Special Issue:

Emerging and Re-emerging Animal Health Challenges in Low and Middle-Income Countries

Prescence and Verification of LasI and LasR Genes in Pseudomonas aeruginosa Causing Urinary Tract Infection in Dogs

Shatha E. Jasim*, Sahar M. Hayyawi

Department of Microbiology, College of Veterinary Medicine, University of Baghdad, Baghdad, Iraq.

Received | August 09, 2025; Accepted | September 27, 2025; Published | October 14, 2025

*Correspondence | Shatha E. Jasim, Department of Microbiology, College of Veterinary Medicine, University of Baghdad, Baghdad, Iraq; Email: [email protected]

Citation | Jasim SE, Hayyawi SM (2025). Prescence and verification of LasI and LasR genes in Pseudomonas aeruginosa causing urinary tract infection in dogs. J. Anim. Health Prod. 13(s1): 558-567.

DOI | https://dx.doi.org/10.17582/journal.jahp/2025/13.s1.558.567

ISSN (Online) | 2308-2801

Copyright: 2025 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

INTRODUCTION

Pseudomonas aeruginosa is frequently cause localized or system-specific infections, such as urinary tract infection, ears, eyes, and occasionally the respiratory system (Mohammad et al., 2024), mastitis in cattle (Al-Taee et al., 2019). It is widely known to cause otitis externa in dogs (Mohammad et al., 2024), wound infections (Raheem and Abdalshheed, 2023), and isolated from urine of dogs affected with malignant tumor (Sahar et al., 2009). Urinary tract infections (UTIs) are the most prevalent diseases in dogs, which are caused by bacterial pathogens (Yu et al., 2020), occurs frequently causing chronic kidney diseases with significant effects on the kidney functions (Mohmoud and Al-Dujaily, 2018). This bacterium regarded as a significant pathogen because its wide variety of resistance mechanisms (Yaseen and Ahmed, 2023; Khames and Ahmed, 2024). It has a vast genome that gives several virulence characteristics, including the ability to form biofilm (Ali et al., 2024), adhered to surfaces by extracellular polymer substances (EPS) called matrix, enables bacteria to survive in a harsh condition, and permits the cells within the biofilm to communicate with each other (Al-Barhawee and Al-Rubyee, 2024). The microbial biofilm is the most efficient and competing expression of the genome in prokaryotic biofilm cells, and being more protected and metabolically efficient, demonstrating tolerance to many stressors through a signaling system controlled by quorum-sensing (QS) system (Lazar and Chifiriuc, 2010; Razzaq et al., 2017) which is a bacterial cell-cell communication system that uses chemical signals to control gene expression levels depended on the cell density manner, it is crucial for pathogenicity, biofilm formation, and antibiotic resistance (Lafta and Sadeq, 2024). Thes chemical signals known as autoinducers (AIs) that bind to specific receptors (Shalata, 2022). Interestingly the genes that contribute to the composition of this system are about 10% of P. aeruginosa genome and for this status are responsible for most of the cellular physiology processes and virulence phenotypes (Schuster and Greenberg, 2006).

In P. aeruginos, a there are seven genes associated with the occurrence of QS which are rhlA, rhlR, rhlI, lasR, lasI, lasB, phzA1 (Mohammed and Zgair, 2022), and the main highly interconnected QS systems are Las, Rhl, Pqs, and Iqs (Shalata, 2022), which are channels interlinked together that used transcriptional regulators such as LasR, RhlR, PqsR, and IqsR, respectively and connected to specific AIs leading to aggravating the expression of the selected genes that cause bacterial virulence (Bhardwaj et al., 2021). This bacterium has two AHL-depended on systems known as LasR/LasI and RhlR/RhlI, which regulate the synthesis and signal transduction of the N-(3-oxo-dodecanoyl)-L-homoserine lactone (OdDHL) and N-butanoyl-L-homoserine lactone (BHL), respectively (Wu and Luo, 2021). The QS system has significant role in this bacterium by increasing its pathogenicity (Hemmati et al., 2024).

This study aimed to investigate biofilm production in clinical P. aeruginosa isolates from dogs suffering UTI, and to detect the occurrence of mutations in16S rRNA in all six P. aeruginosa isolates. Additionally, we aim to determine if experimental infection of mice with diverse P. aeruginosa could induce differing histopathological changes.

MATERIALS AND METHODS

Samples collection

Samples were collected from dogs with suspected urinary tract infection (UTI) of different ages, both genders, and different breads, during the period from February 2024 to June 2024, obtained from the veterinary hospital and veterinary clinics located in various areas of Baghdad. This included 108 urine samples from 108 dogs with suspected UTI by spontaneous urination, collected in a sterile container, marked, and kept in cooling box to perform examination and bacterial diagnosing in the microbiology laboratory in the College of Veterinary Medicine in Baghdad.

General urine examination

This method was performed according to Punia et al., 2018 to detect the UTI in dogs. Taking 5 mL of the urine sample into a test tube and centrifuged at 3000 rpm for 7 min. The supernatant was discarded, placed the sediment on a glass slide for examination under a light microscope at 40× magnification.

Isolation and identification

Based on a loopful of urine spread onto blood agar and MacConkey agars (HiMedia, India), incubated aerobically at 37°C for 24 hrs. Then, isolated the colonies on selective media cetrimide agar and pseudomonas agars (HiMedia, India) to get pure growth (Devnath et al., 2017), after that identified by biochemical tests such as oxidase and catalase, confirmation the isolates using VITEK-2 compact system according to the manufacturer company VITEK-2 technique (BioMerieux, France) was done using a GN colorimetric identification card to conformation the isolates (Hakim et al., 2024; Abed et al., 2024).

Biofilm detection methods

Tube method (qualitative assay): A loopful of the isolated bacteria was inoculated into 5 mL of tryptic soy broth supplemented with 1% glucose and incubated at 37°C for 72 h. The tube was washed with normal saline and air-dried. The dried tube was heat-fixed by passing it through a flame three times. Subsequently, the biofilm was stained with 0.1% crystal violet for 1 h, excess stain was removed, and the tube was rinsed with normal saline and dried in an inverted position. Biofilm formation was confirmed by the presence of a visible layer on the inner walls and at the bottom of the tube (Furtuna et al., 2018).

Congo red method: On Congo red agar, P. aeruginosa isolate was cultured for 48 h at 37°C, black colonies indicated the biofilm formation, while the red colonies indicated non-biofilm formation (Ciocan et al., 2016).

Polymerase chain reaction (PCR): DNA was extracted according to the commercial purification system using (Genomic DNA Mini Kit, Korea) to detect 16S rRNA, LasR and LasI genes. The primers designed are mentioned in Table 1, and the optimum conditions of PCR cycles were: firstly one cycle of initial denaturation at 95ᵒC for 5 min, then 35 cycles of denaturation at 95ᵒC for 45 sec, annealing (16S rRNA at 58ᵒC/ LasR and LasI at 57ᵒC)

 

Table 1: The sequence of primers used in this study.

Primer	Sequence	Primer sequence	GC%	Size of product (bp)	Reference
16s RNA	27F	5'- AGAGTTTGATCCTGGCTCAG- 3'	50.0	1250 bp	(Srinivasanet al., 2015)
	1392R	5'- GGTTACCTTGTTACGACTT- 3’	42.1
LasI	F	5'- CGTGCTCAAGTGTTCAAGG-3'	52.63	295 bp	(Lima et al., 2018)
	R	5'- TACAGTCGGAAAAGCCCAG-3’	52.63
LasR	F	5'- ATGGCCTTGGTTGACGGT -3'	55.56	700 bp	(Azemin et al., 2022)
	R	5'- GCAAGATCAGAGAGTAATAAGACC -3’	44.00

 

for 45 sec, and extension at 72ᵒC for 1 min, at last, final extension at 72ᵒC for 5 min. The PCR products were stained with red stain (Intron, Korea), then electrophoresis on 1.5% agarose and observed under UV trans illuminator. The amplified products were sent for sequencing to Macrogen Inc. (Geumcheon-gu, Seoul, South Korea) using the Sanger’s method. The sequences were compared with the NCBI GenBank database using the basic local alignment search tool (BLAST) to confirm the isolates as P. aeruginosa.

Animal experimental design

A total of 24 mice were divided into three groups each one contains eight mice: first group (G1) of mice was injected with (PBS) as a negative control, second group (G2) mice were infected with biofilm producing P. aeruginosa, third group (G3) mice were infected with non-biofilm producing P. aeruginosa. The dose was given intraperitonially (I/P) (Al-Rasheed et al., 2023), at 0.5 McFarland tube (1.5× 108 CFU/ml) 0.25 ml, then sacrificed on 5th days (Ali, 2019).

Histological examination

Specimens were taken from internal organs (kidney, liver and spleen) of mice, fixed in 10% buffered neutral formalin. According to (Suvarna et al., 2018) a technique of several steps was done for histological examination.

Statistical analysis

Data were analyzed using SAS (Statistical Analysis System - version 9.1). One-way analysis of variance (ANOVA) program was used to detect the percentage of difference groups in study parameters.

RESULTS

In the present study according to the microscopic analysis, the urine samples from which P. aeruginosa was isolated contained pus and bacteria, that is indicative of a urinary tract infection. The bacterial isolation and identification revealed out of 108 urine samples with UTIs the P. aeruginosa isolates were found in 6/108 (5.5%) (Figure 1). The incidence rate of infection in male was higher than females with a rate of 66.6% and 33.33%, respectively (Figure 2). The rate of infection occurred at a high infection rate 100% in adult > 1 year with no infection rate in young ≤1 year.

 

 

The biofilm formation was performed by using tube method and Congo red agar demonstrated that five out of six isolates (5/6, 83.33%) produced biofilm and only one isolate (1/6, 16.66%) failed to produce. In tube method, the positive results to detect the biofilm formation were indicated by a violet-colored layer adhering to the tube wall, while a colorless tube indicated a negative result (Figure 3). Black colonies on Congo red agar indicated the presence of a biofilm layer, while non-biofilm colonies appeared red color (Figure 4).

 

 

The P. aeruginosa confirmed by VITEK-2 system microbiology showed a match 99% (Figure 5), and the bacteria were genetically diagnosed by PCR and automated DNA sequencing to all isolates of P. aeruginosa amplified directed the 16S rRNA gene as in (Figure 6).

The identity of isolates was subsequently confirmed by sequencing the PCR. BLAST analysis showed 99% similarity to reference sequences of P. aeruginosa, including strain OR793893.1. The sequences have been added to the NCBI GenBank database and are available under the accession codes: PP979721.1, PP979722.1, PP979723.1, PP979724.1, PP979725.1, and PP979726.1. In this study the detection of QS genes LasR and LasI was found in 100% of biofilm forming isolates and 100% missing in isolate that do not contain biofilm (Figure 7).

 

 

 

Sequencing analysis of P. aeruginosa 16S rRNA gene was performed by MEGA6 software and showed the changes in nucleotide sequence compared to other globally known sequences. These changes were transition or transversion and are listed in Table 2.

Sequencing analysis of QS genes LasR and LasI in P. aeruginosa (ID: PP979723.1) was performed in MEGA6 software and has no changes in nucleotide sequence of LasR gene and had 100.

Introduction

Identity when compared to other globally known (ID: CP137940.1). On the other hands, LasI gene showed transition mutation in nucleotide sequence when compared to other globally known (ID: CP137912.1) as listed in Table 3.

 

Table 2: Genetic variation at 16S rRNA genes of Pseudomonas aeruginosa.

Identities	Sequence ID with submission	Sequence ID with compare	Nucleotide	Location	Type of substitution	No.
99%	ID: PP979721.1	ID: OR793893.1	G\A	133	Transition	1
99%	ID: PP979722.1	ID: OR793893.1	T\A	208	Transvertion	2
			G\A	536	Transition
			T\A	537	Transvertion
99%	ID: PP979723.1	ID: OR793893.1	T\C	222	Transition	3
			A\C	277	Transvertion
99%	ID: PP979724.1	ID: OR793893.1	A\T	252	Transvertion	4
			C\T	253	Transition
			C\G	563	Transvertion
99%	ID: PP979725.1	ID: OR793893.1	G\T	539	Transvertion	5
99%	ID: PP979726.1	ID: OR793893.1	C\A	563	Transvertion	6

 

Source: P. aeruginosa; 16S rRNA gene.

 

Table 3: Genetic variation at LasR and LasI genes of Pseudomonas aeruginosa.

Identities	Predicted effect	Amino acid change	Nucleotide change	Nucleotide	Location	Type of substitution	Gene	No. of gene
100%	----	------	------	------	-----	------	LasR	1
99%	Missense	Q(Glutamine)\ R(Arginine)	CTG\CCG	T\C	4101403	Transition	LasI	2

 

Source: Pseudomonas aeruginosa (ID: PP979723.1). Sequence ID with compare: 1: LasR=ID: CP137940.1; and 2: LasI=ID: CP137912.1

 

The result of protein conformation of LasR and LasI genes in P. aeruginosa (ID: PP979723.1) showing as three-dimensional (3D) modeling secondary structure, and exposes the location of mutation in only LasI protein as in Figure 8.

 

 

In Ramachandran graph for amino acid in general and local quality estimation with Z score of LasR and LasI genes, the results showed that model evaluation of the amino acid of query protein were in the most favorable energy regions for good quality model (Figure 9). The results also show that the model validation include the local quality estimation with Z score, located within the light or dark gray and blank areas (Figure 10).

 

In histological examination of G1 mice injection with PBS as a negative control showed that the kidney with normal appearance of glomerular tuffet surrounded by Boman space, and normal proximal convoluted tubule (Figure 11A). Liver tissue showed normal central vein surrounded by a regular arrangement of normal hepatocytes and sinusoids (Figure 11B). The spleen has a normal (white pulp) consist of lymphoid follicles with central arteriols surrounded by lymphocytes, and the (red pulp) contains lymphocytes with blood vessels, all of them surrounded by a normal capsule (Figure 11C).

 

In G2 mice infected with P. aeruginosa, produced biofilm there were histological changes in kidney demonstrates severely congested blood vessels, aggregation of mononuclear cells, and cloudy swelling tubules (Figure 11D), the liver showed severe interstitial infiltration with inflammatory cells (lymphocytes and macrophages) with dilated central vein (Figure 11E), in spleen there is an extensive interstitial hemorrhage with the depleted lymphoid follicle, and the presence of necrotic lymphocytes (Figure 11F). In G3 mice infected with P. aeruginosa not produced biofilm there were histological changes in kidney demonstrates enlarged glomeruli surrounded by infiltration of mononuclear cells and tubules cloudy swelling (Figure 11G), the liver showed congested blood vessels, lymphocytic cuffing central vein, sinusoid hemorrhage, and apoptosis (Figure 11H). In spleen there is an increase in megakaryocytic cell, depleted lymphoid follicle with hemorrhage (Figure 11I).

In general, according to the results of this study, only six dogs (6/108, 5.5%) had a UTI caused by P. aeruginosa. This is consistent with another study (Hakim et al., 2024) where they have found 5.3% of dog cases with lower UTI and cystitis were caused by P. aeruginosa isolates. According to another study (Hattab et al., 2021), P. aeruginosa was present in 4.2% of the dogs that had bladder infections, while (Rampacci et al., 2018) isolated 13.4% P. aeruginosa from dogs with UTIs in Italy. The spread of P. aeruginosa in dogs with UTIs varies according to geographic area and underlying medical conditions (Ataya et al., 2023). In this study, the incidence rate of males was higher than females (66.6%), and (33.3%), respectively, occurred at a high infection rate 100% in (adult > 1 Year). However, the study conducted by (Thompson et al., 2011), presented that many reports showed UTIs are more prevalent in older female dogs with a mean age of about 7–8 years.

The genotypic results for the 16S rRNA gene confirmed the diagnosis for all isolates, allowing to conclude that all of them were P. aeruginosa, as expected. Also, the detection of QS genes LasR and LasI was found in 100% of biofilm-forming isolates and 100% missing in isolate that do not contain biofilm. The genes LasI and LasR were tested to know the quorum sensing regulatory system, which is essential for coordinating gene expression related to virulence and biofilm formation (Fernandes et al., 2023).

The substitutions in 16S rRNA gene were found in P. aeruginosa in this study showed transition and transversion substitutions at different locations with 99% identity when compared to other globally known ones. Moreover, the substitution in LasI gene found in P. aeruginosa in this study showed one substitution of Q(Glutamine)/R(Arginine) at location 4101403 was a missense mutation and had been 99% identity when compared with (ID: CP137912.1). In general, these genetic changes may result in a high degree of biofilm formation and serve a supporting role in the formation of high levels of pathogenicity in P. aeruginosa. In the study conducted by de Sousa et al. (2023) they suggest that biofilm production is common among P. aeruginosa isolates from dogs and may play a role in the pathogenesis of the disease, and found LasI gene within 90% of P. aeruginosa isolates from dogs and lasR gene was absence, whereas (Lima et al., 2018) they found 100% of the isolates had lasR gene, and 97.5% had lasI genes.

From previous studies, found limited available data on the prevalence of lasR, lasI virulence genes in P. aeruginosa specifically isolates from dogs, highlighting the importance of this study. Also, some studies investigated the distribution of lasR, lasI genes in P. aeruginosa obtained from humans and the environment (Park and Koo, 2022), they showed the prevalence of virulence genes and found the genes lasR was present in a significant proportion of carbapenem-resistant P. aeruginosa (CRPA) isolates in 96.7% of the isolates. Another study conducted by (O’Connor et al., 2021) investigated the prevalence of virulence genes in 90 environmental P. aeruginosa and found that lasR was presented in 50% of the isolates. The result of protein conformation of LasR and LasI protein in this study revealed there was no change in 3D secondary structure of lasR and distribution the amino acid of query protein were in the most favorable energy regions for a favorable quality model, and located within the black areas with graph of Z score indicated of an effective model, while LasI 3D structure showed the location of mutation, and distribution the amino acid of query protein were in the most favorable energy regions for good quality model and located within the black areas with graph of Z score, these results were differed from (Lima et al., 2018) they revealed there is change in 3D structure of LasR protein with distribution the amino acid of query protein were in the unfavorable energy regions, and negative Z-score indicated of a favorable model.

Plokarz et al. (2022); Zhang et al. (2022) have shown that the studying P. aeruginosa biofilms in dogs enables the researchers to gain a better understanding of how these structures contribute to infection and develop more effective treatments (Rex et al., 2023) revealed that P. aeruginosa possesses four complicated (QS) system used several signals and receptors to regulate virulence and pathogenicity, among which the LasI/ LasR and RhlI/LasR system is regulated by (3-oxo-C12-HSL) and (C4-HSL) respectively, plays a major role in host pathogenesis. The las and rhl quorum-sensing circuitry operate in a hierarchical cascade responsible for regulating the expression of many virulence determinants, secondary metabolites, type 2 secretion system, stationary phase genes and genes involved in biofilm formation (Sánchez-Jiménez et al., 2023). Therefore, the persistence of P. aeruginosa in various environments, including host tissues regulates the synthesis of proteases, toxins, and other exoproducts that contribute to pathogenicity.

The histopathological finding in this study, the G2 mice infected with P. aeruginosa forming biofilm there were histopathological changes in kidney tissue demonstrates severely congested blood vessels, aggregation of mononuclear cells, and cloudy swelling tubules, the liver section showed severe interstitial infiltration with inflammatory cells (lymphocytes and macrophages) with dilated central vein, while spleen tissue shows an extensive interstitial hemorrhage with the depleted lymphoid follicle with the presence of necrotic lymphocytes. In G3 mice infected with P. aeruginosa non-forming biofilm the histopathological changes in kidney tissue demonstrates enlarged glomeruli surrounded by infiltration of mononuclear cells and tubules cloudy swelling, the liver showed congested blood vessels, lymphocytic cuffing central vein, sinusoid hemorrhage, and apoptosis, in addition the spleen section showed an increase in megakaryocytic cell, depleted lymphoid follicle with hemorrhage. These results corresponds to (Mittal et al., 2009) found in their study the severity of lesions induced by four-days old biofilm cells was more as compared to planktonic cells. Although, that planktonic as well as biofilm cells both the cell forms of P. aeruginosa were able to induce chronic renal inflammation in the experimental animals, more significantly, when bacteria and neutrophils interact during the planktonic stage of an infection, the pathogen is typically killed, inflammatory mediators are regulated, neutrophils undergo apoptosis, and acute inflammation is resolved, conversely, the bacterial infection biofilm stage promotes neutrophil necrosis and results in chronic inflammation (Lenda et al., 2019). The reasons for these histopathological changes may be due to the virulence factors of P. aeruginosa that counteract host defenses causing direct damage to the organ tissues or making the bacteria more competitive, this agrees with (Gellatly and Hancock, 2013). Also, this results corresponds to (Alrabia et al., 2024) they showed the presence of cystic dilatation of some renal tubules with cloudy swelling of others, atrophy of some glomeruli with degeneration of some renal tubules, constriction of renal blood vessels, and degenerative changes of some renal tubules were all observed in the kidney tissues of the mice given strain PAO1 injection, also in the liver tissue showed diffuse vacuolation of certain hepatocytes, significant hepatic blood vessel congestion, and focal regions with inflammatory cell infiltration in their liver tissues, and in the spleen there was a localized area of extravasated blood (hemorrhage), splenic blood vessel congestion, and a decrease in white pulp lymphocytes. As well as (Abd Al-Rubai, 2013) appeared kidney aggregation of neutrophils and lymphocytes around congested blood vessels and also between kidney tubules with severe cytoplasmic vacuolation of endothelium cells and others explained congestion of blood vessels with filtration neutrophils between kidney tubules, and showed spleen depletion of white pulp with neutrophil infiltration in the congested red pulp, however, the liver showed granuloma with congestion of the central vein and sinusoids with neutrophils in the lumen as well as necrosis of hepatocytes with an explanation of sinusoids with neutrophils in the lumen added to necrosis hepatocytes (Abd Al-Rubai, 2013). The researchers (Al-Rasheed et al., 2023) presented that the spleen of the mice in the P. aeruginosa infected group showed signs of severe inflammation, the red and white pulps were enlarged, and the characteristic germinal center structures were lost. There were also hemorrhages, clogged blood vessels, inflammatory cell infiltration, and many erythrocytes in the red pulp. The study of (Panpetch et al., 2024) showed that increased gut LPS produced by P. aeruginosa promotes gut permeability destruction resulting in the direct transfer of LPS to hepatocytes in part via portal veins that promote systemic inflammation (inflammation, apoptosis, and increasing oxidative stressors in hepatocytes), adding to that LecA binds to glycoprotein oligosaccharides on the surface of epithelial and endothelial cells to help P. aeruginosa adhere to host cells (Grishin et al., 2015). While the researchers (Hickey, et al., 2018) revealed that the virulence factors promoted by RpoN are siderophore pyoverdine, and the phenazine compound pyocyanin, these factors are a redox-active molecule that causes oxidative stress that damages target cells. On the other hand, it has been demonstrated that the (T3SS) secretion system effectors ExoS and ExoY, cause regions of cell death, which results in defects in the barrier of the epithelial cells (Golovkine et al., 2016).

CONCLUSION

In conclusion, this study highlights the biofilm forming abilities, importance of QS genes, and mutation occurrence of P. aeruginosa isolates from canine UTIs. The relatively low frequency of P. aeruginosa in dogs UTIs indicates that the epidemiology of this bacterium is not significantly impacted by domestic dogs, probably act as an ecological reservoir for the virulent P. aeruginosa that can be harmful. The identification of LasI/ LasR genes was found in P. aeruginosa isolates resulting in thought that these genes are connected to varying levels of intrinsic virulence and pathogenicity that prompting the need for further studies. The main histopathological finding emphasizing that the biofilm-forming strain caused more severe histological changes than non-biofilm-forming strain.

Acknowledgment

The authors express their sincere gratitude to Baghdad University/College of Veterinary Medicine for the support and facilities provided.

Novelty Statement

The study revealed that the P. aeruginosa isolates produced biofilm layer severely affected mice compared to the isolates from non- biofilm layer. Taken together, molecular surveillance identifies that utilizing the LasR and LasI genes at the same time improves the accuracy of detection of P. aeruginosa producing biofilm.

Author’s Contribution

SEJ: Conceptualization, methodology, validation, writing original draft, writing review and editing.

SMH: Conceptualization, methodology, review and editing, supervisor.

Ethical approval

Ethical approval was obtained through the local committee of animal care in the College of Veterinary Medicine, University of Baghdad (Number 279 on 7/2/2024) before starting this study.

Generative AI and AI-assisted technology statement

The authors declare that no Genrative AI was used in the creation of this manuscript.

Conflict of interest

The authors have declared no conflict of interest.

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