A secret weapon against Zika and other mosquitoborne diseases Nina Fedoroff

Zika fever:

our newest dread disease.

What is it? Where’d it come from?

What do we do about it?

Well for most adults,
it’s a relatively mild disease –

a little fever, a little headache,
joint pain, maybe a rash.

In fact, most people who get it
don’t even know they’ve had it.

But the more we find out
about the Zika virus

the more terrifying it becomes.

For example, doctors
have noticed an uptick

of something called Guillain-Barré
syndrome in recent outbreaks.

In Guillain-Barré, your immune system
attacks your nerve cells

it can partially
or even totally paralyze you.

Fortunately, that’s quite rare,
and most people recover.

But if you’re pregnant
when you’re infected

you’re at risk of something terrible.

Indeed, a child with a deformed head.

Here’s a normal baby.

Here’s that infant
with what’s called microcephaly.

a brain in a head that’s too small.

And there’s no known cure.

It was actually doctors
in northeastern Brazil

who first noticed, just a year ago,
after a Zika outbreak,

that there was a peak
in the incidence of microcephaly.

It took medical doctors another year

to be sure that it was caused
by the Zika virus,

but they’re now sure.

And if you’re a “bring on
the evidence” type,

check out this publication.

So where did it come from,
and how did it get here?

And it is here.

Like many of our viruses,
it came out of Africa,

specifically the Zika forest in Uganda.

Researchers at the nearby
Yellow Fever Research Institute

identified an unknown virus
in a monkey in the Zika forest

which is how it got its name.

The first human cases of Zika fever

surfaced a few years later
in Uganda-Tanzania.

The virus then spread through West Africa

and east through equatorial Asia –
Pakistan, India, Malaysia, Indonesia.

But it was still mostly in monkeys
and, of course, mosquitoes.

In fact in the 60 years between the time
it was first identified in 1947 and 2007

there were only 13 reported cases
of human Zika fever.

And then something extraordinary happened
on the tiny Micronesian Yap islands.

There was an outbreak that affected
fully 75 percent of the population.

How did it get there? By air.

Today we have two billion
commercial airline passengers.

An infected passenger can board a plane,
fly halfway around the world

before developing symptoms –
if they develop symptoms at all.

Then when they land, the local mosquitoes
begin to bite them and spread the fever.

Zika fever then next surfaced
in 2013 in French Polynesia.

By December of that year, it was being
transmitted locally by the mosquitoes.

That led to an explosive outbreak in which
almost 30,000 people were affected.

From there it radiated around the Pacific.

There were outbreaks in the Cook
Islands, in New Caledonia,

in Vanuatu, in the Solomon Islands

and almost all the way around to the coast
of South America and Easter Island.

And then, in early 2015,

there was an upsurge of cases
of a dengue-like syndrome

in the city of Natal
in northeastern Brazil.

The virus wasn’t dengue, it was Zika,
and it spread rapidly –

Recife down the coast, a big metropolitan
center, soon became the epicenter.

Well people have speculated that it was
2014 World Cup soccer fans

that brought the virus into the country.

But others have speculated that perhaps
it was Pacific Islanders

participating in championship canoe races

that were held in Rio that year
that brought it in.

Well today, this is only a year later.

The virus is being locally transmitted
by mosquitoes

virtually throughout South America,
Central America, Mexico

and the Caribbean Islands

Until this year, the many
thousands of cases

that have been diagnosed in the US
were contracted elsewhere.

But as of this summer, it’s being
transmitted locally in Miami.

It’s here.

So what do we do about it?

Well, preventing infection

is either about protecting people
or about eliminating the mosquitoes.

Let’s focus on people first.

You can get vaccinated.

You can not travel to Zika areas.

Or you can cover up
and apply insect repellent.

Getting vaccinated is not an option,
because there isn’t a vaccine yet

and there probably won’t be
for a couple of years.

Staying home isn’t
a foolproof protection either

because we now know that
it can be sexually transmitted.

Covering up and applying
insect repellent does work …

until you forget.

(Laughter)

So that leaves the mosquitoes,
and here’s how we control them now:

spraying insecticides.

The protective gear is necessary
because these are toxic chemicals

that kill people as well as bugs.

Although it does take quite a lot more
to kill a person than to kill a bug.

These are pictures from
Brazil and Nicaragua.

But it looks the same in Miami, Florida.

And we of course can spray
insecticides from planes.

Last summer, mosquito control officials
in Dorchester County, South Carolina,

authorized spraying of Naled,
an insecticide,

early one morning,
as recommended by the manufacturer.

Later that day, a beekeeper told reporters

that her bee yard looked
like it had been nuked.

Oops.

Bees are the good guys.

The citizens of Florida protested,
but spraying continued.

Unfortunately, so did the increase
in the number of Zika fever cases.

That’s because insecticides
aren’t very effective.

So are there any approaches that are
perhaps more effective than spraying

but with less downsides
than toxic chemicals?

I’m a huge fan of biological controls,

and I share that view with Rachel Carson,
author of “Silent Spring,”

the book that is credited with starting
the environmental movement.

In this book she tells the story,
as an example,

of how a very nasty insect
pest of livestock

was eliminated in the last century.

No one knows that
extraordinary story today.

So Jack Block and I,
when we were writing an editorial

about the mosquito problem today,
retold that story.

And in capsule form, it’s that pupae –
that’s the immature form of the insect –

were irradiated until they were sterile,
grown to adulthood

and then released from planes
all over the Southwest,

the Southeast and down into Mexico
and into Central America

literally by the hundreds of millions
from little airplanes,

eventually eliminating
that terrible insect pest

for most of the Western Hemisphere.

Our real purpose in writing this editorial

was to introduce readers
to how we can do that today –

not with radiation
but with our knowledge of genetics.

Let me explain.

This is the bad guy: Aedes aegypti.

It’s the most common insect
vector of diseases,

not just Zika but dengue,
Chikungunya, West Nile virus

and that ancient plague, yellow fever.

It’s an urban mosquito,

and it’s the female
that does the dirty work.

She bites to get a blood meal
to feed her offspring.

Males don’t bite; they don’t even
have the mouth parts to bite.

A little British company called Oxitec
genetically modified that mosquito

so that when it mates with a wild female,
its eggs don’t develop to adulthood.

Let me show you.

This is the normal reproductive cycle.

Oxitec designed the mosquito so that
when the male mates with the wild female

the eggs don’t develop.

Sounds impossible?

Well let me show you
just diagrammatically how they do it.

Now this represents the nucleus
of a mosquito cell,

and that tangle in the middle
represents its genome,

the sum total of its genes.

Scientists added a single gene

that codes for a protein represented
by this orange ball

that feeds back on itself
to keep cranking out more of that protein.

The extra copies, however,
go and gum up the mosquitoes' genes,

killing the organism.

To keep it alive in the laboratory
they use a compound called tetracycline.

Tetracycline shuts off that gene
and allows normal development.

They added another little wrinkle
so that they could study what happens.

And that is they added a gene
that makes the insect glow under UV light

so that when they released it
they could follow exactly how far it went

how long it lived
and all of the kinds of data

for a good scientific study.

Now this is the pupal stage,
and at this stage

the females are larger than the males.

That allows them to sort them
into the males and the females

and they allow only the males
to grow to adulthood.

And let me remind you
that males don’t bite.

From there it’s pretty simple.

They take beakers full of male mosquitoes,

load them into milk cartons,
and drive around the city,

releasing them guided by GPS.

Here’s the mayor of a city
releasing the first batch

of what they call the “friendly Aedes.”

Now I wish I could tell you
this is an American city, but it’s not.

It’s Piracicaba, Brazil.

The amazing thing is that in just a year

it brought down the cases
of dengue by 91 percent.

That’s better than any insecticide
spraying can do.

So why aren’t we using this remarkable
biological control in the US?

That’s because it’s a GMO:
a genetically modified organism.

Notice the subtitle here says
if the FDA would let them

they could do the same thing here,
when Zika arrives.

And of course it has arrived.

So now I have to tell you the short form

of the long, torturous story
of GM regulation in the US

In the US, there are three agencies that
regulate genetically modified organisms:

the FDA, the Food and Drug Administration,

the EPA, the Environmental
Protection Agency,

and the USDA, US Department
of Agriculture.

Took these folks two years
to decide that it would be the FDA

that would regulate the genetically
modified mosquito.

And they would do it as a new animal drug,
if that makes any sense.

Took them another five years going back
and forth and back and forth

to convince the FDA
that this would not harm people,

and it would not harm the environment.

They finally gave them, this summer,
permission to run a little test

in the Florida Keys,

where they had been invited years earlier
when they Keys had an outbreak of dengue.

Would that it were that easy.

When the local residents heard

that there would be genetically modified
mosquitoes tested in their community

some of them began to organize protests.

They even organized a petition on
the internet with this cuddly logo,

which eventually accumulated
some 160,000 signatures

And they demanded a referendum

which will be conducted
in just a couple of weeks

about whether the trials
would be permitted at all.

Well it’s Miami that really needs
these better ways of controlling insects.

And there the attitudes are changing.

In fact, very recently a bipartisan group
of more than 60 legislators

wrote to HHS Secretary Sylvia Burwell

asking that she, at the Federal level,
expedite access for Florida

to this new technology.

So the bottom line is this:

biological control of harmful insects

can be both more effective and
very much more environmentally friendly

than using insecticides,
which are toxic chemicals.

That was true in Rachel Carson’s
time; it’s true today.

What’s different is that we have
enormously more information

about genetics than we had then,

and therefore more ability
to use that information

to affect these biological controls.

And I hope that what I’ve done
is aroused your curiosity enough

to start your own inquiry –
not into just GM mosquitoes

but to the other genetically modified
organisms that are so controversial today.

I think if you do that, and you dig down
through all of the misinformation,

and the marketing

on the part of the organic food industry
and the Greenpeaces

and find the science,
the accurate science,

you’ll be surprised and pleased.

Thank you.

(Applause)

寨卡热:

我们最新的可怕疾病。

它是什么? 它是从哪里来的?

我们该怎么办?

嗯,对于大多数成年人来说,
这是一种相对轻微的疾病——

有点发烧、有点头痛、
关节痛,也许还有皮疹。

事实上,大多数得到它的
人甚至不知道他们已经得到它。

但我们
对寨卡

病毒了解得越多,它就越可怕。

例如,
医生注意到最近爆发

的格林-巴利
综合征呈上升趋势。

在格林巴利,您的免疫系统会
攻击您的神经细胞,

它可以部分
甚至完全瘫痪您。

幸运的是,这种情况很少见
,大多数人都能康复。

但如果你在
被感染时怀孕了,你

就有发生可怕事情的风险。

确实,一个头部畸形的孩子。

这是一个正常的婴儿。

这是那个
患有小头畸形的婴儿。

脑袋太小了。

而且没有已知的治愈方法。

实际上

,一年前,
在寨卡病毒爆发后,巴西东北部的医生第一次

注意到
小头畸形的发病率达到顶峰。

医生又花了一年

时间才确定它是
由寨卡病毒引起的,

但他们现在可以确定了。

如果您是“
拿出证据”类型,

请查看此出版物。

那么它是从哪里来的,
又是如何来到这里的呢?

它就在这里。

像我们的许多病毒一样,
它来自非洲,

特别是乌干达的寨卡森林。

附近
黄热病研究所的研究人员

在寨卡森林的一只猴子身上发现

了一种未知病毒,这就是它的名字的由来。

几年后,乌干达-坦桑尼亚出现了首例寨卡热人类病例

该病毒随后传播到西非,

并通过赤道亚洲——
巴基斯坦、印度、马来西亚、印度尼西亚向东传播。

但它仍然主要存在于猴子
身上,当然还有蚊子。

事实上,从
1947 年首次发现到 2007

年的 60 年间,仅报告了 13
例人类寨卡热病例。

然后
在密克罗尼西亚的小雅普岛上发生了一些非同寻常的事情。

一场疫情影响了
75% 的人口。

它是如何到达那里的? 空运。

今天,我们有 20 亿
商业航空公司乘客。

受感染的乘客可以在出现症状之前登上飞机,
飞越半个地球

——
如果他们完全出现症状的话。

然后当它们降落时,当地的蚊子
开始叮咬它们并传播发烧。

寨卡热随后
于 2013 年在法属波利尼西亚出现。

到当年 12 月,它已
通过蚊子在当地传播。

这导致了一场爆炸性的爆发,
近 30,000 人受到影响。

从那里它辐射到太平洋周围。

库克
群岛、新喀里多尼亚

、瓦努阿图、所罗门群岛

以及几乎一直到
南美洲海岸和复活节岛都爆发了疫情。

然后,在 2015 年初,巴西东北部纳塔尔市

的登革热样综合征病例激增

病毒不是登革热,而是寨卡病毒,
而且传播速度很快——

累西腓沿岸,一个大都市
中心,很快成为震中。

好吧,人们推测是
2014年世界杯足球迷

将病毒带入了该国。

但其他人推测,
也许是太平洋岛民

参加了

当年在里约举行的锦标赛独木舟比赛,才
带来了它。

今天,这只是一年后。

该病毒

几乎在整个南美洲、
中美洲、墨西哥

和加勒比群岛通过蚊子在当地传播

直到今年,

在美国确诊的数千例病例是在
其他地方感染的。

但截至今年夏天,它
正在迈阿密本地传播。

它在这里。

那么我们该怎么办呢?

嗯,预防

感染要么是为了保护人,要么是为了
消灭蚊子。

让我们首先关注人。

你可以接种疫苗。

您不能前往寨卡地区。

或者你可以掩盖
并涂抹驱虫剂。

接种疫苗不是一种选择,
因为目前还没有疫苗,

而且可能几年内都不会出现

呆在家里也不
是万无一失的保护措施,

因为我们现在知道
它可以通过性传播。

遮盖并使用
驱虫剂确实有效……

直到您忘记为止。

(笑声)

这样就剩下蚊子了
,这就是我们现在控制它们的方法:

喷洒杀虫剂。

防护装备是必要的,
因为这些有毒化学

物质会杀死人和虫子。

虽然
杀死一个人确实比杀死一只虫子要多得多。

这些是来自
巴西和尼加拉瓜的照片。

但它在佛罗里达州的迈阿密看起来是一样的。

我们当然可以
从飞机上喷洒杀虫剂。

去年夏天
,南卡罗来纳州多切斯特县的蚊子控制官员

授权

在一天清晨
按照制造商的建议喷洒杀虫剂 Naled。

当天晚些时候,一位养蜂人告诉记者

,她的养蜂场看起来
像是被核武器炸毁了。

哎呀。

蜜蜂是好人。

佛罗里达州的市民抗议,
但喷洒仍在继续。

不幸的是,
寨卡热病例的数量也在增加。

那是因为杀虫剂
不是很有效。

那么有什么方法
可能比喷洒更有效,

但缺点
比有毒化学品少吗?

我是生物控制的忠实拥护者

,我与《寂静的春天》的作者雷切尔·卡森(Rachel Carson)分享了这一观点,

该书被誉为发起
了环保运动。

在这本书中,她
以一个例子讲述了上

个世纪如何消灭了一种非常讨厌
的牲畜害虫的故事

。 今天

没有人知道这个
非凡的故事。

所以杰克布洛克和我,
当我们今天写一篇

关于蚊子问题的社论时,
重述了这个故事。

而在胶囊形式中,蛹——
这是昆虫的未成熟形式——

被辐照直到它们不育,
长到成年

,然后从
西南

、东南部、墨西哥
和中美洲的飞机上释放出来。

数以亿计
的小飞机,

最终消灭

了西半球大部分地区的可怕害虫。

我们写这篇社论的真正目的

是向
读者介绍我们今天如何做到这一点——

不是用辐射,
而是用我们的遗传学知识。

让我解释。

这是坏人:埃及伊蚊。

它是最常见的昆虫
病媒,

不仅是寨卡病毒,还有登革热、
基孔肯雅热、西尼罗河病毒

和古老的瘟疫黄热病。

是都市蚊子,

干脏活的是雌性

她咬了一口血
来喂她的后代。

雄性不咬人; 他们甚至
没有嘴巴可以咬。

一家名为 Oxitec 的英国小公司对
这种蚊子进行了基因改造,

因此当它与野生雌性交配时,
它的卵不会发育到成年。

我来给你展示。

这是正常的生殖周期。

Oxitec 设计了蚊子,这样
当雄性与野生雌性交配时,

卵子就不会发育。

听起来不可能?

好吧,让我以
图表的方式向您展示他们是如何做到的。

现在这代表
蚊子细胞的细胞核

,中间的缠结
代表它的基因组,

即基因的总和。

科学家们添加了一个基因

,该基因编码一种
由这个橙色球代表的蛋白质,

这种蛋白质会自我反馈
以不断产生更多的这种蛋白质。

然而,额外的副本
会破坏蚊子的基因,

杀死有机体。

为了让它在实验室里存活,
他们使用了一种叫做四环素的化合物。

四环素关闭该基因
并允许正常发育。

他们又增加了一个小皱纹,
这样他们就可以研究发生了什么。

那就是他们添加了一个基因
,使昆虫在紫外线下发光,

这样当他们释放它时,
他们就可以准确地追踪

它的寿命,
以及所有类型的数据

,以进行良好的科学研究。

现在这是蛹阶段
,在这个

阶段雌性比雄性大。

这使他们可以将它们
分为雄性和雌性,

并且只允许
雄性长到成年。

让我提醒你
,雄性不会咬人。

从那里开始很简单。

他们拿起装满雄性蚊子的烧杯,

将它们装入牛奶盒中,
然后在城市周围行驶,并在

GPS 的引导下释放它们。

这是一个城市的市长
释放第

一批他们所谓的“友好的伊蚊”。

现在我希望我能告诉你
这是一座美国城市,但事实并非如此。

这是巴西的皮拉西卡巴。

令人惊奇的是,在短短一年内

,登革热病例减少了 91%。

这比任何杀虫剂
喷雾都好。

那么为什么我们不在美国使用这种非凡的
生物控制呢?

那是因为它是一种转基因生物:
一种转基因生物。

请注意这里的副标题说,
如果 FDA 允许

他们在寨卡病毒到来时在这里做同样的事情

当然它已经到来了。

所以现在我要告诉你美国转基因监管

漫长而曲折的故事的简短形式

在美国,有三个
监管转基因生物的机构

:FDA、食品和药物管理局

、EPA、环境
保护局

和美国农业部美国
农业部。

这些人花了两年时间
才决定由 FDA

来监管转
基因蚊子。

如果这有意义的话,他们会把它作为一种新的动物药物来做

他们又花了五年的时间来回

反复说服 FDA
这不会伤害人

,也不会伤害环境。

今年夏天,他们终于允许他们在佛罗里达礁岛群
进行一次小测试

,几年前他们曾被邀请在佛罗里达
礁岛群爆发登革热。

会不会那么容易。

当当地居民

听说他们的社区将进行转基因
蚊子测试时,他们中的

一些人开始组织抗议。

他们甚至在互联网上组织了一个
带有这个可爱标志的请愿书

,最终积累了
大约 160,000 个

签名,他们要求

在短短几周内

就是否允许进行审判进行公投。

嗯,迈阿密真的需要
这些更好的控制昆虫的方法。

那里的态度正在改变。

事实上,最近一个
由 60 多名立法者组成的两党小组

写信给 HHS 部长西尔维娅·伯威尔,

要求她在联邦一级
加快佛罗里达州

对这项新技术的使用。

所以底线是这样的:

对有害昆虫的生物控制

比使用
有毒化学物质杀虫剂更有效,也更环保。

在雷切尔·卡森的时代就是这样
。 今天是真的。

不同的是,我们拥有比
当时更多的

遗传学信息

,因此更有
能力使用这些信息

来影响这些生物控制。

我希望我所做
的足以引起你的好奇心

,开始你自己的调查——
不仅仅是转基因蚊子

,还有其他
今天如此有争议的转基因生物。

我认为,如果您这样做,并且深入
挖掘所有错误信息,

以及

有机食品行业
和绿色和平组织的营销,

并找到科学
,准确的科学,

您会感到惊讶和高兴。

谢谢你。

(掌声)