Introduction

Because of the immature immunity of infants and young children, bacterial acquired antibiotic resistance and poor sanitation, Salmonella typhimurium (S. typhimurium) has become the main pathogen in nosocomial and foodborne infection1,2,3. Salmonella typhimurium possesses endotoxin, enterotoxin and extracellular enzymes as well as other pathogenic factors, so that Salmonella typhimurium has strong pathogenicity4,5. After the use of antibiotics, it was easy to make Salmonella typhimurium form into cell wall-defective bacteria named bacterial L forms6,7,8.

BacteriaL L forms still have the ability to cause disease, such as leading to the delay of chronic infection, and decreased susceptibility to antibacterial drugs which act on cell walls9,10. In these experiments, we studied the resistance of Salmonella typhimurium standard strain L forms to advanced cephalosporins and judged the susceptibility degree of Salmonella typhimurium L forms to the third and fourth generation cephalosporins, in order to guide the rational use of clinical antibacterial drugs. The study will provide the basic theory for controlling Salmonella typhimurium infection.

Materials and Methods

Bacterial strain

Salmonella typhimurium standard strain CMCC50115 was purchased from the National Institute for the Control of Pharmaceutical and Biological Products.

Reagents and instruments

Gram staining solution was purchased from Nanjing Jiancheng Bioengineering Institute. Antibiotic Drug sensitive tablets were purchased from OXOID company, UK, including third-generation cephalosporins, such as cefotaxime (CTX), ceftriaxone (CRO), cefoperazone (CFP), ceftazidime (CAZ), and fourth generation cephalosporin cefepim (FEP). Mueller-Hinton (MH) agar was used for determination of bacterial susceptibility to antibiotics by using agar paper diffusion method. 100 ml MH agar medium was prepared and made with 1.7 g agar, 0.2 g beef extract powder, 0.15 g soluble starch, 1.75 g casein hydrolysate, and afterwards regulating pH 7.4, and autoclaving at 121 °C for 15 min. The MH agar medium was inverted into the plate for antibiotic drug susceptibility testing. Soft agar plates for bacterial L forms culture were prepared by using improved MH agar plates with 1% agar and 2% NaCl. A mounted digital microscope (Nikon, Japan) was used for observing bacterial L forms and taking photos of micrographs.

Salmonella typhimurium L form Induction

Salmonella typhimurium was induced into stable L-forms by cefazolin drug discs with 30 µg/tablet. Gram stain was used to observe the microscopic morphology of Salmonella typhimurium and its L forms.

Preparation of Salmonella typhimurium and L form bacterial liquid

The bacteria in the logarithmic growth phase were obtained by conventional bacterial culture. 108 CFU/ml bacterial liquid was prepared with sterile physiological saline to a 0.5 McFarland standard concentration. Salmonella typhimurium L forms were subcultured under cefazolin induction, to obtain fresh cultures. 108 CFU/ml L form bacterial liquid was prepared with sterile 3% NaCl hypertonic saline, and counts were measured by McFarland turbidimetry.

Drug susceptibility test

According to the national clinical test operating protocol for drug susceptibility testing in vitro, the first preparation of test broth was made after culturing at 37 °C for 6 hours. The bacterial turbidity degree was regulated to 0.5 McFarland units. The tested bacteria were scribbled and uniform coating on MH agar and agar disc diffusion method was used for drug susceptibility testing. The five kinds of cephalosporin susceptibility paper disc were evenly affixed to the center and surrounding of the plate aseptically. After the conventional bacterial culture, the diameters of the inhibition zones were measured. Referring to the national antibacterial drug susceptibility test criteria, drug susceptibility was determined specifically.

Statistical analysis

The experiment was repeated three times, and continuous variables are expressed as mean ± standard deviation. Between the two groups the data difference was analyzed by the way of using paired t test. A P value of < 0.05 was considered statistically significant.

Results

Gram staining results

As shown in Fig. 1, the Salmonella typhimurium strain was negative Gram stain and medium size bacillus, and Salmonella typhimurium L forms were negative Gram stain and filamentous bacillus. Salmonella typhimurium L forms were often coiled into groups.

Figure 1
Figure 1
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Gram staining morphological observation of Salmonella typhimurium and its L forms (Gram stain, magnification: 1000×). (A) Salmonella typhimurium is negative Gram stain and medium size bacillus. (B) Salmonella typhimurium L forms are negative Gram stain and filamentous bacillus.

Susceptibility test results

Salmonella typhimurium L forms colonies appeared around drug sensitive paper. The Salmonella typhimurium L forms colonies were tiny and gray, (shown in Fig. 2B). According to the criteria of bacterial drug susceptibility, Salmonella typhimurium standard strain L forms susceptibility to the third-generation cephalosporins, such as cefotaxime (CTX), ceftriaxone (CRO), cefoperazone (CFP) and ceftazidime (CAZ) remained sensitive. Salmonella typhimurium standard strain L forms’ susceptibility to the fourth generation cephalosporin cefepime (FEP) also was maintained at the level of susceptibility. Although the Salmonella typhimurium L forms’ inhibition zones were smaller than the original bacteria, there is no significant difference from the comparison of the Salmonella typhimurium original bacteria and L forms. Results are shown in Fig. 3.

Figure 2
Figure 2
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Drug susceptibility test cultures of Salmonella typhimurium and its L forms. (A) Salmonella typhimurium drug susceptibility test culture. (B) Salmonella typhimurium L forms drug susceptibility test culture.

Figure 3
Figure 3
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Drug susceptibility test results of Salmonella typhimurium and its L forms in connection with different cephalosporins Although the Salmonella typhimurium L forms inhibition zones were smaller than the original bacteria, there is no significant difference from the comparison of the Salmonella typhimurium original bacteria and L forms.

Observation of salmonella typhimurium L form colonies

Salmonella typhimurium L form colonies can appear around drug sensitive paper, showed in Fig. 4A. In the L form colonies, Salmonella typhimurium L forms Gram stain showed negative Gram stain and filamentous bacillus, showed in Fig. 4B.

Figure 4
Figure 4
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Salmonella typhimurium L form colonies appeared around drug sensitive paper. (A) Salmonella typhimurium L forms’ drug susceptibility test culture. The Salmonella typhimurium L forms colonies were tiny and gray around drug sensitive paper. (B) Salmonella typhimurium L forms Gram stain showed negative Gram stain and filamentous bacillus.

Discussion

Salmonella typhimurium, commonly known as food poisoning pathogens, has many virulence factors and antibiotic resistance. It has become one of the major pathogens of nosocomial and foodborne infection and food poisoning. And it is more common in food poisoning and sepsis of infants and young children11,12. Salmonella typhimurium L forms often occur in patients after β-lactam antibiotic treatment, resulting in chronic infection. And bacterial L forms were often detected as a pathogen13,14. Therefore, the study on drug susceptibility of Salmonella typhimurium L forms is important to prevent and control Salmonella typhimurium and its L form infection disease.

Bacterial L-form is a cell wall-deficient type of bacteria, and bacterial cell wall peptidoglycan formation is inhibited under various factors in vivo and in vitro. But Bacterial L forms can still grow and reproduce, and they still had pathogenicity. Cephalosporins act on the bacterial cell wall to inhibit the transpeptidase activity, affect the synthesis of the peptidoglycan layer, and exert a bactericidal effect15,16,17. Cephalosporin antibiotic individuation can induce bacterial variability to L forms and result in prolonged infection in blood and bone marrow. Ceftriaxone is the third generation of cephalosporin antibiotics for the treatment of lower respiratory tract infections, skin and soft tissue infections, sepsis caused by sensitive pathogens. And similar drugs also include ceftazidime, cefotaxime and cefoperazone, as well as cefepime of the fourth generation cephalosporins18,19. This study found that Salmonella typhimurium under cephalosporin treatment can mutate to bacterial L forms, so that the drug inhibition zones of third and fourth generation cephalosporins were reduced. But Salmonella typhimurium L forms remained sensitive to third-generation cephalosporins including cefotaxime, ceftriaxone, cefoperazone and ceftazidime and to the fourth-generation cephalosporin cefepime, in relation to the executive standard of the national antibacterial drug susceptibility test. However, clinical medication may require extended treatment of cephalosporins by means of combination medication with other action route antibiotic, in order to achieve complete pathogen removal, including original bacteria and their bacterial L forms20,21.

Salmonella typhimurium has multi-drug resistance and can naturally resist a variety of antibacterial drugs. The main mechanisms of drug resistance are decreased permeability of the outer membrane, changes in lactamase and penicillin-binding proteins, activation and production of efflux pumps. In recent years, with the increasing number of clinically applied antibacterial drugs, broad-spectrum resistant Salmonella typhimurium bacteria have become more and more widespread22,23,24. Besides the influence of plasmids, the development of drug resistance depends on the type of chromosomal gene and the gene of the strain. Mutations and environmental choices are closely related. The data show that Salmonella typhimurium L forms still have pathogenicity. Salmonella typhimurium L forms have cell wall defects, so that they are more resistant to cephalosporins acting on cell walls than Salmonella typhimurium original bacteria. Cephalosporins alone can induce bacterial L form production, but combined use of antibiotics that act on ribosomes or nucleic acids can prevent the prolongation of disease caused by the production of L-forms. Therefore, a reasonable combination of antimicrobial agents is an effective method to kill all Salmonella typhimurium and reduce the Salmonella typhimurium L forms’ formation.

According to the antibiotic target site of pathogenic bacteria, the action mechanisms of antibiotics are divided into four categories. They inhibit bacterial cell wall synthesis, or affect cytoplasmic membrane permeability, or inhibit protein synthesis (eg. macrolides, aminoglycosides), or inhibit nucleic acid metabolism (eg. quinolone, sulfonamides). Doctors should be careful in choosing antibiotics, which should follow the principle of combination and interaction of antibiotics, in order to control Salmonella typhimurium infection.

Conclusions

The antibiotic susceptibility of Salmonella typhimurium standard strain L forms to the third and forth generation cephalosporins remains sensitive, but its L forms inhibition zones are smaller than the original bacteria. The combined use of multi-antibiotics is a convenient and effective method to reduce Salmonella typhimurium L forms occurrence in order to avoid the occurrence of bacterial L form infection.