Evidence map›Paper›PMID 41044671›Full record

ArticleBMC microbiology2025

Unraveling the pathogenic potential, virulence traits, and antibiotic resistance genes of multidrug-resistant Streptococcus agalactiae strains retrieved from Nile tilapia.

Abdelazeem M Algammal, Mahmoud Mabrok, Bian K Almessiry, Banan Atwah, Amenah S Al-Otaibi, Yehia S Mohamed, Sinclair Steele, Mohamed Enany, Geraldine B Dayrit, Fatma M Yousseff and 1 more

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Pathogens (Basel, Switzerland) · 2026
    Article
  4. CorAVeterinary research · 2026
    Article
  5. Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Abdelazeem M Algammal *Department of Bacteriology, Immunology, and Mycology, Faculty of Veterinary Medicine, Suez Canal University, Ismailia, 41522, Egypt. abdelazeem.algammal@gmail.com.ORCID 0000-0001-5580-1559
Mahmoud Mabrok *Department of Aquatic Animal Medicine, Faculty of Veterinary Medicine, Suez Canal University, Ismailia, 41522, Egypt. dr.mahmoudmabrok@yahoo.com.ORCID 0000-0002-2009-322X
Bian K AlmessiryDepartment of Medical Laboratory, College of Applied Medical Sciences, Taibah University, Yanbu, 46522, Saudi Arabia.
Banan AtwahDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, Umm Al- Qura University, Makkah, 24372, Saudi Arabia.
Amenah S Al-OtaibiDepartment of Biology, Faculty of Science, University of Tabuk, Tabuk, 71491, Saudi Arabia.
Yehia S MohamedDepartment of Pathological Sciences, College of Medicine, Ajman University, 346, Ajman, UAE.
Sinclair SteeleDepartment of Pathological Sciences, College of Medicine, Ajman University, 346, Ajman, UAE.
Mohamed EnanyDepartment of Bacteriology, Immunology, and Mycology, Faculty of Veterinary Medicine, Suez Canal University, Ismailia, 41522, Egypt.
Geraldine B DayritDepartment of Medial Microbiology, College of Public Health, University of the Philippines Manila, Ermita Manila, 1000, Philippines.
Fatma M YousseffDepartment of Clinical Pathology, Agriculture Research Center, Animal Health Research Institute, Ismailia, 41511, Egypt.
Marwa E Abo HashemDepartment of Bacteriology, Immunology, and Mycology, Faculty of Veterinary Medicine, Suez Canal University, Ismailia, 41522, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStreptococcus agalactiae is implicated in severe infections in humans and causes considerable financial losses in the aquaculture industry, particularly in tilapia farming. Given its dual threat to public health and food security, this study was conducted to comprehensively assess the prevalence, molecular identification, multidrug resistance (MDR) patterns, virulence traits, antimicrobial resistance genes, and pathogenic potential of S. agalactiae strains isolated from Oreochromis niloticus. Notably, this study highlights the detection of critical virulence genes (cfb, hylB, lmb, and cylE), which play essential roles in host invasion and immune evasion. In parallel, the presence of resistance determinants such as pbp1A, aac(6')-aph(2''), tetM or tetK, and ermB or ermA underscores the growing threat of antimicrobial resistance in aquatic environments.

methodsA total of 180 Oreochromis niloticus samples-comprising 90 apparently healthy and 90 moribund fish-were collected from private fish farms in Ismailia, Egypt. Clinical and postmortem (PM) examinations, along with bacteriological analysis, were subsequently performed. The recovered isolates were then subjected to molecular identification via 16 S rRNA gene amplification, antibiotic susceptibility testing via standard protocols, and PCR-based screening for key virulence and antimicrobial resistance genes.

resultsAll recovered Streptococcus agalactiae isolates were confirmed by the presence of the species-specific 16 S rRNA gene. The overall prevalence of S. agalactiae among the examined O. niloticus was 10% (18/180), with the brain identified as the primary target organ for infection. PCR analysis revealed that the most frequently detected virulence-associated genes among the isolates were cfb (100%), hylB (82.1%), lmb (78.5%), and cylE (57.1%). Additionally, 35.7% of the S. agalactiae isolates exhibited multidrug resistance (MDR) to seven different antimicrobial classes and harbored resistance genes including pbp1A, aac(6')-aph(2''), tetM, and ermB. Another 17.8% of the isolates were MDR to six antimicrobial classes and carried the pbp1A, tetM, and ermA genes. Pathogenicity assays demonstrated a strong correlation between the presence of virulence genes and the observed mortality rates in experimentally infected fish. Notably, mortality sharply increased within the first 7 days post-inoculation, reaching approximately 73.3%, underscoring the high virulence potential of the recovered strains.

conclusionBriefly, this study highpoints the development of MDR S. agalactiae in O. niloticus, affirming a public health risk. The emerging MDR S. agalactiae strains in O. niloticus frequently harbor the cfb, hylB, lmb, and cylE virulence genes, and the pbp1A, aac(6')aph(2''), tetM or tetK, and ermB or ermA resistance genes.

Indexed as

CichlidsDrug Resistance, Multiple, BacterialFish DiseasesStreptococcal InfectionsStreptococcus agalactiaeAnimalsAnti-Bacterial AgentsBacterial ProteinsEgyptMicrobial Sensitivity TestsVirulenceVirulence FactorsAnti-Bacterial AgentsBacterial ProteinsVirulence FactorsMDR S. agalactiaeMultidrug resistance patternsOreochromis niloticusPathogenicityVirulence genes

Identifiers

PMID41044671
PMCPMC12492693

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.