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- •Contents
- •List of contributors
- •Preface
- •Introduction
- •Materials and methods
- •Plants traditionally used in Colombia as antimicrobials
- •Xanthium strumarium L. (Asteraceae)
- •Guazuma ulmifolia Lam. (Malvaceae)
- •Cymbopogon citratus (DC.) Stapf (Poaceae)
- •Austroeupatorium inulaefolium (Kunth) R.M.King & H.Rob. (Asteraceae)
- •Jacaranda caucana Pittier (Bignoniaceae)
- •Solanum nudum Dunal (Solanaceae)
- •Hymenaea courbaril L. (Leguminosae)
- •Biological evaluation as antimicrobials of plant extracts in Colombia
- •Antibacterial activity
- •Otholobium mexicanum (L.f.) J.W. Grimes. (Fabaceae)
- •Cucurbita moschata Duchesne (Cucurbitaceae)
- •Cymbopogon citratus (DC.) Stapf (Poaceae)
- •Conobea scoparioides (Cham. & Schltdl.) Benth (Scrophulariaceae)
- •Rosmarinus officinalis Govaerts. (Lamiaceae)
- •Antiparasitic activity
- •Miconia theaezans (Bonpl.) Cogn. (Melastomataceae)
- •Annona purpurea Dunal (Annonaceae)
- •Guatteria amplifolia Triana & Planch. (Annonaceae)
- •Annona muricata Linn. (Annonaceae)
- •Austroeupatorium inulifolium (Kunth) R.M. King & H. Rob. (Compositae)
- •Campnosperma panamense Standl. (Anacardiaceae)
- •Huberodendron patinoi Cuatrec. (Bombacaceae)
- •Swinglea glutinosa Merr (Rutaceae)
- •Antiviral activity
- •Annona sp. (Annonaceae)
- •Byrsonima verbascifolia L. DC (Malpighiaceae)
- •Vismia macrophylla Kunth. (Clusiaceae)
- •Mammea americana L. (Calophyllaceae)
- •Maclura tinctoria L. D.Don ex Steud. (Moraceae)
- •Conclusions
- •References
- •Lebanese plants with antimicrobial activity
- •Amaryllidaceae
- •Allium cepa/Allium sativum
- •Anacardiaceae
- •Pistacia species
- •Apiaceae
- •Prangos asperula
- •Asteraceae/Compositae
- •Matricaria species
- •Berberidaceae
- •Berberis libanotica
- •Cannabaceae
- •Humulus lupulus
- •Cistaceae
- •Cistus species
- •Conifers
- •Lamiaceae
- •Phlomis species
- •Cyclotrichium species
- •Salvia species
- •Rosmarinus officinalis
- •Thymol/carvacrol rich species
- •Za’atar plants: Satureja thymbra; Origanum syriacum
- •Different Lamiaceae genera
- •Thymbra spicata
- •Myrtaceae
- •Eucalyptus species
- •Portulacaceae
- •Portulaca oleracea
- •Ranunculaceae
- •Clematis vitalba
- •Nigella sativa
- •Rutaceae
- •Ruta species
- •Rosaceae
- •Rosa damascena
- •Conclusion
- •References
- •Introduction
- •Medicinal plants with antimicrobial properties
- •Amaryllidaceae
- •Allium sativum L.
- •Picea abies (L.) H.Karst.
- •Rosaceae
- •Agrimonia eupatoria L.
- •Prunus spinosa L.
- •Rosa canina L.
- •Rubus fruticosus L.
- •Urticaceae
- •Urtica dioica L.
- •Conclusions
- •References
- •Apiaceae
- •Petroselinum crispum (Mill.) Fuss
- •Asteraceae
- •Achillea millefolium L.
- •Artemisia absinthium L.
- •Calendula officinalis L.
- •Matricaria chamomilla L.
- •Betulaceae
- •Alnus glutinosa (L.) Gaertn.
- •Lamiaceae
- •Lavandula angustifolia Mill.
- •Mentha longifolia (L.) L.
- •Mentha x piperita L.
- •Ocimum basilicum L.
- •Origanum vulgare L.
- •Malvaceae
- •Althaea officinalis L.
- •Malva sylvestris L.
- •Pinaceae
- •Larix decidua Mill.
- •Introduction
- •Pathophysiology of wound healing
- •Wound infection
- •Currently available treatments and products
- •Topical creams
- •Transdermal drug delivery systems
- •Bacteria associated with infections of dermal wounds
- •Bacillus subtilis
- •Staphylococcus aureus
- •Staphylococcus epidermidis
- •Pseudomonas aeruginosa
- •Aloe barberae Dyer
- •Traditional usage
- •Aloe excelsa Berger
- •Traditional usage
- •Aloe ferox Miller
- •Traditional usage
- •Elephantorrhiza elephantina (Burch.) Skeel
- •Traditional usage
- •Erythrina lysistemon Hutch
- •Traditional usage
- •Galenia africana L
- •Traditional usage
- •Grewia occidentalis L
- •Traditional usage
- •Melianthus comosus Vahl.
- •Traditional usage
- •Traditional usage
- •Polystichum pungens (Kaulf.) C. Presl
- •Traditional usage
- •Sutherlandia frutescens (L.) R.Br.
- •Traditional usage
- •Urtica urens L.
- •Traditional usage
- •Aloe species
- •Elephantorrhiza elephantina
- •Erythrina lysistemon
- •Galenia africana
- •Melianthus comosus
- •Plectranthus fruticosus
- •Sutherlandia frutescens
- •Discussion
- •Conclusion
- •Index
- •Glossary
- •References
- •Introduction
- •Background on gonorrhea
- •The causal agent: Neisseria gonorrhoeae
- •Pathogenesis of Neisseria gonorrhoeae and evasion of host immune system
- •Evasion of host immune system via nutrition immunity
- •Coinfections of Neisseria gonorrhoeae
- •Status of available treatments for gonorrhea
- •Aloe ferox
- •Cassia abbreviata
- •Combretum molle
- •Elaeodendron transvaalense
- •Hypoxis hemerocallidea
- •Peltophorum africanum
- •Tabernaemontana elegans
- •Terminalia sericea
- •Conclusion
- •References
- •Introduction
- •Antibacterial properties of different medicinal plants from Pakistan
- •Conclusion
- •References
- •Introduction
- •Traditional medicine for diarrheal diseases in the Mekong Basin
- •The role of traditional medicine in the management of diarrhea
- •The cultural belief system of people living in the Mekong area
- •Pharmacological validation of plants used for diarrhea
- •Models assessing the effect of plants on the signs and symptoms of diarrhea
- •Antidiarrheal effect
- •Spasmolytic activity
- •Models assessing the antimotility and antisecretory activities
- •Antimotility activity
- •Antisecretory activity
- •Models assessing the antiinfective properties
- •Antibacterial activity
- •Antiviral and antiparasitic activity
- •Other models
- •Medicinal plants used for diarrhea in the lower Mekong basin
- •Literature search methodology
- •Overview of the dataset
- •Discussion of some selected plant species
- •Psidium guajava
- •Chromolaena odorata
- •Alstonia scholaris
- •Allium sativum
- •Centella asiatica
- •Punica granatum
- •Caesalpinia sappan
- •Mangifera indica
- •Holarrhena pubescens
- •Oroxylum indicum
- •Conclusion
- •References
- •Introduction
- •Traditional use of medicinal plants in West Africa
- •In vitro antimalarial evaluation of plant extracts
- •In vivo antimalarial evaluation of plant extracts
- •In vitro and in vivo evaluation of antimalarial compounds
- •The case of Artemisia in West Africa
- •Conclusion
- •References
- •Introduction
- •Significance of quorum quenching research
- •Current state of quorum quenching research
- •Quorum sensing versus quorum quenching
- •Biofilms
- •Background on biofilms
- •Biofilms and Mycobacterium tuberculosis
- •Virulence factors
- •Background on virulence factors
- •Virulence factors and Mycobacterium tuberculosis
- •Medicinal plants as quorum quenching agents
- •Medicinal plants and mycobacterial quorum quenching
- •Phytochemicals used in bacterial quorum quenching
- •Conclusion
- •References
- •Introduction
- •Plants as sources of antiinfective agents
- •Bioassay-guided fractionation
- •Metabolomics
- •Methods of detection
- •Data analysis
- •Biochemometrics
- •Metabolomics-driven antiinfective discovery from plants
- •Challenges and future directions
- •Metabolome coverage
- •Annotation/identification
- •Synergy
- •Conclusions
- •References
- •Introduction
- •Taxonomy and DNA barcoding
- •Infectious diseases and antiinfective plants
- •Herbal products, commercialization, and quality issues of antiinfective plants
- •Advancements in quality control methods
- •Materials and methods
- •Results and discussion
- •Embelia ribes—anthelmintic plant
- •Swertia chirayita—antiviral plant
- •Picrorhiza kurroa—antiviral plant
- •Paris polyphylla—anthelmintic plant
- •Saussurea costus—anthelminthic/antiparasitic plant
- •Syzygium aromaticum—antimicrobial plant
- •Andrographis paniculata—antimicrobial plant
- •Future perspectives
- •References
- •Introduction
- •Current situation of microbial infections
- •Microbial natural products as sources of new drugs
- •Endophytic fungi
- •Antimicrobial compounds from endophytic fungi
- •Antibacterial compounds
- •Alkaloids
- •Pyrazin-2-one
- •Piperine
- •Pyrrocidines
- •Bisindoles
- •Peptides
- •Dipeptides
- •Polypeptides
- •Polyketides
- •Chromones
- •Quinones
- •Xanthones
- •Benzofurans
- •Octaketides
- •Benzophenones
- •Terpenoids
- •Antivirulence compounds
- •Antiparasitic compounds
- •Antileishmanial compounds
- •Polyketides
- •Polyketide-alkaloids
- •Terpenoids
- •Antiplasmodial
- •Alkaloids
- •Polyketides
- •Polyketide-alkaloid
- •Polypeptides
- •Terpenoids
- •Antitrypanosomal/antiplasmodial/antileishmanial compounds
- •Polyketides
- •Polypeptides
- •Discussion and conclusion
- •References
- •Introduction
- •Dengue disease
- •Conventional treatment
- •Medicinal plants
- •Introduction
- •Psidium guajava: a potential antidengue medicinal plant
- •A metabolomic approach in antiviral compound identification
- •Objectives
- •Results
- •UHPLC-HRMS-based metabolomics approach
- •Antidengue activity
- •Identification of putative antidengue compounds
- •Antidengue assay of pure authentic standards
- •Discussion
- •Materials and methods
- •Plant collection
- •Leaf extraction
- •Cells and virus
- •Extracts preparation
- •Cell viability assay
- •Virus infection
- •UHPLC-HRMS profiling
- •Data processing
- •Statistical analysis
- •Identification of significant features
- •References
- •Introduction
- •Brief history of Arabic medicine
- •Principles of Arab medicine: theoretical aspects
- •Cutaneous infections and medications
- •Plants and metals useful for skin diseases
- •Toxicity of metals
- •Elementary metal particle
- •Organometallic molecule
- •Metal nanoparticles
- •Conclusion
- •References
- •Introduction
- •General information on improved traditional medicines
- •Definition
- •Regulatory framework
- •Categories of improved traditional medicines
- •Marketing authorization files for ITMs in Mali

A number of chemical fingerprinting studies report essential oil of clove as being
adulterated with inferior quality vegetables and mineral oils. For example,
Bounaas
et al. (2018)
used Fourier-transform infrared spectroscopy method to analyze the
quality of clove essential oil and revealed that the commercial samples were diluted
with vegetables and mineral oils. Furthermore,
Bruno et al. (2019) used the DNA meta-
barcoding method and analyzed food products that contain S. aromaticum (two pro-
ducts) as an ingredient and revealed that none of the products contained S. aromaticum
as labeled.
Andrographis paniculata—antimicrobial plant
Due to its extremely bitter taste, Andrographis paniculata (Burm.f.) Nees (Acanthaceae)
is often referred as “the king of bitters,” and is used as a bitter tonic in Ayurvedic and
other traditionally known health-care systems of India and many other Asian countries.
The genus Andrographis comprises 40 species, and about 26 species of Andrographis
are reported to occur in India (
Neeraja et al., 2015). Traditionally, A. paniculata is used
to treat stomachaches, inflammation, pyrexia, intermittent fevers, as an antidote for
snakebite and poisonous stings of some insects, and to treat dyspepsia, influenza, dysen-
tery, malaria, and respiratory infections (
Hossain, Urbi, Sule, & Rahman, 2014;
Okhuarobo et al., 2014
). Andrographolide (structurally a labdane diterpenoid) is the
major bitter-tasting secondary metabolite and bioactive constituent, reported to have a
broad range of pharmacological effects including antidiarrheal, antihepatitis, anti-HIV,
antimicrobial, antimalarial, cardiovascular, cytotoxic, hepatoprotective, a nd im munosti-
mulatory activities, as well as the effect on sexual dysfunctions (
Hossain et al., 2014;
Okhuarobo et al., 2014
).
The whole plant of A. paniculata is collected in preflowering stages and when dried, it
constitutes the herbal drug. The trade name of A. paniculata in India is Kalmegh and
Nilavembu, and the trade demand for Kalmegh for the year 201415 was approximately
2000 MT (
Goraya & Ved, 2017). In the wild, the species has been assessed as vulnerable
and also reported to be widely cultivated in India. Due to the species complexity, other
species of Andrographis such as A. alata (Vahl) Nees, A. lineata Nees, A. glandulosa Nee s,
A. echioides (L.) Nees, A. serpyllifolia (Vahl) Wight, A. macrobotrys Nees, A. neesiana Wight,
A. elongata (Vahl) T. Anderson, A. nallamalayana J.L. Ellis, and A. wightiana Arn. ex Nees
are used as substitutes and adulterants and are being extensively used in folk medicine
(
Alagesa Boopathi & Andrographis, 2000; Arolla, Cherukupalli, Khareedu, & Vudem,
2015
). Santhosh Kumar et al. (2018) utilized DNA barcoding method to authenticate the
raw herbal drugs traded as Kalmegh (six samples) in India and reported no adulteration.
Similarly,
Osathanunkul et al. (2016) developed high resolution melting coupled with
DNA barcoding method to identify A. paniculata herbal products available in markets in
Thailand. In this study, rbcL DNA barcode loci were used to authenticate 10 commercial
herbal products and it was found that all the tested herbal products melting curves pro-
files were similar to A. paniculata which indicated that all tested products contained the
correct species as labeled (
Osathanunkul et al., 2016). However, another study reported
the presence of Rhinacanthus nasutus (L.) Kurzin three tested products out of 15 products
(
Osathanunkul, Madesis, & De Boer, 2015).
374 11. Value chains and DNA barcoding for the identification of antiinfective medicinal plants
Medicinal Plants as Anti-infectives

Future perspectives
Currently, the World Health Organization guidelines for assessing the quality of
herbal medicines mainly include the methods that ensure the identity and safety of
the raw plant materials by screening a specified chemical marker compound, and by
checking the m icrobiological purity of the herbal products. Most herbal monographs
specify the use of macroscopic and microscopic characterization, phytochemistry-based
analysis of specifi c marker compounds, assays for toxic constituents such as heavy
metals, and the use of different chromatog raphic approaches to detect adulteration.
The appropriate utilization of these quality assurance methods, viz., morphological,
microscopy, phytochemistry, and DNA-based methods for the identification of medicinal
plants heavily depend on various stages of the value chain and are used on the basis
of a case-by-case evaluation, starting from theplantmaterialharvest,storage,andto
the finished herbal products. Though British Pharmacopeia is one of the first to
publish a specific methods section on DNA barcoding that creates a framework for com-
pliance of DNA barcoding with regulatory re quirements, DNA barcoding and metabar-
coding are not yet widespread validated methods for use in the regulatory context of
quality control. A number of studies support its usefulness for herbal product authenti-
cation and pharmacovigilance either as a standard method or as a complementary
method.
In this chapter, we reviewed the development of DNA barcoding in a few selected anti-
infective plants. As a widely accepted method, DNA barcoding has played an important
role in the classification of medicinal plants, the identification of substitutes/adulterants,
and the regulation of the herbal products market. The presence of adulterants and substi-
tutes may be explained by various factors, including but not limited to the deliberate adul-
teration and unintentional substitution that may occur from the early stage of the supply
chain of medicinal plants (i.e., cultivation, transport, and storage), to the manufacturing
process and the commercialization of the final products. It was evident that the antiinfec-
tive plants categorized under any threat status were reported to be more adulterated and
substituted. The existing technical means can effectively identify plant raw materials but
for some processed products (e.g., tablets, pills, oral liquids, and injections, etc.), there is
still a lack of effective, rapid, and standardized identification methods up to now, espe-
cially for the complex herbal products.
In the past, the development of DNA barcoding has been primarily focused on the
selection of c andidate DNA ma rkers and the development of sequence databases.
Although universal plant DNA barcodes have not yet been chosen, most studies utilize
the four markers rbcL, matK, trnH-psbA, and nr-ITS, and the international DNA bar-
code database is maintained by BOLD in Canada (
http://www.boldsystems.org/).
Apart from the identification of specific DNA barcode markers for plants, the chloro-
plast genomes based identification of plants is being developed. Furthermore, the next
and third-generation sequencing technologies have been sophisticated, and the research
of chloroplast (or plastid) genomics of medical plants is underway. In short, DNA bar-
coding has a broad application in the field of pharmacovigilance and it will certainly
help to assure the safety, quality, and efficacy of traditional medicines in countries
around the globe.
375Future perspectives
Medicinal Plants as Anti-infectives

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CHAPTER
12
Fungal endophytes: a source of
antibacterial and antiparasitic
compounds
Romina Pacheco
1
, Sergio Ortiz
1,2
, Mohamed Haddad
1
and
Marieke Vansteelandt
1
1
UMR 152 PharmaDev, Univers ite
´
de Toulouse, IRD, UPS, Toulouse, France
2
UMR 7200
Laboratoire d’Innovation The
´
rapeutique, Universite
´
de Strasbourg, CNRS, Strasbourg Drug
Discovery and Development Institute (IMS), Illkirch-Graffenstaden, France
Introduction
Current situation of microbial infections
The golden era of the antibiotic occurred between the early 1930s and late 1960s, a
period where most of the new classes of drugs were discovered. This period was followed
by an important decline in drug discovery rate along with the increase and emergence of
resistant microbes, including bacteria, viruses, fungi, and parasites (
Aminov, 2010). In
2019 the WHO listed 32 antibiotics in clinical development that were addressed to the list
of priority pathogens, of which only six were considered innovative. Antimicrobial resis-
tance affects health care systems from all countries found in any level of development,
generating a great economic burden while other medical procedures become more risky.
Protozoal diseases such as malaria (Plasmodium spp.), leishmaniasis (Leishmania spp.),
and trypanosomiasis (Trypanosoma spp.) affect mainly tropical and subtropical regions
with great health and economic impacts worldwide. These unicellular eukaryotic organ-
isms are free-living organisms and their developmental stages include intracellular stages
within the host cell or extracellular stages in body fluids, hollow organs, or between cells
in the interstitial space. Additionally, they can possess dormant forms that help them to
survive under extreme conditions over a long period of time. Their transmission is mainly
vector-borne but also fecaloral or predatorprey transmission.
383
Medicinal Plants as Anti-infectives
DOI:
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