₦airaland Forum

Harryjoshua4: faithless generation, when will you acknowledge the great work God is doing in our midst through Tb Joshua.

ceejayluv: There's no vaccine for malaria and HIV as well....

ReubenAbati: [size=18pt]America invested in science

Nigeria invested in Religion.

Ebola came, and Nigerians are praying for American science.

EEDIOTS!!![/size]

MKSON: Several years ago, Ebola virus erupted in Africa, killing thousands without restrain or cure. The medical world was perplexed. A great man of God by the name John G Lake came to the rescue. Laying hands on infected people who were not to be touched. The slightest contact with any secretion from an infected person is all it takes for transmission. But with bare hands, cleaning secretion and curing every victim, John G Lake along with his Holy Ghost filled team, brought to an abrupt end the spread of the deadly virus. When asked by the medical world how he did it. He had this to say: I have the life of God in me, every virus that comes in contact with me dies. He asked them to get an innoculum from an infected person, observe same under a microscope to ascertain viral activities in it. They did and confirmed living and multiplying virus. He then asked them to put the innoculum on his palm and observe under the microscope. This time there were no more activities. ALL WERE DEAD upon contact with him. What a life! Every child of God has this life! He that has the Son has this life! That higher life that put out Ebola in the days of John G Lake will do the same through you in your day! At the Name of Jesus, Ebola will bow out! Stop the fear! Let this message of hope and faith go viral and the Ebola viral spread will stop! Don't disdain the ever living words of Jesus: And these signs shall follow them that believe, in my Name, they shall cast out devils, they shall speak with new tongues, they shall take up serpents, and if they drink any deadly thing (Ebola virus included) it shall not hurt them, they shall lay hand on the sick (those already infected) and they shall recover - Mark 16:15-18.
John G Lake and team are long gone! But I am here, you are here! We can save our world!
We have the life of God in us!
Spread the faith!
Stop the fear!
Spread the life!
Stop the death!
Yes you can!
The world belongs to you!
Cause you belong to Jesus!
Halleluyah

san316: thank u mr enlightened. I guess i can learn a lot from you. But first, know that everything exists and is only discovered over time. So i know the virus has been there. But are you not curious that since 1976, over 20 yrs nw, d virus was nt such a plague until now? Why have we not heard of such massive deaths arising from the virus until recently? Knw that those scientists do research, just as they pick plants that could be useful to man and develop it, that's how they pick up such organisms and harness them for reasons best known to them. If ebola was actually a problem since 1976, then there wlda bin a vaccine already and media campaign wld av been more proactive since then.

viution: Is it a pure breed? How much did you get it?

oluwaseun0sewa: In 2005 more than 250 people lost their lives to chikungunya virus.. BOTH CAN KILL..

oluwaseun0sewa: Over the past few days, Ebola has turned to a household name in every home in Nigeria, The Ministry Of Health is working to find the 70 people which might have possibly had contact with Mr. Sawyer [the dead infected Liberian National] . The main question on people's mind is "Where are those who took the same flight with mr.sawyer.?".. The U.S said that they've found a possible cure for the virus but its not ready for west africa ,Now it seems the U.S now Has a challenge to face with the Chikunguya Virus Outbreak

Chikungunya (English pronunciation: /ˌtʃɪkənˈgʊɲə/ CHI-kən-GUUN-yə; Makonde for "that which bends up" is an infection caused by the Chikungunya virus. It causes an illness with an acute febrile phase lasting two to five days, followed by a longer period of joint pains in the extremities; this pain may persist for years in some cases.[1][2]

The disease is transmitted similarly to dengue fever. It is transmitted to humans by virus-carrying Aedes mosquitoes.[3] Specifically, there are two species of mosquitoes, A. albopictus and A. aegypti, that are extrinsic hosts (vectors) of chikungunya virus. The strain of chikungunya spreading to the US from the Caribbean is most easily spread by A. aegypti. There is concern that this strain of chikungunya could mutate to make the A. albopictus vector more efficient. If this mutation were to occur, chikungunya would be more of a public health concern to the US. The A. albopictus or "Asian Tiger" mosquito is more widespread in the US and is more aggressive than the A. aegypti.[4] It is known that monkeys, apes, and rodents act as a reservoir for the virus.[5] Having rodents as a viral reservoir for chikungunya differs from that of dengue which has only humans and nonhuman primates as hosts.[6]

The best means of prevention is overall mosquito control and in addition, the avoidance of bites by any infected mosquitoes.[7] There is no specific treatment but medications can be used to reduce symptoms.[7] Rest and fluids may also be useful.[8]

Contents

1 Signs and symptoms
1.1 Chronic disease
2 Virology
2.1 Type 1 interferon
3 Diagnosis
4 Prevention
4.1 Vaccine
5 Treatment
5.1 Chronic arthritis
6 Epidemiology
7 History
8 Society and culture
8.1 Biological weapon
9 References
10 Further reading
11 External links

Signs and symptoms

The incubation period of chikungunya disease ranges from one to twelve days, typically two to three. The majority of those infected will develop symptoms.[9] Symptoms include a fever up to 40 °C (104 °F), a petechial or maculopapular rash of the trunk and occasionally the limbs, and arthralgia or arthritis affecting multiple joints.[10] Other nonspecific symptoms can include headache, nausea, vomiting, conjunctivitis, slight photophobia and partial loss of taste.[11] Ocular inflammation from chikungunya may present as iridocyclitis. Retinal lesions may also occur.[12] Pedal edema (swelling of legs) is observed in many people, the cause of which remains obscure as it is not related to any cardiovascular, renal or hepatic abnormalities.

Typically, the fever lasts for two days and then ends abruptly. However, other symptoms—namely joint pain, intense headache, insomnia and an extreme degree of prostration—last for a variable period; usually for about five to seven days.[10] People have complained of joint pains for much longer time periods; some as long as two years, depending on their age.[13][14] Recovery from the disease varies by age. Younger people recover within 5 to 15 days; middle-aged people recover in 1 to 2.5 months. Recovery is longer for the elderly. The severity of the disease as well as its duration is less in younger people and pregnant women. In pregnant women, no untoward effects are noticed after the infection.
Chronic disease

Observations during recent epidemics have suggested chikungunya may cause long-term symptoms following acute infection. During the La Reunion outbreak in 2006, more than 50% of subjects over the age of 45 reported long term musculoskeletal pain[15] with up to 60% of people reporting prolonged arthralgia 3 years following initial infection.[16] A study of imported cases in France reported that 59% of people still suffered from arthralgia two years after acute infection.[17] Following a local epidemic of chikungunya in Italy, 66% of people reported muscles pains, joint pains, or asthenia at one year postacute infection.[18] Long-term symptoms are not an entirely new observation; long-term arthritis was observed following an outbreak in 1979.[19] Common predictors of prolonged symptoms are increased age and prior rheumatological disease.[15][16][18][20] The cause of these chronic symptoms is currently not fully known. Markers of autoimmune or rheumatoid disease have not been found in people reporting chronic symptoms.[16][21] However, some evidence from humans and animal models suggest that chikungunya may be able to establish chronic infections within the host. Viral antigen was detected in a muscle biopsy of a people suffering a recurrent episode of disease three months after initial onset.[22] Additionally, viral antigen and RNA were found in synovial macrophages of a person during a relapse of musculoskeletal disease 18 months post initial infection.[23] Several animal models have also suggested that chikungunya virus may establish persistent infections. In a mouse model, viral RNA was detected specifically in joint-associated tissue for at least 16 weeks post-inoculation, and was associated with chronic synovitis.[24] Similarly, another study reported detection of a viral reporter gene in joint tissue of mice for weeks post-inoculation.[25] In a non-human primate model, chikungunya virus was found to persist in the spleen for at least 6 weeks.[26]
Virology
Chikungunya virus
Emd-5577.jpg
Cryoelectron microscopy reconstruction of chikungunya virus. From EMDB entry EMD-5577[27]
Virus classification
Group: Group IV ((+)ssRNA)
Order: Unassigned
Family: Togaviridae
Genus: Alphavirus
Species: Chikungunya virus

Chikungunya virus is an alphavirus with a positive sense single-stranded RNA genome of approximately 11.6kb. It is a member of the Semliki Forest virus complex and is closely related to Ross River virus, O'nyong'nyong virus and Semliki Forest virus.[28] In the United States it is classified as a Category C priority pathogen[29] and work requires Biosafety Level III precautions.[30]

Human epithelial, endothelial, primary fibroblasts and monocyte-derived macrophages are permissive for chikungunya virus in vitro and viral replication is highly cytopathic but susceptible to type I and II interferon.[31] In vivo, chikungunya virus appears to replicate in fibroblasts, skeletal muscle progenitor cells and myofibers.[22][32][33]
Type 1 interferon

Upon infection with chikungunya, the host's fibroblasts will produce type 1 (alpha and beta) interferon.[34] Mice that lack the interferon alpha receptor die in 2–3 days upon being exposed to 102 chikungunya PFU, while wild type mice survive even when exposed to as much as 106 PFU of the virus.[34] At the same time, mice that are partially type 1 deficient (IFN α/β +/−) are mildly affected and experience symptoms such as muscle weakness and lethargy.[35] Partidos et al. 2011 saw similar results with the live attenuated strain CHIKV181/25. However, rather than dying, the type 1 interferon deficient (IFN α/β −/−) mice were temporarily disabled and the partially type 1 interferon deficient mice did not have any problems.[36]

Several studies have attempted to find the upstream components of the type 1 interferon pathway involved in the host's response to chikungunya infection. So far, no one knows the chikungunya specific pathogen associated molecular pattern.[37] Nonetheless, IPS-1—also known as Cardif, MAVS, and VISA—has been found to be an important factor. In 2011, White et al. found that interfering with IPS-1 decreased the phosphorylation of interferon regulatory factor 3 (IRF3) and the production of IFN-β.[37] Other studies have found that IRF3 and IRF7 are important in an age-dependent manner. Adult mice that lack both of these regulatory factors die upon infection with chikungunya.[38] Neonates, on the other hand, succumb to the virus if they are deficient in one of these factors.[39]

Chikungunya counters the Type I interferon response by producing NS2, a non-structural protein that degrades Rpb and turns off the host cell's ability to transcribe DNA.[40] NS2 interferes with the JAK-STAT signaling pathway and prevents STAT from becoming phosphorylated.[41]
Diagnosis

Common laboratory tests for chikungunya include RT-PCR, virus isolation, and serological tests.

Virus isolation provides the most definitive diagnosis, but takes one to two weeks for completion and must be carried out in biosafety level 3 laboratories.[42] The technique involves exposing specific cell lines to samples from whole blood and identifying chikungunya virus-specific responses.
RT-PCR using nested primer pairs is used to amplify several chikungunya-specific genes from whole blood. Results can be determined in one to two days.[42]
Serological diagnosis requires a larger amount of blood than the other methods, and uses an ELISA assay to measure chikungunya-specific IgM levels. Results require two to three days, and false positives can occur with infection via other related viruses, such as o'nyong'nyong virus and Semliki Forest virus.[42]

Prevention
The Aedes aegypti mosquito biting a person

The most effective means of prevention are protection against contact with the disease-carrying mosquitoes and mosquito control.[7] These include using insect repellents with substances such as DEET (N,N-diethyl-meta-toluamide; also known as N,N'-diethyl-3-methylbenzamide or NNDB), icaridin (also known as picaridin and KBR3023), PMD (p-menthane-3,8-diol, a substance derived from the lemon eucalyptus tree), or IR3535. Wearing bite-proof long sleeves and trousers also offers protection.

In addition, garments can be treated with pyrethroids, a class of insecticides that often has repellent properties. Vaporized pyrethroids (for example in mosquito coils) are also insect repellents. Securing screens on windows and doors will help to keep mosquitoes out of the house. In the case of the day-active Aedes aegypti and Aedes albopictus, however, this will have only a limited effect, since many contacts between the mosquitoes and humans occur outside.
Vaccine

There are currently no approved vaccines available. A phase II vaccine trial used a live, attenuated virus, developing viral resistance in 98% of those tested after 28 days and 85% still showed resistance after one year.[43] However, 8% of people reported transient joint pain and attenuation was found to be due to only two mutations in the E2 glycoprotein.[44] Alternative vaccine strategies have been developed and shown efficacy in mouse models but have so far not reached clinical trials.[45][46]
Treatment

Currently there is no specific treatment.[7] Attempts to relieve the symptoms include the use of NSAIDs such as naproxen, paracetamol (acetaminophen) and fluids.[7] Aspirin is not recommended.[47]
Chronic arthritis

In those who have more than two weeks of arthritis, ribavirin may be useful.[7] The effect of chloroquine is not clear.[7] It does not appear to help acute disease but there is tentative evidence that it might help the chronic arthritis.[7] Steroids do not appear useful either.[7]
Epidemiology
Cases of chikungunya fever (between 1952 and 2006) have been reported in the countries depicted in red on this map. Since 2006, local transmission has occurred in areas within Taiwan, Australia, the Caribbean and Venezuela, and the United States.

Chikungunya virus is an alphavirus closely related to the o'nyong'nyong virus,[48] the Ross River virus in Australia, and the viruses that cause eastern equine encephalitis and western equine encephalitis.[49]

Three genotypes of this virus have been described: West African, East/Central/South African and Asian genotypes.[50]

Chikungunya is generally spread through bites from Aedes aegypti mosquitoes, but recent research by the Pasteur Institute in Paris has suggested chikungunya virus strains in the 2005-2006 Reunion Island outbreak incurred a mutation that facilitated transmission by Asian tiger mosquito (Aedes albopictus).[51]

Concurrent studies by arbovirologists at the University of Texas Medical Branch in Galveston, Texas, confirmed definitively that enhanced chikungunya virus infection of A. albopictus was caused by a point mutation in one of the viral envelope genes (E1).[52][53] Enhanced transmission of chikungunya virus by A. albopictus could mean an increased risk for chikungunya outbreaks in other areas where the Asian tiger mosquito is present. A recent epidemic in Italy was likely perpetuated by A. albopictus.[54]

In Africa, chikungunya is spread via a sylvatic cycle in which the virus largely resides in other primates in between human outbreaks.[49]

On 28 May 2009 in Changwat Trang of Thailand where the virus is endemic, the provincial hospital decided to deliver by Caesarean section a male baby from his chikungunya-infected mother, Khwanruethai Sutmueang, 28, a Trang native, to prevent mother-fetus virus transmission. However, after delivering the baby, the physicians discovered the baby was already infected with the virus, and put him into intensive care because the infection had left the baby unable to breathe by himself or to drink milk. The physicians presumed the virus might be able to be transmitted from a mother to her fetus, but without laboratory confirmation.[55]
History
Main article: Chikungunya outbreaks

The word chikungunya is thought to derive from a description in the Makonde language, meaning "that which bends up", of the contorted posture of people affected with the severe joint pain and arthritic symptoms associated with this disease.[56] The disease was first described by Marion Robinson[57] and W.H.R. Lumsden[58] in 1955, following an outbreak in 1952 on the Makonde Plateau, along the border between Mozambique and Tanganyika (the mainland part of modern day Tanzania).

According to the initial 1955 report about the epidemiology of the disease, the term chikungunya is derived from the Makonde root verb kungunyala, meaning to dry up or become contorted. In concurrent research, Robinson glossed the Makonde term more specifically as "that which bends up". Subsequent authors apparently overlooked the references to the Makonde language and assumed the term derived from Swahili, the lingua franca of the region. The erroneous attribution of the term as a Swahili word has been repeated in numerous print sources. Many erroneous spellings of the name of the disease are in common use.

Since its discovery in Tanganyika, Africa, in 1952, chikungunya virus outbreaks have occurred occasionally in Africa, South Asia, and Southeast Asia, but recent outbreaks have spread the disease over a wider range.

The first recorded outbreak of this disease may have been in 1779.[59] This is in agreement with the molecular genetics evidence that suggests it evolved around the year 1700.[60]

In December 2013, chikungunya was confirmed on the Caribbean island of St. Martin with 66 confirmed cases and suspected cases of around 181.[61] This outbreak is the first time in the Western Hemisphere that the disease has spread to humans from a population of infected mosquitoes.[62] By January 2014, the Public Health Agency of Canada reported that cases were confirmed on the British Virgin Islands, Saint-Barthélemy, Guadeloupe, and Martinique.[63] In April 2014, chikungunya was also confirmed in the Dominican Republic by the Centers for Disease Control and Prevention (CDC).[64] By the end of April, it had spread to 14 countries in all, including St. Lucia, and Haiti where an epidemic was declared.[65][66]

By the end of May 2014, over ten imported cases of the virus had been reported in the United States by people traveling to Florida from areas where the virus is endemic.[67]

On June 2014 six cases of the virus were confirmed in Brazil, two in the city of Campinas in the state of São Paulo. The six cases are Brazilian army soldiers who had recently returned from Haiti, where they were participating in the reconstruction efforts.United Nations Stabilisation Mission in Haiti.[68] The information was officially released by Campinas municipality health secretary that has taken the appropriate actions.[69]

On June 11, 2014, a case was reported in Forsyth County, North Carolina.[70]

On June 16, 2014, Florida had a cumulative 42 cases.[71]

On June 17, 2014,Puerto Rico had confirmed 13 cases of the Chikungunya virus.[72]

On June 17, 2014, Mississippi State Department of Health officials confirmed they are investigating the first potential case in a Mississippi resident who recently travelled to Caribbean nation of Haiti.[73]

On June 19, 2014, the virus had spread to Georgia, USA.[74]

On June 24, 2014, a case was reported in Poinciana, Polk County, Florida.[71]

On June 25, 2014, the Arkansas Health Department confirmed one person from the Natural State is carrying Chikungunya.[75]

On June 26, 2014, a case was reported in Jalisco, Mexico.[76]

On July 17, 2014, the first chikungunya case acquired in the United States were reported in Florida by the Centers for Disease Control and Prevention.[77] Since 2006 over 200 cases have been reported in the United States but only in people who had traveled to other countries. This is the first time the virus was passed by mosquitoes to a person on the U.S. mainland.[78]

http://en.wikipedia.org/wiki/Chikungunya

jokaf: The Servant of God @ CCT. DELIVERANCE MINISTRIES , in his Thursday message today, says that; “Ebola is not for children of God”,

He said there are three class of people on this earth
1. Children of God- Thos Serving God in spirit and in truth.
2. Children of God-devil - Those Claiming to be children of God but doing the things of the devil
3. Children of the devil - Those who are worshiping the devil

He said God is about to prove himself in the lives of those who truly serve him.
According to his sermon this afternoon, "HOW TO ESCAPE THE PRESENT SATANIC WEAPON OF DESTRUCTION CALLED EBOLA"
He said this is the time for everyone to choose who is their father, he said anyone who choose God as his father and work in the ways of God, can never be affected with Ebola, because whoever is a true child of God like SHEDRACK, MEDSHARK AND ABEDNEGO, they will surely carry the spirit of God in them.
He read the book of 1 John 4 V 4- Ye are of Gods, little children, and have overcome them: because greater is he that is in you, than he that is in the world.
And Deuteronomy 7 V15- And the Lord will take away from thee all sickness and will put none of the evil diseases of the Egypt, which thou knowest, upon thee; but will lay them upon all them that hate thee.

He explained 5 ways to escape from Ebola virus
1. We must choose where we belong-Joshua 24V15- And if it is evil in your eyes to serve the LORD, choose this day whom you will serve, whether the gods your fathers served in the region beyond the River, or the gods of the Amorites in whose land you dwell. But as for me and my house, we will serve the LORD.”
2. Walk before the Lord like Abraham-Gen 17 V1
3. Keep the ways of the Lord- Psalm 18V21
4. We should be ready to worship the Lord in spirit and in truth- John 4V24
5. We should be ready to save souls for God

Thousands of MFM members across the world are
expected to attend the annual convention and anointing
service scheduled for October.

newspapers: Even Pst E.A Adeboe advices members to watch and pray http://www.divanaija.com.ng/pastor-e-adeboye-addresses-rccg-ebola-disease/

Image123: 1. Nora is frustrated.
2. i'm not ALWAYS defending most of pastor Adeboye's actions. It don't stop me from talking in his favor once in a while.
3. i don't recall the fault i covered on this thread. Please remind us or are you lying?
4. Do you believe everything the news says?
5. Nora is frustrated.

Image123: Take it easy, i can almost assure you that pastor Adeboye is not here on nairaland. Find something of value to do to cure your frustrations.

lomprico: The americans dint stand up n pray b4 the got the ZMapp serum, they Got up and worked to the found d cure. Mofos like the op is looking for who to take advantage of in d name of God. Smh! africa can never develop.

Smoothchic: Nora and Apatheist, what wrong has the pastor done? I suggest u guys just shut up and stop allowing demons to speak through you if you guys have nothing encouraging to say.

Chanchit: Haba, na Adeboye carry Ebola enter Nigeria..? This insult too much na..

Adeboye told the pastors that all those who fasted for 100 days the last time should have no fear of Ebola as the disease would not get to them.

Of course the pentecostals are as guilty as the roman catholics. There is no perfect church organisation anywhere. What remains true is the body of Christ and it has as members all who believe and accept the finished work of Christ irrespective of the name on the building where they congregate to worship God.

dazzlingd: Pls, wen reading the bible, don't jst pick a verse dat appeals to u, read the whole chapter and understand everyting dat happened there and led to a particular statement being made...."Will a man rob God, ye have robbed me in tithe" if u understand wat led to this statement, den u will knw it has bin misinterpreted & does nt apply to tithes being collected in churches 2day

No one is against giving bt giving on a false believe is nt jst right. U sud give cheerfully at all times & whrevr u are.

So many tins are misinterpreted in d bible and pastors today use dem to preach, it's left to u to seek the truth.

AONO: i dont think u have a good parent cos if u do u will not talk to dis man like dis and for your information dis man can single handedly finance osun state budget.

redsun: I don't think they are interested. They can't be bothered with Africa except for explootations and epidemics.

Africans are not included in world game of respect and dignity. They are seem as the world's plague. As a people that have to be laboriously carried along.

sarmiie: perharps i ddnt post my point well...d que is rhetorical; most nigerians definately know dt zimbabwe is in southern africa (due to our knowledge of dia issues) bt cant locate it on a map.........its nt selfishness, is it??

Do u get my point now sir??