Alessandra Iannuzzi

Dr. Alessandra Iannuzzi

Institute for Animal Production System in Mediterranean Environment, National Research Council
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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12 March 2021 in Animals
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Journal Article
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AIAlessandra Iannuzzi
Alessandra Iannuzzi
Pietro ParmaPietro Parma
Pietro Parma
Prof IannuzziProf Iannuzzi
Prof Iannuzzi
After discovering the Robertsonian translocation rob(1;29) in Swedish red cattle and demonstrating its harmful effect on fertility, the cytogenetics applied to domestic animals have been widely expanded in many laboratories in order to find relationships between chromosome abnormalities and their phenotypic effects on animal production. Numerical abnormalities involving autosomes have been rarely reported, as they present abnormal animal phenotypes quickly eliminated by breeders. In contrast, numerical sex chromosome abnormalities and structural chromosome anomalies have been more frequently detected in domestic bovids because they are often not phenotypically visible to breeders. For this reason, these chromosome abnormalities, without a cytogenetic control, escape selection, with subsequent harmful effects on fertility, especially in female carriers. Chromosome abnormalities can also be easily spread through the offspring, especially when using artificial insemination. The advent of chromosome banding and FISH-mapping techniques with specific molecular markers (or chromosome-painting probes) has led to the development of powerful tools for cytogeneticists in their daily work. With these tools, they can identify the chromosomes involved in abnormalities, even when the banding pattern resolution is low (as has been the case in many published papers, especially in the past). Indeed, clinical cytogenetics remains an essential step in the genetic improvement of livestock.

30 April 2008 in Cytogenetic and Genome Research
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Journal Article
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RCR. Cassata
R. Cassata
AIAlessandra Iannuzzi
Alessandra Iannuzzi
Pietro ParmaPietro Parma
Pietro Parma
LLL. De Lorenzi
L. De Lorenzi
VPV. Peretti
V. Peretti
GMG.P. Di Meo
G.P. Di Meo
The aim of this study was to estimate prognostic factors in a Dalmatian dog with bilateral cryptorchidism and hypospadias. Cytogenetic and molecular analyses revealed a normal karyotype (2n = 78,XY) and the presence of SRY, INSL3 and RXFP2 genes with a normal DNA sequence for SRY and RXFP2, while the INSL3 sequence differed slightly from the normal one due to a heterozygous nucleotide change involving amino acid 22 of the INSL3 dog precursor protein. Levels of plasmatic testosterone were only 0.01 ng/ml, while FSH and LH serum levels were not detectable. After the human chorionic gonadotropin (hCG) test, the serum testosterone level was 0.01 ng/ml. Therefore, the phenotypic aetiology of this subject can not be well-defined because cryptorchidism and hypospadias were frequent clinical features with high genetic heterogeneity.

20 August 2010 in Sexual Development
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Journal Article
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LLL. De Lorenzi
L. De Lorenzi
VGV. Genualdo
V. Genualdo
AIAlessandra Iannuzzi
Alessandra Iannuzzi
GMG.P. Di Meo
G.P. Di Meo
APAngela Perucatti
Angela Perucatti
Prof IannuzziProf Iannuzzi
Prof Iannuzzi
A 4-year-old male horse of Friesian breed with normal body conformation, development and libido, and showing an evident ventral penis deviation with hypospadias, underwent both cytogenetic and genetic investigation. Although the karyotype showed normal male arrangement (2n = 64,XY), one telomere of horse (ECA) chromosome 1 was shorter than both the other one and those of a normal horse (control), as revealed by CBA- and RBA-banding, and by Ag-NOR and FISH-mapping techniques using telomere PNA probes. Genetic investigation of the SRY and MAMLD1 coding sequences revealed a normal SRY sequence and a mutation in the MAMLD1 gene sequence: a homozygous change (C>A) was found, leading to the synthesis of an isoleucine, instead of a leucine. Although it is difficult to find a strict correlation between hypospadias and the genetic defects revealed by this investigation, this study is the first to be performed in a hypospadic horse using both cytogenetic and genetic investigation.

30 April 2008 in Cytogenetic and Genome Research
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Journal Article
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GMG.P. Di Meo
G.P. Di Meo
APAngela Perucatti
Angela Perucatti
ROSSELLA DI PALOROSSELLA DI PALO
ROSSELLA DI PALO
AIAlessandra Iannuzzi
Alessandra Iannuzzi
FCF. Ciotola
F. Ciotola
Prof IannuzziProf Iannuzzi
Prof Iannuzzi
Thirteen male river buffaloes, 119 females with reproductive problems (which had reached reproductive age but had failed to become pregnant in the presence of bulls) and two male co-twins underwent both clinical and cytogenetic investigation. Clinical analyses performed by veterinary practitioners revealed normal body conformation and external genitalia for most females. However, some subjects showed some slight male traits such as large base horn circumference, prominent withers and tight pelvis. Rectal palpation revealed damage to internal sex adducts varying between atrophy of Mullerian ducts to complete lack of internal sex adducts (with closed vagina). All bulls had normal karyotypes at high resolution banding, while 25 animals (23 females and 2 male co-twins) (20.7%) with reproductive problems were found to carry the following sex chromosome abnormalities: X monosomy (2 females); X trisomy (1 female); sex reversal syndrome (2 females); and free-martinism (18 females and 2 males). All female carriers were sterile.

17 October 2014 in PLOS ONE
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Journal Article
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PAPauciullo Alfredo
Pauciullo Alfredo
APAngela Perucatti
Angela Perucatti
GCGianfranco Cosenza
Gianfranco Cosenza
AIAlessandra Iannuzzi
Alessandra Iannuzzi
DIDomenico Incarnato
Domenico Incarnato
Prof IannuzziProf Iannuzzi
Prof Iannuzzi
The main goal of this study was to develop a comparative multi-colour Zoo-FISH on domestic ruminants metaphases using a combination of whole chromosome and sub-chromosomal painting probes obtained from the river buffalo species (Bubalus bubalis, 2n = 50,XY). A total of 13 DNA probes were obtained through chromosome microdissection and DOP-PCR amplification, labelled with two fluorochromes and sequentially hybridized on river buffalo, cattle (Bos taurus, 2n = 60,XY), sheep (Ovis aries, 2n = 54,XY) and goat (Capra hircus, 2n = 60,XY) metaphases. The same set of paintings were then hybridized on bovine secondary oocytes to test their potential use for aneuploidy detection during in vitro maturation. FISH showed excellent specificity on metaphases and interphase nuclei of all the investigated species. Eight pairs of chromosomes were simultaneously identified in buffalo, whereas the same set of probes covered 13 out 30 chromosome pairs in the bovine and goat karyotypes and 40% of the sheep karyotype (11 out of 27 chromosome pairs). This result allowed development of the first comparative M-FISH karyotype within the domestic ruminants. The molecular resolution of complex karyotypes by FISH is particularly useful for the small chromosomes, whose similarity in the banding patterns makes their identification very difficult. The M-FISH karyotype also represents a practical tool for structural and numerical chromosome abnormalities diagnosis. In this regard, the successful hybridization on bovine secondary oocytes confirmed the potential use of this set of probes for the simultaneous identification on the same germ cell of 12 chromosome aneuploidies. This is a fundamental result for monitoring the reproductive health of the domestic animals in relation to management errors and/or environmental hazards.

1 April 2018 in Food and Chemical Toxicology
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Journal Article
Closed access
APAngela Perucatti
Angela Perucatti
VGViviana Genualdo
Viviana Genualdo
PAPauciullo Alfredo
Pauciullo Alfredo
CICiro Iorio
Ciro Iorio
DIDomenico Incarnato
Domenico Incarnato
AIAlessandra Iannuzzi
Alessandra Iannuzzi