Luisa Lanfranco

Luisa Lanfranco

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Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 July 2020 in Nature Reviews Microbiology
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Andrea GenreAndrea Genre
Andrea Genre
LLLuisa Lanfranco
Luisa Lanfranco
Silvia PerottoSilvia Perotto
Silvia Perotto
Paola BonfantePaola Bonfante
Paola Bonfante

16 November 2011 in New Phytologist
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ETE. Tisserant
E. Tisserant
AKA. Kohler
A. Kohler
PDP. Dozolme‐Seddas
P. Dozolme‐Seddas
Raffaella BalestriniRaffaella Balestrini
Raffaella Balestrini
karim benabdellahkarim benabdellah
karim benabdellah
FMFrancis Martin
Francis Martin

28 May 2018 in New Phytologist
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LLLuisa Lanfranco
Luisa Lanfranco
VFValentina Fiorilli
Valentina Fiorilli
CGCaroline Gutjahr
Caroline Gutjahr

1 September 2007 in Molecular Plant-Microbe Interactions®
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Raffaella BalestriniRaffaella Balestrini
Raffaella Balestrini
JGJorge Gómez-Ariza
Jorge Gómez-Ariza
LLLuisa Lanfranco
Luisa Lanfranco
Paola BonfantePaola Bonfante
Paola Bonfante
The establishment of a symbiotic interaction between plant roots and arbuscular mycorrhizal (AM) fungi requires both partners to undergo significant morphological and physiological modifications which eventually lead to reciprocal beneficial effects. Extensive changes in gene expression profiles recently have been described in transcriptomic studies that have analyzed the whole mycorrhizal root. However, because root colonization by AM fungi involves different cell types, a cell-specific gene expression pattern is likely to occur. We have applied the laser microdissection (LMD) technology to investigate expression profiles of both plant and fungal genes in Lycopersicon esculentum roots colonized by Glomus mosseae. A protocol to harvest arbuscule-containing cells from paraffin sections of mycorrhizal roots has been developed using a Leica AS LMD system. RNA of satisfactory quantity and quality has been extracted for molecular analysis. Transcripts for plant phosphate transporters (LePTs), selected as molecular markers for a functional symbiosis, have been detected by reverse-transcriptase polymerase chain reaction assays and associated to distinct cell types, leading to novel insights into the distribution of LePT mRNAs. In fact, the transcripts of the five phosphate transporters (PTs) have been detected contemporaneously in the same arbusculated cell population, unlike from the neighboring noncolonized cells. In addition, fungal H+ATPase (GmHA5) and phosphate transporter (GmosPT) mRNAs were found exclusively in arbusculated cells. The discovery that five plant and one fungal PT genes are consistently expressed inside the arbusculated cells provides a new scenario for plant–fungus nutrient exchanges.

25 August 2011 in The ISME Journal
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Stefano GhignoneStefano Ghignone
Stefano Ghignone
ASAlessandra Salvioli
Alessandra Salvioli
IAIulia Anca
Iulia Anca
Erica LUMINIErica LUMINI
Erica LUMINI
GOGiuseppe Ortu
Giuseppe Ortu
Paola BonfantePaola Bonfante
Paola Bonfante
As obligate symbionts of most land plants, arbuscular mycorrhizal fungi (AMF) have a crucial role in ecosystems, but to date, in the absence of genomic data, their adaptive biology remains elusive. In addition, endobacteria are found in their cytoplasm, the role of which is unknown. In order to investigate the function of the Gram-negative Candidatus Glomeribacter gigasporarum, an endobacterium of the AMF Gigaspora margarita, we sequenced its genome, leading to an ∼ 1.72-Mb assembly. Phylogenetic analyses placed Ca. G. gigasporarum in the Burkholderiaceae whereas metabolic network analyses clustered it with insect endobacteria. This positioning of Ca. G. gigasporarum among different bacterial classes reveals that it has undergone convergent evolution to adapt itself to intracellular lifestyle. The genome annotation of this mycorrhizal-fungal endobacterium has revealed an unexpected genetic mosaic where typical determinants of symbiotic, pathogenic and free-living bacteria are integrated in a reduced genome. Ca. G. gigasporarum is an aerobic microbe that depends on its host for carbon, phosphorus and nitrogen supply; it also expresses type II and type III secretion systems and synthesizes vitamin B12, antibiotics- and toxin-resistance molecules, which may contribute to the fungal host's ecological fitness. Ca. G. gigasporarum has an extreme dependence on its host for nutrients and energy, whereas the fungal host is itself an obligate biotroph that relies on a photosynthetic plant. Our work represents the first step towards unraveling a complex network of interphylum interactions, which is expected to have a previously unrecognized ecological impact.

22 December 2017 in Journal of Experimental Botany
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LLLuisa Lanfranco
Luisa Lanfranco
VFValentina Fiorilli
Valentina Fiorilli
FVFrancesco Venice
Francesco Venice
PBPaola Bonfante
Paola Bonfante
Strigolactones (SLs) first evolved as regulators of simple developmental processes in very ancient plant lineages, and then assumed new roles to sustain the increasing biological complexity of land plants. Their versatility is also shown by the fact that during evolution they have been exploited, once released in the rhizosphere, as a communication system towards plant-interacting organisms even belonging to different kingdoms. Here, we reviewed the impact of SLs on soil microbes, paying particular attention to arbuscular mycorrhizal fungi (AMF). SLs induce several responses in AMF, including spore germination, hyphal branching, mitochondrial metabolism, transcriptional reprogramming, and production of chitin oligosaccharides which, in turn, stimulate early symbiotic responses in the host plant. In the specific case study of the AMF Gigaspora margarita, SLs are also perceived, directly or indirectly, by the well-characterized population of endobacteria, with an increase of bacterial divisions and the activation of specific transcriptional responses. The dynamics of SLs during AM root colonization were also surveyed. Although not essential for the establishment of this mutualistic association, SLs act as positive regulators as they are relevant to achieve the full extent of colonization. This possibly occurs through a complex crosstalk with other hormones such as auxin, abscisic acid, and gibberellins.