Evidence map›Paper›PMID 42338158›Full record

ArticleMicrobiologyOpen2026

Facing Antimicrobial Resistance and Virulence in Streptococcus agalactiae During Late Pregnancy: Evaluation of Lactobacilli as a Supportive Approach.

Astri D Tagueha, Giulia Radocchia, Daniela Scribano, Matteo Lo Scalzo, Giacinto Panella, Serena Schippa, Giovanni Gherardi, Roberta Creti, Ilaria Marani, Giovanna Alfarone and 7 more

Abstract read
In one paragraph

Article in MicrobiologyOpen, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Astri D TaguehaDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
Giulia RadocchiaDepartment of Life Science, Health, and Health Professions, Link Campus University, Rome, Italy.ORCID 0009-0003-8317-5083
Daniela ScribanoDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.ORCID 0000-0002-2901-265X
Matteo Lo ScalzoDepartment of Human Sciences and Promotion of the Quality of Life, San Raffaele Open University, Rome, Italy.
Giacinto PanellaU.O.C Patologia Clinica, Ospedale Fabrizio Spaziani, Frosinone, Italy.
Serena SchippaDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.ORCID 0000-0003-1572-2623
Giovanni GherardiDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Roberta CretiDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Ilaria MaraniDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Giovanna AlfaroneDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Monica ImperiDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Massimiliano MarazzatoDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
Lucia NencioniDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Institute Pasteur Italia-Cenci Bolognetti Foundation, Rome, Italy.ORCID 0000-0003-4427-4823
Paola ChecconiDepartment of Human Sciences and Promotion of the Quality of Life, San Raffaele Open University, Rome, Italy.ORCID 0000-0001-7518-5730
Dolores LimongiDepartment of Human Sciences and Promotion of the Quality of Life, San Raffaele Open University, Rome, Italy.
Anna Teresa PalamaraDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.ORCID 0000-0001-8330-4381
Cecilia AmbrosiDepartment of Human Sciences and Promotion of the Quality of Life, San Raffaele Open University, Rome, Italy.ORCID 0000-0003-2163-1613

Funding

HARH5W, Sapienza Università di Roma RD12318AAC3B4A3EItalian Ministry of Health Ricercacorrente,IRCCSSanRaffaeleRoma,00166Rome,ItalyMinistero dell'Istruzione, dell'UniversitÀ e della Ricerca PRIN 2022Ministero dell'Istruzione, dell'UniversitÀ e della Ricerca PRIN 2022HARH5WMinistry of Health, Sapienza UniversitÀ di Roma RD12318AAC3B4A3E
6 · The paper itself

Abstract

Streptococcus agalactiae (Group B streptococcus, GBS) remains a major cause of neonatal sepsis and meningitis, despite the success of intrapartum antibiotic prophylaxis. However, the rising trend of antimicrobial resistance and the emergence of hypervirulent lineages highlight the need for complementary, innovative prophylactic strategies. This study aimed to characterize the resistance and virulence repertoire of colonizing GBS isolates and to assess the antagonistic potential of selected Lactobacillus strains under conditions mimicking the vaginal niche. We performed integrated phenotypic, genotypic, and functional analysis of 31 clinical GBS isolates collected during routine pre-partum screening, focusing on antimicrobial susceptibility, hemolytic and aggregation phenotypes, capsular serotypes, pilus island profiles, and virulence genes. The collection included MDR isolates, strains exhibiting inducible clindamycin resistance and high-level gentamicin resistance, as well as hypervirulent ST-17 related lineages, with marked heterogeneity in β-hemolytic activity and aggregation phenotypes linked to specific combinations of capsule, pilus, and virulence genes. In co-culture experiments with HeLa cells, individual Lactobacillus strains exerted strong, strain-dependent inhibition of GBS, preserving epithelial cell viability, and impairing pathogen adhesion by up to 98%. Importantly, the multi-strain Lactobacillus combination provided broader and more consistent antagonistic activity, including against MDR, inducible clindamycin-resistant, hypervirulent ST-17-associated, and strongly hemolytic GBS isolates. Although these findings are preliminary, being derived from a limited number of isolates and an in vitro model, they support the promising potential of rationally selected multi-strain Lactobacillus formulations as a strategy to reduce colonization by high-risk GBS lineages and warrant further investigation.

Indexed as

Drug Resistance, BacterialLactobacillusPregnancy Complications, InfectiousStreptococcal InfectionsStreptococcus agalactiaeAnti-Bacterial AgentsAntibiosisBacterial AdhesionFemaleHeLa CellsHumansMicrobial Sensitivity TestsPregnancyVaginaVirulenceVirulence FactorsAnti-Bacterial AgentsVirulence Factorsantibiotic‐resistanceLactobacillipregnancyStreptococcus agalactiaevirulence

Identifiers

PMID42338158
PMCPMC13291431

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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 OpenQuestion graph.