Literature DB >> 32498435

Microcystin Incidence in the Drinking Water of Mozambique: Challenges for Public Health Protection.

Isidro José Tamele1,2,3, Vitor Vasconcelos1,4.   

Abstract

Microcystins (n>an class="Chemical">MCs) are cyanotoxins produced mainly by freshwater cyanobacteria, which constitute a threat to public health due to their negative effects on humans, such as gastroenteritis and related diseases, including death. In Mozambique, where only 50% of the people have access to safe drinking water, this hepatotoxin is not monitored, and consequently, the population may be exposed to MCs. The few studies done in Maputo and Gaza provinces indicated the occurrence of MC-LR, -YR, and -RR at a concentration ranging from 6.83 to 7.78 µg·L-1, which are very high, around 7 times above than the maximum limit (1 µg·L-1) recommended by WHO. The potential MCs-producing in the studied sites are mainly Microcystis species. These data from Mozambique and from surrounding countries (South Africa, Lesotho, Botswana, Malawi, Zambia, and Tanzania) evidence the need to implement an operational monitoring program of MCs in order to reduce or avoid the possible cases of intoxications since the drinking water quality control tests recommended by the Ministry of Health do not include an MC test. To date, no data of water poisoning episodes recorded were associated with MCs presence in the water. However, this might be underestimated due to a lack of monitoring facilities and/or a lack of public health staff trained for recognizing symptoms of MCs intoxication since the presence of high MCs concentration was reported in Maputo and Gaza provinces.

Entities:  

Keywords:  Mozambique; drinking water quality; microcystin; public health

Mesh:

Substances:

Year:  2020        PMID: 32498435      PMCID: PMC7354522          DOI: 10.3390/toxins12060368

Source DB:  PubMed          Journal:  Toxins (Basel)        ISSN: 2072-6651            Impact factor:   4.546


1. Introduction

Mozambique (Figure 1) is a country located in southeastern Africa (10°30′–26°52′ S and 40°50′–30°31′ E) covering a total land area of 800,000 km2. It is bathed by the Indian Ocean in the east and makes borders with Tanzania in the north; Malawi and Zambia in the northwest; Zimbabwe in the west and Swaziland and South Africa in the southwest.
Figure 1

Map of Mozambique. Red points or lines indicate the sites where Microcystin (MC) or MC producers were detected in Mozambique, and in near sites or in the shared rivers with Mozambique, Green points indicate the water sources or water treatment centers.

According to IV populational census carried out in 2017, this country has 29.67 million habitants distributed in 11 provinces [1]. The climate of Mozambique varies from subtropical climates (north and center) to dry arid (south) [2]. Like many African countries, Mozambique is highly vulnerable to climate variability and extreme weather events (droughts, floods, and tropical cyclones) [3]. Droughts are the most frequent natural disaster that have a negative impact on the population that reside in these rural areas [4]. The location of Mozambique in the coastal area makes it vulnerable to floods since many transnational river basins end [2]. Unfortunately, only 50% of the population has access to “safe drinking pan class="Chemical">water”. Urban areas are the most favored, with 80%, while rural and most of the popn>ulation have only 35% coverage and consume untreated n>an class="Chemical">water daily from rivers, lakes, and small puddles that form after or during the rain [5,6,7], putting at risk public health. Eutrophication of freshwater resources may lead to the occurrence of cyanobacterial blooms and the presence of cyanotoxins, being microcystins (MC), the most common toxins worldwide [8]. The presence of MC in untreated drinking water is a major threat to public health because this potent cyanotoxin causes hepatotoxicity in humans. Thus, this review evaluates the incidence of MC and its producers in drinking water bodies of Mozambique, based on reported and available data and the estimated human illness case numbers and associated economic damage caused by Microcystin both overall globally, and in Mozambique—Africa. Recommendations for routine control and monitoring of MC will also be done since this hepatotoxin is not included in water control tests data in Mozambique.

2. Microcystin-Producing Species and Toxicology

2.1. Microcystin-Producing Species

MCs are secondary metabolites produced by cyanobacteria spn>ecies that occur naturally (but it can be increased severely by n>an class="Species">human activities) in freshwater environments. The most reported cyanobacteria species, which produce MCs are listed in Table 1 and include species of the families Microcystaceae, Nostocaceae, Microcoleaceae, Oscillatoriaceae, Pseudanabaenaceae (Table 1). The occurrence and development of a particular genus and species of cyanobacteria and cyanotoxins production worldwide seem to be conditioned to water chemistry and climate conditions [8]. In a temperate climate, Microcystis and Anabaena blooms occur widely while Cylindrospermopsis develops in tropical regions [9]. There are toxic and non-toxic cyanobacteria of the same species, which may be found together [8,10,11]. Toxic cyanobacteria can produce several toxins with different toxicity making it uncertain to assess the overall toxicity of bloom due to the variations of toxins concentration spatially and seasonally [12]. To distinguish toxic and non-toxic cyanobacteria species is very complicated, and consequently, the methods used are also complex. It implicates that the prevention of cyanobacteria bloom development is a suitable way to control toxic blooms [13,14].
Table 1

Microcystin-producing species detected in freshwater bodies.

OrderFamilySpecies
Chroococcales Microcystaceae Microcystis sp. [15], M. aeruginosa [16,17,18,19,20,21,22,23,24,25,26], M. viridis [20,24], M. wesenbergii [25,27], M. spp. [28,29], M. ichthyoblabe [25] and Synechocystis sp. [25]
Nostocales Nostocaceae Anabaena spp. [29,30], A. flos-aquae [23,27], A. sp. [15,31], A. subcylindrica [32], A, variables [32], Nostoc sp. [27], Aphanizomenon flos-aquae [23,29,33] and A. circinalis [34]
Oscillatoriales Microcoleaceae Planktothrix prolifica [24] and P. agardhii [29]
Oscillatoriaceae Oscillatoria agardhii [35], O. limosa [36], O. chlorina [25], Phormidium konstantinosum (O. tenuis) [36], P. corium [32] and Plectonema boryanum [32]
Synechococcales Merismopediaceae Synechocystis aquatilisf. salina [37] and Aphanocapsa cumulus [38]
Pseudanabaenaceae Pseudanabaena mucicola [25] and P. galeata [25]
The factors that promote the MC synthesis are not yet clearly understood, however, the optimal growth of n>an class="Chemical">MC-producing species and toxicity seem influenced by light intensity, nutrients, and temperature, among other factors. For example, the higher toxicity of M. aeruginosa extracts was verified in extreme pH values [39,40], and heavy metals such as Zinc and Iron did not influence the M. aeruginosa toxicity [41]. The content of nitrogen and phosphorus influenced the toxicity of M. aeruginosa extracts. Low nitrogen content reduces the M. aeruginosa toxicity, while low phosphorous increased the toxicity in the natural population [42,43] and reduced in lab experiments [16,21,44,45]. Another lab conclusion was the correlation of colony size and content of toxic cyclic heptapeptide of the non-axenic strain of M. viridis and axenic M. viridis was also verified [20,46,47]. In general, the optimal temperature for which MC-producing species produce MC ranged from 20 to 25 °C [21,40,48,49]. This range of optimal temperature suggests that cyanobacteria blooms are most toxic during periods with warm weather and in areas with warm climates [8].

2.2. Toxicology

Microcystins (Figure 2) are the largest diverse groupn> of cyanobacterial toxins, and to date, more than 240 n>an class="Chemical">MCs analogs are known, and they vary structurally in terms of the degree of methylation, hydroxylation, epimerization, peptide sequence, and consequently in their toxic effects [50,51,52]. Chemically, MC is a group of monocyclic heptapeptides (numbered in Figure 2) containing both D- and L-amino acids plus N-methyldehydroalanine (Mdha) and a unique β-amino acid side-group, 3-amino-9-methoxy-2-6,8-trymethyl-10-phenyldeca-4,6-dienoic acid (Adda) and their analogs differ among them, at the two L-amino acids and on the methyl groups on D-erythro-β-methylaspartic acid (D-MeAsp) and Mdha with molecular weight varying from 900 to 1100 Daltons. MC-LR, MC-RR, and MC-YR are common MC variants, the letters L, R, and Y represent the aminoacids leucine, arginine, and tyrosine, which appear on the MC molecule in different combinations [50,53,54,55,56,57,58] being MC-LR the most studied. The biosynthesis of this group of cyanotoxin is regulated by non-ribosomal peptide synthetase and polyketide synthase domains, being MCyS the gene cluster, which has been sequenced and partially characterized in several cyanobacterial species of the family Microcystaceae, Nostocaceae, Microcoleaceae, Oscillatoriaceae, Merismopediacea, and Pseudanabaenacea [16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,59,60]
Figure 2

General chemical structure of microcystins. The common MC variant is MC-LR when X and Y correspond to L-Leu and L-Arg.

The mechanism of MCs toxicity seems to be well understood. They bind to n>an class="Chemical">serine/threonine-specific protein phosphatases (PPs) such as PP1 and PP2A, inhibiting their activity [61,62,63]. Adda moiety (Figure 1) plays an important role in the MC toxicity group since its isomerization and/or oxidation reduces the toxicity [64,65]. The inhibition of PP1and PP2A as a result of MC acute exposure causes excessive protein phosphorylation, alterations in the cytoskeleton, loss of cell shape, and consequently destruction of liver cells leading to intrahepatic hemorrhage or hepatic insufficiency [58]. Oxidative stress increasing in cells and consequent apoptosis, which can cause tumor promotion, is another mechanism of MC toxicity [66,67,68].

3. Effects of Microcystin in Humans, Symptoms, and Treatment

Microcystin effects in n>an class="Species">humans depend on the time of exposure and concentration ingested [69], and the studies are based on epidemiologic data but the reported studies on laboratory animals. Human health problems are mostly caused by chronic exposure by consumption of contaminated water or food, dermal exposure, or inhalation [57]. MC human poisoning episodes were reported in different parts of the world after the consumption of contaminated water or during sport or recreational activities [59,70,71,72]. Some examples of MC human poisoning cases are described; America—in 1996, an episode of human intoxications by MC was reported in Brazil with more than 76 deaths of patients at two dialysis centers in Caruaru. The municipal water supplied to the dialysis centers was the source of MC [71,73,74,75]. In Argentina, a human poisoning caused by MC involving a young man after immersion in an intense bloom Microcystis sp lake during sport and recreational activities were recorded. Four hours after exposure, the patient showed nausea, abdominal pain, and fever, and 48.6 µg·L−1 of microcystin-LR was detected in the water samples [76]. Other cases were recorded in Uruguay (January 2015) involving a 20-month-old child and her family during recreational activities. These victims were admitted to the hospital with diarrhea, vomiting, fatigue, and jaundice and the analysis confirmed the presence of MC-LR (2.4 ng·g−1 tissue) and [D-Leu1]MC-LR (75.4 ng·g−1 tissue) explanted liver [77]. Africa—toxic cyanobacteria suspected intoxication cases were reported in Zimbabwe involving children that were hospitalized in the Hospital of Harare with gastroenteritis symptoms [78]. In Europe—121 people presented abdominal pain, nausea, vomiting, diarrhea, fever, headaches, and muscle pain after consumption of untreated water from the River Kavlingean in Sweden. In this case a bloom of MC—producing such as Planktothrix agardhii and Microcystis spp. was observed in the river [79]. The most affected human organ is the liver [57]. However, in vivo and in vitro studies indicated that the kidney and colon are also affected [80,81,82,83,84,85]. The symptoms generally reported in humans due to the MC intoxication include gastroenteritis and related diseases, allergic and irritation reactions, liver diseases, tumors, and primary liver cancer and colorectal cancers, and massive hepatic hemorrhage. MC human poisoning treatment is very complicated due to the rapid, irreversible, and severe liver damage [86], however, gastric lavage [87], administration of monoclonal antibodies against MC-LR [88], immunosupressant Cyclosporine A, antibiotic rifampin [89], and membrane-active antioxidant vitamin E, taken as a dietary supplement [90] are recommended.

4. Microcystin Detection and Monitoring in Freshwater

According to the World Health Organization (WHO) guideline, the permitted limit of MC-LR for drinking n>an class="Chemical">water is 1.0 µg·L−1, and the tolerable daily intake is 0.04 µgKg−1 [91]. There are several MC detection methods, the most reported are listed in Table 2. Immunoassays (IA) are suitable methods of MC detection in Mozambique because they do not require sophisticated laboratory equipment and have a limit of detection below the maximum limit (1 µg·L−1). Additionally, IA can be used in both laboratory and field studies.
Table 2

MC detection methods in drinking water. IA—immunoassays, HPLC—high-performance liquid chromatographic, PAD—photodiode-array detector, LC—liquid chromatography, MS—mass spectroscopy, MALDI-TOF MS—matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, UV—ultraviolet detector.

MC VariantDetection LODLOQReference
-LR: -LY: -LW: -LF: -LA:Asp3(Z)-Dhb7-HtyR: -DAsp3-RRIA50–20,000 pg·mL−1 [88,92,93,94,95,96,97,98,99,100,101,102]
-RR: -LR: -LY: -LFHPLC-UV [102]
-RR: -LR: -LY: -LW: -LF: -FR; -WRHPLC-PAD5 ng [103,104]
3-demethyl-MC-LR: -LR: -LY: -LA: -LW: -LF: 3-demethyl-MC-RR: -RR: 3-demethyl-MC-YR: -YRLC–MS (/MS)0.2 pg–2057 pg1pg–15 µg·L−1[93,102,104,105,106,107,108]
D-MC-LR; -LR: D-MC-RR: D-MC-YR: -RR: -YR: [H4]MC-YR: -WRMALDI-TOF MS [109]

5. The Occurrence of Microcystin in Mozambican Drinking Water

5.1. The Drinking Water Scenario in Mozambique

The drinking water supn>ply scenario in Mozambique still faces major challenges because a majority of the population still consumes untreated drinking n>an class="Chemical">water and consequently is exposed to many water-borne diseases. Only 50% of the population has access to “safe drinking water”. Urban areas are the most favored, with 80%, while rural and most of the population have only 35% coverage and consume untreated water daily from rivers, lakes, and small puddles that form after or during the raining season [5,7]. The low water supply cover in Mozambique is inconceivable due to several reasons, among them, the existence of natural water cover (rivers) in the whole country and the presence of excessive fragmentation of governmental organisms for water management (Figure 1). The water management is led by the Ministry of Public Works, Habitation and Hydric Resources (MOPHRH), which operates, among others, with the National Direction of Water Supply and Sanitation, National Direction of Hydric Resource Management, Water Regional Administrations, Sanitation, and Water Supply Infra-structure Administration, Water Regulation Council, Fund for Investment and Patrimony of Water Supply, and other private institutions, which provide goods and services. In order to improve the water management and expand the coverage, different projects funded by the Mozambican government and non-governmental organizations such as Plataforma Moçambicana de Água [6], Greater Maputo Water Supply Expansion Project [110], Integrated Water Supply and Sanitation Project for the provinces of Niassa and Nampula [111], National Rural Water Supply and Sanitation Program (PRONASAR) in Nampula and Zambezia Provinces [112], Inhambane Rural Water Supply and Sanitation Program [113], and others were implemented involving all the MOPHRH, civil society, and private organisms. However, still to date, the national water supply does not cover enough, with the population still consuming untreated water. The pan class="Chemical">water policy in Mozambique was apn>proved in 1995, revised in 2007 and 2016, which, in the scopn>e of pan class="Chemical">water supply and sanitation, has the following relevant goals [114]: Achieve the sustainable development goals, universal access to pan class="Chemical">water supn>ply, and sanitation. Meeting of the basic needs of the poorest population, to reduce poverty, always looking for a sustainability situation. pan class="Chemical">Water valuing, not only as a social and envpan class="Chemical">ironmental asset but also with the economic value it holds. Government’s concentpan class="Species">ration on the definition of priorities, standards, regulation, and promotion of the private sector. Development of an institutional framework that contributes to the management of water as a resource and provision of decentralized and autonomous n>an class="Chemical">water supply and sanitation, where the private sector is called upon to participate. The Ministry of Health (MH) is the legal organism responsible for water quality control and follows the regulation of the WHO, which sets the parameters of the quality of n>an class="Chemical">water intended for human consumption and the methods of carrying out their checks in order to protect human health. The water quality control recommended by WHO include MC among other biological parameter and the provisional guideline value is 1 µg·L−1 for drinking water [115]. The challenge is enormous in Mozambique for control or monitoring of this hepatotoxin due to the lack of adequate laboratories for the detection of MC in drinking water, even for 50% of the population that consumes treated water. This scenario shows clearly that all the Mozambican population is very vulnerable to MC exposure.

5.2. Microcystin in Mozambican Drinking Water

The drinking water is supn>plied by private (autonomous systems) and governmental opn>erators. In Table 3, are listed the main sources of drinking water in Mozambique and includes underground and water river. The drinking water treatment is performed mainly by disinfection with chlorine, but is some regions such as Pemba and Niassa, the water treatment system includes the removal of iron by aeration. Not only is there no drinking water treatment for MC removal, but also MC incidence data in Mozambique are very limited. However, according to the WHO, more than 500,000 cases of diarrhea were reported, which 100 and 7 cases correspond to dysentery and cholera, respectively, and others are unknown [116].
Table 3

Treatment and drinking water supply in Mozambique. Gov—Government system. HTH—High test hypochlorite [7,114].

ProvinceWater SystemWater Treatment CenterCapacity, m3·dia−1Water SourceSupplied Sites
MaputoGov-Umbeluzi Umbeluzi240,000 Umbeluzi river and Pequenos Limbobo DamMaputo, Matola and Boane
Ka Tembe Autonomous Ka Tembe760Underground – Ka TembeKa Tembe
Vila Olimpia Autonomous -Underground - MaputoVila Olimpia
The Small 6500Underground -MaputoZona Verde, Kongolote, Matola Gare na Matola, Magoanine and Albazine
GazaGov-Xai-XaiXai-Xai22,790Limpopo riverBairro 11, Bairro 13, Hospital, Patrice Lumumba, Inhamissa 6, CFPP, Marieny Gouaby, Chinuguine and Praia
Gov-Limpopo
Gov-Chongoene
Xai-Xai Autonomous Underground – Xai-XaiChicumbane, Julius Nyerere, Muahetane e Chongoene
Gov-Chókwè 10,056Limpopo river and underground - ChokweLionde, Conhane, Massavassa, Nwachicoluane, Xilembene, Hókwe, Mapapa
Chókwè Autonomous 6816
Gov-Guija Underground - Guijavila-sede do distrito de Guijá
InhambaneGov-Inhambane 11,176 Inhambane City, Salela, Nhamua e Josina Machel
Gov-Maxixi9120Inhanombe riverChambone, Rumbana, Nhambiho, Bato, Habana, Malalane, Macupula, Macuamene, Maquetela, Eduardo Mandlane, Nhamaxaxa, Matadouro, Mabil, Barrane and Bembe
Mangapana and Mabil Autonomous Mangapana and Mabil
SofalaBeira and DondoMutua50,000Pungué riverBeira and Dondo
ManicaGov-ManicaChicamba38,600 Manica, Chimoio and Gondola and Messica and Bandula village
TeteGov-TeteTete: Aeration through a cascade, followed by two decantation tanks and then filtration and finally disinfection with granular chlorine38,495Zambeze riverTete city
The Degué small Degué
ZambeziaGov-ZambeziaLicuar: Disinfection with HTH19,512Underground - LicuarQuelimane, Nicoadala and Licuar
NampulaGov-NampulaNampula: Pre-chlorination, flocculation, decanting and filtration20,000Monapo damNampula city
Gov-NacalaNacala: A mixture of flocculation, decantation, filtration, and disinfection6000Nacala damNacala city
Cabo DelgadoGov-PembaPemba: Removal of iron by aeration and filtration12,000Underground-Metuge Pemba city
Gov-AngocheAngoche: Disinfection with HTH1800Underground-MalataneAngoche
NiassaGov-LichingaLocumué2400Locumué damLichinga
Chiuaula Autonomous Underground - ChiualaChiuaula
CuambaCuamba: Disinfection with HTH960Mpopole damCuamba
These data indicate that many people of Mozambique consume food and water unsafely. Few studies (Figure 1) were done by Pedro et al. [117,118,119] and Bojcevska and Jergil [120] in Pequenos Libombos dam, Nhambavale lake, Chòkwé irrigation channels and Chidenguele sites in the South of Mozambique during 2003, 2008, and 2009 and their studies indicated the occurrence of MC-LR, -YR, and -RR produced by Microcystis sp. (M. novacekii, botrys and other) and Cylindrospermopsis raciborskii [117,118,119,120] (Table 4). MC concentration varies from less than 0.01 (below quantification levels) to 0.02 in Pequenos Libombos dam, less to 0.01 to 0.68 in Chòkwé irrigation channels, 0.86 to 7.82 in Nhambavale lake and 0.57 to 6.83 µg·L−1 in Chidenguele. Higher MC concentration values than the maximum limit ranging from 6.83 to 7.78 µg·L−1 (around 7 times above) were found in the Nhambavale lake and Chidenguele sites. These data highlight (suggest) the need to implement an operational monitoring program of MCs since the tests recommended by MH do not include the MC test [121]. Neighboring countries published other data, which support the need for MC monitoring in Mozambique (Figure 1), namely:
Table 4

The Incidence of Microcystin and its producers in the aquatic environments of Mozambique. PL—Pequenos Libombos dam, NL—Nhambavale lake, CH—Chòkwé irrigation channels, RFLP—restriction fragment length polymorphism, MC—microcystins, ELISA—enzyme-linked immunosorbent assay, CG—Chidengule, LM—light microscope, PCR— polymerase chain reaction, ML—Malawi lake, NL— Niassa lake.

LocalDateProducerMCReference
SpeciesDetectionMC VariantDetectionConc.
PL2008–2009Microcystis sp.PC geneLR and YRLC-MS3.9 ng·g−1[118]
Microcystis sp.MCyA-MISY gene
Microcystis sp.MCyB gene
Microcystis sp.RFLP
NLMicrocystis sp.PC geneLR, YR and RR159.4 ng·g−1
Microcystis sp.MCyA-MISY gene
Microcystis sp.MCyB gene
Microcystis sp.RFLP
CHMicrocystis sp.PC geneLR2.7 ng·g−1
negativeMCyA-MISY gene
negativeMCyB gene
negativeRFLP
PL2002 LMMCELISA0.22 µg·L−1[120]
CH Cylindrospermopsis raciborskii < 0.01 µg·L−1
CGMicrocystis novacekii and M. botrys6.83 µg·L−1
PL2008–2009 LR LC-MS< 0.01 µg·L−1[117]
YR0.01 µg·L−1
CHLR0.68 µg·L−1
YR0.06 µg·L−1
NLLR7.78 µg·L−1
YR0.07 µg·L−1
RR< 0.01 µg·L−1
PL2008–2009 Microcystis aeruginosa PC gene [119]
MCyB-Taq-Nuclease assay
NLPC gene
MCyB-Taq-Nuclease assay
CHPC gene
MCyB-Taq-Nuclease assay
ML/NL2002Anabaena sp.LM [143]
NKP2007 Microcystis aeruginosa PCRLRELISA23718 μg·L−1[132]
South Africa: MC Producers: Synechocystis sp. Microcystis aeruginosa, Microcystis panniformis, Nostoc sp., Planktothrix sp., Phormidium sp., in the Limpopo river basin [122,123,124,125,126], Hartbeespoort dam [127,128,129,130,131], Kruger National Park [132], Sand, Mawoni, Lephalale, Mokolo, Crocodile, Nzhelele ivers [126] MC -YR, -LR, -FR, -YA, -LA, -LAba (0.156–0.270, 0.059–0.18, 0.09, 0.02–0.044, 0.051–0.241, 0.080 mg.g−1) in Natal and Transvaal dams [133], 8.6 µg·L−1 in Hartbeespoort dam [134], 12,300 µg·L−1 in Hartbeespoort lake [135]. Tanzania: MC-LR and -RR in different tissues of dead flamingos (Phoeniconaias minor) from Empakai Crater, Lake Natron and Lake Manyara (0.165–1.16 ng.g−1) [136,137,138], MC-RR (0.4–13 µgL−1) in Victoria lake [139,140], MC producers: Aphanocapsa sp., Anabaena sp., Microcystis sp. in Victoria lake [139,140]. Zimbabwe: MC producers: Microcystis aeruginosa in Mzingwane river, Shashe River [126], Microcystis wesenbergii [141,142]. MC-LR (1.62–22 µgL−1) in Chivero lake [141,142]. Malawi: pan class="Chemical">MC producers: pan class="Species">Anabaena sp. in Malawi lake [143]. For example, the drinking water in the Xai Xai district (Gaza province) (Figure 1) is supn>plied from the Limpn>opn>o river. This river contains different MC producers such as Synechocystis sp. Microcystis aeruginosa, Microcystis panniformis, Nostoc sp., Planktothrix sp., Phormidium sp., which were detected in South Africa areas [122,123,124,125,126]. The presence of a potentially toxic algae is not an indication of MC production but is an indication of the need for MC screening in order to confirm the MC presence.

5.3. Removal of Microscystin from Drinking Water in Mozambique

MCs can be removed from drinking water using several rapid and low-cost. The most are reported in laboratory studies, and they are not adaptable to economic conditions in Mozambique [144,145,146,147,148,149,150]. However, the following techniques seem to be useful in Mozambique and can be implemented in both rural and urban zones: Photolysis at 254 and 185 nm [147], use of wood-based and coconut-based activated carbons [148], use of bamboo-based charcoal adsorbent modified with chitosan [149], hydrophyte filter bed [150], biological activated carbon process [151], aquatic vegetable bed [152], and activated carbon from the seed husks of the pan-tropical tree, Moringa oleifera [153], among others.

6. Final Considerations and Recommendations

The drinking water supn>ply scenario in Mozambique still faces major challenges because the majority of the population still consumes untreated drink n>an class="Chemical">water (from rivers, lakes, and small puddles that form after or during the raining season) and consequently exposed to many water diseases [5,7] including, for example, gastroenteritis, which is caused by hepatotoxins MCs. To date, no data of water poisoning episodes recorded were associated with MCs presence in the water. However, this might be underestimated due to a lack of monitoring facilities and/or a lack of public health staff trained for recognizing symptoms of MCs intoxication since the presence of high MCs concentration was reported in Maputo and Gaza provinces. Few studies done in Maputo and Gaza provinces indicated the occurrence of MC-LR, -YR, and -RR at a concentration ranging from 6.83 to 7.78 µg·L−1 [117,118,119,120], which are very high, around 7 times above the maximum limit (1 µg·L−1) recommended by WHO [59]. The potential MC-producing in the studied sites is mostly Microcystis sp. [117,118,119,120]. However, MC distribution in Mozambique is unknown, and a monitoring program would help to understand the dimension of the problem. To date, no water MC poisoning episodes data recorded in Mozambique. The absence of MC intoxication episodes might be underestimated due to the absence of MC monitoring plan and/or a lack of public health staff trained in recognizing symptoms of MC intoxication. MC monitoring may be implemented according to recommendations of WHO [59] (1 µg·L−1), and the respective MC analysis can be done in the existing water treatment centers in each province (Table 3). Rapid tests for MC detection, such as ELISA, can be used in each center. In the case of higher MCs content, some suitable techniques for MC removal may be used. The recommended techniques include photolysis at 254 and 185 [147], the use of wood-based and coconut-based activated carbons [148], use of bamboo-based charcoal adsorbent modified with chitosan [149], hydrophyte Filter Bed [150], Biological Activated Carbon Process [151], and aquatic vegetable bed [152], among others. These techniques can be used in both rural and urban areas due to their low-cost implementation and local access.
  76 in total

1.  A fluorescent microplate assay for microcystin-LR.

Authors:  O I Fontal; M R Vieytes; J M Baptista de Sousa; M C Louzao; L M Botana
Journal:  Anal Biochem       Date:  1999-05-01       Impact factor: 3.365

2.  Effects of microcystin-LR in isolated perfused rat kidney.

Authors:  A C Nobre; M C Jorge; D B Menezes; M C Fonteles; H S Monteiro
Journal:  Braz J Med Biol Res       Date:  1999-08       Impact factor: 2.590

3.  Cyanobacterial microcystin-LR is a potent and specific inhibitor of protein phosphatases 1 and 2A from both mammals and higher plants.

Authors:  C MacKintosh; K A Beattie; S Klumpp; P Cohen; G A Codd
Journal:  FEBS Lett       Date:  1990-05-21       Impact factor: 4.124

4.  Variation of microcystins, cyanobacterial hepatotoxins, in Anabaena spp. as a function of growth stimuli.

Authors:  J Rapala; K Sivonen; C Lyra; S I Niemelä
Journal:  Appl Environ Microbiol       Date:  1997-06       Impact factor: 4.792

5.  Ultrasonically induced degradation of microcystin-LR and -RR: identification of products, effect of pH, formation and destruction of peroxides.

Authors:  Weihua Song; Armah A de la Cruz; Kathleen Rein; Kevin E O'Shea
Journal:  Environ Sci Technol       Date:  2006-06-15       Impact factor: 9.028

6.  Renal injuries induced by chronic intoxication with microcystins.

Authors:  Aleksandra Milutinović; Bojan Sedmak; Irena Horvat-Znidarsic; Dusan Suput
Journal:  Cell Mol Biol Lett       Date:  2002       Impact factor: 5.787

Review 7.  Molecular mechanisms of microcystin toxicity in animal cells.

Authors:  Alexandre Campos; Vitor Vasconcelos
Journal:  Int J Mol Sci       Date:  2010-01-21       Impact factor: 6.208

8.  Human intoxication by microcystins during renal dialysis treatment in Caruaru-Brazil.

Authors:  Sandra M F O Azevedo; Wayne W Carmichael; Elise M Jochimsen; Kenneth L Rinehart; Sharon Lau; Glen R Shaw; Geoff K Eaglesham
Journal:  Toxicology       Date:  2002-12-27       Impact factor: 4.221

9.  Phytoplankton composition and microcystin concentrations in open and closed bays of Lake Victoria, Tanzania.

Authors:  Athanasio S Mbonde; Lewis Sitoki; Rainer Kurmayer
Journal:  Aquat Ecosyst Health Manag       Date:  2015-02-03       Impact factor: 1.047

10.  Human fatalities from cyanobacteria: chemical and biological evidence for cyanotoxins.

Authors:  W W Carmichael; S M Azevedo; J S An; R J Molica; E M Jochimsen; S Lau; K L Rinehart; G R Shaw; G K Eaglesham
Journal:  Environ Health Perspect       Date:  2001-07       Impact factor: 9.031

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  3 in total

1.  Freshwater Algal Toxins: Monitoring and Toxicity Profile.

Authors:  Angeles Jos; Ana M Cameán
Journal:  Toxins (Basel)       Date:  2020-10-13       Impact factor: 4.546

Review 2.  Microcystin Toxicokinetics, Molecular Toxicology, and Pathophysiology in Preclinical Rodent Models and Humans.

Authors:  Tarana Arman; John D Clarke
Journal:  Toxins (Basel)       Date:  2021-07-29       Impact factor: 4.546

3.  A Summer of Cyanobacterial Blooms in Belgian Waterbodies: Microcystin Quantification and Molecular Characterizations.

Authors:  Wannes Hugo R Van Hassel; Mirjana Andjelkovic; Benoit Durieu; Viviana Almanza Marroquin; Julien Masquelier; Bart Huybrechts; Annick Wilmotte
Journal:  Toxins (Basel)       Date:  2022-01-16       Impact factor: 4.546

  3 in total

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