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Exploring the antimicrobial and antibiofilm activities of Artocarpus heterophyllus Lam. against Pseudomonas aeruginosa PAO1

  • Authors:
    • Muskan Soni
    • Naji Naseef Pathoor
    • Akshaya Viswanathan
    • Geetha Royapuram Veeraragavan
    • Pitchaipillai Sankar Ganesh
  • View Affiliations

  • Published online on: July 11, 2024     https://doi.org/10.3892/wasj.2024.265
  • Article Number: 50
  • Copyright : © Soni et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].

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Abstract

Pseudomonas aeruginosa (P. aeruginosa) is an opportunistic pathogen accountable for severe illness and mortality among immunocompromised individuals due to its extraordinary resistance to antibiotics. The regulation of pathogenic traits in P. aeruginosa is governed by a quorum sensing (QS) signaling molecule named acyl homoserine lactone (AHL). The present study investigated the inhibitory effects of the compound, Artocarpus heterophyllus Lam (A. heterophyllus), on the number of AHL‑dependent components produced by P. aeruginosa (PAO1). A. heterophyllus is considered as a beneficial natural compound with notable inhibitory effects on several pathogens. The present study investigated the antimicrobial and antibiofilm activities of A. heterophyllus against PAO1 through in vitro experiments, including minimum inhibitory concentration tests, biofilm inhibition assays and growth curve analysis. The results demonstrated that the methanolic extract of A. heterophyllus at a concentration of 10 mg/ml effectively inhibited PAO1. Additionally, the extract exhibited a 55.12% biofilm inhibitory effect at the lowest sub‑inhibitory concentration of 2.5 mg/ml, without affecting planktonic cell growth. On the whole, the findings of the present study indicate the prospective significance of A. heterophyllus as an anti‑pathogenic agent, which is effective in reducing QS‑dependent infection in PAO1.

Introduction

Pseudomonas aeruginosa (P. aeruginosa), a Gram-negative, aerobic pathogen, infects both immunocompetent and immunocompromised hosts. It can lead to a variety of community-acquired illnesses, including pneumonia, osteomyelitis-causing puncture wounds, folliculitis, urinary tract infections, septicemia, endocarditis and otitis externa (swimmer's ear) (1). Exopolysaccharide, lytic enzymes, such as protease and elastase, pyocyanin pigment formation and motility are all necessary for the pathogenic activity of P. aeruginosa (2-4).

Quorum sensing (QS) depends on protein systems that synthesize auto inducer (AI). P. aeruginosa uses four primary QS systems, each of which is linked with its unique autoinducer: 3-oxododecanoyl-L-homoserine lactone (3-oxo-C12-HSL), N-butanoyl homoserine lactone (C4-HSL), 2-heptyl-3-hydroxy-4-quinolone (Pseudomonas quinolone signal) and 2-(2-hydroxy-phenyl)-thiazole-4-carbaldehyde (integrated quorum sensing signal) (5). When these acyl-homoserine lactone (AHL) molecules bind to their respective receptors, LasR and RhlR induce the expression of pathogenic traits (2,6). The RhlI/RhlR system regulates rhamnolipid expression, while the LasI/LasR system also significantly contributes to virulence factors (7). The synchronized expression of these factors in response to QS enables bacteria to adapt to shifts in population density and environmental conditions. Targeting and disrupting these QS systems with antimicrobial compounds may be a promising approach with which to combat P. aeruginosa infections. The production of virulence factors frequently reduces the efficacy of a number of antibiotics, resulting in increased bacterial pathogenicity and a mortality rate of 18 to 61% in patients (8).

Natural products have long been a source of novel pharmacological compounds, and there is a renewed interest in examining them as potential candidates for drugs, particularly in the fight against antimicrobial resistance (9). Plant-based bioactive compounds can suppress disease pathogenesis-related genes by disrupting QS-associated virulence factors and preventing biofilm formation. Research findings indicate that natural products exert synergistic effects when combined with antibiotics against microbial pathogens (10,11). A wide range of natural products with medicinal properties, including flavonoids (e.g., curcumin and quercetin), quinones (e.g., plumbagin), alkaloids (e.g., piperine), triterpenoids and essential oil phenols (e.g., eugenol and thymol), have been shown to be effective against certain bacteria (9). Some of these products have been demonstrated to be potent antibacterial and antibiofilm agents; they can also inhibit cell attachment and adhesion, and suppress the production of virulence factors, inhibit polymer matrix formation, and thus disrupt the QS network (12,13). Therefore, determining potent QS inhibitors is essential, ideally sourced from natural sources.

Artocarpus heterophyllus Lam. (A. heterophyllus), belonging to the family Moraceae, produces the largest edible fruit among evergreen trees, commonly known as jackfruit. This species yields more fruit than any other fruit tree species. However, despite its abundance, the leaves of the jackfruit tree (A. heterophyllus) are often regarded as agro-industrial waste. Only a small proportion of the total biomass is utilized, primarily as cattle fodder, and occasionally, for managing asthma, diarrhea and dermatitis. Traditional medicine has extensively utilized the fruits, leaves and bark of the jackfruit tree due to their various medicinal properties. These include anticarcinogenic, antibacterial, antifungal, anti-inflammatory, wound-healing and hypoglycemic qualities (14). According to research, A. heterophyllus contains bioactive compounds, such as alkaloids, flavonoids, phenolic acids and terpenoids, which are known for their antimicrobial properties. These compounds have the potential to limit the growth and survival of pathogenic microbes, either individually or in combination (15). It has been previously demonstrated that flavonoids, particularly artonin and artocapones, exhibit anti-plasmodial activity (16). Additionally, the methanolic extract of dried A. heterophyllus leaf powder has been shown to exhibit potent antibacterial properties against a variety of microbes, including Escherichia coli (E. coli) and Salmonella enterica (S. enterica) (17). Furthermore, ethyl acetate extracts from unutilized parts of the jackfruit have been found to exhibit optimal antibacterial activity against Xanthomonas axonopodis, with the peels exhibiting the most potent inhibitory effects, followed by the fiber and the core exhibiting the least potent effects (18). Additionally, it has been reported that A. heterophyllus exhibits antimicrobial activity against certain foodborne pathogens (19). In a previous study, it was found that the seed powder extract of A. heterophyllus, which is used in the green synthesis of silver nanoparticles (AgNPs) from an aqueous solution of silver nitrate (AgNO3), contains jacalin (20). This lectin constitutes more than half of the proteins in the jackfruit crude seed extract and has a variety of biological activities. The resulting AgNPs demonstrate potent antibacterial activity against both Gram-positive and -negative bacteria, suggesting potential applications in nanomedicine (20). In the study conducted by Sato et al (21), it was found that artocarpin, extracted from A. heterophyllus, demonstrated potent antibacterial activity against cariogenic bacteria, with minimum inhibitory concentration (MIC) values ranging from 3.13 to 12.5 µg/ml. At this MIC, the compound effectively inhibited the growth of cariogenic bacteria (21). Furthermore, Sun et al (22) found that artocarpin exerted selective cytotoxic effects on human colon cancer cells. It attenuated anchorage-independent growth, inhibited colon cancer cell growth and caused G1 phase cell cycle arrest, followed by apoptotic and autophagic death (22).

It has also been shown that isolated bioactive compounds from A. heterophyllus fruits exert anti-inflammatory effects. Jackfruit contains flavonoids, which can inhibit the production of inflammatory chemicals from mast cells, neutrophils and macrophages (23). Prakash et al (24) documented in their study that A. heterophyllus contains compounds, such as morin, dihydromorin, cynomacurin, artocarpin, isoartocarpin, cycloartocarpin, artocarpesin, oxydihydroartocarpesin, artocarpetin, betulinic acid, artocarpanone and heterophylol. These compounds have been found to be beneficial in treating fever, boils, wounds, skin diseases, convulsions, diuretic conditions, constipation, ophthalmic disorders and snake bites (24). Fernando et al (25) found that a hot water extract of A. heterophyllus leaves significantly improved glucose tolerance in both normal and diabetic subjects when taken orally in doses of 20 g/kg.

Numerous studies have focused on A. heterophyllus as an achievable source of starch. Tulyathan et al (26) reported that jackfruit seeds contain ~20% starch on a dry basis, the recovery yield of starch extracted from jackfruit seeds was ~77%, indicating that it could be a valuable source of starch for the food and pharmaceutical industries (26). These properties highlight the potential of A. heterophyllus. The primary aim of the present study was to examine the effects of A. heterophyllus on P. aeruginosa (PAO1). To the best of our knowledge, the anti-quorum sensing (anti-QS) properties of A. heterophyllus are unexplored in relation to P. aeruginosa.

The present study aimed to investigate the antimicrobial and antibiofilm properties of A. heterophyllus against PAO1. The objective was to evaluate the effectiveness of A. heterophyllus in preventing and disrupting biofilm formation by this common pathogen.

Materials and methods

Sample collection

In the present study, which was conducted from January to October, 2023, A. heterophyllus was obtained from an indigenous botanical garden in Chennai, Tamil Nadu, India. A qualified botanist examined the plant and confirmed its authenticity. The leaves were cleaned with water and allowed to dry naturally for 1 week. To prepare the extract, 10 g A. heterophyllus leaf powder were mixed with 50 ml methanol and distributed across two maceration containers for 48 h, with occasional shaking using a shaker. Following the extraction process, the resulting suspension was filtered through No. 1 filter paper (Whatman, HiMedia Laboratories, LLC) and placed over a funnel lined with a white muslin cloth. The methanol solvent was then evaporated from the filtrate using a hot water bath set precisely at 50˚C. The dehydrated filtrate was measured, and the dried substance was weighed before being stored at 4˚C for later use.

Bacterial strain and growth condition

The culture of Pseudomonas aeruginosa (PAO1) samples utilized in the present study was generously provided by Dr Busi Siddhardha from Pondicherry University, Puducherry, Tamil Nadu, India. The samples were sub-cultured in Luria Bertani (LB) broth (HiMedia Laboratories, LLC). PAO1 cultures were then incubated at 37˚C in a shaking incubator set at 100 rpm for 24 h. Characteristic growth patterns were observed on LB agar and Nutrient agar. To verify the identity of PAO1, a preliminary identification was conducted by laboratory personnel at Saveetha Dental College and Hospital in Chennai, Tamil Nadu, India, utilizing the VITEK 2 automated system. As previously described by David H. Pincus (BioMérieux, Inc.), the biochemical reactions of the bacterial isolate were compared to a comprehensive database to provide accurate identification (27). In addition, various phenotypic tests, including Gram staining, catalase, oxidase, motility and citrate utilization, were conducted and documented based on standard microbiological investigations, as previously described by others (28). The bacterial cultures underwent routine sub-culturing for experimental use.

Antimicrobial activity and antibiotic susceptibility testing (AST)

The agar well-diffusion method, an established technique, was employed to evaluate the antibacterial activity of A. heterophyllus (29). The bacterial culture of PAO1 was spread onto Mueller Hinton agar (MHA) (HiMedia Laboratories, LLC) using a swab moistened with the bacterial suspension. Subsequently, a well with a diameter of 8 mm was punched into the MHA medium using a sterile cork borer, and a well was filled with 50 µl A. heterophyllus extract, while water served as a control in another well. The plate was then incubated upright at 37˚C for a 24 h. Following incubation, the zone of inhibition around the wells was measured using a Vernier caliper on a mm scale to detect the antibacterial activity of the A. heterophyllus extract.

Subsequently, the antibiotic susceptibility of PAO1 was assessed using the Kirby-Bauer disk diffusion method (30). Using this standard technique, the authors were able to determine the susceptibility of PAO1 to various antibiotics. Initially, the culture of PAO1 was evenly distributed onto MHA plates using a sterile swab saturated with the bacterial suspension. Subsequently, these plates were subjected to testing with a comprehensive panel of conventional antibiotics, including colistin, tobramycin, ciprofloxacin, azlocillin, aminoglycosides, netilmicin, piperacillin and carbenicillin (HiMedia Laboratories, LLC).

Evaluation of MIC

A 2-fold broth dilution method was used to determine the MIC of A. heterophyllus extract against PAO1. The assessment was carried out at concentrations ranging from 10 to 0.01 mg/ml. The MIC for the methanol extract was determined using established protocols (31,32). In brief, 20 µl PAO1 broth culture with the cell mass equivalent of 0.5 McFarland turbidity standard (1.5x108 CFU/ml) was filled in tubes containing LB broth. Following the successive dilution with A. heterophyllus extract, each of the tubes underwent incubation at 37˚C for 24 h. Following incubation, 40 µl 2,3,5-triphenyl tetrazolium chloride (HiMedia Laboratories, LLC) was added to each tube to check for color changes and confirm the results. The minimum concentration that caused no growth (no color change) was recorded as the MIC. Additional antibiofilm studies were carried out in accordance with these findings.

Crystal violet biofilm inhibition assay

To determine the effects of A. heterophyllus extract on PAO1 biofilm formation, the crystal violet staining assay was used (32). An overnight culture of PAO1 (20 µl) was added to a microtiter plate containing 180 µl fresh LB medium, and the A. heterophyllus extract was added in a concentration-dependent manner (ranging from 5 to 0.009 mg/ml). The mixture was incubated for 48 h at 37˚C. Following incubation, the surface-adherent biofilm was stained with a 0.1% crystal violet solution (HiMedia Laboratories, LLC) at room temperature for 2 min, and the planktonic cells were washed away with sterile distilled water. After 10 min, the CV-bound biofilm was eluted in 200 µl 70% ethanol. A UV-Vis spectrophotometer (JASCO UV/Vis, India) was used to determine the concentration of the eluted CV by measuring the crystal violet intensity at 520 nm. The percentage of inhibition was then calculated using the following equation: Control optical density (OD) 520 nm-treated OD 520 nm/control OD 520 nm x100.

Bacterial growth curve

The growth curve analysis was conducted following previously established protocols (33). The concentration of 2.5 mg/ml A. heterophyllus was selected based on the crystal violet biofilm inhibition assay, which indicated that this concentration inhibited PAO1 biofilm formation by 55.12%. Subsequently, the present study wished to confirm its influence on bacterial growth at the same concentration through growth curve experiments to determine whether it inhibited growth as well. To encapsulate, the present study delved into the growth dynamics of PAO1 bacteria under dual conditions, with or without the presence of A. heterophyllus, at a concentration of 2.5 mg/ml. The cultures were meticulously incubated at 37˚C, with hourly recordings of OD at 600 nm spanning a duration of up to 24 h.

Statistical evaluation

Each experiment was carried out three times, with statistical significance rigorously demonstrated for both the growth curve analysis and biofilm quantification. The Student's t-test with GraphPad prism 10.1.0 software (Dotmatics) served as the tool for statistical analysis. A P-value <0.05 was considered to indicate a statistically significant difference.

Results

Bacterial identification of PAO1

The VITEK 2 system accurately confirmed the identity of the bacterial strain as PAO1 with high confidence. The biochemical profile aligned with the expected characteristics for PAO1, thus validating the initial identification methods (34). The morphological profiling of the bacterial isolates further supported the findings, revealing distinct morphotypes consistent with PAO1. Notably, Gram staining revealed the characteristic Gram-negative, rod-shaped morphology of PAO1 (Fig. 1A). Additionally, the identity of PAO1 was further confirmed by positive results in catalase (Fig. 1B), oxidase (Fig. 1C), motility (Fig. 1D) and citrate utilization (Fig. 1E) tests.

Antimicrobial susceptibility and AST

The present study initially examined the antimicrobial activity of A. heterophyllus extract against PAO1, indicated by a measured zone of inhibition with a recorded diameter of 8 mm, highlighting its potent efficacy (Fig. 2). Subsequent AST, conducted in accordance with the Clinical and Laboratory Standards Institute (CLSI) Guidelines 2022(35), unveiled PAO1 resistance to a majority of tested drugs, including colistin, ciprofloxacin, piperacillin and azlocillin (Table I).

Table I

Antibiogram of PAO1 against several antibiotics.

Table I

Antibiogram of PAO1 against several antibiotics.

Serial no.AntibioticsP. aeruginosa (PAO1)
1Tobramycin22.3±2.9
2AzlocillinR
3 Aminoglycosides15±0.9
4Netilmicin18±1.1
5PiperacillinR
6ColistinR
7CiprofloxacinR
8Carbenicillin16±1.1

[i] Values represent the mean inhibition zone diameter (mm) ± standard deviation for P. aeruginosa (PAO1) isolates tested. R, resistance to the antibiotic; P. aeruginosa, Pseudomonas aeruginosa.

Antibacterial activity of A. heterophyllus at the MIC level

By employing a 2-fold serial dilution method, the present study explored the antibacterial potential of the A. heterophyllus extract across a spectrum ranging from 10 to 0.019 mg/ml. Notably, at the end point concentration of 10 mg/ml, the inhibition of PAO1 growth was observed (Table II), suggestive of the promising antimicrobial efficacy of A. heterophyllus against PAO1. This prompted further investigation into the anti-biofilm properties of the A. heterophyllus extract at sub-MIC concentrations.

Table II

Minimum inhibitory concentration.

Table II

Minimum inhibitory concentration.

Serial no.Two-fold dilution concentration (mg/ml)Growth measureda
110-
25+
32.5+
41.25+
50.62+
60.312+
70.156+
80.078+
90.039+
100.019+

[i] Methanol extract of A. heterophyllus inhibited PAO1 growth at a final concentration of 10 mg/ml.

[ii] aThe growth measured refers to the presence (+) or absence (-) of visible growth in the microbial culture following exposure to the respective two-fold dilution concentrations (mg/ml) of A. heterophyllus. A. heterophyllus, Artocarpus heterophyllus.

Effect on biofilm formation

The present study investigated the ability of A. heterophyllus, at concentrations ranging from 5 to 0.009 mg/ml, to inhibit PAO1 biofilm formation using 0.1% crystal violet dye on a static microtiter plate. The findings indicated that the A. heterophyllus extract significantly reduced biofilm formation when PAO1 was exposed to concentrations of 2.5 and 1.25 mg/ml, resulting in reductions of 55.12 and 26%, respectively. In the control, no biofilm inhibition was observed (without A. heterophyllus extract) (Fig. 3). Therefore, conducting a bacterial growth curve analysis will further assess the efficacy of the A. heterophyllus extract at these same concentrations.

Bacterial growth curve analysis

The growth curve was analyzed both with and without A. heterophyllus. The results revealed that A. heterophyllus at a concentration of 2.5 mg/ml did not inhibit bacterial growth (Fig. 4). The spectrophotometric analysis revealed no noticeable disparity between the control and treated bacterial cells at 600 nm. These findings suggest that A. heterophyllus does not exert inhibitory effects on bacterial growth at a concentration of 2.5 mg/ml under the tested conditions. However, it does exhibit inhibitory effects specifically on biofilm formation.

Discussion

Gram-negative bacteria primarily cause infections and form biofilms due to the activity of QS signaling molecules. However, treating infections caused by biofilm-forming P. aeruginosa poses a considerable challenge due to bacterial resistance to traditional antibiotics (36). The AHL molecule plays a crucial role in the pathogenesis of P. aeruginosa, and inhibiting its activity holds promise for mitigating the pathogenicity of this pathogen.

The present study evaluated the potency of A. heterophyllus, which contains bioactive compounds, such as alkaloids, flavonoids, phenolic acids and terpenoids, and examined whether it has the ability to reduce AHL-dependent factors production in PAO1. In the study by Khan et al (17), A. heterophyllus, which contains flavonoids, was shown to exert an inhibitory effect on several bacteria, including E. coli and S. enterica (17). Similarly, a recent study by Alam et al (37) demonstrated that the plant-derived extract, Berginia ciliata, which also contains flavonoids, inhibited the pathogenic bacteria PAO1(37).

The present study evaluated the antibiofilm activities of A. heterophyllus extract against PAO1. The preliminary findings indicated that A. heterophyllus effectively inhibited biofilm formation at the lowest concentration of 10 mg/ml. The current data support the findings of the study by Sivagnanasundaram and Karunanayake (38), which reported that A. heterophyllus had potent bactericidal activity against E. coli at 3 mg/ml, and the presence of phytosterols and terpenoids was reported (38). In another study, it was found that artocarpin, extracted from A. heterophyllus, inhibited the growth of Streptococcus mutans at an MIC of 1.95 µg/ml by altering cell membrane permeability, leading to the release of intracellular proteins (39). The study by Sato et al (21) demonstrated that artocarpin exhibited potent antibacterial activity against cariogenic bacteria, with MIC values ranging from 3.13 to 12.5 µg/ml. At these MIC levels, artocarpin was able to inhibit the growth of cariogenic bacteria (21).

In the present study, A. heterophyllus extract inhibited QS-dependent biofilm formation in PAO1 at concentrations below the MIC. The crystal violet biofilm inhibition assay revealed that at a concentration of 2.5 mg/ml, the A. heterophyllus extract significantly reduced biofilm formation (Fig. 3). Vijayaraghavan et al (40) reported that peel waste from jackfruit was identified as a source for anaerobic biohydrogen production and exhibited potential for removing toxic dyes and chemicals from wastewater released by the textile and pharmaceutical industries. Moreover, Majik et al (41) reported that natural pyrrolidine alkaloid (R)-Bgugaine extracted from Arisarum vulgare, which decreased the biofilm density by 83%, also inhibited the pyocyanin pigmentation, LasA protease and rhamnolipid production of PAO1(41). Similarly, Vijayakumar and Ramanathan (42) reported that the tropical plant Musa acuminata contains flavonoids and 5-hydroxymethylfurfural, which inhibited P. aeruginosa biofilm formation at a concentration of 400 µg/ml. Furthermore, methanolic extract from the leaves and stems of A. heterophyllus contains chromones and flavonoids that have anti-proliferative activity. These compounds have been shown to exert significant inhibitory effects against various human cancer cells, with IC50 values ranging from 0.36±0.02 to 22.09±0.16 µM (43). A previous study found that flavonoids act to inhibit bacterial movement and reduce biofilm formation in P. aeruginosa, while also inhibiting the production of bacterial toxins in Staphylococcus aureus (44).

In the present study, growth curve analysis conducted in the presence of A. heterophyllus extract at a concentration of 2.5 mg/ml, as depicted in Fig. 4, indicated that A. heterophyllus did not impede bacterial growth. These results suggest that, under the conditions tested, A. heterophyllus does not exert inhibitory effects on bacterial growth at the specified concentration. However, it is noteworthy that A. heterophyllus does demonstrate inhibitory effects specifically on biofilm formation. Rashmi et al (45) conducted a growth curve experiment using antibiofilm concentrations. The results of their study revealed that the growth pattern of P. aeruginosa with and without treatment of Alternaria alternata extract at three concentrations did not impede bacterial growth. However, the extract exhibited inhibitory effects specifically on biofilm formation (45).

Taken together, the results of the present study suggest that the methanol extract of A. heterophyllus inhibits the QS system in PAO1 by targeting the LasI/LasR and RhlI/RhlR systems, possibly due to the presence of bioactive compounds. However, additional research is warranted to identify active components within A. heterophyllus extract that may harbor anti-QS and anti-biofilm producing properties.

In conclusion, A. heterophyllus was found to exhibit notable potential in disrupting the QS pathways in PAO1. Specifically, it targets the LasI/LasR and RhlI/RhlR systems. By inhibiting the production of autoinducer molecules, such as 3-oxo-C12-HSL and C4-HSL, or by preventing their binding to the LasR and RhlR receptors, A. heterophyllus downregulates the expression of genes critical for virulence and biofilm formation (Fig. 5A). This interference leads to a reduction in extracellular polymeric substance production and impaired biofilm development (Fig. 5B). Additionally, the extract introduction enhances antibiotic penetration and immune defense effectiveness (Fig. 5C).

The results of the present study suggest that the significant inhibition of the QS system in PAO1 by A. heterophyllus is likely due to its bioactive compounds, such as alkaloids, flavonoids, phenolic acids and terpenoids. The methanol extract of A. heterophyllus demonstrates considerable potential in restoring the effectiveness of antibiotics by facilitating their penetration through the compromised biofilm structure of PAO1. By degrading the biofilm matrix, this extract can render the infectious bacteria more accessible to immune defense.

Considering the broad availability of jackfruit in India and the versatile use of all of its parts, including wood and latex, which are known to have therapeutic properties, there is significant potential for scientific research into its medicinal benefits. The present study highlights the importance of exploring plant-based compounds for enhancing current antimicrobial therapies and addressing the challenges posed by P. aeruginosa biofilm-associated infections. Further research with various formulations would be beneficial in improving the pharmacological therapeutic applications of the identified compounds, particularly their anti-QS and anti-biofilm properties. Despite being historically neglected, jackfruit is gaining recognition for its medicinal properties, and continued research is essential to unlock its full potential as an antibiotic adjuvant. In conclusion, A. heterophyllus could serve as a valuable antibiotic adjuvant, offering promising strategies to prevent or treat chronic infections caused by P. aeruginosa. This underscores the importance of plant-based compounds in addressing the growing challenge of antibiotic resistance and biofilm-associated infections.

Acknowledgements

Not applicable.

Funding

Funding: No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

MS collected, managed the data and participated in the writing of the manuscript. AV and NNP participated in writing the proposal, performing data collection and in the writing of the manuscript. RVG and PSG were involved in data curation, data analysis and in revising the manuscript. RVG and PSG confirm the authenticity of all the raw data. All authors have read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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September-October 2024
Volume 6 Issue 5

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Spandidos Publications style
Soni M, Naseef Pathoor N, Viswanathan A, Veeraragavan G and Sankar Ganesh P: Exploring the antimicrobial and antibiofilm activities of <em>Artocarpus heterophyllus</em> Lam. against <em>Pseudomonas aeruginosa</em> PAO1. World Acad Sci J 6: 50, 2024.
APA
Soni, M., Naseef Pathoor, N., Viswanathan, A., Veeraragavan, G., & Sankar Ganesh, P. (2024). Exploring the antimicrobial and antibiofilm activities of <em>Artocarpus heterophyllus</em> Lam. against <em>Pseudomonas aeruginosa</em> PAO1. World Academy of Sciences Journal, 6, 50. https://doi.org/10.3892/wasj.2024.265
MLA
Soni, M., Naseef Pathoor, N., Viswanathan, A., Veeraragavan, G., Sankar Ganesh, P."Exploring the antimicrobial and antibiofilm activities of <em>Artocarpus heterophyllus</em> Lam. against <em>Pseudomonas aeruginosa</em> PAO1". World Academy of Sciences Journal 6.5 (2024): 50.
Chicago
Soni, M., Naseef Pathoor, N., Viswanathan, A., Veeraragavan, G., Sankar Ganesh, P."Exploring the antimicrobial and antibiofilm activities of <em>Artocarpus heterophyllus</em> Lam. against <em>Pseudomonas aeruginosa</em> PAO1". World Academy of Sciences Journal 6, no. 5 (2024): 50. https://doi.org/10.3892/wasj.2024.265