosa | A. baumannii | E. coli$ | - | A. baumannii | A. baumannii | A. baumannii | P. aeruginosa | |
| 19 | Stool | E. coli ° | E. coli | E. coli° | - | - | - | - | M. morganii |
| Skin | E. coli ° | - | - | - | - | - | - | - | |
| 20 | Stool | K. pneumoniae# | K. pneumoniae | K. pneumoniae | K. pneumoniae# | K. pneumoniaeAC | K. pneumoniae | - | - |
| Skin | - | K. pneumoniae# | K. pneumoniae | K. pneumoniae | K. pneumoniae | K. pneumoniae | - | K. pneumoniae# | |
| 21 | Stool | E. coli | E. coli ** | E. coli | E. coli | E. coli ** | E. coli | -AC | K. pneumoniae |
| Skin | E. coli | - | E. coli | - | - | - | E. coli ** | E. coli |
E. coli = Escherichia coli; A. baumannii = Acinetobacter baumannii, K. aerog. = Klebsiella aerogenes; K. oxytoca = Klebsiella oxytoca; K. pn. = K. pneumoniae = Klebsiella pneumoniae; E. cloacae = Enterobacter cloacae; M. morganii = Morganella morganii. # These K. pneumoniae isolates were sequence type 15 belonging to the same cluster.AC = amoxicillin/clavulanate, C = cefuroxime. * All isolates were sequence type 131 belonging to cluster 1. ** All isolates were sequence type 131 belonging to cluster 5. § All isolates were sequence type 131 belonging to cluster 3. ° All isolates were sequence type 131 belonging to cluster 2. & All isolates were sequence type 354. $ All isolates were sequence type 38. Isolates of patients who did not complete the study are not shown.
References
- Thorpe, K.E.; Joski, P.; Johnston, K.J. Antibiotic-resistant infection treatment costs have doubled since 2002, now exceeding $2 billion annually. Health Aff. 2018, 37, 662–669. [Google Scholar] [CrossRef] [PubMed]
- Ray, S.; Anand, D.; Purwar, S.; Upadhye, K.V.; Gupta, P.; Dhar, D. Association of high mortality with extended-spectrum beta-lactamase (esbl) positive cultures in community acquired infections. J. Crit. Care 2018, 44, 255–260. [Google Scholar] [CrossRef] [PubMed]
- Donskey, C.J. The role of the intestinal tract as a reservoir and source for transmission of nosocomial pathogens. Clin. Infect. Dis. 2004, 39, 219–226. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ruppe, E.; Armand-Lefevre, L.; Estellat, C.; Consigny, P.H.; El Mniai, A.; Boussadia, Y.; Goujon, C.; Ralaimazava, P.; Campa, P.; Girard, P.M.; et al. High rate of acquisition but short duration of carriage of multidrug-resistant enterobacteriaceae after travel to the tropics. Clin. Infect. Dis. 2015, 61, 593–600. [Google Scholar] [CrossRef]
- Isendahl, J.; Giske, C.G.; Hammar, U.; Sparen, P.; Tegmark, W.K.; Ternhag, A.; Naucler, P. Temporal dynamics and risk factors for bloodstream infection with extended-spectrum beta-lactamase-producing bacteria in previously-colonized individuals: National population-based cohort study. Clin. Infect. Dis. 2019, 68, 641–649. [Google Scholar] [CrossRef]
- Ruscher, C.; Pfeifer, Y.; Layer, F.; Schaumann, R.; Levin, K.; Mielke, M. Inguinal skin colonization with multidrug-resistant bacteria among residents of elderly care facilities: Frequency, persistence, molecular analysis and clinical impact. Int. J. Med. Microbiol. 2014, 304, 1123–1134. [Google Scholar] [CrossRef]
- March, A.; Aschbacher, R.; Dhanji, H.; Livermore, D.M.; Bottcher, A.; Sleghel, F.; Maggi, S.; Noale, M.; Larcher, C.; Woodford, N. Colonization of residents and staff of a long-term-care facility and adjacent acute-care hospital geriatric unit by multiresistant bacteria. Clin. Microbiol. Infect. 2010, 16, 934–944. [Google Scholar] [CrossRef]
- Rooney, P.J.; O’Leary, M.C.; Loughrey, A.C.; McCalmont, M.; Smyth, B.; Donaghy, P.; Badri, M.; Woodford, N.; Karisik, E.; Livermore, D.M. Nursing homes as a reservoir of extended-spectrum beta-lactamase (esbl)-producing ciprofloxacin-resistant escherichia coli. J. Antimicrob. Chemother. 2009, 64, 635–641. [Google Scholar] [CrossRef] [Green Version]
- Cochard, H.; Aubier, B.; Quentin, R.; van der Mee-Marquet, N.; Reseau des Hygienistes du, C. Extended-spectrum beta-lactamase-producing enterobacteriaceae in french nursing homes: An association between high carriage rate among residents, environmental contamination, poor conformity with good hygiene practice, and putative resident-to-resident transmission. Infect. Control Hosp. Epidemiol. 2014, 35, 384–389. [Google Scholar]
- Leitner, E.; Zechner, E.; Ullrich, E.; Zarfel, G.; Luxner, J.; Pux, C.; Pichler, G.; Schippinger, W.; Krause, R.; Zollner-Schwetz, I. Low prevalence of colonization with multidrug-resistant gram-negative bacteria in long-term care facilities in graz, austria. Am. J. Infect. Control 2018, 46, 76–80. [Google Scholar] [CrossRef]
- Huttner, B.; Haustein, T.; Uckay, I.; Renzi, G.; Stewardson, A.; Schaerrer, D.; Agostinho, A.; Andremont, A.; Schrenzel, J.; Pittet, D.; et al. Decolonization of intestinal carriage of extended-spectrum beta-lactamase-producing enterobacteriaceae with oral colistin and neomycin: A randomized, double-blind, placebo-controlled trial. J. Antimicrob. Chemother. 2013, 68, 2375–2382. [Google Scholar] [PubMed] [Green Version]
- Saidel-Odes, L.; Polachek, H.; Peled, N.; Riesenberg, K.; Schlaeffer, F.; Trabelsi, Y.; Eskira, S.; Yousef, B.; Smolykov, R.; Codish, S.; et al. A randomized, double-blind, placebo-controlled trial of selective digestive decontamination using oral gentamicin and oral polymyxin e for eradication of carbapenem-resistant klebsiella pneumoniae carriage. Infect. Control Hosp. Epidemiol. 2012, 33, 14–19. [Google Scholar] [CrossRef] [PubMed]
- Tascini, C.; Sbrana, F.; Flammini, S.; Tagliaferri, E.; Arena, F.; Leonildi, A.; Ciullo, I.; Amadori, F.; Di Paolo, A.; Ripoli, A.; et al. Oral gentamicin gut decontamination for prevention of kpc-producing klebsiella pneumoniae infections: Relevance of concomitant systemic antibiotic therapy. Antimicrob. Agents Chemother. 2014, 58, 1972–1976. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Tacconelli, E.; Mazzaferri, F.; de Smet, A.M.; Bragantini, D.; Eggimann, P.; Huttner, B.D.; Kuijper, E.J.; Lucet, J.C.; Mutters, N.T.; Sanguinetti, M.; et al. Escmid-eucic clinical guidelines on decolonization of multidrug-resistant gram-negative bacteria carriers. Clin. Microbiol. Infect. 2019, 25, 807–817. [Google Scholar] [CrossRef] [Green Version]
- Saidani, N.; Lagier, J.C.; Cassir, N.; Million, M.; Baron, S.; Dubourg, G.; Eldin, C.; Kerbaj, J.; Valles, C.; Raoult, D.; et al. Faecal microbiota transplantation shortens the colonisation period and allows re-entry of patients carrying carbapenamase-producing bacteria into medical care facilities. Int. J. Antimicrob. Agents 2019, 53, 355–361. [Google Scholar] [CrossRef] [Green Version]
- Bilinski, J.; Grzesiowski, P.; Sorensen, N.; Madry, K.; Muszynski, J.; Robak, K.; Wroblewska, M.; Dzieciatkowski, T.; Dulny, G.; Dwilewicz-Trojaczek, J.; et al. Fecal microbiota transplantation in patients with blood disorders inhibits gut colonization with antibiotic-resistant bacteria: Results of a prospective, single-center study. Clin. Infect. Dis. 2017, 65, 364–370. [Google Scholar] [CrossRef]
- Huttner, B.D.; de Lastours, V.; Wassenberg, M.; Maharshak, N.; Mauris, A.; Galperine, T.; Zanichelli, V.; Kapel, N.; Bellanger, A.; Olearo, F.; et al. A 5-day course of oral antibiotics followed by faecal transplantation to eradicate carriage of multidrug-resistant enterobacteriaceae: A randomized clinical trial. Clin. Microbiol. Infect. 2019, 25, 830–838. [Google Scholar] [CrossRef] [Green Version]
- Sanders, M.E. Probiotics: Definition, sources, selection, and uses. Clin. Infect. Dis. 2008, 46 (Suppl. 2), S58–S61. [Google Scholar] [CrossRef] [Green Version]
- Brunel, A.S.; Guery, B. Multidrug resistant (or antimicrobial-resistant) pathogens—Alternatives to new antibiotics? Swiss Med. Wkly 2017, 147, w14553. [Google Scholar]
- Walker, W.A. Mechanisms of action of probiotics. Clin. Infect. Dis. 2008, 46 (Suppl. 2), S87–S91. [Google Scholar] [CrossRef]
- Hachimura, S.; Totsuka, M.; Hosono, A. Immunomodulation by food: Impact on gut immunity and immune cell function. Biosci. Biotechnol. Biochem. 2018, 82, 584–599. [Google Scholar] [CrossRef] [PubMed]
- Hopkins, M.J.; Macfarlane, G.T. Nondigestible oligosaccharides enhance bacterial colonization resistance against clostridium difficile in vitro. Appl. Environ. Microbiol. 2003, 69, 1920–1927. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Koning, C.J.; Jonkers, D.M.; Stobberingh, E.E.; Mulder, L.; Rombouts, F.M.; Stockbrugger, R.W. The effect of a multispecies probiotic on the intestinal microbiota and bowel movements in healthy volunteers taking the antibiotic amoxycillin. Am. J. Gastroenterol. 2008, 103, 178–189. [Google Scholar] [CrossRef] [PubMed]
- Zollner-Schwetz, I.; Zechner, E.; Ullrich, E.; Luxner, J.; Pux, C.; Pichler, G.; Schippinger, W.; Krause, R.; Leitner, E. Colonization of long term care facility patients with mdr-gram-negatives during an acinetobacter baumannii outbreak. Antimicrob. Resist. Infect. Control 2017, 6, 49. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Der KRINKO, E. Hygienemaßnahmen bei infektionen oder besiedlung mit multiresistenten gramnegativen stäbchen. Bundesgesundheitsblatt; Springer: Berlin/Heidelberg, Germany, 2012; pp. 1311–1354. [Google Scholar]
- Stadlbauer, V. Immunosuppression and probiotics: Are they effective and safe? Benef. Microbes. 2015, 6, 823–828. [Google Scholar] [CrossRef]
- Schlager, S.; Lepuschitz, S.; Ruppitsch, W.; Ableitner, O.; Pietzka, A.; Neubauer, S.; Stöger, A.; Lassnig, H.; Mikula, C.; Springer, B.; et al. Petting zoos as sources of shiga toxin-producing escherichia coli (stec) infections. Int. J. Med. Microbiol. 2018, 308, 927–932. [Google Scholar] [CrossRef]
- Lepuschitz, S.; Schill, S.; Stoeger, A.; Pekard-Amenitsch, S.; Huhulescu, S.; Inreiter, N.; Hartl, R.; Kerschner, H.; Sorschag, S.; Springer, B.; et al. Whole genome sequencing reveals resemblance between esbl-producing and carbapenem resistant klebsiella pneumoniae isolates from austrian rivers and clinical isolates from hospitals. Sci. Total Environ. 2019, 662, 227–235. [Google Scholar] [CrossRef]
- Diancourt, L.; Passet, V.; Verhoef, J.; Grimont, P.A.; Brisse, S. Multilocus sequence typing of klebsiella pneumoniae nosocomial isolates. J. Clin. Microbiol. 2005, 43, 4178–4182. [Google Scholar] [CrossRef] [Green Version]
- Klymiuk, I.; Bilgilier, C.; Stadlmann, A.; Thannesberger, J.; Kastner, M.T.; Hogenauer, C.; Puspok, A.; Biowski-Frotz, S.; Schrutka-Kolbl, C.; Thallinger, G.G.; et al. The human gastric microbiome is predicated upon infection with helicobacter pylori. Front. Microbiol. 2017, 8, 2508. [Google Scholar] [CrossRef] [Green Version]
- McKenna, P.; Hoffmann, C.; Minkah, N.; Aye, P.P.; Lackner, A.; Liu, Z.; Lozupone, C.A.; Hamady, M.; Knight, R.; Bushman, F.D. The macaque gut microbiome in health, lentiviral infection, and chronic enterocolitis. PLoS Pathog. 2008, 4, e20. [Google Scholar] [CrossRef] [Green Version]
- Callahan, B.J.; McMurdie, P.J.; Rosen, M.J.; Han, A.W.; Johnson, A.J.; Holmes, S.P. Dada2: High-resolution sample inference from illumina amplicon data. Nat. Methods 2016, 13, 581–583. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bolyen, E.; Rideout, J.R.; Dillon, M.R.; Bokulich, N.A.; Abnet, C.C.; Al-Ghalith, G.A.; Alexander, H.; Alm, E.J.; Arumugam, M.; Asnicar, F.; et al. Reproducible, interactive, scalable and extensible microbiome data science using qiime 2. Nat. Biotechnol. 2019, 37, 852–857. [Google Scholar] [CrossRef] [PubMed]
- Quast, C.; Pruesse, E.; Yilmaz, P.; Gerken, J.; Schweer, T.; Yarza, P.; Peplies, J.; Glockner, F.O. The silva ribosomal rna gene database project: Improved data processing and web-based tools. Nucleic Acids Res. 2013, 41, D590–D596. [Google Scholar] [CrossRef] [PubMed]
- Price, M.N.; Dehal, P.S.; Arkin, A.P. Fasttree 2--approximately maximum-likelihood trees for large alignments. PLoS ONE 2010, 5, e9490. [Google Scholar] [CrossRef] [PubMed]
- Katoh, K.; Standley, D.M. Mafft multiple sequence alignment software version 7: Improvements in performance and usability. Mol. Biol. Evol. 2013, 30, 772–780. [Google Scholar] [CrossRef] [Green Version]
- Chen, L.; Reeve, J.; Zhang, L.; Huang, S.; Wang, X.; Chen, J. Gmpr: A robust normalization method for zero-inflated count data with application to microbiome sequencing data. PeerJ 2018, 6, e4600. [Google Scholar] [CrossRef]
- Indra, A.; Schmid, D.; Huhulescu, S.; Simons, E.; Hell, M.; Stickler, K.; Allerberger, F.; Austrian, C.d.S.G. Clostridium difficile ribotypes in austria: A multicenter, hospital-based survey. Wien. Klin. Wochenschr. 2015, 127, 587–593. [Google Scholar] [CrossRef] [Green Version]
- Coman, M.M.; Verdenelli, M.C.; Cecchini, C.; Silvi, S.; Orpianesi, C.; Boyko, N.; Cresci, A. In vitro evaluation of antimicrobial activity of lactobacillus rhamnosus imc 501((r)), lactobacillus paracasei imc 502((r)) and synbio((r)) against pathogens. J. Appl. Microbiol. 2014, 117, 518–527. [Google Scholar] [CrossRef]
- Ljungquist, O.; Kampmann, C.; Resman, F.; Riesbeck, K.; Tham, J. Probiotics for intestinal decolonization of esbl-producing enterobacteriaceae: A randomized, placebo-controlled clinical trial. Clin. Microbiol. Infect. 2020, 26, 456–462. [Google Scholar] [CrossRef]
- O’Neill, C.A.; Monteleone, G.; McLaughlin, J.T.; Paus, R. The gut-skin axis in health and disease: A paradigm with therapeutic implications. Bioessays 2016, 38, 1167–1176. [Google Scholar] [CrossRef]
- Bowe, W.P.; Logan, A.C. Acne vulgaris, probiotics and the gut-brain-skin axis—Back to the future? Gut. Pathog. 2011, 3, 1. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Gueniche, A.; Philippe, D.; Bastien, P.; Reuteler, G.; Blum, S.; Castiel-Higounenc, I.; Breton, L.; Benyacoub, J. Randomised double-blind placebo-controlled study of the effect of lactobacillus paracasei ncc 2461 on skin reactivity. Benef. Microbes 2014, 5, 137–145. [Google Scholar] [CrossRef] [PubMed]
- Reygagne, P.; Bastien, P.; Couavoux, M.P.; Philippe, D.; Renouf, M.; Castiel-Higounenc, I.; Gueniche, A. The positive benefit of lactobacillus paracasei ncc2461 st11 in healthy volunteers with moderate to severe dandruff. Benef. Microbes 2017, 8, 671–680. [Google Scholar] [CrossRef] [PubMed]
- Bar-Yoseph, H.; Hussein, K.; Braun, E.; Paul, M. Natural history and decolonization strategies for esbl/carbapenem-resistant enterobacteriaceae carriage: Systematic review and meta-analysis. J. Antimicrob. Chemother. 2016, 71, 2729–2739. [Google Scholar] [CrossRef]
- Wachholz, P.A.; Nunes, V.D.S.; Polachini do Valle, A.; Jacinto, A.F.; Villas-Boas, P.J.F. Effectiveness of probiotics on the occurrence of infections in older people: Systematic review and meta-analysis. Age Ageing 2018, 47, 527–536. [Google Scholar] [CrossRef] [Green Version]
Figure 1.
Study timeline.
Figure 2.
Percentage of patients colonized by multidrug-resistant Gram negative (MRGN) bacteria in stool (n = 12) during and after a 12 week probiotic treatment.
Figure 2.
Percentage of patients colonized by multidrug-resistant Gram negative (MRGN) bacteria in stool (n = 12) during and after a 12 week probiotic treatment.
Figure 3.
Percentage of patients colonized by MRGN bacteria on skin of the inguinal region (n = 7) during and after a 12 week probiotic treatment.
Figure 3.
Percentage of patients colonized by MRGN bacteria on skin of the inguinal region (n = 7) during and after a 12 week probiotic treatment.
Figure 4.
Stool microbiome analysis. (a) Statistically significant increase of the genus Enterococcus at the end of probiotic treatment (t2) compared with start (t1), p = 0.00642. (b) Statistically significant increase of the genus Ruminococcaceae at week 24 (t3) compared with start (t1), p = 0.02. Skin microbiome analysis. (c) Statistically significant increase of the genus Actinotignum at the end of probiotic treatment (t2) compared with start (t1), p = 0.00201. (d) Statistically significant increase of the genus Aerococcus at the end of probiotic treatment (t2) compared with start (t1), p = 0.005654.
Figure 4.
Stool microbiome analysis. (a) Statistically significant increase of the genus Enterococcus at the end of probiotic treatment (t2) compared with start (t1), p = 0.00642. (b) Statistically significant increase of the genus Ruminococcaceae at week 24 (t3) compared with start (t1), p = 0.02. Skin microbiome analysis. (c) Statistically significant increase of the genus Actinotignum at the end of probiotic treatment (t2) compared with start (t1), p = 0.00201. (d) Statistically significant increase of the genus Aerococcus at the end of probiotic treatment (t2) compared with start (t1), p = 0.005654.
Table 1.
Clinical characteristics of all 21 patients enrolled.
| Characteristics | ACU | Geriatric Wards |
|---|---|---|
| Number of patients | 12 | 9 |
| Age (years, median, range) | 59 (19–80) | 86 (77–100) |
| Gender, n (%) | ||
| Male | 8 (66) | 5 (55) |
| Female | 4 (33) | 4 (45) |
| Comorbidities, n (%) | ||
| Parkinson’s disease | 0 | 2 (22) |
| Coronary heart disease | 0 | 2 (22) |
| Dementia | 0 | 7 (77) |
| Functional status, n (%) | ||
| Bedridden | 12 (100) | 2 (22) |
| Bowel incontinence, n (%) | 12 (100) | 6 (66) |
| Bladder incontinence, n (%) | 12 (100) | 4 (45) |
| Gastrostomy, n (%) | 12 (100) | 1 (11) |
| Antibiotic treatment, n (%) | ||
| During probiotic | 5 (41) | 0 |
| After probiotics | 3 (25) | 0 |
ACU = apallic care unit.
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Share and Cite
MDPI and ACS Style
Zollner-Schwetz, I.; Scarpatetti, M.; Pichler, G.; Pux, C.; Klymiuk, I.; Trajanoski, S.; Krause, R. Effect of a Multispecies Probiotic on Intestinal and Skin Colonization by Multidrug-Resistant Gram-Negative Bacteria in Patients in a Long-Term Care Facility: A Pilot Study. Nutrients 2020, 12, 1586. https://0-doi-org.brum.beds.ac.uk/10.3390/nu12061586
AMA Style
Zollner-Schwetz I, Scarpatetti M, Pichler G, Pux C, Klymiuk I, Trajanoski S, Krause R. Effect of a Multispecies Probiotic on Intestinal and Skin Colonization by Multidrug-Resistant Gram-Negative Bacteria in Patients in a Long-Term Care Facility: A Pilot Study. Nutrients. 2020; 12(6):1586. https://0-doi-org.brum.beds.ac.uk/10.3390/nu12061586
Chicago/Turabian StyleZollner-Schwetz, Ines, Monika Scarpatetti, Gerald Pichler, Christian Pux, Ingeborg Klymiuk, Slave Trajanoski, and Robert Krause. 2020. "Effect of a Multispecies Probiotic on Intestinal and Skin Colonization by Multidrug-Resistant Gram-Negative Bacteria in Patients in a Long-Term Care Facility: A Pilot Study" Nutrients 12, no. 6: 1586. https://0-doi-org.brum.beds.ac.uk/10.3390/nu12061586
Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.
