African Journal of
Microbiology Research

  • Abbreviation: Afr. J. Microbiol. Res.
  • Language: English
  • ISSN: 1996-0808
  • DOI: 10.5897/AJMR
  • Start Year: 2007
  • Published Articles: 5000

Full Length Research Paper

Lactobacillus acidophilus and Bifidobacteria spp having antibacterial and antiviral effects on chronic HCV infection

Nanis G. Allam
  • Nanis G. Allam
  • Department of Botany, Microbiology Section, Faculty of Science, Tanta University, Egypt.
  • Google Scholar
Mohamed L. Salem
  • Mohamed L. Salem
  • Department of Zoology, Immunology and Biotechnology Unit, Faculty of Science, Center of Excellence in Cancer Research Tanta University, Egypt.
  • Google Scholar
Hassan Elbatae
  • Hassan Elbatae
  • Hepatology, Tropical Diseases Medicine, Kafr Elsheikh University, Egypt.
  • Google Scholar
Maii Moustafa Nabieh
  • Maii Moustafa Nabieh
  • Department of Botany, Microbiology Section, Faculty of Science, Tanta University, Egypt.
  • Google Scholar

  •  Received: 25 November 2018
  •  Accepted: 11 January 2019
  •  Published: 07 February 2019


Hepatitis C virus is a serious hepatic disease that could be developed into hepatocellular carcinoma. Previously, some probiotic strains showed a natural therapeutic activity against the fatty liver disorder. Therefore, it could make sense to evaluate the antiviral and antibacterial responses to probiotics as Lactobacillus acidophilus and Bifidobacteria spp. in patients with chronic hepatitis C virus. Twenty (20) patients with chronic hepatitis C (both gender in age 47± 5 years) were treated with capsule that contains probiotics (L. acidophilus and Bifidobacterium spp.). They administered one capsule per day for a month before HCV treatment; blood and urine samples were collected before and after the given treatment and they were processed for a quantitative estimation of HCV by PCR, identification of bacteria by VITEK2 system and 16S r RNA gene sequencing assay. Moreover, the estimation of antibacterial activity of probiotics by antibiotic sensitivity test, counts of leukocytes, CD3+ T cells and CD56+ natural killer cells by flowcytometry, DGAT1 by ELISA. Administration of probitics enhanced the treatment response rate to HCV treatments pegylated IFN-α and ribavirin by 25% and showed an antibacterial activity against five species of the most common infectious bacteria in chronic HCV patients which were identified by this study. CD3+ cells counts and CD56+ natural killer cells were increased. L. acidophilus and Bifidobacterium spp. can act as a supportive supplement with antiviral and antibacterial activities; we recommend Probiotics side by side with HCV treatments.


Key words: Hepatitis C virus, Lactobacillus acidophilus and Bifidobacteria spp., CD3+, CD56+, pegylated IFN-α and ribavirin.


Hepatitis C virus (HCV) is a leading cause of pathogenesis of liver disease including chronic  hepatitis, fibrosis, cirrhosis, hepatocellular carcinoma, liver failure and death. Currently, no effective vaccineis available for
HCV infection (Dore et al., 2014). The most recent estimates of disease burden show about 185 million infections worldwide (Hanafiah et al., 2013).
One of the most common HCV drug therapies was pegylated interferon (IFN) and ribavirin combination therapy, but it was limited to about 55% of patients with a lower efficacy and associated with severe side effects (Lam et al., 2014). Recently, Sovaldi®, alone or in combination with IFN and ribavirin, has also been introduced as a new treatment modality with promising antiviral effects (Heathcote and Main, 2005; Gane et al., 2013).
However, exploring new therapeutic protocol, especially those that can improve the existing ones and lower their toxicity can have significant impact on the anti-viral responses. One of the promising modalities is natural products as well as probiotics that have potential anti-toxic effects on liver functions (Gratz et al., 2010).
Probiotics are defined as live microorganisms which are consumed as food or therapeutic supplements with beneficial effects on the health (Bermudez-Britet et al., 2012; Kechagia et al., 2013; Martin et al., 2013). For instance, Lactobacilli and befidobacteria are beneficial in the treatment of intestinal micro-flora disturbance by increasing gut permeability and re-establishment of the microbial equilibrium (Deye et al., 2016; Bischoff et al., 2014; Goldenberg et al., 2013). With this regard, it was found that Lactobacilli and bifidobacteria provide antibacterial activity against common pathogenic bacteria such as Escherichia coli, Staphylcoccus aureus and Salmonella typhimurium ((Bali et al., 2011; Butel et al., 2014), Enterobacteriaceae species, Klebsiella and E. coli. Indeed, these gram negative bacteria as well as gram-positive bacteria including S. aureus are the most common pathogenic bacteria in patients with chronic HCV, which is considered as secondary bacterial infections (Carrion et al., 2009; Jalan et al., 2014).
Triacylglycerol synthesis is catalyzed by acyl-CoA: diacylglycerol acyltransferase  (DGAT) enzymes,  DGAT1  and  DGAT2 (Harris et al., 2011). DGAT1,  an enzyme  involved  in  triglyceride  synthesis  and  luminal  LD  maturation,  targets  core  to lipid droplets LDs and bounded with NS5B in active HCV replication (Camus et al., 2013). Its absence or inhibition leads to the inhibition of viral assembly and production (Herker et al., 2010).
Besides their anti-bacterial activities, recent studies showed that both Lactobacilli and bifidobacteria have different immunomodulatory effects, including increasing phagocytosis NK cell activity (Yuan and Walker, 2004; Candore et al., 2008; Rask et al., 2013), IgG and IgA synthesis (Stagg et al., 2004; Tsai et al., 2012), production of cytokines (Th1 or Th2) in both in vivo and in vitro systems, the development and maturation of mucosal and systemic NKT cells (Villamil et al., 2002; Pagnini et al., 2010). The cytotoxic effects of natural killer (NK; CD3-CD56dim) cells against virally infected cells caused   inhibition   of  HCV  replication  as  well  as  their cytotoxicity against hepatocellular carcinoma (HCC) (Doskali et al., 2011). The effects of probiotics on these cells are paramount significance; especially these NK cells can activate multiple elements of janus kinase/signal transducer and transcription (JAK/STAT) pathway, resulting in an induction of endogenous IFN-alpha/beta expression in hepatocytes and enhancement of anti-HCV cell-mediated immunity (Ye et al., 2009). Additionally, probiotic bacteria differentially activated dendretic cells (DCs) in vitro and induced CD4+ T cells (Hart et al., 2003). With these beneficial effects, probiotics have been recommended for use as biological safe product drug system by FDA (Degnan, 2008; Snydman, 2008).
This study aimed to enhance utilize L.acidophilus and Bifidobacteria spp. as a supportive supplement to the treatment strategy based on Pegylated IFN-α and ribavirin which provides antibacterial, antiviral effect, reduce DGAT1 and improving the immune response rate. Subsequently, increase the treatment response rate to HCV treatment. 


This study was adopted on 40 selective patients (males and females) with chronic HCV who were diagnosed by a specialist physician that selected them according to a mean age of 47± 5 years and their positive results of HCV antibody antigen test and polymerase chain reaction (PCR) estimation which showed high viral load. The exclusion criteria included liver cirrhoses, HCC, hepatitis B virus (HBV), diabetes and/or renal impairment. Patients were recruited from the Virology Unit, El-Obour Hospital, Kafr El-sheikh, Egypt.
Ethical approval
This study had an approval letter from the ethical committee, Faculty of Medicine, Tanta University, Egypt.
Treatment strategies involved in the study
L. acidophilus and Bifidobacteria spp combination (1.5 billion cells) were used in this study in the form of a capsule (Phillips’® Colon Health, Bayer Health Care, USA). The ingredients included potato starch, gelatin, and silicon dioxide. The probiotics with long term benefit takes longer within the host body to colonize in the gut, colon or the small intestine. The process may take days to months with the least reported being 2-3 weeks as mentioned by Swanson (2013). Three groups (A, B and C) were designed in this study. Group A included healthy volunteers as controls who took the capsule once a day for one month. Group B included chronic hepatitis C patients who took the capsule once a day for one month before treatment with pegylated IFN-α and ribavirin (single interferon injection weekly for 12 weeks). Group C of chronic hepatitis C patients was treated with only pegylated IFN-α and ribavirin (12 weeks). Patients were followed up clinically during the time course of the experiment.
Samples collection and duration of study
Blood  and  urine samples were collected from the patient groups in the time range from October 2013 to April 2014. Ten samples were collected before and after capsule supplementation on (day 1, and day 30) from healthy volunteers as controls (group A). Twenty samples were collected before and after the given treatment strategies on day 1, 30 then day 120 in the groups B and C.
Reagents and materials
The following media were used. 1) Nutrient agar (Thomas et al., 1977) pH was adjusted to 5.0); 2) Mannitol salt agar (Koch, 1942) (Final pH: 7.4 ± 0.2 at 25°C); 3) MacConky agar (pH 7.4 ± 0.2 at 25°C). Gram stain (crystal violet, gram's iodine solution, acetone/ethanol (50:50 v: v), 0.1% basic fuchsin solution). VITEK 2 system (Funke, 1998), (bioMerieux Inc., Hazelwood, MO) VITEK 2 Cassette Loaded with Cards and Suspension Tubes being loaded Into the Automatic Transport System.                  
Antibiotics used for antibacterial sensitivity test (Barry, 1979) included the following: nitrofurantion (F), doxycyclin (DA), OFloxacin (OFX), Nalidexic acid (NA), Vancomycine (VA), Tetracycline (TE), Erythromycin (E), Amplicilin sulbactam (SAM), Imipenem (IPM), Amikacin (AK), chloraphenicol (C), Ciprofloxacin (CIP), Levofloxacin (LEV), Piperacillin-tazobactam (TPZ), sulfamethoxazole (SXT), Cefuroxime (CXM), Cefataxime (CTX), Amoxicilin calvulinic acid (AMC).
The QIAGEN gel extraction kit for 16S rRNA gene sequencing (Stackebrandt, 1992) was purchased from Sigma (Sigma Scientific Services Co., Cairo, Egypt).
Antibodiesm used were Anti-human CD3 and CD56 monoclonal antibodies (BD Biosciences, SanJose, CA, USA) were used for immunophenotype analysis.
BD FACS was used for lysing solution for RBCs lysis and PBS buffer solution for washing and suspension. EDTA tubes were used as anticoagulant tubes for blood collection. Sterilizing Petri dishes and swabs were used.
Quantitative estimation of HCV RNA
Blood samples were used for RNA extraction. 20 μL of the extracted RNA was added to 30 μL of Master Mix in each 0.1 mL microtube and test was performed in automated instrument (HVD Auto Q server) (Bièche, 1998). A standard curve was automatically drawn with software using five quantification standard concentrations of HCV-RNA to analyze the viral RNA load.
Isolation of bacteria from patients with chronic HCV and antibacterial responses to Lactobacillus acidophilus and Bifidobacteria spp.
Isolation of bacteria from urine samples was performed on nutrient agar inoculated with 100 µl of each urine sample and incubated at 37°C for 18-24 h. Investigation of the isolated bacteria by Gram reaction was performed, eventually pure subculture of gram positive and gram negative were cultured in 20 mL of sterilized Macconky and Mannitol media, respectively, at 37°C for 18-24 h. The load of pathogenic bacteria was observed by detection of CFU/ml based on this equation CFU/mL = (no. of colonies x dilution factor) / volume of culture plate. Moreover, the numbers of the infected patients were recorded before and after the capsule administration in the three groups.
Identification of isolated bacteria
VITEK 2 system
This system provided 64  identification  tests  processed   for identification of isolated bacterial strains while, BioMerieux VITEK® 2 system version: 06.01 was used as lactase, alkalinization, growth under inhibition conditions like oxidase, enzyme hydrolysis acidification test. Sufficient numbers of pure colonies were transferred into 3.0 mL of sterile saline, a special rack (cassette) of the suspended microorganism; the identification cards were placed in slots that moved to the optical system where readings were observed each 15 min. Then the data were recorded.
Antibacterial sensitivity test (AST) (Kirby Bauer technique)
Sterile Petri plates with 20 mL of sterilized MacConkey and Mannitol agar were inoculated with 100 μL of each isolated bacteria; the antibiotics discs were placed on plates and incubated for 18-24 h at 37°C. Inhibition zones diameters were recorded in mm according to the Clinical and Laboratory Standards Institute (CLSI, 2013).
16S r RNA gene sequences identification
PCR was performed in a thermal cycler (Bio-Rad MJ Research, Hercules, USA). The 50 μL reaction mixture consisted of,  5 μL  of  10  ×  Taq  buffer  (100  mM  Tris-HCl,  500  mM KCl pH 8.3),2.5  U  of  Taq  DNA  polymerase,  20 ng of  genomic  DNA, 200 μM dNTP, 10 p moles each universal primers, Forward primer CAAACAGGATTAGATACCCTG, reverse primer CGCGAAGAACCTTACC and  2.0  mM  MgCl2.  Amplification started with  initial  denaturation  for  5  min at  94°C, followed  by  25  cycles  of  denaturation  for  30 s at 94°C , annealing temperature of primers for 30  s at 50°C,  and  extension  for  1  min at  72°C .  The last extension for 15 min at 72°C was used.  Submarine  agarose gel  electrophoresis in 1.2%  agarose  gel  pre-staining with  ethidium  bromide  at  8  V/cm was used for analyzing 5  μL  of  the  amplified  product, gel doc UV transilluminator was used for visualizing the PCR product (Imran and Abd-Al-Kareem, 2016). The QIAGEN gel extraction kit serves as a gel purified for the amplified PCR product.  GATC  Company  using  ABI  3730xl  DNA  sequence used  forward  and  reverse  primers  for the sequencing of a total  of  100  ng/μL  concentration  of  16S  rRNA amplified product (Sigma  Scientific Services Co., Cairo, Egypt).
Flow cytometric analysis
Fresh venous blood samples were collected on EDTA tubes and100 µl was stained by human mAbs in staining tubes using the recommended concentrations by the manufactures. The stained samples were incubated at 4°C in the dark for 20 min, and then RBCs were lysed by adding BD FACS or ACK lysing solution (1x) for 15 min then centrifugation at 1250 rpm for 5 min. Then, the supernatant containing lysed RBCs was discarded and the cells were washed using PBS buffer solution. The cells were acquired on FACS Calibur or FACS Canto II (BD Biosciences, San Jose, CA, USA) and analyzed using FACSDiva, Cell Quest (BD Biosciences) and Flow jo software (Givan et al., 2011).
White blood cells
A total number of leukocytes, differential lymphocytes, monocytes and neutrophils were identified by using fully automated instrument (CBC Swelab Alpha three part differential).
Determination of DGAT1 enzyme level
Enzyme-linked   Immunosorbent   Assay Kit   for    Diacylglycerol-O- Acyltransferase Homolog 1 (DGAT1) .Organism Species: Homo sapiens (Human). This assay has high sensitivity and excellent specificity for detection of DGA T1.
Statistical analysis
The clinical data were recorded for the study and analyzed for each patient. The statistical presentation analysis of the present study was conducted using the mean, standard deviation, Chi-square test by software SPSS V.20. Standard student "t test" was used to test significance of the differences between means *P≤ 0.05, **P≤ 0.01.


The antiviral effect of probiotics by HCV PCR assays result
The antiviral effect of L. acidophilus and Bifidobacteria spp. capsule was determined by HCV PCR assay for three groups (Group A, B and C). The outcome data illustrated that L. acidophilus and Bifidobacteria spp increased the number of responded patients to the IFN-α and ribavirin treatment about 95 % in group B  compared to their number in group C about  70 % which was treated with only IFN-α and ribavirin treatment compared to the control group A which was negative (Figure 1; Table 1A,B).
Antibacterial activity of treatment with Lactobacillus acidophilus and Bifidobacteria spp.
The secondary infectious bacteria in patients with chronic HCV (groups B and C) were compared to that in the group A of healthy people which revealed no bacterial growth. It was found that, the number of patients and the load of isolated bacteria before oral administration of the probiotic capsules were higher than after administration.  The loads of Gram positive and negative bacteria were reduced to 43.2 and 76%, respectively in urine samples as a response to probiotic administration in group B; the number of infected patients was reduced by 60% after probiotic supplementation. On the other hand, group C did not show any enhancement as it is nearly the same percentage of both the number of patients and the bacterial load after as well as before any treatments.
Identification of Isolated bacteria using VITEK 2 system      
The microscopic investigation of Gram reaction revealed presence of G+ve isolates in cocci form especially Staphylococci form while G-ve isolates were bacilli. They were cultured on selective media for further biochemical  identification by VITEK 2 system. Five main bacterial pathogens were identified in patients with chronic HCV as S. lentus, S. aureus, Klebsiella pneumonia, P. aeruginosa and  E. coli.
Antibacterial sensitivity of the isolated bacteria
It was found that the investigated antibiotics against isolated bacterial species revealed different inhibition zones with variable degrees of resistance. P. aeruginosa was resistant against the following antibiotics: Ofloxacin (OFX), nalidixic acid (NA), chloramphenicol (C), levofloxacin (LEV), norfloxacin (NOR), furantoin (F), and ampilicillin+sulbactam (SAM). Moreover, among 5 isolated S. aureus, isolate number 2 was the most resistant against doxycyclin (DA), Nalidexic acid (NA), erythromycin (E), chloramphenicol (C), amikacin (AK), piperacillin-tazobactam (TPZ), amoxicilin calvulinic acid (AMC) (Figures 2 and 3).
16S rRNA bacterial identification
The 16S rRNA gene sequence proved that S. aureus number 2 (highly antibiotic resistant) is subsp. strain N315 16S ribosomal RNA with identity about 89%, and the phylogenetic tree was constructed as illustrated in Figure 4.
Analysis of CD3+ and CD56+ cells counts
Treatment with L. acidophilus and Bifidobacteria spp. resulted in significant enhancement in the numbers of CD56+  NK  cells  (P values  =  0.001)  and  CD3+ T  cells (Figures 5 and 6; Table 2).
It was found that the counts of CD3+ and CD56+ cells in healthy individuals group A were more than group B before oral administration of probiotics. CD3+ and CD56+cells counts increased after probiotic capsule administration in both groups A and B. In group B, their production slightly increased than group A after probiotic administration, but level of CD3+ cells in Group A was more than Group B, group C did not undergo this test as they did not take probiotics (Figure 7; Tables 3, 4).
White blood cells 
The differential count of Leucocytes (WBCs), including monocytes , lymphocytes and granulocytes, increased after oral administration of the probiotics capsules in group B by 8.7%, while total WBCs count before probiotics capsule administration was 6.33%  compared to group A (healthy individuals) controls as they did not show observed change after probiotics administration. This parameter was not measured in group C as it did not take probiotics (Figure 8).
Subsequently, probiotics enhanced the immune responses by increasing the immune cells that produce T lymphocytes (CD3+), natural killer cells (CD56+), monocytes, Basophiles and eosinophiles, thus strengthening immune defenses against both bacterial and viral infections.
Inhibition of DGAT1 reduces HCV viral production
The outcome data illustrated that the concentration of DGAT1 enzyme was reduced as a result of probiotics capsule administration inside the same group B (chronic HCV patients) from 528 up to 373 ng/ mml (Table 5). More evidence was observed after three months of the treatment protocols in group (B) DGAT1 concentration was about  373  ng /mml  lesser  compared  to group (C) who treated only with pegylated IFN and it was 1038 ng/mml higher with a significance P. value = 0.05*. 
P. value= 0.01-0.05 showed significant result, Mean + SD showed the mean and standard error, gpc = chronic HCV patients (only IFN), gpB = chronic HCV patients (probiotics plus IFN), as shown it increased with a significance P. value = 0.05*.
On the other hand,  the  presented  study  revealed  the  correlation between the level of DGAT1 and HCV infection which was determined in group (C) of patients treated  with  only  pegylated  IFN-α  and  ribavirin without probiotics capsule, while the concentration of DGAT1 enzyme increased from 624 up  to  1038 ng/mml. DGAT1 concentration in group (A) was 302 ng/mml less than its concentration in group (B) which  was 528 ng/mml (Table 6).



In this work, we performed a study providing a principle and clinical guidance that aimed to reduce HCV severity in a representative group of Egyptian patients with chronic HCV infection (where HCV genotype 4 was dominant). The patients were treated with L. acidophilus and Bifidobacteria spp. a month before starting the conventional therapy with IFN-α and ribavirin which was the available therapy at the time  of  study.  However the benefits of probiotics were the main objective of this study and developing new treatments which are various latterly (Servin, 2004). It was assessed the probiotic treatments on three main parameters, including the viral titer, the secondary bacterial infections, as well as the count of immune cells and their differential numbers and phenotypes. It was found that treatment with L. acidophilus and Bifidobacteria spp. induced antiviral and antibacterial activities and increased the immune cell numbers. These pilot studies indicate that probiotics can be used as an adjuvant system during conventional HCV therapy.
The outcome data in vivo demonstrated that the most common secondary bacterial infections associated with chronic HCV patients were S. lentus, S. aureus, K. pneumonia, P. aeruginosa and  E. coli from the investigated HCV patients in the current study showed resistance against common used antibiotics especially P. aeruginosa and strain No 2 S. aureus.  The bacterial load and the numbers of the infected patients with bacteria remarkably reduced in response to oral administration probiotic capsules. This is in line with prior studies which detected antibacterial activity of Lactobacilli and Bifidobacteria in the laboratory against common disease pathogens such as S. typhimurium, E. coli and S. aureus that proved what Hor and Liong (2014) and Hütt (2006) noted. The identification with VITEK 2 system as a precise automated technique was used to identify the isolated pathogens into P. aeuroginosa, E. coli, S. lentus, S. aureus, K. pneumonia. This is consistent with prior studies (Garcia-Valdecasas et al., 2009; Kawano et al., 2015) which showed that E. coli, Klebsiella, and Enterobacteriaceae species were the most common pathogenic bacteria in patients with chronic HCV infection. As expected, the group of healthy people A showed no bacterial growth on both of media. In the same connection, Jacobs et al. (2009); (Sikorska and Smoragiewicz, 2013) illustrated and explained the mechanism of the antibacterial activity of Lactobacillus strains. The activity was correlated to production of metabolites such as lactic and acetic acid and that reduced the pH. In the same context, Reis et al. (2012), Ibrahim et al. (2010) explained the activity of Probiotic cell free supernatant by presence of acetic acid, lactic acid, organic acids, hydrogen peroxide, diacetyl, phenols and bacteriocins using GC-Mass.
It has been established that HCV patients are immunocompromised since viral infection causes several symptoms by time related to severity of the infection and progression of the disease. Subsequently, the immuno-compromised patients develop fibroses followed by cirrhosis and end up by HCC. Throughout all these stages several biochemical changes have been noticed including decreasing of albumin, increasing of liver enzymes, liver dysfunction, immune dysfunction, diarrhea, respiration and digestion difficulties (Ibrahim et al., 2010). Due   to  these   dysfunction  several  other   side   effects emerge which are related to secondary bacterial infection.
Another objective of this study was to investigate whether treating with probiotics can also enhance the immune responses through increasing the counts of immune cells CD3+ and CD56+. Also it was to investigate the antibacterial effects of probiotics on the load of pathogenic bacteria that included G +ve or G-ve bacteria which was an evidence. Moreover, treatment with probiotics capsule (one per day for a month before IFN-α) resulted in improving the treatment response rate of chronic HCV patients that reflected by PCR assay result. These data suggest that probiotic can be used as a supportive therapy to the treatment of HCV infection whether it based on IFN-α treatment only or with Sovaldi and IFN-α protocol. With this regard, it has been found in preclinical and clinical studies that administration of probiotics enhanced the innate and adaptive immune defenses (Ye et al., 2009), including phagocytosis, NK cell activity, IgG, IgA) (Chen and Morgan, 2006) as well as induction of Th1 and Th2 both in vivo and in vitro systems, while maintaining the balance between the strength of the Th2-like response, and Th1/like response. In line with these studies on the effect of exogenous probiotics, endogenous probiotics (gut microbiota) have been reported to control systemic NKT cells (Tsai et al., 2012). Other studies showed that probiotics, including, Lactobacillus and Bifidobacterium, increased expression level of the activation molecule CD69 on CD4+ (Th) and CD3+CD56+ (NKT cells) (Takeda et al., 2013; Kim et al., 2008).
Additionally, probiotics are considered by FDA as biological products which are safe (Doskali et al., 2011; Snydman, 2008) with protecting and supporting the liver and the immune function (Gratz et al., 2010). As a result of this clinical study, the level of DGAT1 after probiotic capsule and treatment by IFN-α injection group (B) was less than its level after treatment by IFN-α injection only group(c) with P value = 0.005* significance. DGAT1 enzyme level  catalyzes the fat droplet formation, where probiotics decrease the fat droplet formation that in agree with (Hung et al., 2017)  and DGAT1 enzyme which involved in lipoprotein coat structure of HCV particle (Blaising and Pécheur, 2013) and as a result the virus could not replicate or escape from the immunity defense. 


In conclusion, oral administration of L. acidophilus and Bifidobacteria spp. before treatment with IFN-α and ribavirin associated with significant antiviral activity, and antibacterial effects result in enhancement of the immune status and antibacterial metabolites. 


This study recommends prescription  of probiotic side by side twith HCV treatment due to the antiviral and antibacterial effects of probiotics. Moreover it enhanced the immune response against the viral and bacterial infection. It is recommended to work on other probiotic species and study its role in the treatment of HCV infection.


The authors declare that they have no conflict of interest.



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